Maria Teresa Landi | Academic Influence

Maria Teresa Landi's AcademicInfluence.com Rankings

Maria Teresa Landi

Medical

#2054

World Rank

#2448

Historical Rank

Oncology

#246

World Rank

#254

Historical Rank

Epidemiology

#690

World Rank

#718

Historical Rank

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Medical

Maria Teresa Landi's Degrees

Bachelors Biology University of Milan
Doctorate Medicine University of Milan
PhD Epidemiology University of Milan

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Why Is Maria Teresa Landi Influential?

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According to Wikipedia, Maria Teresa Landi is an Italian epidemiologist and oncologist who researches genetic and environmental determinants of lung cancer and melanoma. At the National Cancer Institute, she is a senior investigator in the integrative tumor epidemiology branch and a senior advisor for genomic epidemiology. Landi is an associate professor of epidemiology at the Johns Hