Kari Hemminki

Kari Hemminki's AcademicInfluence.com Rankings

Kari Hemminki

Philosophy

#2201

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#3818

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#484

World Rank

#900

Historical Rank

philosophy Degrees

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Philosophy

Kari Hemminki's Degrees

PhD Medical Genetics University of Helsinki
Doctorate Medicine University of Helsinki

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Kari Hemminki's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

TERT Promoter Mutations in Familial and Sporadic Melanoma (2013) (1539)
Highly Recurrent TERT Promoter Mutations in Human Melanoma (818)
Genome-wide association study identifies five susceptibility loci for glioma (2009) (781)
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types (2009) (613)
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 (2008) (578)
Patterns of metastasis in colon and rectal cancer (2016) (575)
Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish family‐cancer database (2002) (509)
Metastatic sites and survival in lung cancer. (2014) (501)
Incidence trends and risk factors of carcinoid tumors (2001) (368)
Polymorphisms in DNA repair and metabolic genes in bladder cancer. (2003) (363)
New common variants affecting susceptibility to basal cell carcinoma (2009) (321)
Spontaneous abortions and malformations in the offspring of nurses exposed to anaesthetic gases, cytostatic drugs, and other potential hazards in hospitals, based on registered information of outcome. (1985) (304)
Polymorphisms within micro-RNA-binding sites and risk of sporadic colorectal cancer. (2007) (285)
A study of occupational exposure to antineoplastic drugs and fetal loss in nurses. (1985) (282)
DNA adducts, mutations and cancer. (1993) (280)
TERT promoter mutations in bladder cancer affect patient survival and disease recurrence through modification by a common polymorphism (2013) (279)
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility (2011) (261)
The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk. (2002) (257)
Risk of second primary cancer among patients with head and neck cancers: A pooled analysis of 13 cancer registries (2008) (255)
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk (2010) (253)
Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia: results from the Swedish Family-Cancer Database. (2004) (252)
Genetic polymorphisms in DNA repair genes and possible links with DNA repair rates, chromosomal aberrations and single-strand breaks in DNA. (2003) (246)
Metastatic spread in patients with gastric cancer (2016) (242)
Vascular Endothelial Growth Factor Polymorphisms in Relation to Breast Cancer Development and Prognosis (2005) (238)
Cancer in twins: genetic and nongenetic familial risk factors. (1997) (234)
BRAF mutations are common somatic events in melanocytic nevi. (2004) (233)
The nation-wide Swedish family-cancer database--updated structure and familial rates. (2001) (230)
Modification of cancer risks in offspring by sibling and parental cancers from 2,112,616 nuclear families (2001) (227)
BRAF mutations in metastatic melanoma: a possible association with clinical outcome. (2003) (225)
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. (2007) (222)
Molecular and genetic damage in humans from environmental pollution in Poland (1992) (221)
Risk of second cancer among women with breast cancer (2006) (220)
Familial risk in testicular cancer as a clue to a heritable and environmental aetiology (2004) (217)
DNA adducts : identification and biological significance (1994) (217)
Familial associations of rheumatoid arthritis with autoimmune diseases and related conditions. (2009) (208)
ESMO Consensus Conference on testicular germ cell cancer: diagnosis, treatment and follow-up (2018) (205)
TERT promoter mutations in cancer development. (2014) (205)
Autoimmunity and susceptibility to Hodgkin lymphoma: a population-based case-control study in Scandinavia. (2006) (200)
A genome-wide association study of Hodgkin Lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21, and 10p14 (GATA3) (2010) (194)
Organic solvents and cancer (1997) (191)
Single nucleotide polymorphisms in breast cancer. (2004) (191)
Association of DNA repair polymorphisms with DNA repair functional outcomes in healthy human subjects. (2006) (188)
Detection of polycyclic aromatic hydrocarbon-DNA adducts in white blood cells of foundry workers. (1988) (187)
The epidemiology of metastases in neuroendocrine tumors (2016) (185)
Sunscreen Use and Duration of Sun Exposure: a Double-Blind, Randomized Trial (1999) (181)
Risk of Cancer Following Hospitalization for Type 2 Diabetes (2010) (179)
Second primary neoplasms in 633,964 cancer patients in Sweden, 1958–1996 (2001) (179)
Cancer risk of air pollution: epidemiological evidence. (1994) (177)
Second primary cancers in thyroid cancer patients: a multinational record linkage study. (2006) (176)
Cancer risks in first‐generation immigrants to Sweden (2002) (176)
Familial aggregation of Hodgkin lymphoma and related tumors (2004) (175)
TERT promoter mutations: a novel independent prognostic factor in primary glioblastomas. (2015) (174)
Cancer Incidence among Finnish Workers Exposed to Halogenated Hydrocarbons (1995) (173)
Opinion: The balance between heritable and environmental aetiology of human disease (2006) (168)
Evaluation of SNPs in miR‐146a, miR196a2 and miR‐499 as low‐penetrance alleles in German and Italian familial breast cancer cases (2010) (168)
Low expression of hexokinase-2 is associated with false-negative FDG-positron emission tomography in multiple myeloma. (2017) (166)
Sibling risks in cancer: clues to recessive or X-linked genes? (2001) (164)
Tonsillar and other upper aerodigestive tract cancers among cervical cancer patients and their husbands (2000) (164)
Methods for detecting DNA damaging agents in humans : applications in cancer epidemiology and prevention (1988) (163)
Autoimmune diseases associated with non-Hodgkin lymphoma: a nationwide cohort study. (2014) (163)
Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma (2014) (162)
Chromosome 7p11.2 (EGFR) variation influences glioma risk. (2011) (161)
Familial risks for nonmedullary thyroid cancer. (2005) (160)
Spontaneous abortions among women exposed to organic solvents. (1990) (157)
Tamoxifen-induced DNA adducts in endometrial samples from breast cancer patients. (1996) (156)
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk (2011) (155)
DNA adducts in lymphocytes and granulocytes of smokers and nonsmokers detected by the 32P-postlabelling assay. (1991) (153)
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk (2013) (150)
Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker. (2008) (148)
DNA adducts in human environmentally exposed to aromatic compounds in an industrial area of Poland. (1990) (147)
Effect of common B-RAF and N-RAS mutations on global gene expression in melanoma cell lines. (2005) (146)
Laboratory work and pregnancy outcome. (1994) (146)
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. (2013) (144)
Spontaneous abortions and congenital malformations among the wives of men occupationally exposed to organic solvents. (1989) (143)
Monitoring occupational exposure to carcinogens: detection by 32P-postlabelling of aromatic DNA adducts in white blood cells from iron foundry workers. (1988) (141)
Occupational exposure to anticancer drug--potential and real hazards. (1985) (140)
Familial characteristics of autoimmune and hematologic disorders in 8,406 multiple myeloma patients: A population‐based case‐control study (2006) (139)
Familial Risks for Type 2 Diabetes in Sweden (2009) (139)
Familial carcinoid tumors and subsequent cancers: A nation‐wide epidemiologic study from Sweden (2001) (139)
Detection of benzo(a)pyrene:DNA adducts in human white blood cells. (1985) (139)
Does solar exposure, as indicated by the non-melanoma skin cancers, protect from solid cancers: vitamin D as a possible explanation. (2007) (137)
Childhood cancer and parental occupation in Finland. (1981) (136)
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma (2016) (136)
Familial and second primary pancreatic cancers: A nationwide epidemiologic study from Sweden (2003) (134)
Second primary neoplasms among 53 159 haematolymphoproliferative malignancy patients in Sweden, 1958–1996: a search for common mechanisms (2001) (134)
The Swedish Family‐Cancer Database 2009: prospects for histology‐specific and immigrant studies (2010) (134)
Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. (2010) (129)
Dectin-1 and DC-SIGN Polymorphisms Associated with Invasive Pulmonary Aspergillosis Infection (2012) (128)
Cancer risks in Nordic immigrants and their offspring in Sweden. (2002) (128)
A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk (2010) (127)
Autoimmune disease in individuals and close family members and susceptibility to non-Hodgkin's lymphoma. (2008) (124)
Cancer risks in Crohn disease patients. (2009) (124)
B-RAF and N-RAS Mutations Are Preserved during Short Time In Vitro Propagation and Differentially Impact Prognosis (2007) (124)
The epidemiology of Graves' disease: evidence of a genetic and an environmental contribution. (2010) (122)
Spontaneous abortions in hospital staff engaged in sterilising instruments with chemical agents. (1982) (120)
Aromatic DNA adducts, micronuclei and genetic polymorphism for CYP1A1 and GST1 in chimney sweeps. (1994) (120)
BRAF and NRAS mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. (2005) (120)
Familial association between type 1 diabetes and other autoimmune and related diseases (2009) (120)
Familial risks in cervical cancer: Is there a hereditary component? (1999) (118)
Mutations and polymorphisms in TP53 gene--an overview on the role in colorectal cancer. (2012) (118)
MDM2 SNP309 and cancer risk: a combined analysis. (2007) (117)
Detecting homozygous deletions in the CDKN2A(p16(INK4a))/ARF(p14(ARF)) gene in urinary bladder cancer using real-time quantitative PCR. (2003) (116)
Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin (2011) (113)
Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus (2010) (113)
Survival in cancer of unknown primary site: population-based analysis by site and histology. (2012) (112)
Micronuclei in humans induced by exposure to low level of ionizing radiation: influence of polymorphisms in DNA repair genes. (2005) (112)
DNA repair genetic polymorphisms and risk of colorectal cancer in the Czech Republic. (2008) (112)
In situ repair of cyclobutane pyrimidine dimers and 6-4 photoproducts in human skin exposed to solar simulating radiation. (1999) (111)
Biomarkers of styrene exposure in lamination workers: levels of O6-guanine DNA adducts, DNA strand breaks and mutant frequencies in the hypoxanthine guanine phosphoribosyltransferase gene in T-lymphocytes. (1995) (110)
Significant impact of promoter hypermethylation and the 540 C>T polymorphism of CDKN2A in cutaneous melanoma of the vertical growth phase. (2002) (110)
Biomarkers of polycyclic aromatic hydrocarbon-DNA damage and cigarette smoke exposures in paired maternal and newborn blood samples as a measure of differential susceptibility. (2001) (110)
Magnetic fields of video display terminals and spontaneous abortion. (1992) (110)
Familial cancers in a nationwide family cancer database: age distribution and prevalence. (1999) (109)
Relationship between hprt mutant frequency, aromatic DNA adducts and genotypes for GSTM1 and NAT2 in bus maintenance workers. (1995) (109)
Cancer risks in hairdressers: Assessment of carcinogenicity of hair dyes and gels (2003) (109)
Reduced fertility among women exposed to organic solvents. (1995) (109)
Attributable risks of familial cancer from the Family-Cancer Database. (2002) (107)
Age‐specific familial risks in common cancers of the offspring (1998) (107)
A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults (2008) (107)
Paternal occupational lead exposure and spontaneous abortion. (1991) (107)
Risk factors and age‐incidence relationships for contralateral breast cancer (2000) (107)
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
Familial risk and familial survival in prostate cancer (2012) (105)
Familial risk for non-Hodgkin lymphoma and other lymphoproliferative malignancies by histopathologic subtype: the Swedish Family-Cancer Database. (2005) (103)
Cancer risk among patients hospitalized for Type 1 diabetes mellitus: a population‐based cohort study in Sweden (2010) (103)
A single nucleotide polymorphism in the 3′untranslated region of the CDKN2A gene is common in sporadic primary melanomas but mutations in the CDKN2B, CDKN2C, CDK4 and p53 genes are rare (2001) (103)
Second primary cancers among 109 000 cases of non-Hodgkin's lymphoma (2005) (102)
Effects of paternal occupational exposure on spontaneous abortions. (1991) (102)
Cancer risk in hospitalized rheumatoid arthritis patients. (2008) (101)
Spontaneous abortions among female chemical workers in Finland (1980) (100)
Polymorphisms and haplotype structures in genes for transforming growth factor β1 and its receptors in familial and unselected breast cancers (2004) (99)
Parental age and risk of sporadic and familial cancer in offspring: implications for germ cell mutagenesis. (1999) (99)
Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk. (2007) (99)
Effects of ultrasound, shortwaves, and physical exertion on pregnancy outcome in physiotherapists. (1990) (99)
Spontaneous abortions among women working in the pharmaceutical industry. (1986) (98)
Influence of education level on breast cancer risk and survival in Sweden between 1990 and 2004 (2008) (98)
Single nucleotide polymorphisms in the XPG gene: Determination of role in DNA repair and breast cancer risk (2003) (98)
Spontaneous abortions and congenital malformations among women exposed to tetrachloroethylene in dry cleaning. (1989) (97)
TERT promoter mutations in melanoma survival (2016) (97)
Risk of second malignant neoplasms after childhood leukemia and lymphoma: an international study. (2007) (96)
Comparability of cancer identification among Death Registry, Cancer Registry and Hospital Discharge Registry (2012) (96)
Incidence trends of squamous cell and rare skin cancers in the Swedish national cancer registry point to calendar year and age-dependent increases. (2010) (96)
Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin. (2005) (95)
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women. (2009) (95)
Update on genetic predisposition to colorectal cancer and polyposis. (2019) (95)
The CCND1 870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma (2013) (95)
p53 autoantibodies predict subsequent development of cancer (2005) (95)
Socioeconomic factors in cancer in Sweden (2003) (95)
Somatic alterations in the melanoma genome: A high‐resolution array‐based comparative genomic hybridization study (2010) (94)
Second malignancies among survivors of germ‐cell testicular cancer: A pooled analysis between 13 cancer registries (2007) (94)
XPD exon 10 and 23 polymorphisms and DNA repair in human skin in situ. (2001) (93)
Aromatic DNA adducts in foundry workers in relation to exposure, life style and CYP1A1 and glutathione transferase M1 genotype. (1997) (93)
Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9 (2003) (93)
Second primary cancers after sporadic and familial colorectal cancer. (2001) (92)
Glutathione S-transferase mu1 and N-acetyltransferase 2 genetic polymorphisms and exposure to tobacco smoke in nonsmoking and smoking lung cancer patients and population controls. (1998) (92)
Association of HLA‐DRB1, interleukin‐6 and cyclin D1 polymorphisms with cervical cancer in the Swedish population—A candidate gene approach (2009) (91)
Covalent modification of DNA by antineoplastic agents. (1984) (91)
Risk of inflammatory bowel disease in first‐ and second‐generation immigrants in Sweden: A nationwide follow‐up study (2011) (91)
Inorganic Arsenic and Basal Cell Carcinoma in Areas of Hungary, Romania, and Slovakia: A Case–Control Study (2012) (90)
Promoter polymorphisms in matrix metalloproteinases and their inhibitors: few associations with breast cancer susceptibility and progression (2007) (90)
Smoking-related DNA adducts: 32P-postlabeling analysis of 7-methylguanine in human bronchial and lymphocyte DNA. (1993) (90)
Analysis of G1/S checkpoint regulators in metastatic melanoma (2000) (90)
Influence of education level on cancer survival in Sweden. (2008) (89)
Familial risk of cancer by site and histopathology (2003) (88)
Tumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes (2010) (87)
Time to pregnancy among the wives of men exposed to organic solvents. (1998) (87)
CDH1 mutations are present in both ductal and lobular breast cancer, but promoter allelic variants show no detectable breast cancer risk (2002) (87)
Association between genetic polymorphisms and biomarkers in styrene-exposed workers. (2001) (86)
Familial risks in testicular cancer as aetiological clues. (2006) (86)
International conference on health hazards and biological effects of welding fumes and gases (1986) (86)
Sporadic colorectal cancer and individual susceptibility: a review of the association studies investigating the role of DNA repair genetic polymorphisms. (2007) (85)
Risk of Second Primary Cancer among Esophageal Cancer Patients: a Pooled Analysis of 13 Cancer Registries (2008) (85)
Level of education and the risk of cancer in Sweden. (2003) (85)
Death causes in breast cancer patients. (2012) (85)
Familial and attributable risks in cutaneous melanoma: effects of proband and age. (2003) (84)
Genome-wide association study on differentiated thyroid cancer. (2013) (84)
Somatic Mutations in Exocrine Pancreatic Tumors: Association with Patient Survival (2013) (84)
Dna adducts, mutations, and cancer 2000. (2000) (84)
Second primary neoplasms among 53 159 haematolymphoproliferative malignancy patients in Sweden, 1958-1996: a search for common mechanisms. (2001) (84)
Autoimmune disease and subsequent digestive tract cancer by histology. (2012) (83)
Incidence and survival in non-hereditary amyloidosis in Sweden (2012) (83)
Smoking and the occurrence of congenital malformations and spontaneous abortions: multivariate analysis. (1983) (82)
Research Recommendations for Selected IARC-Classified Agents (2010) (82)
Risk of cancer at sites other than the breast in Swedish families eligible for BRCA1 or BRCA2 mutation testing. (2004) (81)
Familial risks and temporal incidence trends of multiple myeloma. (2006) (81)
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2018) (81)
Selective estrogenic effects of a novel triphenylethylene compound, FC1271a, on bone, cholesterol level, and reproductive tissues in intact and ovariectomized rats. (2000) (81)
Cancer risks in ulcerative colitis patients (2008) (81)
7-Methylguanine levels in DNA of smokers' and non-smokers' total white blood cells, granulocytes and lymphocytes. (1992) (81)
Loss of heterozygosity in tumour-adjacent normal tissue of breast and bladder cancer. (2001) (80)
Familial risks in nervous-system tumours: a histology-specific analysis from Sweden and Norway. (2009) (80)
National database of familial cancer in Sweden (1998) (80)
Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray (2008) (80)
Familial liver and gall bladder cancer: a nationwide epidemiological study from Sweden (2003) (80)
Congenital malformations by the parental occupation in finland (1980) (79)
How common is familial cancer? (2008) (79)
Polymorphisms of the GSTP1 and GSTM1 genes and PAH‐DNA adducts in human mononuclear white blood cells (2000) (79)
Biomonitoring of occupational exposure to styrene in a plastics lamination plant. (1999) (79)
Cancer risk in hospitalized sarcoidosis patients: a follow-up study in Sweden. (2009) (79)
Mutations in TERT promoter and FGFR3 and telomere length in bladder cancer (2015) (79)
Excess lung cancer among workers exposed to lead. (1995) (78)
Human DNA adducts of 1,3-butadiene, an important environmental carcinogen. (2000) (78)
Cancer risks to spouses and offspring in the family‐cancer database (2001) (78)
Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study (2017) (78)
The XPD 751Gln allele is associated with an increased risk for esophageal adenocarcinoma: a population-based case-control study in Sweden. (2006) (78)
IARC Monographs: 40 Years of Evaluating Carcinogenic Hazards to Humans (2015) (78)
Correlation of mutagenicity and 4-(p-nitrobenzyl)-pyridine alkylation by epoxides (1979) (78)
Risk of nervous system cancer among workers exposed to lead. (1996) (77)
An evaluation of styrene genotoxicity using several biomarkers in a 3-year follow-up study of hand-lamination workers. (1999) (77)
Cancer risk in patients hospitalized with polymyalgia rheumatica and giant cell arteritis: a follow-up study in Sweden. (2010) (77)
Effect of autoimmune diseases on risk and survival in female cancers. (2012) (77)
Estimation of genetic and environmental components in colorectal and lung cancer and melanoma (2001) (75)
Genetic variation in adipokine genes and risk of colorectal cancer. (2009) (75)
Styrene oxide-induced HPRT mutations, DNA adducts and DNA strand breaks in cultured human lymphocytes. (1995) (74)
Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism. (2005) (74)
Selective deletion of exon 1β of the p19ARF gene in metastatic melanoma cell lines (1998) (74)
Correspondence re: Risch, N.: Genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol. Biomark. Prev., 10: 733-741, 2001. (2002) (74)
5-Fluorouracil-based chemotherapy for colorectal cancer and MTHFR/MTRR genotypes. (2011) (73)
Familial testicular cancer and second primary cancers in testicular cancer patients by histological type. (2001) (73)
Extrapolation of the evidence on teratogenicity of chemicals between humans and experimental animals: chemicals other than drugs. (1985) (73)
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. (2008) (73)
Modulation of DNA adduct levels in human mononuclear white blood cells and granulocytes by CYP1A1 CYP2D6 and GSTM1 genetic polymorphisms. (1998) (73)
Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case–control study (2007) (73)
Subsequent primary malignancies after endometrial carcinoma and ovarian carcinoma (2003) (72)
TERT promoter mutations and telomere length in adult malignant gliomas and recurrences (2015) (72)
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk (2004) (72)
Inherited genetic susceptibility to multiple myeloma (2014) (71)
Cytogenetic markers, DNA single-strand breaks, urinary metabolites, and DNA repair rates in styrene-exposed lamination workers. (2004) (71)
Second primary malignancies in patients with male breast cancer (2005) (71)
The disialosyl group of glycoproteins. Occurrence in different tissues and cellular membranes. (1977) (71)
Familial risk for colorectal cancers are mainly due to heritable causes. (2004) (71)
Kidney cancer in the Swedish Family Cancer Database: familial risks and second primary malignancies. (2002) (71)
Inherited predisposition to early onset lung cancer according to histological type (2004) (71)
Familial relationships in thyroid cancer by histo‐pathological type (2000) (71)
Subsequent cancers after in situ and invasive squamous cell carcinoma of the skin. (2000) (71)
Age specific and attributable risks of familial prostate carcinoma from the family‐cancer database (2002) (70)
Spontaneous abortions by occupation and social class in Finland. (1980) (70)
Markers of individual susceptibility and DNA repair rate in workers exposed to xenobiotics in a tire plant (2004) (70)
What do prostate cancer patients die of? (2011) (70)
Binding of metabolites of cyclophosphamide to DNA in a rat liver microsomal system and in vivo in mice. (1985) (70)
Risk of subsequent solid tumors after non-Hodgkin's lymphoma: effect of diagnostic age and time since diagnosis. (2008) (69)
Cancer risk in hospitalised psoriasis patients: a follow-up study in Sweden (2009) (69)
Patterns of autoimmunity and subsequent chronic lymphocytic leukemia in Nordic countries. (2006) (68)
Carcinogen-DNA adducts and gene mutation in foundry workers with low-level exposure to polycyclic aromatic hydrocarbons. (1994) (68)
Seasonal variation of aromatic DNA adducts in human lymphocytes and granulocytes. (1993) (68)
High familial risks for cerebral palsy implicate partial heritable aetiology. (2007) (67)
Age-specific risk of incident prostate cancer and risk of death from prostate cancer defined by the number of affected family members. (2010) (67)
Familial Lung Cancer and Aggregation of Smoking Habits: A Simulation of the Effect of Shared Environmental Factors on the Familial Risk of Cancer (2005) (67)
Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study (2006) (67)
Re: detection of Epstein-Barr virus in invasive breast cancers. (1999) (67)
Melanocortin receptor 1 variants and melanoma risk: A study of 2 European populations (2009) (67)
Interleukin promoter polymorphisms and prognosis in colorectal cancer. (2008) (66)
The detection of increased amounts of the extracellular domain of the epidermal growth factor receptor in serum during carcinogenesis in asbestosis patients. (1994) (66)
Familial risks of cancer as a guide to gene identification and mode of inheritance (2004) (66)
Gastroschisis and omphalocele in Finland in the 1970s: prevalence at birth and its correlates. (1982) (66)
Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer (2013) (66)
Familial risk of early and late onset cancer: nationwide prospective cohort study (2012) (66)
Familial Aggregation and Heterogeneity of Non-Hodgkin Lymphoma in Population-Based Samples (2005) (66)
Biological monitoring of exposure to polycyclic aromatic hydrocarbon in an electrode paste plant. (1994) (65)
Association of prolactin and its receptor gene regions with familial breast cancer. (2006) (65)
Subsequent autoimmune or related disease in asthma patients: clustering of diseases or medical care? (2010) (65)
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s Lymphoma (2013) (65)
Time to pregnancy among the wives of men occupationally exposed to lead. (2000) (65)
Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant. (2006) (65)
Association of Inherited Variation in Toll-Like Receptor Genes with Malignant Melanoma Susceptibility and Survival (2011) (65)
Population Landscape of Familial Cancer (2015) (64)
Mutations in the CDKN2A ( p16INK4a ) gene in microdissected sporadic primary melanomas (1998) (64)
TLR-3 polymorphism is an independent prognostic marker for stage II colorectal cancer. (2011) (64)
Genetic risks caused by occupational chemicals. Use of experimental methods and occupational risk group monitoring in the detection of environmental chemicals causing mutations, cancer and malformations. (1979) (63)
Quantifying the carcinogenicity of antineoplastic drugs. (1988) (63)
Effect of age on the formation and repair of UV photoproducts in human skin in situ. (2000) (63)
Endogenous and background DNA adducts by methylating and 2-hydroxyethylating agents. (1999) (63)
Familial breast cancer in the family‐cancer database (1998) (63)
Parental occupational exposure and spontaneous abortions in Finland. (1984) (63)
Polycyclic aromatic hydrocarbon-DNA adducts in white blood cells and urinary 1-hydroxypyrene in foundry workers. (1993) (63)
Cancer risks among long-standing spouses (2002) (63)
Time trends in the incidence of cervical and other genital squamous cell carcinomas and adenocarcinomas in Sweden, 1958-1996. (2002) (62)
The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study (2008) (62)
Prevalence of overweight and obesity in adults from North Africa. (2014) (62)
Familial risks in nervous system tumors. (2003) (62)
The ‘Common Disease-Common Variant’ Hypothesis and Familial Risks (2008) (62)
The population impact of familial cancer, a major cause of cancer (2014) (62)
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions (2009) (61)
Time to pregnancy among the wives of Finnish greenhouse workers. (2003) (61)
SNP_tools: A compact tool package for analysis and conversion of genotype data for MS-Excel (2009) (61)
Consanguinity and genetic diseases in North Africa and immigrants to Europe. (2014) (60)
Concordance of survival in family members with prostate cancer. (2008) (60)
Multiple primary cancers as clues to environmental and heritable causes of cancer and mechanisms of carcinogenesis. (2004) (60)
Cancer risk in hospitalised asthma patients (2009) (60)
Polymorphisms in the KDR and POSTN Genes: Association with Breast Cancer Susceptibility and Prognosis (2006) (60)
Cancer risk in patients with type 2 diabetes mellitus and their relatives (2015) (59)
Serum oncoproteins and growth factors in asbestosis and silicosis patients (1992) (59)
Effect of type 2 diabetes predisposing genetic variants on colorectal cancer risk. (2012) (59)
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. (2010) (59)
Genetic status of cell cycle regulators in squamous cell carcinoma of the oesophagus: the CDKN2A (p16(INK4a) and p14(ARF) ) and p53 genes are major targets for inactivation. (2002) (59)
MC1R variants associated susceptibility to basal cell carcinoma of skin: Interaction with host factors and XRCC3 polymorphism (2007) (59)
Styrene Metabolism, Genotoxicity, and Potential Carcinogenicity (2006) (59)
Risk of breast cancer in families of multiple affected women and men (2012) (59)
Aurora kinases A and B and familial breast cancer risk. (2007) (59)
The impact of type 2 diabetes mellitus on cancer‐specific survival (2012) (58)
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1 (2016) (58)
Cancer risk in patients hospitalised for Graves’ disease: a population-based cohort study in Sweden (2010) (58)
Community study of spontaneous abortions: Relation to occupation and air pollution by sulfur dioxide, hydrogen sulfide, and carbon disulfide (1982) (57)
Risk of Second Cancer in Hodgkin Lymphoma Survivors and Influence of Family History (2017) (57)
Ultraviolet B-induced DNA damage in human skin and its modulation by a sunscreen. (1998) (57)
Familial Risks for Cervical Tumors in Full and Half Siblings: Etiologic Apportioning (2006) (57)
Number of Siblings and the Risk of Lymphoma, Leukemia, and Myeloma by Histopathology (2006) (57)
Association of genetic polymorphisms in ESR2, HSD17B1, ABCB1, and SHBG genes with colorectal cancer risk. (2011) (57)
Selective Estrogenic Effects of a Novel Triphenylethylene Compound, FC1271a, on Bone, Cholesterol Level, and Reproductive Tissues in Intact and Ovariectomized Rats1. (2000) (57)
Loss of heterozygosity at chromosome 9p21 (INK4-p14ARF locus): homozygous deletions and mutations in the p16 and p14ARF genes in sporadic primary melanomas. (1999) (56)
DNA adducts among personnel servicing and loading diesel vehicles. (1994) (56)
Spontaneous abortions among women employed in the metal industry in Finland (1980) (56)
Birth order, family size, and the risk of cancer in young and middle-aged adults (2001) (56)
A genetic study of Hodgkin's lymphoma: an estimate of heritability and anticipation based on the familial cancer database in Sweden (2000) (56)
Skin cancer and non-Hodgkin's lymphoma as second malignancies. markers of impaired immune function? (2003) (56)
Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic (2009) (56)
Association of NCOA3 Polymorphisms with Breast Cancer Risk (2005) (56)
Familial risk of cancer: data for clinical counseling and cancer genetics. (2004) (55)
Subsequent risk of hospitalization for neuropsychiatric disorders in patients with rheumatic diseases: a nationwide study from Sweden. (2008) (55)
Second primary cancers in patients with nasopharyngeal carcinoma: a pooled analysis of 13 cancer registries (2007) (55)
Genetic epidemiology of multistage carcinogenesis. (2001) (55)
Frequent DPH3 promoter mutations in skin cancers (2015) (55)
High levels of dipyrimidine dimers are induced in human skin by solar-simulating UV radiation. (1998) (55)
Low birthweight, congenital malformations, and spontaneous abortions among dry-cleaning workers in Scandinavia. (1990) (55)
Concordant and discordant familial cancer: Familial risks, proportions and population impact (2017) (55)
Familial risks in cancer of unknown primary: tracking the primary sites. (2011) (55)
Clinical genetic counselling for familial cancers requires reliable data on familial cancer risks and general action plans (2004) (55)
Familial gastrointestinal carcinoid tumours and associated cancers. (2009) (54)
Genetic epidemiology of cancer: From families to heritable genes (2004) (54)
DNA adducts and related biomarkers in populations exposed to environmental carcinogens (1992) (54)
Identification of alkylation products of styrene oxide in single- and double-stranded DNA. (1988) (54)
Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer. (2005) (54)
Familial risk of cancer: Data for clinical counseling and cancer genetics (2004) (54)
Age of onset in familial cancer. (2008) (53)
Alkylation products of DNA bases by simple epoxides. (1980) (53)
p53 mutations in urinary bladder cancer (2001) (53)
Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer. (2006) (53)
Congenital malformations and maternal occupation in Finland: multivariate analysis. (1981) (53)
Reactions of ethyleneimine with guanosine and deoxyguanosine. (1984) (53)
Familial risk of cancer shortly after diagnosis of the first familial tumor. (2005) (53)
Polymorphisms in the IGF-1 and IGFBP3 promoter and the risk of breast cancer (2005) (52)
A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer (2012) (52)
Familial Association of Inflammatory Bowel Diseases With Other Autoimmune and Related Diseases (2010) (52)
Chromosomal damage among medical staff occupationally exposed to volatile anesthetics, antineoplastic drugs, and formaldehyde. (2013) (52)
Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis? (2009) (52)
Attributable risks for familial breast cancer by proband status and morphology: A nationwide epidemiologic study from Sweden (2002) (52)
Multiple primary cancers of the colon, breast and skin (melanoma) as models for polygenic cancers (2001) (52)
Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis. (2008) (52)
VHL gene alterations in renal cell carcinoma patients: novel hotspot or founder mutations and linkage disequilibrium (2001) (52)
Cancer incidence among Finnish workers exposed to aromatic hydrocarbons (1998) (51)
Incidence and familial risks in pituitary adenoma and associated tumors. (2007) (51)
Increased risk of hepatobiliary cancers after hospitalization for autoimmune disease. (2014) (51)
Hprt mutant frequency and aromatic DNA adduct level in non-smoking and smoking lung cancer patients and population controls. (1999) (51)
Exposure of bus and taxi drivers to urban air pollutants as measured by DNA and protein adducts. (1994) (51)
Influence of polymorphism in DNA repair and defence genes on p53 mutations in bladder tumours. (2006) (51)
Spectrum of styrene-induced DNA adducts: the relationship to other biomarkers and prospects in human biomonitoring. (2002) (51)
DNA Repair Gene and MTHFR Gene Polymorphisms as Prognostic Markers in Locally Advanced Adenocarcinoma of the Esophagus or Stomach Treated with Cisplatin and 5-Fluorouracil-Based Neoadjuvant Chemotherapy (2011) (51)
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2018) (50)
Clinical landscape of cancer metastases (2018) (50)
Cancer risks in second‐generation immigrants to Sweden (2002) (50)
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (50)
Molecular and genetic damage in humans from environmental pollution in Poland (1993) (50)
Effects of methylene chloride, trichloroethane, trichloroethylene, tetrachloroethylene and toluene on the development of chick embryos. (1979) (50)
Constraints for genetic association studies imposed by attributable fraction and familial risk. (2006) (50)
Transplacental carcinogens and mutagens: childhood cancer, malformations, and abortions as risk indicators. (1980) (50)
Functional TLR5 genetic variants affect human colorectal cancer survival. (2013) (50)
DNA adducts, strand breaks and micronuclei in mice exposed to styrene by inhalation. (2001) (50)
Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches (2015) (50)
Tobacco smoke-associated N7-alkylguanine in DNA of larynx tissue and leucocytes. (1996) (49)
Characterization of reaction products between styrene oxide and deoxynucleosides and DNA. (1986) (49)
Comparison of alkylation rates and mutagenicity of directly acting industrial and laboratory chemicals (1980) (49)
Associations between small intestine cancer and other primary cancers: An international population‐based study (2006) (49)
Site‐specific survival rates for cancer of unknown primary according to location of metastases (2013) (49)
Shared familial aggregation of susceptibility to autoimmune diseases. (2009) (49)
32P-postlabeling of DNA adducts of styrene-exposed lamination workers. (1993) (49)
Measurement by 32P-postlabelling of 7-methylguanine levels in white blood cell DNA of healthy individuals and cancer patients treated with dacarbazine and procarbazine. Human data and method development for 7-alkylguanines. (1991) (49)
Deciphering the 8q24.21 association for glioma. (2013) (49)
Familial risk for gastric carcinoma: an updated study from Sweden (2007) (48)
Low frequency of BRAF and CDKN2A mutations in endometrial cancer (2005) (48)
Immunologic measurement of polycyclic aromatic hydrocarbon-albumin adducts in foundry workers and roofers. (1991) (48)
MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from the Czech Republic. (2011) (48)
MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia. (2005) (48)
Polymorphisms in the Estrogen Receptor Beta Gene and Risk of Breast Cancer: No Association (2003) (48)
Mutations in the BRAF and N-ras genes in childhood acute lymphoblastic leukaemia (2005) (48)
Second cancers after testicular cancer diagnosed after 1980 in Sweden. (2010) (48)
Data on the carcinogenicity of chemicals in the IARC Monographs programme. (1985) (47)
Polymorphisms within microRNA-binding sites and risk of sporadic colorectal cancer (2008) (47)
Socio-economic status and overall and cause-specific mortality in Sweden (2008) (47)
Familial Breast Cancer: Scope for More Susceptibility Genes? (2003) (47)
Effect of autoimmune diseases on risk and survival in histology-specific lung cancer (2012) (47)
No Evidence for Anticipation in Lymphoproliferative Tumors in Population-Based Samples (2005) (47)
Risk of second malignant neoplasms among lymphoma patients with a family history of cancer (2006) (46)
Persistence of O6-guanine DNA adducts in styrene-exposed lamination workers determined by 32P-postlabelling. (1994) (46)
Survival in ovarian cancer patients by histology and family history (2008) (46)
Interlaboratory comparison of the 32P-postlabelling assay for aromatic DNA adducts in white blood cells of iron foundry workers. (1989) (46)
Familial cancer risks in offspring from discordant parental cancers (1999) (46)
Risk of familial classical Hodgkin lymphoma by relationship, histology, age, and sex: a joint study from five Nordic countries. (2015) (46)
Incidence trends and familial risks in invasive and in situ cutaneous melanoma by sun‐exposed body sites (2003) (46)
Risk factors for cancers of unknown primary site: Results from the prospective EPIC cohort (2014) (46)
DNA adducts caused by tamoxifen and toremifene in human microsomal system and lymphocytes in vitro. (1995) (46)
TERT promoter mutations in clear cell renal cell carcinoma (2015) (46)
Timing and rates of synthesis of early histone mRNA in the embryo of Strongylocentrotus purpuratus. (1983) (45)
Effect of monosubstituted epoxides on chromosome aberrations and SCE in cultured human lymphocytes. (1981) (45)
Ala228 variant of trail receptor 1 affecting the ligand binding site is associated with chronic lymphocytic leukemia, mantle cell lymphoma, prostate cancer, head and neck squamous cell carcinoma and bladder cancer (2006) (45)
Mutations, tissue accumulations, and serum levels of p53 in patients with occupational cancers from asbestos and silica exposure (1997) (45)
Familial risks for asthma among twins and other siblings based on hospitalizations in Sweden (2007) (45)
Aromatic DNA adducts in larynx biopsies and leukocytes. (1994) (45)
Chromosomal damage in peripheral blood lymphocytes of newly diagnosed cancer patients and healthy controls. (2010) (45)
Histone gene switch in the sea urchin embryo. Identification of late embryonic histone messenger ribonucleic acids and the control of their synthesis. (1979) (45)
Time Trends and Occupational Risk Factors for Peritoneal Mesothelioma in Sweden (2003) (45)
Risk of thyroid cancer in first-degree relatives of patients with non-medullary thyroid cancer by histology type and age at diagnosis: a joint study from five Nordic countries (2013) (45)
Celiac disease confers a 1.6-fold increased risk of asthma: a nationwide population-based cohort study. (2011) (45)
DNA adducts of 1,3‐butadiene in humans: Relationships to exposure, GST genotypes, single‐strand breaks, and cytogenetic end points (2001) (45)
Reproductive Effects of Chemical Exposures in Health Professions (1995) (45)
Spontaneous abortions in an industrialized community in Finland. (1983) (45)
Nasopharyngeal and hypopharyngeal carcinoma risk among immigrants in Sweden (2010) (45)
Postlabeling and immunoassay analysis of polycyclic aromatic hydrocarbons--adducts of deoxyribonucleic acid in white blood cells of foundry workers. (1990) (45)
Risks for familial and contralateral breast cancer interact multiplicatively and cause a high risk. (2007) (44)
Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk. (2014) (44)
Increases in Adult Life Expectancy in Rural South Africa : Valuing the Scale-Up of HIV Treatment (44)
Reactions of nitrogen mustards with DNA. (1986) (44)
Seasonal variation of DNA adduct pattern in human lymphocytes analyzed by 32P-HPLC. (1996) (44)
Cancer characteristics in Swedish families fulfilling criteria for hereditary nonpolyposis colorectal cancer. (2005) (44)
Studies of biomarkers in aluminum workers occupationally exposed to polycyclic aromatic hydrocarbons. (1995) (44)
Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer. (2002) (44)
Cancers in the first-degree relatives of children with brain tumours (2000) (44)
Familial Risk of Ischemic and Hemorrhagic Stroke: A Large-Scale Study of the Swedish Population (2006) (44)
Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer. (2005) (44)
Does the breast cancer age at diagnosis differ by ethnicity? A study on immigrants to Sweden. (2011) (44)
Cancer risks in twins: Results from the Swedish family‐cancer database (2002) (44)
Single nucleotide polymorphisms in chromosomal instability genes and risk and clinical outcome of breast cancer: a Swedish prospective case-control study. (2009) (43)
Exposure to low environmental levels of benzene: evaluation of micronucleus frequencies and S-phenylmercapturic acid excretion in relation to polymorphisms in genes encoding metabolic enzymes. (2011) (43)
Differential interactions between GSTM1 and NAT2 genotypes on aromatic DNA adduct level and HPRT mutant frequency in lung cancer patients and population controls. (2001) (43)
Genetic polymorphisms and possible gene-gene interactions in metabolic and DNA repair genes: effects on DNA damage. (2006) (43)
A case–control study of childhood leukaemia and paternal occupational contact level in rural Sweden (2002) (43)
Cutaneous melanoma patients have normal repair kinetics of ultraviolet-induced DNA repair in skin in situ. (2000) (43)
Tamoxifen-induced DNA adducts in leucocytes of breast cancer patients. (1997) (43)
Prostate cancer screening, changing age‐specific incidence trends and implications on familial risk (2005) (43)
Time to Pregnancy Among Women Occupationally Exposed to Lead (1995) (42)
Clinical course of bladder neoplasms and single nucleotide polymorphisms in the CDKN2A gene (2003) (42)
Determination of allele frequency in pooled DNA: comparison of three PCR-based methods. (2005) (42)
Uptake, distribution, and formation of hemoglobin and DNA adducts after inhalation of C2-C8 1-alkenes (olefins) in the rat. (1995) (42)
Insulin pathway related genes and risk of colorectal cancer: INSR promoter polymorphism shows a protective effect. (2007) (42)
Assessment of methods and results of reproductive occupational epidemiology: spontaneous abortions and malformations in the offspring of working women. (1983) (42)
Familial risks for cancer as the basis for evidence-based clinical referral and counseling. (2008) (42)
Survival in breast cancer is familial (2008) (42)
Analysis of 153,115 patients with hematological malignancies refines the spectrum of familial risk. (2019) (42)
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma (2014) (42)
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer. (2006) (41)
Biologic monitoring of exposure to chemical mutagens in the occupational environment. (1982) (41)
Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia (2011) (41)
Subsequent COPD and lung cancer in patients with autoimmune disease (2011) (41)
Seasonal variations in levels of DNA adducts and X-spots in human populations living in different parts of Poland. (1993) (41)
Detection of increased amounts of the extracellular domain of the c‐erbB‐2 oncoprotein in serum during pulmonary carcinogenesis in humans (1994) (41)
Separation of 7-methyl- and 7-(2-hydroxyethyl)-guanine adducts in human DNA samples using a combination of TLC and HPLC. (1996) (41)
A candidate CpG SNP approach identifies a breast cancer associated ESR1‐SNP (2011) (41)
Familial colorectal adenocarcinoma and hereditary nonpolyposis colorectal cancer: a nationwide epidemiological study from Sweden (2001) (40)
Paternal occupational lead exposure and congenital malformations. (1992) (40)
Reaction products of styrene oxide with guanosine in aqueous media. (1984) (40)
SNPs in ultraconserved elements and familial breast cancer risk. (2009) (40)
Familial and second lung cancers: a nation-wide epidemiologic study from Sweden. (2003) (40)
Age-incidence relationships and time trends in cervical cancer in Sweden (2004) (40)
Genetic Epidemiology--science and ethics on familial cancers. (2001) (40)
Nucleic acid adducts of chemical carcinogens and mutagens (1983) (40)
Combined effect of low-penetrant SNPs on breast cancer risk (2011) (40)
Autoimmune disease and subsequent urological cancer. (2013) (40)
Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma (2012) (39)
Infectious diseases in North Africa and North African immigrants to Europe. (2014) (39)
Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis. (2009) (39)
Search for familial clustering of multiple myeloma with any cancer (2016) (39)
Methods for testing familial aggregation of diseases in population‐based samples: application to hodgkin lymphoma in swedish registry data (2004) (39)
Gastro-intestinal atresias in Finland in 1970-79, indicating time-place clustering. (1988) (39)
Cancer in husbands of cervical cancer patients. (2000) (39)
Fluorescence study of DNA alkylation by epoxides. (1979) (39)
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype. (2014) (39)
Postlabeling analysis of polycyclic aromatic hydrocarbon-DNA adducts in white blood cells of foundry workers. (1991) (39)
Genome-wide investigation of gene–environment interactions in colorectal cancer (2013) (39)
Gender‐specific incidence trends in lung cancer by histological type in Sweden, 1958–1996 (2001) (39)
Determination of malonaldehyde-modified 2'-deoxyguanosine-3'-monophosphate and DNA by 32P-postlabelling. (1992) (38)
Parental Cancer as a Risk Factor for Brain Tumors (Sweden) (2001) (38)
Structural chromosomal aberrations as potential risk markers in incident cancer patients. (2015) (38)
Occupation and bladder cancer: a cohort study in Sweden (2005) (38)
Cancer Risk in Relatives of Testicular Cancer Patients by Histology Type and Age at Diagnosis: A Joint Study from Five Nordic Countries. (2015) (38)
Familial risks for common diseases: etiologic clues and guidance to gene identification. (2008) (38)
Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk (2006) (37)
Molecular and cellular alterations in tobacco smoke-associated larynx cancer. (1999) (37)
Biologic markers in risk assessment for environmental carcinogens (1991) (37)
Effect of constitutional pigmentation on ultraviolet B-induced DNA damage in fair-skinned people. (2000) (37)
Do discordant cancers share familial susceptibility? (2012) (37)
Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer. (2012) (37)
Sibling risk of pediatric obstructive sleep apnea syndrome and adenotonsillar hypertrophy. (2009) (37)
Risk for familial breast cancer increases with age (2002) (37)
Analysis of UV-induced DNA photoproducts by 32P-postlabelling. (1995) (37)
Reply to: "On cancer risks in second‐generation immigrants to Sweden" (2002) (37)
Familial colorectal adenocarcinoma from the Swedish family‐cancer database (2001) (36)
Lifestyle and cancer: effect of parental divorce (2006) (36)
Bladder cancer in cancer patients: population-based estimates from a large Swedish study (2009) (36)
BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study (2007) (36)
Photoadaptation to ultraviolet (UV) radiation in vivo: photoproducts in epidermal cells following UVB therapy for psoriasis. (2000) (36)
Second primary breast cancer in men (2001) (36)
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. (2014) (36)
Risk for contralateral breast cancers in a population covered by mammography: effects of family history, age at diagnosis and histology (2007) (36)
Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis (2014) (36)
The GH1/IGF-1 axis polymorphisms and their impact on breast cancer development (2007) (36)
Nationwide data base on medically diagnosed spontaneous abortions in Finland. (1988) (36)
Application of the chicken embryo in testing for embryotoxicity: thiurams. (1982) (36)
Allelic losses demonstrate monoclonality of multifocal bladder tumors (2000) (36)
Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer. (2007) (36)
Age‐ and time‐dependent changes in cancer incidence among immigrants to Sweden: colorectal, lung, breast and prostate cancers (2012) (36)
The updated Swedish family-cancer database used to assess familial risks of prostate cancer during rapidly increasing incidence (2006) (36)
A gene-wide investigation on polymorphisms in the ABCG2/BRCP transporter and susceptibility to colorectal cancer. (2008) (36)
Aromatic DNA adducts in lymphocytes of humans working at high and low traffic density areas. (1996) (36)
Mesothelioma incidence seems to have leveled off in Sweden (2003) (36)
Polymorphisms in XPD, XPC and the risk of death in patients with urinary bladder neoplasms (2007) (36)
Occupation and Upper Aerodigestive Tract Cancers: A Follow-Up Study in Sweden (2005) (35)
A functional promoter polymorphism in the TERT gene does not affect inherited susceptibility to breast cancer. (2009) (35)
Aromatic DNA adducts in white blood cells of coke workers (1990) (35)
Cancer of unknown primary (CUP): does cause of death and family history implicate hidden phenotypically changed primaries? (2012) (35)
Adenine N3 is a main alkylation site of styrene oxide in double-stranded DNA. (2000) (35)
Consensus Pathways Implicated in Prognosis of Colorectal Cancer Identified Through Systematic Enrichment Analysis of Gene Expression Profiling Studies (2011) (35)
Association between the germline MC1R variants and somatic BRAF/NRAS mutations in melanoma tumors. (2010) (35)
Association between number of siblings and nervous system tumors suggests an infectious etiology (2006) (35)
Polymorphisms in genes involved in GH1 release and their association with breast cancer risk. (2006) (35)
The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer. (2006) (34)
Genetic variation in genes encoding for polymerase ζ subunits associates with breast cancer risk, tumour characteristics and survival (2011) (34)
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci (2017) (34)
Associations between ocular melanoma and other primary cancers: An international population‐based study (2007) (34)
Use of pyrosequencing to detect clinically relevant polymorphisms of genes in basal cell carcinoma. (2004) (34)
Lifestyle and cancer: effect of widowhood and divorce. (2003) (34)
Variants at the 9p21 locus and melanoma risk (2013) (34)
Time trends and familial risks in squamous cell carcinoma of the skin. (2003) (34)
Familial risks in in situ cancers from the Family-Cancer Database. (1998) (33)
Familial risks for amyotrophic lateral sclerosis and autoimmune diseases (2009) (33)
Obesity and familial obesity and risk of cancer (2011) (33)
Aromatic DNA adducts in white blood cells of foundry workers. (1988) (33)
Familial Risks for Epilepsy among Siblings Based on Hospitalizations in Sweden (2006) (33)
A pooled analysis of second primary pancreatic cancer. (2006) (33)
Risk for incident and fatal prostate cancer in men with a family history of any incident and fatal cancer. (2012) (33)
Familial multiple primary lung cancers: a population-based analysis from Sweden. (2005) (33)
The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer. (2006) (33)
Tumour necrosis factor-alpha (TNF-alpha) in patients who have asbestosis and develop cancer. (1995) (33)
Genotoxic exposures of potroom workers. (1999) (33)
Embryotoxicity of industrial chemicals on the chicken embryo: dithiocarbamates. (1983) (33)
Kaposi sarcoma and Merkel cell carcinoma after autoimmune disease (2012) (32)
Second primary neoplasms after 19281 endocrine gland tumours: aetiological links? (2001) (32)
Second primary cancers after anogenital, skin, oral, esophageal and rectal cancers: Etiological links? (2001) (32)
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma (2016) (32)
Chromosomal aberrations in tire plant workers and interaction with polymorphisms of biotransformation and DNA repair genes. (2008) (32)
7-Alkylguanine adducts of styrene oxide determined by 32P-postlabeling in DNA and human embryonal lung fibroblasts (HEL). (1996) (32)
Time trends in incidence, causes of death, and survival of cancer of unknown primary in Sweden (2012) (32)
Familial risk for esophageal cancer: an updated epidemiologic study from Sweden. (2006) (32)
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2017) (32)
Influence of family size and birth order on risk of cancer: a population-based study (2011) (32)
Familial association of prostate cancer with other cancers in the Swedish Family‐Cancer Database (2005) (32)
Familial risk for histology-specific bone cancers: an updated study in Sweden. (2006) (32)
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study (2010) (32)
Alkylation of guanosine by phosphoramide mustard, chloromethine hydrochloride and chlorambucil. (2009) (32)
Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma. (2010) (32)
Effects of parental occupational exposure to solvents and lead on spontaneous abortion. (1992) (31)
Calcium binding to brain plasma membranes. (1974) (31)
32P-postlabeling of N-7, N2 and O6 2'-deoxyguanosine 3'-monophosphate adducts of styrene oxide. (1991) (31)
Death Receptor 4 Variants and Colorectal Cancer Risk (2006) (31)
PAI-1 −675 4G/5G polymorphism as a prognostic biomarker in breast cancer (2008) (31)
The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer. (2004) (31)
Copy number variation in patients with cervical artery dissection (2012) (31)
Familial and second esophageal cancers: A nation‐wide epidemiologic study from Sweden (2002) (31)
Identification of the major tamoxifen-DNA adducts in rat liver by mass spectroscopy. (1999) (31)
Effect of multiplicity, laterality, and age at onset of breast cancer on familial risk of breast cancer: a nationwide prospective cohort study (2014) (31)
Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants (2012) (31)
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma (2017) (31)
Mammographic screening is dramatically changing age-incidence data for breast cancer. (2004) (31)
Colorectal cancer patients: what do they die of? (2012) (31)
Familial risk of non-Hodgkin lymphoma by sex, relationship, age at diagnosis and histology: a joint study from five Nordic countries (2016) (30)
Risks among siblings and twins for childhood acute lymphoid leukaemia: results from the Swedish Family-Cancer Database (2002) (30)
High constant incidence rates of second primary cancers of the head and neck: A pooled analysis of 13 cancer registries (2011) (30)
Molecular epidemiology of VHL gene mutations in renal cell carcinoma patients: relation to dietary and other factors. (2002) (30)
Distribution and risk of the second discordant primary cancers combined after a specific first primary cancer in German and Swedish cancer registries. (2015) (30)
Familial risks in second primary breast cancer based on a family cancer database. (1999) (30)
Do polymorphisms and haplotypes of mismatch repair genes modulate risk of sporadic colorectal cancer? (2008) (30)
The role of various biomarkers in the evaluation of styrene genotoxicity. (2003) (30)
Renal cell carcinoma as first and second primary cancer: etiological clues from the Swedish Family-Cancer Database. (2011) (30)
Familial risks of aortic aneurysms among siblings in a nationwide Swedish study (2006) (30)
Spontaneous abortions among women employed in the plastics industry. (1985) (29)
Serum oncoproteins in asbestosis patients. (1995) (29)
Survival in cancer patients hospitalized for inflammatory bowel disease in Sweden (2011) (29)
Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression (2016) (29)
Second primary cancers in patients with acute lymphoblastic, chronic lymphocytic and hairy cell leukaemia (2019) (29)
Risks of second primary cancer among patients with major histological types of lung cancers in both men and women (2010) (29)
Familial risks for colorectal cancer show evidence on recessive inheritance (2005) (29)
Time trends in survival from cancer of unknown primary: small steps forward. (2013) (29)
Modification of menopausal hormone therapy-associated colorectal cancer risk by polymorphisms in sex steroid signaling, metabolism and transport related genes. (2011) (29)
Micronuclei in Cord Blood Lymphocytes and Associations with Biomarkers of Exposure to Carcinogens and Hormonally Active Factors, Gene Polymorphisms, and Gene Expression: The NewGeneris Cohort (2013) (29)
Childhood Cancer and Parental Occupation in the Swedish Family-Cancer Database (2001) (29)
Higher risk of primary cancers after polycythaemia vera and vice versa (2011) (29)
Serum oncogene proteins in foundry workers. (1990) (29)
Bladder cancer: allelic deletions at and around the retinoblastoma tumor suppressor gene in relation to stage and grade. (2000) (29)
Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms. (2018) (29)
Toxicity of styrene and styrene oxide on chick embryos. (1977) (28)
Incorporation of detailed family history from the Swedish Family Cancer Database into the PCPT risk calculator. (2015) (28)
Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk. (2005) (28)
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer (2015) (28)
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival (2014) (28)
32P-postlabelling method for the detection of 7-alkylguanine adducts formed by the reaction of different 1,2-alkyl epoxides with DNA. (1995) (28)
Influence of GSTM1, GSTT1, GSTP1 and NAT2 genotypes on the p53 mutational spectrum in bladder tumours (2005) (28)
The in vivo levels of DNA alkylation products in human lymphocytes are not age dependent: an assay of 7-methyl- and 7-(2-hydroxyethyl)-guanine DNA adducts. (2002) (28)
No association between MDM2 SNP309 promoter polymorphism and basal cell carcinoma of the skin (2007) (28)
The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells (2015) (28)
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome (2011) (28)
Metabolism and genotoxicity of styrene. (1981) (28)
Systematic enrichment analysis of gene expression profiling studies identifies consensus pathways implicated in colorectal cancer development (2011) (28)
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. (2014) (28)
Age of onset in familial breast cancer as background data for medical surveillance (2009) (28)
Immigrant health, our health. (2014) (28)
Low‐risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients (2010) (28)
DNA-binding products of nornitrogen mustard, a metabolite of cyclophosphamide. (1987) (27)
Urinary sulfur containing metabolites after administration of ethanol, acetaldehyde and formaldehyde to rats. (1982) (27)
Stabilities of 7-alkylguanosines and 7-deoxyguanosines formed by phosphoramide mustard and nitrogen mustard. (1986) (27)
Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas. (2015) (27)
Liver and gallbladder cancer in immigrants to Sweden. (2010) (27)
Depurination and imidazole ring-opening in nucleosides and DNA alkylated by styrene oxide. (1988) (27)
Multiple primary (even in situ) melanomas in a patient pose significant risk to family members. (2014) (27)
DNA and protein adducts. (1995) (27)
Demonstration of UV-dimers in human skin DNA in situ 3 weeks after exposure. (2002) (27)
ARLTS1 variants and risk of colorectal cancer. (2006) (27)
DNA adducts in humans related to occupational and environmental exposure to aromatic compounds. (1990) (27)
Familial risks for main neurological diseases in siblings based on hospitalizations in Sweden. (2006) (27)
Familial prostate cancer from the family-cancer database. (2000) (27)
Subsequent leukaemia in autoimmune disease patients (2013) (27)
Apparent Anticipation and Heterogeneous Transmission Patterns in Familial Hodgkin's and Non-Hodgkin's Lymphoma: Report from a Study Based on Swedish Cancer Database (2001) (27)
Morphological types of breast cancer in family members and multiple primary tumours: is morphology genetically determined? (2002) (26)
The effect of maternally inhaled styrene on embryonal and foetal development in mice and Chinese hamsters. (2009) (26)
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer (2006) (26)
A population-based study of familial cutaneous melanoma (2001) (26)
Obstructive sleep apnea syndrome in siblings: an 8-year Swedish follow-up study. (2008) (26)
Smoking and body mass index as risk factors for subtypes of cancer of unknown primary (2015) (26)
Familial association of pancreatic cancer with other malignancies in Swedish families (2009) (26)
Heritable and environmental components in cervical tumors (2006) (26)
Separation of transforming amino acid-substituting mutations in codons 12, 13 and 61 the N-ras gene by constant denaturant capillary electrophoresis (CDCE). (1995) (26)
Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer (2012) (26)
Cyclobutane thymidine dimers are present in human urine following sun exposure: quantitation using 32P-postlabeling and high-performance liquid chromatography. (2001) (26)
Socio-economic and occupational risk factors for gastric cancer: a cohort study in Sweden (2006) (26)
The Swedish Family-Cancer Database: Update, Application to Colorectal Cancer and Clinical Relevance (2005) (26)
Cancer incidence among Iranian immigrants in Sweden and Iranian residents compared to the native Swedish population. (2010) (26)
Familial risks for chronic obstructive pulmonary disease among siblings based on hospitalisations in Sweden (2008) (26)
Does the time interval between first and last birth influence the risk of endometrial and ovarian cancer? (2011) (26)
ARLTS1 variants and melanoma risk (2006) (26)
Case–control study in basal cell carcinoma of the skin: single nucleotide polymorphisms in three interleukin promoters pre‐analysed in pooled DNA (2006) (26)
Carcinogenicity of quinoline, styrene, and styrene-7,8-oxide. (2018) (26)
In situ repair of cyclobutane pyrimidine dimers in skin and melanocytic nevi of cutaneous melanoma patients (2002) (25)
Power and limits of modern cancer diagnostics: cancer of unknown primary. (2012) (25)
Familial invasive and in situ squamous cell carcinoma of the skin (2003) (25)
Variants at chromosome 20 (ASIP locus) and melanoma risk (2013) (25)
Risk of second malignant neoplasms after childhood central nervous system malignant tumours: an international study. (2008) (25)
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 (2018) (25)
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk (2015) (25)
Ethnic differences in incidence of type 1 diabetes among second-generation immigrants and adoptees from abroad. (2010) (25)
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 (2018) (25)
Are twins at risk of cancer: results from the Swedish family-cancer database. (2005) (25)
Urinary Thymidine Dimer as a Marker of Total Body Burden of UV-Inflicted DNA Damage in Humans (2005) (25)
Styrene: from characterisation of DNA adducts to application in styrene-exposed lamination workers. (1995) (25)
p53 intron 7 polymorphisms in urinary bladder cancer patients and controls. Stockholm Bladder Cancer Group. (2000) (25)
A gene-wide investigation on polymorphisms in the taste receptor 2R14 (TAS2R14) and susceptibility to colorectal cancer (2010) (25)
Activity of enzymes related to neurotransmission in neuronal and glial fractions. (1973) (25)
Age at diagnosis and age at death in familial prostate cancer. (2009) (25)
The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A (2015) (25)
Impact of functional germline variants and a deletion polymorphism in APOBEC3A and APOBEC3B on breast cancer risk and survival in a Swedish study population (2015) (25)
A single‐nucleotide polymorphism in the XPG gene, and tumour stage, grade, and clinical course in patients with nonmuscle‐invasive neoplasms of the urinary bladder (2006) (25)
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology (2018) (25)
Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression (2009) (25)
SNP microarray analysis for genome-wide detection of crossover regions (2005) (25)
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family (2018) (25)
Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients. (2009) (24)
UV-induced photoproducts in human skin explants analysed by TLC and HPLC-radioactivity detection. (1995) (24)
Parental cancer as a risk factor for nine common childhood malignancies (2001) (24)
Obligation for cell line authentication: Appeal for concerted action (2010) (24)
Genetic variants in C‐type lectin genes are associated with colorectal cancer susceptibility and clinical outcome (2013) (24)
Bladder Neoplasms--Regions at Chromosome 9 with Putative Tumour Suppressor Genes (2003) (24)
Familial sarcoma: challenging pedigrees (2003) (24)
Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer (2013) (24)
Population attributable fractions for ovarian cancer in Swedish women by morphological type (2007) (24)
Modulation of DNA repair capacity and mRNA expression levels of XRCC1, hOGG1 and XPC genes in styrene-exposed workers. (2010) (24)
Cancer in immigrants as a pointer to the causes of cancer. (2014) (24)
Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer. (2000) (24)
Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity (2010) (24)
Interaction of breast cancer and melanoma genotypes (1997) (24)
Endometrial cancer: population attributable risks from reproductive, familial and socioeconomic factors. (2005) (24)
Styrene oxide as a stereochemical probe for the mechanism of aralkylation at different sites on guanosine. (1988) (24)
Assay of different photoproducts after UVA, B and C irradiation of DNA and human skin explants. (1996) (24)
Incidence of celiac disease among second-generation immigrants and adoptees from abroad in Sweden: evidence for ethnic differences in susceptibility (2011) (24)
Risks of breast, endometrial, and ovarian cancers after twin births. (2007) (24)
Effects of screening for breast cancer on its age‐incidence relationships and familial risk (2005) (24)
Genetic Polymorphisms in Host Innate Immune Sensor Genes and the Risk of Nasopharyngeal Carcinoma in North Africa (2013) (24)
Inherited susceptibility to bleomycin-induced micronuclei: correlating polymorphisms in GSTT1, GSTM1 and DNA repair genes with mutagen sensitivity. (2008) (24)
Effect of a detailed family history of melanoma on risk for other tumors: a cohort study based on the nationwide Swedish Family-Cancer Database. (2014) (24)
Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events (2005) (24)
Preparation of plasma membranes from isolated cells of newborn rat brain. (1973) (24)
Association of polymorphisms and haplotypes in the human growth hormone 1 (GH1) gene with breast cancer. (2005) (24)
New aspects in the biomonitoring of occupational exposure to styrene (2002) (24)
Familial risk of small intestinal carcinoid and adenocarcinoma. (2013) (24)
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects. (2015) (24)
Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma (2012) (24)
Depurination from DNA of 7-methylguanine, 7-(2-aminoethyl)-guanine and ring-opened 7-methylguanines. (1989) (24)
Etiologic impact of known cancer susceptibility genes. (2008) (23)
Spontaneous abortions and reproductive selection mechanisms in the rubber and leather industry in Finland (1983) (23)
Preferential binding of benzo[a]pyrene into nuclear matrix fraction. (1979) (23)
Risk of other Cancers in Families with Melanoma: Novel Familial Links (2017) (23)
Association of childhood acute lymphoblastic leukaemia with cancers in family members (2005) (23)
Kinetics of formation of specific styrene oxide adducts in double-stranded DNA. (2001) (23)
Emigration flows from North Africa to Europe. (2014) (23)
Clustering of concordant and discordant cancer types in Swedish couples is rare. (2011) (23)
Serum levels of growth-factor receptors, egfr and Neu in asbestosis patients - a follow-up-study. (1994) (23)
Predictive and Prognostic Clinical Variables in Cancer Patients Treated With Adenoviral Oncolytic Immunotherapy. (2016) (23)
Levels and repair of cyclobutane pyrimidine dimers and 6-4 photoproducts in skin of sporadic basal cell carcinoma patients. (2000) (23)
Toxicity of rubber chemicals towards three-day chicken embryos. (1983) (23)
Protective Effects of Tanning on Cutaneous DNA Damage in situ (2001) (23)
Familial clustering of cancer at human papillomavirus‐associated sites according to the Swedish Family‐Cancer Database (2007) (23)
Concordant and discordant associations between rheumatoid arthritis, systemic lupus erythematosus and ankylosing spondylitis based on all hospitalizations in Sweden between 1973 and 2004. (2008) (23)
Familial cancer risks to offspring from mothers with 2 primary breast cancers: Leads to cancer syndromes (2000) (23)
Occupational chemicals tested for teratogenicity (1980) (22)
Familial risks of ovarian cancer by age at diagnosis, proband type and histology (2018) (22)
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease (2015) (22)
Familial relationships in squamous cell carcinoma of the skin. (2000) (22)
Sex‐specific familial risks of urinary bladder cancer and associated neoplasms in Sweden (2009) (22)
DNA Adducts in Biomonitoring (1995) (22)
Familial and second gastric carcinomas (2002) (22)
Differences in global gene expression in melanoma cell lines with and without homozygous deletion of the CDKN2A locus genes (2006) (22)
Cancer risks in women who had children with different partners from the Swedish Family-Cancer Database (2002) (22)
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population (2020) (22)
Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes (2000) (22)
Site‐specific cancer deaths in cancer of unknown primary diagnosed with lymph node metastasis may reveal hidden primaries (2013) (22)
Embryotoxic effects of phtalic acid derivatives, phosphates and aromatic oils used in the manufacturing of rubber on three day chicken embryos. (1983) (22)
Death causes in breast cancer patients. (2012) (22)
Familial risks in invasive and in situ cervical cancer by histological type (2001) (22)
Genetic predisposition for multiple myeloma (2020) (22)
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression (2018) (22)
University and medical education and the risk of cancer in Sweden (2004) (21)
FAMILIAL RISK FOR LUNG CANCER BY HISTOLOGY AND AGE OF ONSET: EVIDENCE FOR RECESSIVE INHERITANCE (2005) (21)
Time Trends and Occupational Risk Factors for Pleural Mesothelioma in Sweden (2003) (21)
Familial mortality and familial incidence in cancer. (2011) (21)
Assay for nucleoside and nucleotide binding of a potent mutagen, 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone. (1991) (21)
Familial risks for migraine and other headaches among siblings based on hospitalizations in Sweden (2005) (21)
Surveillance Bias in Cancer Risk After Unrelated Medical Conditions: Example Urolithiasis (2017) (21)
Primary cancers following squamous cell carcinoma of the skin suggest involvement of Epstein-Barr virus. (2000) (21)
Subsequent brain tumors in patients with autoimmune disease. (2013) (21)
Preparation of viable and morphologically intact cells from newborn rat brain. (1972) (21)
Associations between autoimmune conditions and hepatobiliary cancer risk among elderly US adults (2019) (21)
Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays. (2006) (21)
Familial papillary renal cell tumors and subsequent cancers: a nationwide epidemiological study from Sweden. (2003) (21)
Embryotoxicity of industrial chemicals on the chicken embryo: thiourea derivatives. (2009) (21)
Incidence and mortality in epithelial ovarian cancer by family history of any cancer (2011) (21)
Polymorphisms in the genes of the urokinase plasminogen activation system in relation to colorectal cancer. (2007) (21)
Polymorphisms in the growth hormone receptor: A case‐control study in breast cancer (2006) (20)
Familial Associations Between Prostate Cancer and Other Cancers. (2017) (20)
Second primary cancers in non‐Hodgkin lymphoma: Bidirectional analyses suggesting role for immune dysfunction (2018) (20)
Size of histone gene transcripts in different embryonic stages of the sea urchin, Strongylocentrotus purpuratus. (1978) (20)
Styrene oxide-induced 2'-deoxycytidine adducts: implications for the mutagenicity of styrene oxide. (2000) (20)
Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk (2011) (20)
Overview on health research ethics in Egypt and North Africa. (2014) (20)
p53 mutations in larynx cancer. (1994) (20)
Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population (2016) (20)
Nonendocrine cancers associated with benign and malignant parathyroid tumors. (2011) (20)
Binding of cisplatin to specific sequences of human DNA in vitro. (1988) (20)
Reproductive hazards and plastics industry. (1984) (20)
Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer. (2001) (20)
Familial risk for soft tissue tumors: a nation-wide epidemiological study from Sweden (2008) (20)
Familial bladder cancer and the related genes (2011) (20)
Familial breast carcinoma risks by morphology (2002) (20)
Spontaneous abortions in hospital sterilising staff (1983) (20)
Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways (2019) (20)
Some properties of brain cell suspensions prepared by a mechanical-enzymic method. (1970) (20)
Correlations of alkylating activity and mutagenicity in bacteria of cytostatic drugs. (2009) (20)
A Comprehensive Meta-analysis of Case–Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma (2016) (20)
Risk of subsequent invasive breast carcinoma after in situ breast carcinoma in a population covered by national mammographic screening (2004) (20)
Cancer risks in childhood and adolescence among the offspring of immigrants to Sweden (2002) (20)
Familial clustering of ovarian and endometrial cancers. (2004) (19)
Familial renal cell carcinoma from the Swedish Family-Cancer Database. (2011) (19)
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer (2013) (19)
Ethnic variation in genotype frequencies of a p53 intron 7 polymorphism. (2001) (19)
Genotypes, haplotypes and diplotypes of three XPC polymorphisms in urinary-bladder cancer patients. (2010) (19)
Interaction between functional polymorphic variants in cytokine genes, established risk factors and susceptibility to basal cell carcinoma of skin. (2011) (19)
Relationships between familial risks of cancer and the effects of heritable genes and their SNP variants. (2005) (19)
Validity Aspects of Exposure and Outcome Data in Reproductive Studies (1995) (19)
Reactions of 'bay-region' and non-'bay-region' diol-epoxides of benz(a)anthracene with DNA: evidence indicating that the major products are hydrocarbon-N2-guanine adducts. (1980) (19)
Familial associations of female breast cancer with other cancers (2017) (19)
Estimates of heritable and environmental components of familial breast cancer using family history information (2007) (19)
Morbidity and mortality in gynecological cancers among first‐ and second‐generation immigrants in Sweden (2012) (19)
Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis (2013) (19)
Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases (2013) (19)
A genome-wide association study identi fi es risk loci for childhood acute lymphoblastic leukemia at 10 q 26 . 13 and 12 q 23 . 1 (2017) (19)
Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer (2012) (19)
DNA adducts in human nasal mucosa and white blood cells from smokers and non-smokers. (1997) (19)
Malignant melanoma--a genetic overview. (2009) (19)
Cancer incidence, trends, and survival among immigrants to Sweden: a population-based study (2015) (19)
HLA and KIR Associations of Cervical Neoplasia (2018) (19)
Familial melanoma by histology and age: joint data from five Nordic countries. (2014) (18)
Polymorphisms in NQO1 and the clinical course of urinary bladder neoplasms (2007) (18)
Colorectal cancer risk and patients’ survival: influence of polymorphisms in genes somatically mutated in colorectal tumors (2014) (18)
Genetic variation of acquired structural chromosomal aberrations. (2018) (18)
Reactions of -propiolactone, -butyrolactone and ?-butyrolactone with nucleic acids (1981) (18)
Re: Association between endothelin receptor B nonsynonymous variants and melanoma risk. (2006) (18)
Hodgkin lymphoma after autoimmune diseases by age at diagnosis and histological subtype. (2014) (18)
Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts (2016) (18)
Embryotoxicity of sixteen industrial amines to the chicken embryo (1983) (18)
Metabolic gene variants associated with chromosomal aberrations in healthy humans (2015) (18)
Origin of B-Cell Neoplasms in Autoimmune Disease (2016) (18)
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS) (2017) (18)
Direct evidence for a polygenic etiology in familial multiple myeloma. (2017) (18)
Risk of cancer of unknown primary after hospitalization for autoimmune diseases (2015) (18)
Bortezomib‐induced peripheral neuropathy: A genome‐wide association study on multiple myeloma patients (2018) (18)
Risk of incident and fatal melanoma in individuals with a family history of incident or fatal melanoma or any cancer (2011) (18)
Allelotyping of pooled DNA with 250 K SNP microarrays (2007) (18)
Familial association of specific histologic types of ovarian malignancy with other malignancies (2004) (18)
Familial upper aerodigestive tract cancers: incidence trends, familial clustering and subsequent cancers. (2003) (18)
Male breast cancer: risk to daughters (1999) (17)
Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism (2017) (17)
Identification of guanine-adducts of carcinogens by their fluorescence. (1980) (17)
Relative turnover of tubulin subunits in rat brain. (1973) (17)
Effect of autoimmune diseases on mortality and survival in subsequent digestive tract cancers. (2012) (17)
Differential gene expression in melanocytic nevi with the V600E BRAF mutation (2007) (17)
Age‐time risk patterns of solid cancers in 60 901 non‐Hodgkin lymphoma survivors from Finland, Norway and Sweden (2014) (17)
DNA repair and cyclin D1 polymorphisms and styrene-induced genotoxicity and immunotoxicity. (2005) (17)
Composition and synthesis of plasma membranes and smooth endoplasmic reticulum in isolated cells of newborn rat brain. (1973) (17)
Embryotoxic effects of acrolein, methacrylates, guanidines and resorcinol on three day chicken embryos. (2009) (17)
Risk of transitional-cell carcinoma of the bladder in first- and second-generation immigrants to Sweden (2010) (17)
Occupational risk factors for kidney cancer: a cohort study in Sweden (2005) (17)
Spontaneous abortions among rubber workers and congenital malformations in their offspring. (1983) (17)
32P-postlabelling analysis of isomeric 7-alkylguanine adducts of styrene oxide. (1997) (17)
Familial risks of hospitalization for Parkinson’s disease in first-degree relatives: a nationwide follow-up study from Sweden (2006) (17)
New cancer susceptibility loci: Population and familial risks (2008) (17)
Implications of results of molecular epidemiology on DNA adducts, their repair and mutations for mechanisms of human cancer. (2004) (17)
Population attributable risks for breast cancer in Swedish women by morphological type (2008) (17)
Coffee consumption not associated with risk of pancreas cancer in Finland. (1995) (17)
Familial risks in nervous system tumours: joint Nordic study (2010) (17)
Life style and cancer: Effect of divorce (2002) (17)
Subsequent cancers in patients diagnosed with cancer of unknown primary (CUP): etiological insights? (2012) (17)
Risk of Second Primary Cancers in Multiple Myeloma Survivors in German and Swedish Cancer Registries (2016) (17)
Preventable breast cancer is postmenopausal (2010) (17)
Familial invasive and borderline ovarian tumors by proband status, age and histology (2003) (17)
Novel somatic mutations in the VHL gene in Swedish archived sporadic renal cell carcinomas. (1999) (17)
Molecular genetic analysis of NBS1 in German melanoma patients (2007) (17)
The effect of having an affected parent or sibling on invasive and in situ skin cancer risk in Sweden. (2009) (17)
Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer (2018) (17)
Biological monitoring in surveillance of exposure to genotoxicants. (1983) (17)
Dimethylnitrosamine adducts excreted in rat urine. (1981) (17)
Characterization of neuronal and glial fractions separated in sucrose and ficoll media. (1971) (17)
Identification of 1-Adenine DNA Adducts in Workers Occupationally Exposed to Styrene (2001) (17)
Familial risks for nerve, nerve root and plexus disorders in siblings based on hospitalisations in Sweden (2006) (17)
Familial association of colorectal adenocarcinoma with cancers at other sites. (2004) (17)
Skilled use of DNA polymorphisms as a tool for polygenic cancers. (2002) (17)
Survival in cancer patients with previous hospitalization for sarcoidosis: a Swedish population-based cohort study during 1964-2006. (2011) (16)
TP53-binding protein variants and breast cancer risk: a case-control study (2005) (16)
DNA adducts and mutations in occupational and environmental biomonitoring. (1997) (16)
Familial risks for depression among siblings based on hospitalizations in Sweden (2008) (16)
Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden (2020) (16)
Ultraviolet radiation-induced photoproducts in human skin DNA as biomarkers of damage and its repair. (2001) (16)
Esophageal cancer risk among immigrants in Sweden (2011) (16)
Binding of styrene oxide to amino acids, human serum proteins and hemoglobin. (1986) (16)
A rapid fluorescence based multiplex polymerase chain reaction — single‐strand conformation polymorphism method for p53 mutation detection (2000) (16)
c‐MYC Asn11Ser is associated with increased risk for familial breast cancer (2005) (16)
Runs of homozygosity and inbreeding in thyroid cancer (2016) (16)
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. (2018) (16)
Sites of reaction of glutaraldehyde and acetaldehyde with nucleosides (1984) (16)
Survival patterns among lymphoma patients with a family history of lymphoma. (2008) (16)
Prostate cancer incidence and survival in immigrants to Sweden (2013) (16)
Parental lung cancer as predictor of cancer risks in offspring: Clues about multiple routes of harmful influence? (2006) (16)
Risks of papillary and follicular thyroid cancer among immigrants to Sweden (2011) (16)
Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta‐analysis (2017) (16)
Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer (2013) (16)
Micronuclei, DNA single-strand breaks and DNA-repair activity in mice exposed to 1,3-butadiene by inhalation. (2006) (16)
Epidemiology, genetics and treatment of multiple myeloma and precursor diseases (2021) (16)
POMC and TP53 genetic variability and risk of basal cell carcinoma of skin: Interaction between host and genetic factors. (2011) (16)
7-Alkylguanine adduct levels in urine, lungs and liver of mice exposed to styrene by inhalation. (2006) (16)
Familial polycythemia vera: results from the Swedish Family-Cancer Database (2001) (16)
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma (2018) (16)
Incidence of cancer of unknown primary in Sweden: analysis by location of metastasis (2012) (16)
Socioeconomic and Occupational Risk Factors for Pancreatic Cancer:: A Cohort Study In Sweden (2006) (16)
Embryotoxicity of benzothiazoles, benzenesulfohydrazide, and dithiodimorpholine to the chicken embryo (1982) (16)
32P-postlabelling of 7-methyl-dGMP ring-opened 7-methyl-dGMP and platinated dGpdG. (1990) (16)
Autoimmune diseases and hematological malignancies: Exploring the underlying mechanisms from epidemiological evidence. (2020) (16)
32P-postlabelling of N6-adenine adducts of epoxybutanediol in vivo after 1,3-butadiene exposure. (1998) (16)
Association of ocular melanoma with breast cancer but not with cutaneous melanoma: Results from the Swedish family‐cancer database (2001) (16)
Risk of asthma and autoimmune diseases and related conditions in patients hospitalized for obesity (2012) (16)
Carcinogenic chemicals in the occupational environment. (1993) (16)
A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer (2020) (16)
Location of metastases in cancer of unknown primary are not random and signal familial clustering (2016) (15)
A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: Results from the IMMEnSE consortium and meta-analysis (2016) (15)
Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study (2014) (15)
Mesothelioma incidence has leveled off in Sweden (2007) (15)
Systematic Pathway Enrichment Analysis of a Genome-Wide Association Study on Breast Cancer Survival Reveals an Influence of Genes Involved in Cell Adhesion and Calcium Signaling on the Patients’ Clinical Outcome (2014) (15)
The Swedish Family-Cancer Database (2005) (15)
Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk (2007) (15)
Variation in the risk for liver and gallbladder cancers in socioeconomic and occupational groups in Sweden with etiological implications (2005) (15)
Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients (2018) (15)
Integrin genes and susceptibility to human melanoma. (2012) (15)
Copy number variations of GSTT1 and GSTM1, colorectal cancer risk and possible effect modification of cigarette smoking and menopausal hormone therapy (2012) (15)
Prognostic significance of homozygous deletions and multiple duplications at the CDKN2A (p16INK4a)/ARF (p14ARF) locus in urinary bladder cancer (2006) (15)
Molecular epidemiology and cancer prevention. (1990) (15)
DNA adduct formation in the human nasal mucosa as a biomarker of exposure to environmental mutagens and carcinogens. (1996) (15)
Population-based study of familial medullary thyroid cancer (2004) (15)
Breast cancer risk in women who fulfill high-risk criteria: at what age should surveillance start? (2010) (15)
Familial risks in urolithiasis in the population of Sweden (2018) (15)
Prostate cancer survivors: Risk and mortality in second primary cancers (2018) (15)
Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis (2017) (15)
Cancer risk and mortality in asthma patients: A Swedish national cohort study (2015) (15)
Distribution of estrogen receptors in hen oviduct chromatin fractions in the course of DNAase II digestion. (1977) (15)
Influence of Genetic Variants in Type I Interferon Genes on Melanoma Survival and Therapy (2012) (15)
Familial Risks and Mortality in Second Primary Cancers in Melanoma (2018) (15)
Ethnic differences in breast cancer risk and survival: A study on immigrants in Sweden (2013) (15)
Synthesis and stability of 2'-deoxyguanosine 3'-monophosphate adducts of dimethyl sulfate, ethylene oxide and styrene oxide. (1990) (15)
Biological monitoring in the identification of the cancer of individuals exposed to chemical carcinogens. (1981) (15)
Reaction kinetics of alkyl epoxides with DNA and other nucleophiles. (1994) (15)
Human estrogen receptor beta 548 is not a common variant in three distinct populations. (2003) (15)
Prostate cancer risk assessment model: a scoring model based on the Swedish Family-Cancer Database (2012) (15)
Second malignancies after childhood noncentral nervous system solid cancer: Results from 13 cancer registries (2011) (15)
32P-postlabelling/HPLC analysis of various styrene-induced DNA adducts in mice (2001) (15)
A Population-Based Study of Familial Central Nervous System Hemangioblastomas (2001) (14)
Survival in bladder and renal cell cancers is familial. (2008) (14)
Risk of multiple primary cancers in nasal cancer patients. (2001) (14)
Analysis of cigarette-smoke-induced DNA adducts by butanol extraction and nuclease P1-enhanced 32P-postlabeling in human lymphocytes and granulocytes. (1993) (14)
Risks of Subarachnoid Hemorrhage in Siblings: A Nationwide Epidemiological Study from Sweden (2007) (14)
Localization of ATPase in bovine retinal outer segments. (1975) (14)
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci (2017) (14)
Re: Familial clustering of Hodgkin lymphoma and multiple sclerosis. (2005) (14)
Regional, socioeconomic and occupational groups and risk of hospital admission for multiple sclerosis: a cohort study in Sweden (2008) (14)
Case-control estimation of the impact of oncolytic adenovirus on the survival of patients with refractory solid tumors. (2015) (14)
Reactions of formaldehyde with guanosine. (1981) (14)
Familial renal cell cancer appears to have a recessive component (2004) (14)
Search for multiple myeloma risk factors using Mendelian randomization. (2020) (14)
Familial risks of breast and prostate cancers: does the definition of the at risk period matter? (2010) (14)
Testing of quantitative parameters in the 32P-postlabelling method. (1993) (14)
Cancer incidence among Turkish, Chilean, and North African first-generation immigrants in Sweden compared with residents in the countries of origin and native Swedes (2013) (14)
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma (2019) (14)
Hydrolysis and rearrangement of O6-substituted guanosine products resulting from reaction of guanosine with styrene oxide (1986) (14)
Familial cancer in Sweden Population-based study (1997) (14)
Familial association of histology specific breast cancers with cancers at other sites (2004) (14)
Survival in cancer patients hospitalized for psoriasis: a population‐based cohort study in Sweden (2011) (14)
Cancer of unknown primary is associated with diabetes (2015) (14)
Causes of death in patients with extranodal cancer of unknown primary: searching for the primary site (2014) (14)
DNA binding of tamoxifen and its analogues: identification of the tamoxifen-DNA adducts in rat liver. (1998) (14)
Spontaneous Abortion as Risk Indicator in Metal Exposure (1983) (14)
Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families. (2008) (14)
Gene-environment studies: any advantage over environmental studies? (2007) (14)
Reactions of methylnitrosourea, epichlorohydrin, styrene oxide and acetoxyacetylaminofluorene with polyamino acids. (1983) (14)
Histology-specific risks in testicular cancer in immigrants to Sweden. (2010) (14)
Could polymorphisms in ATP-binding cassette C3/multidrug resistance associated protein 3 (ABCC3/MRP3) modify colorectal cancer risk? (2008) (13)
Comparison of (32)P-postlabeling and high-resolution GC/MS in quantifying N7-(2-Hydroxyethyl)guanine adducts. (1999) (13)
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes (2016) (13)
Reproductive health of working women: spontaneous abortions and congenital malformations. (1985) (13)
Covalent binding of 2-acetylaminofluorene, 2-aminofluorene, and N-hydroxy-2-acetylaminofluorene to rat liver nuclear DNA and protein in vivo and in vitro. (1980) (13)
Modification of second cancer risk after malignant melanoma by parental history of cancer (2008) (13)
Embryotoxicity of acrolein, acrylonitrile and acryl-amide in developing chick embryos (1979) (13)
DNA adducts of nitrogen mustards and ethylene imines. (1994) (13)
Socioeconomic/occupational risk factors for lymphoproliferative diseases in Sweden. (2006) (13)
Abundant lipophilic DNA adducts in human tissues. (1998) (13)
Analysis of tamoxifen-induced DNA adducts by 32P-postlabelling assay using different chromatographic techniques. (1997) (13)
Polyadenylic acid in RNA extracted by thermal phenol fractionation from chick embryo brain and liver. (1974) (13)
32P-postlabelling analysis of DNA adducts in humans: adduct distribution and method improvement. (1994) (13)
Ring-opened 7-methylguanine nucleotides are resistant to nuclease P1 digestion and good substrates to polynucleotide kinase. (1989) (13)
A population-based comparison of second primary cancers in Germany and Sweden between 1997 and 2006: clinical implications and etiologic aspects (2013) (13)
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma (2019) (13)
DNA photodamage induced by UV phototherapy lamps and sunlamps in human skin in situ and its potential importance for skin cancer. (2001) (13)
A population-based study of familial soft tissue tumors. (2001) (13)
Effect of the spectral range of a UV lamp on the production of cyclobutane pyrimidine dimers in human skin in situ (2003) (13)
32P-postlabelling of 2-hydroxyethylated, ethylated and methylated adducts of 2'-deoxyguanosine 3'-monophosphate. (1990) (13)
Repair of UV Dimers in Skin DNA of Patients with Basal Cell Carcinoma (2008) (13)
Occupational Risks for Nasal Cancer in Sweden (2004) (13)
Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival (2019) (13)
Risk of Cancer among the Offspring of Women Who Experienced Parental Death during Pregnancy (2007) (13)
Risk of second primary cancer following myeloid neoplasia and risk of myeloid neoplasia as second primary cancer: a nationwide, observational follow up study in Sweden. (2018) (13)
Association of brain tumours with other neoplasms in families. (2004) (13)
Embryotoxic effects of eight organic peroxides and hydrogen peroxide on three-day chicken embryos. (1984) (13)
Familial Risks and Proportions Describing Population Landscape of Familial Cancer (2021) (13)
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans. (2016) (13)
32P-postlabelling of diastereomeric 7-alkylguanine adducts of butadiene monoepoxide. (1996) (13)
Survival in non-Hodgkin’s lymphoma by histology and family history (2009) (12)
Age-Dependent Metastatic Spread and Survival: Cancer of Unknown Primary as a Model (2016) (12)
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes (2019) (12)
Searching for the missing heritability of complex diseases (2011) (12)
Persistence of 7-(2-hydroxyethyl)guanine± DNA adducts in rats exposed to ethene by inhalation (1997) (12)
Genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches Cancer Epidemiol. Biomark (2002) (12)
Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing (2019) (12)
Familial [corrected] transmission of coronary heart disease: a cohort study of 80,214 Swedish adoptees linked to their biological and adoptive parents. (2011) (12)
Gender effects in familial cancer (2002) (12)
The Single Nucleotide Polymorphism IVS 1 + 309 in Mouse Double Minute 2 Does Not Affect Risk of Familial Breast Cancer (2006) (12)
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance (2019) (12)
Familial Associations in Testicular Cancer with Other Cancers (2018) (12)
575 Genetic polymorphisms of DNA repair and biotransformation genes and possible links with chromosomal aberrations and single-strand breaks in DNA (2003) (12)
DNA adducts in biomonitoring. (1995) (12)
Second cancers and causes of death in patients with testicular cancer in Sweden (2019) (12)
A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 (NPAS2) is not associated with breast cancer risk (2011) (12)
Familial risk of endometrial cancer after exclusion of families that fulfilled Amsterdam, Japanese or Bethesda criteria for HNPCC. (2004) (12)
Lifestyle and cancer: protection from a cancer‐free spouse (2000) (12)
Association of first ocular melanoma with subsequent cutaneous melanoma: Results from the Swedish Family‐Cancer Database (2003) (12)
Seasonal and regional variations of asthma and association with osteoporosis: possible role of vitamin D in asthma (2010) (12)
Re: familial multiple myeloma: a family study and review of the literature. (2002) (12)
Breast and prostate cancer: familial associations (2010) (12)
Environmental pollution and human exposure to polycyclic aromatic hydrocarbons in the east Baltic region. (1999) (11)
Surveying the Genomic Landscape of Colorectal Cancer (2009) (11)
Comparison of TLC- and HPLC-32P-postlabelling assay for cisplatin-DNA adducts. (1994) (11)
Properties of 7-substituted deoxyguanosines formed by cis-diamminedichloroplatinum(II). (1986) (11)
Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera (2017) (11)
Occurrences of Leukemia Subtypes by Socioeconomic and Occupational Groups in Sweden (2005) (11)
Re: Detection of Epstein-Barr Virus in Invasive Breast Cancers. (1999) (11)
Postlabelling HPLC analysis of lipophilic DNA adducts from human lung. (1997) (11)
A case–control study of childhood acute lymphoblastic leukaemia and polymorphisms in the TGF‐β and receptor genes (2009) (11)
Re: Prostate cancer in fathers with fewer male offspring: the Jerusalem Perinatal Study cohort. (2007) (11)
Embryotoxicity and teratogenicity of styrene and styrene oxide on chick embryos enhanced by trichloropropylene oxide. (2009) (11)
Survival in Familial Pancreatic Cancer (2008) (11)
Cancer risk in amyloidosis patients in Sweden with novel findings on non-Hodgkin lymphoma and skin cancer. (2014) (11)
DNA adducts as a marker for cancer risk? (2001) (11)
Cancer risks in men who had children with different partners from the Swedish Family-Cancer Database (2002) (11)
Familial blood vessel tumors and subsequent cancers. (2007) (11)
Estimating risks of common complex diseases: familial and population risks (2007) (11)
Risk of second primary cancers in women diagnosed with endometrial cancer in German and Swedish cancer registries (2017) (11)
Proper controls for SNP studies? (2002) (11)
Genetics of gallbladder cancer. (2017) (11)
Familial risk of urological cancers: data for clinical counseling (2004) (11)
The Molecular Epidemiology of Growth Signal Transduction Proteins (1995) (11)
Genetic factors influencing the risk of multiple myeloma bone disease (2015) (11)
Synthesis of chromatin proteins in resting and stimulated human lymphocyte populations. (1975) (11)
Impact of family history of cancer on risk and mortality of second cancers in patients with prostate cancer (2018) (11)
Differential responses of free and bound polysomes to inhibitors and neuroactive substances in vitro (1972) (11)
Common cancers share familial susceptibility: implications for cancer genetics and counselling (2016) (11)
Alkylation of anionic DNA bases by styrene 7,8-oxide (1999) (11)
Accumulation of calcium by retinal outer segments. (1975) (11)
Familial risks of psychotic disorders and schizophrenia among siblings based on hospitalizations in Sweden (2009) (11)
32P-postlabelling of bulky human DNA adducts enriched by different methods including immunoaffinity chromatography. (1996) (11)
Age-specific familial risks for renal cell carcinoma with evidence on recessive heritable effects. (2004) (10)
Does immigration play a role in the risk of gastric cancer by site and by histological type? A study of first-generation immigrants in Sweden (2011) (10)
Nuclear receptor coregulator SNP discovery and impact on breast cancer risk (2009) (10)
Second gastric cancers among patients with primary sporadic and familial cancers in Sweden (2006) (10)
Survival in colon and rectal cancers in Finland and Sweden through 50 years (2021) (10)
Second primary malignancies in females with primary fallopian tube cancer (2007) (10)
Interindividual variation in the level of DNA and protein adducts in humans (1991) (10)
Purification of surface membranes from immature brain cells. (1973) (10)
A bias in genotyping the ERBB2 (HER2) Ile655Val variant. (2005) (10)
Risk for incident and fatal prostate cancer in men with a family history of any incident and fatal cancer. (2012) (10)
Co-Morbidity between Early-Onset Leukemia and Type 1 Diabetes – Suggestive of a Shared Viral Etiology? (2012) (10)
FLUORESCENCE PROPERTIES OF ALKYLATED GUANINE DERIVATIVES (1981) (10)
N-nitrosodimethylamine and 7-methylguanine DNA adducts in tissues of rats fed Chinese salted fish. (1995) (10)
32P-postlabelling of DNA adducts in styrene oxide-modified DNA and in workers exposed to styrene. (1993) (10)
Multiple regions with allelic loss at chromosome 3 in superficial multifocal bladder tumors. (2001) (10)
Bleomycin‐induced chromosomal damage and shortening of telomeres in peripheral blood lymphocytes of incident cancer patients (2018) (10)
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma (2014) (10)
Progress in survival in renal cell carcinoma through 50 years evaluated in Finland and Sweden (2021) (10)
Re: Integrin β3 Leu33Pro Homozygosity and Risk of Cancer (2004) (10)
Re: "Familial risk of multiple sclerosis: a nationwide cohort study". (2006) (10)
The prevalence of loss of heterozygosity in chromosome 3, including FHIT, in bladder cancer, using the fluorescent multiplex polymerase chain reaction (2001) (10)
DNA adduct formation by tamoxifen and structurally-related compounds in rat liver (1998) (10)
The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias: Etiologic Implications (2016) (10)
Does the risk of stomach cancer remain among second-generation immigrants in Sweden? (2012) (10)
Risk of lung cancer by histology among immigrants to Sweden. (2012) (10)
Second primary malignancies among patients with soft tissue tumors in Sweden (2006) (10)
Human exposure to potentially carcinogenic compounds. (1984) (10)
Prostate cancer as a first and second cancer: effect of family history (2009) (10)
Polyglutamine repeat length in the NCOA3 does not affect risk in familial breast cancer. (2005) (10)
Genetic variation in ALCAM and other chromosomal instability genes in breast cancer survival (2011) (10)
Familial risks for eye melanoma and retinoblastoma: results from the Swedish Family-Cancer Database (2006) (10)
Familiar transmission of coronary heart disease: A cohort study of 80,214 Swedish adoptees linked to their biological and adoptive parents (2011) (10)
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer (2021) (10)
Heritability estimates on Hodgkin’s lymphoma: a genomic- versus population-based approach (2014) (10)
Second primary cancer after female breast cancer: Familial risks and cause of death (2018) (10)
Familial risks for hospitalization with endocrine diseases. (2008) (10)
Familial risks of second primary cancers and mortality in ovarian cancer patients (2018) (10)
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study (2018) (9)
The risk of contralateral breast cancer in daughters of women with and without breast cancer (2016) (9)
Future research directions in the use of biomarkers. (1996) (9)
Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients (2019) (9)
Ultraviolet photoproduct levels in melanocytic nevi and surrounding epidermis in human skin in situ. (2002) (9)
Mesothelioma is a killer of urban men in Sweden (2003) (9)
Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications. (2011) (9)
Second primary cancers in patients with invasive and in situ squamous cell skin carcinoma, Kaposi sarcoma and Merkel cell carcinoma: role for immune mechanisms? (2020) (9)
Characterization of proteins and glycoproteins of surface membranes isolated from immature brain cells. (1972) (9)
Functional germline variants in driver genes of breast cancer (2017) (9)
Risk of subsequent cancers in renal cell carcinoma survivors with a family history. (2014) (9)
Familial associations of lymphoma and myeloma with autoimmune diseases (2017) (9)
Excretion kinetics of the DNA adducts of cis-diamminedichloroplatinum(II) formed in vitro in rat urine. (1988) (9)
Polymorphisms within base and nucleotide excision repair pathways and risk of differentiated thyroid carcinoma. (2016) (9)
Assessment of methods and results of reproductive occupational epidemiology: spontaneous abortions and malformations in the offspring of working women (1983) (9)
Genetic epidemiology of colorectal cancer and associated cancers. (2020) (9)
Turnover of actin in rat brain. (1973) (9)
Significance of DNA and protein adducts. (1992) (9)
Effect of autoimmune diseases on mortality and survival in subsequent digestive tract cancers. (2012) (9)
Alteration of p53 gene structure and function in laryngeal squamous cell cancer (2006) (9)
Polymorphic insertion of additional repeat within an area of direct 8 bp tandem repeats in the 5'-untranslated region of the p53R2 gene and cancer risk. (2001) (9)
Separate deamination mechanisms for isomeric styrene oxide induced N1-adenine adducts. (1999) (9)
Risk of Kaposi sarcoma among immigrants to Sweden. (2014) (9)
Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach (2017) (9)
Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis. (2014) (9)
Telomere length in circulating lymphocytes: Association with chromosomal aberrations (2015) (9)
Labelling of histones and nonhistones in lung nuclear matrix and chromatin fractions. (1977) (9)
Quantitation of the 32P-postlabeling reaction using cyclic N1,N2 and C8 modified deoxyguanosine 3'-monophosphates as substrates. (1991) (9)
Survival in familial and non-familial breast cancer by age and stage at diagnosis. (2016) (9)
DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancer. (1999) (9)
VHL down-regulation and differential localization as mechanisms in tumorigenesis. (2003) (9)
Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis (2020) (9)
Power and limits of modern cancer diagnostics: cancer of unknown primary. (2012) (9)
Second cancer risk following Hodgkin lymphoma (2017) (9)
NBN and XRCC3 genetic variants in childhood acute lymphoblastic leukaemia. (2014) (9)
STR Markers for Kinship Analysis (2006) (9)
Identification of miRSNPs associated with the risk of multiple myeloma (2017) (9)
DNA damage, DNA repair rates and mRNA expression levels of cell cycle genes (TP53, p21(CDKN1A), BCL2 and BAX) with respect to occupational exposure to styrene. (2011) (8)
Increased frequency of LOH on chromosome 9 in sporadic primary melanomas is associated with increased patient age at diagnosis. (2000) (8)
A simple-to-use method incorporating genomic markers into prostate cancer risk prediction tools facilitated future validation. (2015) (8)
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells (2015) (8)
Assessment of cancer hazard from environmental pollution in Silesia. (1996) (8)
Re: markers of DNA repair and susceptibility to cancer in humans: an epidemiologic review. (2000) (8)
Second primary cancers in non‐Hodgkin lymphoma: Family history and survival (2020) (8)
Loss of heterozygosity and microsatellite instability in larynx cancer. (1997) (8)
Risk of thyroid cancer in relatives of patients with medullary thyroid carcinoma by age at diagnosis. (2013) (8)
Sensitive 32P-HPLC technique shows base sequence dependent differences in photolesion repair in human keratinocytes. (1998) (8)
Familial associations of male breast cancer with other cancers (2017) (8)
Modification of risk for subsequent cancer after female breast cancer by a family history of breast cancer (2008) (8)
MyelomA Genetics International Consortium (2012) (8)
Importance of tumor location and histology in familial risk of upper gastrointestinal cancers: a nationwide cohort study (2018) (8)
Impact of immigration on HIV-1 molecular epidemiology in West Africa, Maghreb and Southern Europe. (2014) (8)
Reactivity, SCE induction and mutagenicity of benzyl chloride derivatives (1983) (8)
Binding of the estradiol receptor to hen oviduct nuclei and chromatin. (1976) (8)
Use of Monozygotic Twins in Search for Breast Cancer Susceptibility Loci (2001) (8)
Alkylation of rat serum proteins by dimethylnitrosamine and acetylaminofluorene. (1980) (8)
Genetic variation associated with chromosomal aberration frequency: A genome‐wide association study (2018) (8)
Incidence of multiple primary malignancies among patients with bone cancers in Sweden (2006) (8)
genes are major targets for inactivation (2002) (8)
Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans (2014) (8)
Stability of 7-alkyldeoxyguanosines of trichloropropylene oxide, epichlorohydrin and glycidol. (2009) (8)
Aromatic deoxyribonucleic acid adducts in white blood cells of foundry and coke oven workers. (1988) (8)
Kinetics of reaction of cis-diamminedichloroplatinum(II) with DNA. (1989) (8)
Epistatic effect of TLR3 and cGAS‐STING‐IKKε‐TBK1‐IFN signaling variants on colorectal cancer risk (2019) (8)
Mortality causes in cancer patients with type 2 diabetes mellitus (2012) (8)
Association of colorectal adenoma with other malignancies in Swedish families (2008) (8)
Familial risk of pleural mesothelioma increased drastically in certain occupations: A nationwide prospective cohort study. (2018) (8)
Chromatin proteins of large and small brain nuclei (1976) (8)
Mono- and bifunctional binding of cis-diamminedichloroplatinum(II) to dinucleotides. (1987) (8)
Parental cancer as a risk factor for bone cancer: a nation-wide study from Sweden. (2002) (8)
Correspondence: SEMA4A variation and risk of colorectal cancer (2016) (8)
Risk of familial breast cancer is not increased after pregnancy (2008) (8)
Second primary malignancies among women with uterine sarcoma. (2012) (8)
Use of chemical, biochemical, and genetic markers in cancer epidemiology and risk assessment. (1992) (8)
Sites of reaction of propane sultone with guanosine and DNA. (1983) (8)
Risk of second primary cancers after malignant mesothelioma and vice versa. (2016) (8)
Protein composition of chromatin subfractions prepared from chick embryos. (1977) (7)
Quantitative estimation and prediction of cancer risk: review of existing activities. (1999) (7)
Familial associations of monoclonal gammopathy of unknown significance with autoimmune diseases (2016) (7)
Occupational cancer and carcinogenesis. (1981) (7)
Incidence, mortality and survival in malignant pleural mesothelioma before and after asbestos in Denmark, Finland, Norway and Sweden (2021) (7)
An estimation of the exposure of the population in Finland to suspected chemical carcinogens (1983) (7)
OCCUPATIONAL EXPOSURE TO ANTICANCER DRUGS (1985) (7)
Finnish and Swedish genotypes and risk of cancer in Sweden (2003) (7)
Unique properties of cisplatin in reactions with nucleophiles. (1986) (7)
Use of DNA adducts in the assessment of occupational and environmental exposure to carcinogens. (1991) (7)
Re: Sunscreen use and duration of sun exposure: a double-blind, randomized trial. (1999) (7)
Determination of cis-diamminedichloroplatinum (II) in plasma proteins and hemoglobin of cancer patients (1989) (7)
Alkylation of guanosine and 4-(p-nitrobenzyl)-pyridine by styrene oxide analogues in vitro (1981) (7)
A population-based assessment of the clustering of breast cancer in families eligible for testing of BRCA 1 and BRCA 2 mutations (2005) (7)
Incidence trends in lung and bladder cancers in the Nordic Countries before and after the smoking epidemic (2021) (7)
Associated cancers in parents and offspring of polycythaemia vera and myelofibrosis patients (2009) (7)
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases (2012) (7)
Thalassemia and sickle cell anemia in Swedish immigrants: Genetic diseases have become global (2015) (7)
Do GST Polymorphisms Modulate the Frequency of Chromosomal Aberrations in Healthy Subjects? (2009) (7)
Genotoxicity of epoxides and epoxy compounds. (1984) (7)
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts (2017) (7)
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk (2009) (7)
Kinetics of hydrolysis in vitro of nornitrogen mustard, a metabolite of phosphoramide mustard and cyclophosphamide (1987) (7)
Consideration of family history of cancer in medical routine: a survey in the primary care setting in Germany (2014) (7)
Multiple melanomas after treatment for Hodgkin lymphoma in a non-Dutch p16-Leiden mutation carrier with 2 MC1R high-risk variants. (2006) (7)
Determination of cisplatin in blood compartments of cancer patients. (1988) (7)
Do Reproductive Factors Influence T, N, and M Classes of Ductal and Lobular Breast Cancers? A Nation-Wide Follow-Up Study (2013) (7)
Development of a 32P-postlabeling assay for 7-methylguanines in human DNA. (1993) (7)
Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor (2020) (7)
A population-based assessment of the clustering of breast cancer in families eligible for testing of BRCA1 and BRCA2 mutations. (2005) (7)
Inherited variants in genes somatically mutated in thyroid cancer (2017) (7)
Formation of phosphodiesters in thymidine monophosphate by styrene oxide. (1984) (7)
Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer (2021) (7)
Increased cancer risk in the offspring of women with colorectal carcinoma (2001) (7)
Familial risks for gallstones in the population of Sweden (2017) (7)
Simultaneous detection of the exon 10 polymorphism and a novel intronic single base insertion polymorphism in the XPD gene using single strand conformation polymorphism. (2003) (7)
Incidence, mortality and survival in multiple myeloma compared to other hematopoietic neoplasms in Sweden up to year 2016 (2021) (7)
Contribution of the Defective BRCA1, BRCA2 and CHEK2 Genes to the Familial Aggregation of Breast Cancer: a Simulation Study Based on the Swedish Family-Cancer Database (2004) (7)
Measurement of 7-methyl- and 7-(2-hydroxyethyl)-guanine DNA adducts in white blood cells of smokers and non-smokers (1998) (7)
The molecular epidemiology of oncoproteins. Serum p53 protein in patients with asbestosis. (1996) (7)
Pedigree based DNA sequencing pipeline for germline genomes of cancer families (2016) (7)
Modification of cancer risk in offspring by parental cancer (Sweden) (2004) (7)
Levels of DNA damage (Micronuclei) in patients suffering from chronic kidney disease. Role of GST polymorphisms. (2018) (7)
DNA adduct formation by tamoxifen and structurally-related compounds in rat liver. (1997) (7)
Loci associated with genomic damage levels in chronic kidney disease patients and controls. (2020) (7)
A novel polymorphism (‐88 C>A) in the 5′ UTR of the p53R2 gene (2001) (7)
Familial Ovarian Cancer Clusters with Other Cancers (2018) (7)
Covalent binding of styrene oxide to amino acids, human serum proteins and hemoglobin. (1986) (7)
Cytogenetic aberrations in multiple myeloma are associated with shifts in serum immunoglobulin isotypes distribution and levels (2018) (6)
High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk (2007) (6)
Familial risks in and between stone diseases: sialolithiasis, urolithiasis and cholelithiasis in the population of Sweden (2018) (6)
Familial Clustering, Second Primary Cancers and Causes of Death in Penile, Vulvar and Vaginal Cancers (2019) (6)
Gene–Environment Interactions in Cancer (2006) (6)
How fast are UV-dimers repaired in human skin DNA in situ? (2002) (6)
Familial risk for colon and rectal cancers (2004) (6)
Characterization of the major DNA adducts in the liver of rats chronically exposed to tamoxifen for 18 months. (2000) (6)
Breast Cancer Histology in Immigrants to Sweden: Do Ethnic Differences Exist? (2012) (6)
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. (2019) (6)
Some quantitative considerations about DNA adduct enrichment procedures for 32P-postlabelling. (1992) (6)
Analysis of deoxyribonucleic acid adducts in workers. (1992) (6)
Survival trends in solid cancers in the Nordic countries through 50 years. (2022) (6)
DNA adducts and other biological markers in risk assessment for environmental carcinogens. (1991) (6)
DNA adducts in environmental, occupational and life-style studies in human biomonitoring. (1996) (6)
Shared familial risk factors between cancer and RA patients. (2007) (6)
Reactions of beta-propiolactone, beta-butyrolactone and gamma-butyrolactone with nucleic acids. (1981) (6)
Macromolecular adducts and related biomarkers in biomonitoring and epidemiology of complex exposures. (1990) (6)
A 32P-postlabelling assay for DNA adducts induced by cis-diamminedichloroplatinum(II). (1994) (6)
Familial association of leukemia with colorectal cancer. (2004) (6)
Alkylation of nucleic acid bases by epoxides and glycidyl ethers. (1980) (6)
Familial Associations of Colorectal Cancer with Other Cancers (2017) (6)
Association of genetic polymorphisms in ESR 2 , HSD 17 B 1 , ABCB 1 , and SHBG genes with colorectal cancer risk (2011) (6)
Collection and use of family history in oncology clinics. (2014) (6)
Familial risks for diseases of myoneural junction and muscle in siblings based on hospitalizations and deaths in sweden. (2006) (6)
In vitro characterization of DNA adducts formed by foundry air particulate matter. (1996) (6)
Long- and medium-term carcinogenicity studies in animals and short-term genotoxicity tests. (1999) (6)
Joint occurrence of Merkel cell carcinoma and non-Hodgkin lymphomas in four Nordic countries (2015) (6)
Molecular analysis of occupational cancer: infrequent p53 and ras mutations in renal‐cell cancer in workers exposed to gasoline (1997) (6)
Re: Risk of subsequent cancer following breast cancer in men. (2002) (6)
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP 13 with familial breast cancer (2006) (6)
Nervous system tumors in adult immigrants to Sweden by subsite and histology (2011) (6)
Evidence of Inbreeding in Hodgkin Lymphoma (2016) (6)
Familial associations for rheumatoid autoimmune diseases (2020) (6)
DNA adducts in experimental cancer research (1986) (6)
Coding variants in NOD-like receptors: An association study on risk and survival of colorectal cancer (2018) (6)
Familial myeloid leukemias from the Swedish Family-Cancer Database. (2002) (6)
Reaction products of styrene oxide with deoxynucleosides and DNA in vitro. (1986) (6)
Multiple myeloma: family history and mortality in second primary cancers (2018) (6)
Use of twins in search for tumor suppressor genes (1997) (6)
Increase in Years of Life after Eliminating Causes of Death: Significance for Health Priorities (1976) (6)
Influence of family history on risk of second primary cancers and survival in patients with squamous cell skin cancer (2019) (5)
Second Primary Cancers After Liver, Gallbladder and Bile Duct Cancers, and These Cancers as Second Primary Cancers (2021) (5)
Quantitative aspects of 32P-postlabeling. (1991) (5)
Serum growth factors in asbestosis patients (2009) (5)
Environmental Carcinogens: Assessment of Exposure and Effect (1993) (5)
Synthesis of RNA containing polyadenylic acid in resting and stimulated human lymphocytes. (1975) (5)
Characterization of rare germline variants in familial multiple myeloma (2020) (5)
Carbon disulfide is not mutagenic in bacteria or Drosophila. (1981) (5)
Urinary excretion products of formaldehyde in the rat. (1984) (5)
Phosphodiester cleavage in apurinic dinucleotides. (1988) (5)
Telomere length in peripheral blood lymphocytes related to genetic variation in telomerase, prognosis and clinicopathological features in breast cancer patients. (2020) (5)
Inbreeding and homozygosity in breast cancer survival (2015) (5)
Exposure limits and medical surveillance in occupational health. (1982) (5)
Myeloproliferative disorders in Sweden: Incidence trends and multiple tumors. (2009) (5)
Linking data to study reproductive effects of occupational exposures. (1986) (5)
[Environmental and genetic causes of cancer]. (2000) (5)
Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer. (2004) (5)
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer (2021) (5)
The non-random distribution of UV-induced photoproducts in the nuclear matrix and non-matrix DNA fractions. (1996) (5)
Familial Cancer: How to Successfully Recruit Families for Germline Mutations Studies? Multiple Myeloma as an Example. (2019) (5)
Prescription of antimicrobial drugs by general practitioners (1974) (5)
32P-postlabelling analysis of 1,3-butadiene-induced DNA adducts in vivo and in vitro (2000) (5)
Familial cancer risks in affected sibships: Results from the Swedish Family‐Cancer Database (2000) (5)
Familial risks for hospitalized Graves' disease and goiter. (2009) (5)
Familial Associations of Colon and Rectal Cancers With Other Cancers (2019) (5)
Distribution of estrogen receptors in subfractions of hen oviduct chromatin. (1976) (5)
Breast cancer genomics based on biobanks. (2011) (5)
Incidence Differences Between First Primary Cancers and Second Primary Cancers Following Skin Squamous Cell Carcinoma as Etiological Clues (2020) (5)
Dose-dependence and stability of cisplatin binding to tissue DNA and blood proteins in rats. (1989) (5)
32P-postlabelling with high-performance liquid chromatography for analysis of abundant DNA adducts in human tissues. (1999) (5)
Incidence and survival in oral and pharyngeal cancers in Finland and Sweden through half century (2022) (4)
Protein binding, sister chromatid exchange and expression of oncogene proteins in patients treated with cisplatinum (cisDDP)-based chemotherapy (1990) (4)
Transplacental Toxicity of Environmental Chemicals (1986) (4)
Quantitative and kinetic examination of 32P-postlabeling of etheno-substituted nucleotides. (1991) (4)
Long‐term incidence and survival trends in cancer of the gallbladder and extrahepatic bile ducts in Denmark, Finland, Norway and Sweden with etiological implications related to Thorotrast (2022) (4)
Short article: Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy (2018) (4)
Long Non-Coding RNA and microRNA Interplay in Colorectal Cancer and Their Effect on the Tumor Microenvironment (2022) (4)
Synthesis of oviduct nuclear and chromatin proteins during steroid induced differentiation. (1975) (4)
Incorporation of 3 H-leucine into insoluble proteins of neuronal and glial cell fractions in vitro. (1973) (4)
Is risk of pleural mesothelioma an environmental risk outside Turkey? A study on immigrants to Sweden. (2010) (4)
Surveying germline genomic landscape of breast cancer (2009) (4)
Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (4)
The Genetic Basis of Cancer (2005) (4)
Brain cancers in siblings of salivary gland cancer patients suggest viral etiology? (2007) (4)
Specific radioactivities of protein discs in a polyacrylamide gel. (1971) (4)
The costs of diseases and violence in Finland in 1972. (1977) (4)
Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases (2020) (4)
Non-Hodgkin lymphoma in familial amyloid polyneuropathy patients in Sweden. (2013) (4)
GWAS-Identified Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer (2014) (4)
Measurement of cyclobutane thymidine dimers in melanocytic nevi and surrounding epidermis in human skin in situ. (2002) (4)
Incidence trends in bladder and lung cancers between Denmark, Finland and Sweden may implicate oral tobacco (snuff/snus) as a possible risk factor (2021) (4)
The 9 p 21 . 3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN 2 A (2015) (4)
Second primary cancers after cancer of unknown primary in Sweden and Germany: efficacy of the modern work-up (2013) (4)
Bladder and upper urinary tract cancers as first and second primary cancers (2021) (4)
Estrogen receptors and ovalbumin genes in hen oviduct chromatin fractions. (1976) (4)
Chromosomal damage and telomere length in peripheral blood lymphocytes of cancer patients. (2020) (4)
Correlation analysis of production and photoisomerization of epidermal urocanic acid versus induction and repair of DNA photoproducts in the human skin in situ. (2002) (4)
Is family history associated with improved survival in patients with gastric cancer? (2012) (4)
Genetic and Environmental Factors in Carcinogenesis (2003) (4)
Search for AL amyloidosis risk factors using Mendelian randomization. (2021) (4)
Methylation of neuronal and glial macromolecules by methylnitrosourea and dimethylnitrosamine in vivo (1979) (4)
Incidence differences for gallbladder cancer between occupational groups suggest an etiological role for alcohol (2005) (4)
32P-postlabeling of 7-methylguanine adducts in DNA. (1990) (4)
Correction: Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study (2018) (4)
International Journal of Cancer: Editorial (2009) (4)
Effects of colchicine and cytochalasin B on labelling and enzyme activities of brain plasma membranes. (1973) (4)
Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example (2020) (3)
Comparison of Familial Clustering of Anogenital and Skin Cancers Between In Situ and Invasive Types (2019) (3)
Toward a Better Working Life. international Evaluation of the Finnich Institute of Occupational health (1997-2003) (2004) (3)
Use of molecular biology techniques in cancer epidemiology. (1992) (3)
Long‐term incidence in hepatocellular carcinoma and intrahepatic bile duct cancer in Denmark, Finland, Norway and Sweden, role of Thorotrast? (2022) (3)
Survival trends in hematological malignancies in the Nordic countries through 50 years (2022) (3)
Familial Urinary Bladder Cancer with Other Cancers. (2018) (3)
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. (2021) (3)
Purification of surface membranes from rat brain cells. (1975) (3)
ARLTS1 polymorphisms and basal cell carcinoma of the skin (2007) (3)
Survival in bladder and upper urinary tract cancers in Finland and Sweden through 50 years (2022) (3)
Familial risks in understanding type 1 diabetes genetics (2012) (3)
Rearrangement and Deletion of the PAX5 Gene in Pediatric Acute B-Cell Lineage Lymphoblastic Leukemia. (2007) (3)
GSTM1 AND NAT2 GENETIC POLYMORPHISMS AND EXPOSURE TO TOBACCO SMOKE IN NONSMOKING AND SMOKING LUNG CANCER PATIENTS AND POPULATION CONTROLS (1998) (3)
Significance of DNA adduct studies in the early phase of carcinogenesis (1994) (3)
Lifestyle and Cancer (2003) (3)
Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer (2007) (3)
Do inflammatory bowel disease and cancer share susceptibility: a family study. (2008) (3)
Epidemiological and experimental applications to occupational cancer prevention. (1989) (3)
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1 (2020) (3)
Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer (2021) (3)
Serum epidermal growth factor receptor and p53 as predictors of lung cancer risk in the ATBC study. (1999) (3)
Familial Risks Between Urolithiasis and Cancer (2018) (3)
B‐RAF mutations in tumors from melanoma‐breast cancer families (2005) (3)
Comparison of Six Statistics of Genetic Association Regarding Their Ability to Discriminate between Causal Variants and Genetically Linked Markers (2011) (3)
Re: characterization of hereditary nonpolyposis colorectal cancer families from a population-based series of cases. (2001) (3)
Measurement and Monitoring of Individual Exposures (1990) (3)
Familial Risks for Diseases of Myoneural Junction and Muscle in Siblings Based on Hospitalizations and Deaths in Sweden (2006) (3)
Does immigration play a role in the risk of pancreatic cancer? A study on immigrants to Sweden. (2010) (3)
Association between tumor characteristics and second primary cancers with cutaneous melanoma survival: A nationwide cohort study (2020) (3)
TERT promoter mutations in actinic keratosis before and after treatment (2020) (3)
Cervical, vaginal and vulvar cancer incidence and survival trends in Denmark, Finland, Norway and Sweden with implications to treatment (2022) (3)
Incorporation of radioactive leucine and fucose in brain plasma membrane proteins fractionated by polyacrylamide gel electrophoresis. (1974) (3)
Risk of cancer of unknown primary among immigrants to Sweden (2012) (3)
Histological concordance in familial central nervous system tumors: Evidence from nationwide Swedish Family-Cancer Database. (2015) (3)
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden (2021) (3)
Binding of benzo(a)pyrene into lung and thymocyte nuclear fractions. (1979) (3)
Shared susceptibility for celiac disease and inflammatory bowel disease? (2008) (3)
Epidemiology, Risk Factors, and Survival in CUP: Pointers to Disease Mechanisms (2016) (3)
Ancestral susceptibility to colorectal cancer. (2012) (3)
Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer (2021) (3)
Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK / ERK and PI 3 K / AKT Signaling Pathways (2019) (3)
Application of the 32P-postlabelling technique to detect DNA-adducts by cisplatin and methylating agents. (1990) (3)
Null Results in Brief Polyglutamine Repeat Length in the NCOA 3 Does Not Affect Risk in Familial Breast Cancer (2005) (3)
Re: "underlying genetic models of inheritance in established type 2 diabetes associations". (2010) (3)
Functional dissection of inherited non-coding variation influencing multiple myeloma risk (2022) (3)
Re: Hemminki,K., Dickey,C., Karlsson,S., Bell,D., Hsu,Y., Tsai,W.-Y., Mooney,L.A., Savela,K. and Perera,F.P. (1997) Aromatic DNA adducts in foundry workers in relation to exposure, lifestyle and CYP1A1 and glutathione transferase M1 genotype. Carcinogenesis, 18, 345-350. (2000) (3)
Re: Risks of cancer and families. (2006) (3)
Other cancers in lung cancer families are overwhelmingly smoking-related cancers (2017) (3)
Foreword: Euro-Mediterranean partnership and EUNAM. (2014) (3)
Familial Risks for Liver, Gallbladder and Bile Duct Cancers and for Their Risk Factors in Sweden, a Low-Incidence Country (2022) (3)
Polymorphisms within Autophagy-Related Genes Influence the Risk of Developing Colorectal Cancer: A Meta-Analysis of Four Large Cohorts (2021) (2)
Poly(A)-containing RNA in embryonic chick tissues. (1976) (2)
CTNNB1 mutations, TERT polymorphism and CD8+ cell densities in resected hepatocellular carcinoma are associated with longer time to recurrence (2022) (2)
Activated Hepatic Stellate Cells in Hepatocellular Carcinoma: Their Role as a Potential Target for Future Therapies (2022) (2)
Cancer Predisposition Genes in Cancer-Free Families (2020) (2)
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans. (2020) (2)
Family History of Head and Neck Cancers (2021) (2)
Formation of UV-photoadducts during DNA purification. (1995) (2)
Personal comorbidities and their subsequent risks for liver, gallbladder and bile duct cancers (2022) (2)
Genetics of inflammatory bowel disease: population aspects. (2008) (2)
Distribution of enzymes related to transmission in neurons and glia (1972) (2)
Labelling kinetics of RNA containing poly(a) in liver subcellular fractions (1975) (2)
Survival in Colon, Rectal and Small Intestinal Cancers in the Nordic Countries through a Half Century (2023) (2)
Incidence and survival in laryngeal and lung cancers in Finland and Sweden through a half century (2022) (2)
Long-term survival trends for primary liver and pancreatic cancers in the Nordic countries (2022) (2)
Second Primary Cancers in Melanoma Patients Critically Shorten Survival (2020) (2)
A rare large duplication of MLH1 identified in Lynch syndrome (2021) (2)
Preparation of surface membranes from isolated cells of newborn rat brain. (1973) (2)
Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Myeloma Patients? (2022) (2)
The challenges of understanding cancer of unknown primary (2013) (2)
Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis (2009) (2)
Special section editorial: Cancer incidence in five continents including Africa (2015) (2)
Screening detected prostate cancers in type 2 diabetics (2011) (2)
Detection of Methylation Damage in DNA of Gastric Cancer Tissues Using 32P‐Postlabelling Assay (1999) (2)
Trisomy 8q and partial trisomy 22 in a 43‐year‐old man with moderate intellectual disability, epilepsy and large cell non‐Hodgkin lymphoma (2006) (2)
What Is the Major Prognostic Factor in Tumor–Node–Metastasis Staging of Pancreatic Adenocarcinoma? (2010) (2)
Dimethylnitrosamine adducts excreted in rat urine. (1982) (2)
Demographic effects of the elimination of selected causes of death in Finland (Finnish) (1974) (2)
[Biological monitoring of exposure to carcinogens]. (1981) (2)
Pesticide residues in food: how much and how safe? (1982) (2)
Melanocortin receptor 1 variants and melanoma risk – a study on two European populations (2008) (2)
Borderline Ovarian Tumors Share Familial Risks with Themselves and Invasive Cancers (2018) (2)
Survival in common cancers defined by risk and survival of family members (2011) (2)
Population Landscape of Familial (2015) (2)
The influence of N-7 platination and methylation on the stability of deoxyguanosine and deoxyguanylyl-(3'-5')-deoxyguanosine. (1990) (2)
Controls need to be selected for the type of SNP study (2002) (2)
Use of monozygotic twins in search for breast cancer susceptibility loci. (2001) (2)
Abstract 2743: Cancer risk in relatives of testicular cancer patients by histology type and age at diagnosis: a joint study from five Nordic countries (2015) (1)
Prevalence of the GFI1-36N SNP in Multiple Myeloma Patients and Its Impact on the Prognosis (2021) (1)
Reproductive hazards in industry: Identification and prevention (1988) (1)
The Asthma Family Tree: Evaluating Associations Between Childhood, Parental, and Grandparental Asthma in Seven Chinese Cities (2021) (1)
Variants at the 9p21 locus and melanoma risk (2013) (1)
Use of registered data in studies of occupational exposure and pregnancy outcome (1988) (1)
Familial risks between giant cell arteritis and Takayasu arteritis and other autoimmune diseases in the population of Sweden (2020) (1)
Determination of the levels of cis-diammine-dichloroplatinum(II) in plasma proteins, hemoglobin and white cell DNA of cancer patients (1989) (1)
Types of second primary cancer influence overall survival in cutaneous melanoma (2021) (1)
Toxicity of rubber chemicals in the chicken embryo. How to interpret results from animal tests. (1983) (1)
32P-postlabelling of DNA adducts in white blood cells of foundry workers. (1989) (1)
Differential distribution of oestrogen receptors in subfractions of oviduct chromatin. (1977) (1)
T- and B-Cells in the Inner Invasive Margin of Hepatocellular Carcinoma after Resection Associate with Favorable Prognosis (2022) (1)
RE: Familial Cancer Clustering of Urothelial Cancer: A Population-Based Case-Control Study. (2018) (1)
[Estimation of aromatic DNA adduct levels in laryngeal tumors in relation to cancer staging]. (1995) (1)
Abstract 801: Chromosomal damage as markers of genotoxicity and carcinogenesis (2016) (1)
The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression (2018) (1)
Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2019) (1)
Tumour necrosis factor-a (TNF-a) in patients who have asbestosis and develop cancer (2005) (1)
Time to pregnancy among the wives of men exposed to inorganic lead (1999) (1)
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2018) (1)
Comparison of survival of patients with metastases from known versus unknown primaries: survival in metastatic cancer (2013) (1)
Erratum: Cheompreventative effect of dietary flavonoid morin on chemically induced rat tongue carcinogenesis. (International Journal of Cancer (1999) 83 (381-6)) (2001) (1)
Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer (2022) (1)
Subsequent cancers in patients diagnosed with cancer of unknown primary (CUP): etiological insights? (2012) (1)
Environment and genetics in the etiology of gastrointestinal tract cancers (2007) (1)
Special section editorial (2014) (1)
32P-postlabelling of aromatic DNA adducts in peripheral blood, lung and tumour tissue of lung cancer patients (1992) (1)
Repeat polymorphisms in ESR 2 and AR and colorectal cancer risk and prognosis : results from a German population-based case-control study (2014) (1)
Association between the B-RAF/N-RAS mutations, the CDKN2A alterations and the MC1R variants in melanoma (2006) (1)
Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium (2020) (1)
INTERNATIONAL COURSE ON HEALTH AND IMMIGRATION (2014) (1)
Family history of early onset acute lymphoblastic leukemia is suggesting genetic associations (2021) (1)
Sources, Nature and Levels of Indoor Air Pollutants (1993) (1)
GASTROINTESTINAL ATRESIAS AND BORRELIOSIS (1989) (1)
Polygenic susceptibility to papillary thyroid cancer: detection of the main genetic signature in Italian patients (2019) (1)
Correction: Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival (2019) (1)
Editorial (2009) (1)
[Pregnancy in health care personnel handling cancer medications]. (1986) (1)
Association of NCOA3 (AIB1) polymorphisms with breast cancer risk (2005) (1)
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations (2021) (1)
Survival in gastric and esophageal cancers in the Nordic countries through a half century. (2023) (1)
Comment on: Association of a common variant of the CASP8 gene with reduced risk of breast cancer. Author's reply (2005) (1)
Mutational risks of smoking. A review (1980) (1)
Search for familial clustering of cancer in monoclonal gammopathy of unknown significance (2016) (1)
Maternal and paternal transmission of type 2 diabetes (2011) (1)
Propylene oxide ( PO ) (1)
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2018) (1)
Cancer incidence among Finnish workers exposed to aromatic hydrocarbons. (1998) (1)
Clinical and molecular features associated with long-term survival of elderly patients with glioblastoma. (2017) (1)
Smoking and metabolism phenotype interact with inorganic arsenic in causing bladder cancer (2016) (1)
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma (2019) (1)
Intake of inorganic arsenic from food in hungary, Romania and Slovakia (2016) (1)
Causes of death in patients with extranodal cancer of unknown primary: searching for the primary site (2014) (1)
Utilization of energy reserves by cells isolated from newborn rat brain. (1974) (1)
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study (2022) (1)
Determinants of unfavorable presentation of primary cutaneous melanoma. (2011) (1)
Monitoring of telomere dynamics in peripheral blood leukocytes in relation to colorectal cancer patients’ outcomes (2022) (1)
An investigation of DNA damage and DNA repair in chemical carcinogenesis triggered by small-molecule xenobiotics and in cancer: Thirty years with the comet assay. (2022) (1)
Genetic variation in adipokine genes and risk of colorectal cancer (European Journal of Endocrinology vol. 160 (6) (933-940)) (2009) (1)
Familial Risk of Asthma for Children with Affected Family Members in Multiple Generations (2020) (1)
415: Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma (2014) (1)
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study (2018) (1)
Magnetic fields of video display terminals and spontaneous abortion (1993) (1)
Familial risks of age-related macular degeneration. (2011) (1)
Incidence and survival in oral and pharyngeal cancers in Finland and Sweden through half century (2022) (1)
The prospects of the development of the method for monitoring of occupational exposure to some alkylating agents. (1991) (1)
Cisplatin binding to plasma proteins and hemoglobin in cancer patients. (1989) (1)
Causes of death in patients with extranodal cancer of unknown primary (0)
List of Participants: Steering committee (*) and experts (in alphabetical order): (1998) (0)
Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients (2019) (0)
Expression Quantitative Trait Loci Reveal Regulatory Regions Important In The Pathogenesis of Multiple Myeloma (2013) (0)
Abstract 2740: Familial Hodgkin lymphoma by relationship, sex, age and histology: a joint study from five Nordic countries (2015) (0)
OP-JNCS180071 1..7 (2019) (0)
The association between genetically elevated polyunsaturated fatty acids and risk of cancer (2023) (0)
Abstract 2549: Familial risk of upper gastrointestinal cancers by tumor location (2016) (0)
Issue Information (2018) (0)
Issue Information (2019) (0)
Monitoring of workers in industries for exposure to carcinogens (1983) (0)
Genotype frequencies and risk estimates of polymorphisms related to T 2 D in the DACHS study population (2012) (0)
Np 63 α and YB-1 functional interaction regulates proliferation and survival of normal and transformed keratinocytes (2013) (0)
Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci (2016) (0)
[Effects of the working environment on fetuses]. (1982) (0)
Surveillance Bias in Cancer Risk After Unrelated Medical Conditions: Example Urolithiasis (2017) (0)
Understanding the agreement of histology of familial testicular tumors. (2010) (0)
Epidemiology and genetics of familial cancer (2017) (0)
with breast cancer risk (2006) (0)
Polymorphisms in the CRK gene and their association with breast cancer risk (2005) (0)
Issue Information (2019) (0)
Issue Information (2020) (0)
Effect of parental history of cancer on the development of second neoplasms after lymphoma at the same site than the parents (2008) (0)
Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (0)
Second Primary Cancers After Kidney Cancers, and Kidney Cancers as Second Primary Cancers (2021) (0)
P-070: A pleiotropy scan on multiple myeloma survival (2022) (0)
GWAS-Identi ﬁ ed Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer Epidemiology,Biomarkers&Prevention (2014) (0)
N-7 guanine DNA adducts, SSB and DNA repair determined in cell cultures treated with styrene and styrene oxide (1996) (0)
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family (2018) (0)
GENOME-WIDE ASSOCIATION STUDY OF HODGKIN LYMPHOMA IDENTIFIES HISTOLOGY-SPECIFIC ASSOCIATIONS AND TRANSCRIPTIONAL REGULATORS OF DISEASE SUSCEPTIBILITY (2017) (0)
Issue Information (2018) (0)
Disease Etiology And Prevention: Old And New Lessons From Immigrant Studies (2010) (0)
Contents Vol. 20, 2001 (2001) (0)
Issue Information (2019) (0)
Familial Associations in Testicular Cancer with Other Cancers (2018) (0)
CTNNB1 mutations, TERT polymorphism and CD8+ cell densities in resected hepatocellular carcinoma are associated with longer time to recurrence (2022) (0)
Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma (2022) (0)
CLEP_A_230149 105..112 (2020) (0)
Binding of Tubulin to Substituted Sepharose. (1976) (0)
Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2019) (0)
Genetic Epidemiology: Editorial (2001) (0)
Power and limits of modern cancer diagnostics: cancer of unknown primary. (2017) (0)
578 Biomerkers of susceptibility and DNA damage in humans exposed to chronic low level of ionizing radiation (2003) (0)
Survival patterns among Hodgkin lymphoma patients with a family history of lymphoma (2007) (0)
SIR of type 1 diabetes among second immigrations by parental birth region Parental birth region One parent from abroad Both parents from abroad (2010) (0)
' s response to reviews Transcription factor 7-like 2 ( TCF 7 L 2 ) variant is associated with familial breast cancer risk : a Title : case-control study (2006) (0)
DNA-bound polycyclic aromatic hydrocarbons in white blood cell DNA of foundry workers (1987) (0)
61 Influence of polymorphism-modified gene expression on breast cancer survival (2010) (0)
[Mutational hazards of smoking]. (1980) (0)
Family history of any cancer for childhood leukemia patients in Sweden (2021) (0)
Overview on population screening for carriers with germline BRCA mutation in China (2022) (0)
Are population level familial risks and germline genetics meeting each other? (2023) (0)
[Formaldehyde as an environmental toxin]. (1983) (0)
Biallelic Inactivation of Multiple Tumor Suppressors Is Associated with Early Relapse after Stem Cell Transplant in Newly Diagnosed Myeloma (2019) (0)
Theranostics Nanomedicine Applications for Colorectal Cancer and Metastasis: Recent Advances (2023) (0)
Survival in melanoma in the nordic countries into the era of targeted and immunological therapies. (2023) (0)
Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer (2021) (0)
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression? (2023) (0)
MPTH-23. LONG-TERM SURVIVAL WITH GLIOBLASTOMA IN THE ELDERLY (2016) (0)
[Risks in the work environment of medical personnel]. (1983) (0)
Issue Information (2018) (0)
Polymorphic microRNA binding sites within candidate genes are associated with the risk of colorectal cancer (2008) (0)
622 Genetics of familial cancer (2010) (0)
Hydrolysis and Rearrangement of O6-Substituted Guanosine Products Resulting from Reaction of Guanosine with Styrene Oxide. (1987) (0)
factor AKAP13 with familial breast cancer (2005) (0)
Familial Risks Between Urolithiasis and Cancer Hemminki , Kari 2018-0215 (0)
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2010) (0)
Correspondence re: Zheng et al, Haplotype of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study. 11: 640-645, 2002. (2003) (0)
Issue Information (2018) (0)
A rare large duplication of MLH1 identified in Lynch syndrome (2021) (0)
Role of the estradiol in the development of papillary thyroid carcinoma in women (2016) (0)
Incidence trends in bladder and lung cancers between Denmark, Finland and Sweden may implicate oral tobacco (snuff/snus) as a possible risk factor (2021) (0)
Title COGENT ( COlorectal cancer GENeTics ) : An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (0)
A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer (2021) (0)
SEMA 4 A variation and risk of colorectal cancer (2016) (0)
84 DNA repair, cell cycle control and risk of cancer (2003) (0)
Anticancer agents : qualitative and quantitative aspects (2019) (0)
In reply [6] (2005) (0)
Re: Multifocality in testicular germ cell tumors Y. Ehrlich, M. Konichezky, O. Yossepowitch and J. Baniel J Urol 2009, 181: 1114-1120. (2010) (0)
Subject Index Vol. 20, 2001 (2001) (0)
From exposure to target dose: Examples from occupational setting (1998) (0)
Familial Risks Between Urolithiasis and Cancer (2018) (0)
Abstract 2556: Family history of colorectal cancer in half-siblings as important as in siblings (2016) (0)
Kinetics of hydrolysis of nornitrogen mustard, a metabolite of phosphoramide mustard and cyclophosphamide (1987) (0)
Issue Information (2018) (0)
Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2019) (0)
SHORT REPORT Polymorphisms in the growth hormone receptor: A case-control study in breast cancer (2006) (0)
Correction: Inherited variants in genes somatically mutated in thyroid cancer (2018) (0)
New cancer susceptibility loci: Population and familial risks (International Journal of Cancer (2008) 123, (1726-1729)) (2009) (0)
Binding of benzo(a)pyrene into nuclear subfractions in rat tissues (1978) (0)
MON-486 Polygenic Susceptibility to Papillary Thyroid Cancer in Italian Subjects (2020) (0)
Issue Information (2020) (0)
Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia (0)
Binding for cis-diamminedichloroplatinum (II) to dinucleotides (1987) (0)
Edinburgh Research Explorer SEMA4A variation and risk of colorectal cancer (2018) (0)
Family History of Prostate Cancer During Rapidly Increasing Incidence (2009) (0)
Monitoring of aromatic DNA adducts in white blood cells of foundry workers by 32P-postlabelling (1989) (0)
Correction: Familial risks of ovarian cancer by age at diagnosis, proband type and histology (2018) (0)
Recommendations for Selected IARC-Classified Agents (2010) (0)
Overview on health research ethics in North Africa (2022) (0)
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6 (2022) (0)
GWAS-Identified Variants for Obesity Do Not Influence the Risk of Developing Multiple Myeloma: A Population-Based Study and Meta-Analysis (2023) (0)
Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients (2018) (0)
CORDBLOOD ACRYLAMIDE AND GLYCIDAMIDE HAEMOGLOBIN ADDUCTS, METABOLIC POLYMORPHISMS AND MICRONUCLEUS FREQUENCY (2011) (0)
Genetic Epidemiology?Science and Ethics on Familial Cancers, (2001) (0)
Alkylation of DNA bases by epoxides: propylene oxide, glycidol, epichlorohydrin, trichloropropylene oxide and styrene oxide (1980) (0)
Issue Information (2019) (0)
Determining the Appropriate Risk-Adapted Screening Age for Familial Breast Cancer. (2020) (0)
Profound impact of sample processing delay on gene expression of multiple myeloma plasma cells (2015) (0)
Clinical prognostic markers of non-seminomatous germ cell tumours: an insight from Swedish Family-Cancer Database. (2010) (0)
Genetic signature of differentiated thyroid carcinoma susceptibility: a machine learning approach (2022) (0)
Exchange of brain organelle proteins with soluble cytoplasmic proteins in vitro. (1972) (0)
exposed to organic solvents . Time to pregnancy among the wives of men (1998) (0)
Methodological issues m the use of biomarkers (1995) (0)
Incidence, Mortality and Survival Trends in Breast Cancers Coincident with Introduction of Mammography in the Nordic Countries (2022) (0)
Meeting abstracts from the Annual Conference on Hereditary Cancers 2016 (2017) (0)
Familial Ovarian Cancer Clusters with Other Cancers (2018) (0)
Subject Index Vol. 29, 2007 (2007) (0)
Deregulation of critical cell cycle regulatory genes in melanocytic nevi with the B-RAF V600E mutation (2006) (0)
Association between TAS2R38 gene polymorphisms and colorectal cancer risk (2011) (0)
Erratum: Power and limits of modern cancer diagnostics: Cancer of unknown primary [Ann Oncol, 23, (2012), (760-764)] doi:10.1093/annonc/mdr369 (2017) (0)
Detection of DNA adducts by postlabelling with 3H-acetic anhydride. (1988) (0)
Issue Information (2018) (0)
Autoimmune diseases as comorbidities for liver, gallbladder, and biliary duct cancers in Sweden (2023) (0)
Reactivity and guanosine adducts of alkylating cytostatic drugs (1983) (0)
Development of a 32 P-Postlabeling Assay for 7-Methylguanines in Human DNA by Riitta Mustonen , ' Asta Forsti , Paivi Hietanen , 2 and Kari Hemminki (2006) (0)
Testicular and prostate cancers: genetic and environmental factors (2010) (0)
Familial Associations of Colorectal Cancer with Other Cancers (2017) (0)
Determination of adducts between styrene oxide and N-7 guanine with acetylation method in vitro (1987) (0)
Labelling of oviduct nuclear and nucleolar proteins during estrogen induced differentiation (1976) (0)
Molecular Analysis of Breast Cancer in MZ Twins (2001) (0)
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes (2019) (0)
and SHBG genes with colorectal cancer risk 2 (2011) (0)
Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population (2016) (0)
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (2017) (0)
Report from the working group on occupational cancer. (1993) (0)
Quantitative Estimation and Prediction of Risk at the International Agency for Research on Cancer (1994) (0)
Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example (2020) (0)
Risk of NextMelanoma in PatientsWith Familial and SporadicMelanoma by Number of PreviousMelanomas (2015) (0)
Epidemiology of Amyloidosis and Genetic Pathways to Diagnosis and Typing (2021) (0)
GBV-C in HIV-HCV Coinfection, Low Liver-Related Mortality But High Overall Mortality (2008) (0)
Abstract 5524: Prostate cancer risk assessment model (PCRAM): a scoring model based on the Swedish Family-Cancer Database (2012) (0)
DNA adducts and genotypes of drug metabolizing enzymes in workers exposed to PAH and styrene (1994) (0)
Characterization of rare germline variants in familial multiple myeloma (2021) (0)
indicating time-place cluster inFinland in 1970-79, (1988) (0)
Relationship between DNA adduct level in larynx and cancer staging in larynx tissues (1996) (0)
Survival patterns among chronic lymphocytic leukemia and other lymphoma patients with family history of lymphoma (2007) (0)
ARLTS 1 polymorphisms and basal cell carcinoma of the skin (2007) (0)
Early effects of estrogen on the synthesis of oviduct nuclear proteins. (1977) (0)
Prevalence of overweight and obesity in adults from (2014) (0)
Issue Information (2019) (0)
Abstract 1290: Survival in familial breast cancer: Novel findings based on a nationwide prospective cohort study (2014) (0)
Cervical, vaginal and vulvar cancer incidence and survival trends in Denmark, Finland, Norway and Sweden with implications to treatment (2022) (0)
Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338)) (2010) (0)
Long‐term survival trends in solid cancers in the Nordic countries marking timing of improvements (2022) (0)
Chromosome 7p11.2(EGFR) and 7q36.1(XRCC2) variants influence glioma risk (2011) (0)
Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera (2017) (0)
Smoking Overlooked as an Important Risk Factor for Squamous Cell Carcinoma—Reply (2004) (0)
A novel germline mutation in the POT1 gene predisposes to familial non-medullary thyroid cancer (2020) (0)
Abstract 1832: Associations between ovarian cancer and other malignant neoplasms in an international population-based study (2010) (0)
Use of exposure information and animal cancer data in the prevention of environmental and occupational cancer. (1991) (0)
Contents Vol. 29, 2007 (2007) (0)
Advances in Brief Ultraviolet B-induced DNA Damage in Human Skin and Its Modulation by a Sunscreen 1 (2006) (0)
New developments in the 32P-postlabelling analysis of DNA adducts (1998) (0)
945: Increased overall risk of cancer in patients with type 2 diabetes mellitus, but not their siblings or spouses (2014) (0)
Alterations of CDKN2A, p53 and related cell cycle regulatory genes in esophageal squamous cell carcinoma (2001) (0)
The impact of hormone replacement therapy on the incidence of breast cancer in Norway (2005) (0)
PO-057 Genetic interaction and pathway based discovery of key regulators in multiple myeloma (2018) (0)
Genotoxicity of tobacco smoke demonstrated by molecular alterations leading to larynx cancer (1998) (0)
Influence of human TLR and NLR genetic variants on colorectal cancer - involvement of commensal bacterial detection, gut immunity or microbiome diversity? (HUM1P.311) (2015) (0)
IDENTIFICATION AND FUNCTIONAL CHARACTERIZATION OF GERMLINE GENETIC VARIANTS PREDISPOSING TO DIFFERENTIATED THYROID CANCER RISK (2020) (0)
Second primary cancers among individuals with rare skin tumors may provide etiologic clues (2007) (0)
CLINICAL STUDY Genetic variation in adipokine genes and risk of colorectal cancer (2009) (0)
Genome-wide investigation of gene–environment interactions in colorectal cancer (2012) (0)
Influence of family history on risk of second primary cancers and survival in squamous cell skin cancer patients (2019) (0)
VI.5 Tamoxifen-DNA Adducts in Breast Cancer Patients (1998) (0)
Abstract 4578: Excision DNA repair: a biomarker of colorectal cancer onset and its chemotherapy (2015) (0)
Familial Risks for Main Neurological Diseases in Siblings Based on Hospitalizations in Sweden (2006) (0)
MAMMOGRAPHIC SCREENING AND THE INCIDENCE OF BREAST CANCER (2017) (0)
Issue Information (2019) (0)
Risk Of Second Malignant Neoplasms After Rare Childhood Solid Tumors: Up To 50 Years Of Follow-Up In 11 Countries (2010) (0)
Abstract 2855: Estrogen transport, metabolism, binding and signalling related single nucleotide polymorphisms modulate menopausal hormone therapy effect on risk of colorectal cancer (2010) (0)
[Molecular epidemiology--applications in cancer research]. (1992) (0)
Repeat polymorphisms in ESR2 and ARand colorectal cancer risk and prognosis: results from a German population-based case-control study (2014) (0)
Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology (2018) (0)
Runs of homozygosity and inbreeding in thyroid cancer (2016) (0)
PPARGC1A, PPARGC1B and EP300 with familial breast cancer (2006) (0)
Are Twins at Risk of Cancer: Results From the Swedish Family-Cancer Database (2005) (0)
Re: Mark N. Brook, Holly Ní Raghallaigh, Koveela Govindasami, et al. Family History of Prostate Cancer and Survival Outcomes in the UK Genetic Prostate Cancer Study. Eur Urol 2023;83:257-66. (2023) (0)
Identification of candidate predisposing factors in familial polycythemia vera with exome sequencing (2016) (0)
O XVI B.1 DNA adduct studies in human populations (1997) (0)
Issue Information (2018) (0)
Abstract 559: Patterns ofTelomerase reverse transcriptase(TERT) promoter mutations in melanoma and bladder cancer (2014) (0)
Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (2019) (0)
Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk (2022) (0)
Imatinib Mesylate May Improve Fasting Blood Glucose in Diabetic Ph Chronic Myelogenous Leukemia Patients Responsive to Treatment (2013) (0)
Author’s response to reviews Title: INFORMING PATIENTS ABOUT THEIR MUTATION TESTS: CDKN2A c.256G>A IN MELANOMA AS AN EXAMPLE Authors: (2020) (0)
Author ' s response to reviews Title : Influence of family size and birth order on risk of cancer : a population-based study (2010) (0)
Familial associations for Addison’s disease and between Addison’s disease and other autoimmune diseases (2020) (0)
Malignant Melanoma–a Genetic Overview (2009) (0)
Reply to “No major impact of mammography screening on the age specific incidence rates of breast cancer in the Netherlands” (2006) (0)
Brief report Veriﬁcation of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood (2010) (0)
Issue Information (2019) (0)
Alkylation of DNA bases by epoxides (1980) (0)
Risk of second cancers among people with thyroid cancer - treatment effects or common aetiology? (2005) (0)
Abstract 4172: Identification of familial Hodgkin lymphoma predisposing genes by whole genome sequencing (2019) (0)
7503-114079-1-Sp (2016) (0)
Response to letter entitled: Re: Survival trends in solid cancers in the Nordic countries through 50 years. (2023) (0)
Issue Information (2017) (0)
A novel polymorphism (-88 C>A) in the 5′ UTR of the p53R2 gene Communicated by Mark H. Paalman Online Citation: Human Mutation, Mutation and Polymorphism Report #200 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr200.pdf Acknowledgments: This work was supported by a research grant (2001) (0)
[Life expectancy of the population and the influence of most occuring causes of death]. (1974) (0)
Abstract 23: Functional DNA repair tests and their perspectives in molecular epidemiology (experience with subjects exposed to carcinogens and in cancer patients). (2012) (0)
Multiple myeloma: family history and mortality in second primary cancers (2018) (0)
Pedigree based DNA sequencing pipeline for germline genomes of cancer families (2016) (0)
[Nerve cell connections]. (1975) (0)
59 Colorectal cancer: candidate gene approach using obesity associated genes that show ancestral susceptibility (2010) (0)
Null Results in Brief GWAS-Identi fi ed Common Variants for Obesity Are Not Associated with the Risk of Developing Colorectal Cancer (2014) (0)
Explorer COGENT ( COlorectal cancer GENeTics ) : an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2017) (0)
Biologic Markers inRiskAssessment forEnvironmental Carcinogens (1991) (0)
RNA metabolism in chick oviduct during oestrogen stimulation. (1976) (0)
Single nucleotide polymorphisms within Mucin-type O-glycan genes are associated with colorectal cancer survival. (2018) (0)
Functional germline variants in driver genes of breast cancer (2017) (0)
The development of an ELISA for the detection of styrene-oxide-modified DNA (1983) (0)
Response: Methods for second primary cancers evaluation have to be standardized (2017) (0)
Issue Information (2018) (0)
Colorectal cancer risk and patients’ survival: influence of polymorphisms in genes somatically mutated in colorectal tumors (2014) (0)
Survival in Lung Cancer in the Nordic Countries Through A Half Century (2023) (0)
Reply from Authors re: Marc C. Smaldone, Veda N. Giri, Robert G. Uzzo. Familial Clustering of Sporadic Kidney Cancer: Insufficient Evidence to Recommend Routine Screening in Unaffected Kin. Eur Urol 2011;60:994–5 (2011) (0)
Increase in Years of Life after Eliminating Causes of Death: Significance for Health Priorities (1976) (0)
Abstract 2625: Is familial risk of cancer limited to relatively early onset cases (2012) (0)
Aurora-A Polymorphisms in Multiple Myeloma: Implications On Chromosomal Instability (2012) (0)
Polylysine titration of rat liver chromatin fractions after DNase II digestion. (1977) (0)
IS 21 Identification of very small embryonic like ( VSEL ) stem cells in adult bone marrow — implications for aging (2007) (0)
955: Functional germline variants in driver genes of breast cancer (2014) (0)
[Reduction of the mortality rate in traffic acciddent in 1974 compared with the mortality rate in tuberculosis and with infant death]. (1975) (0)
Impact of family history of cancer on risk and mortality of second cancers in patients with prostate cancer (2018) (0)
Sporadic colorectal cancer: From genetic make-up to complex phenotypic measurement, from risk determination to prognostic markers (2015) (0)
Biological monitoring in the estimation of the cancer risk (1982) (0)
Identification of carcinogen-guanosine adducts by fluorescencespectroscopy (1980) (0)
144 Polymorphisms of DNA repair and biotransformation genes and possible relationships with immunological response (2003) (0)
Survival in hematological malignancies in the Nordic countries through a half century with correlation to treatment (2023) (0)

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What Schools Are Affiliated With Kari Hemminki?

Kari Hemminki is affiliated with the following schools:

Karolinska Institute
University of Helsinki
Institute of Cancer Research
Tampere University
Charles University
Lund University
Pomeranian Medical University in Szczecin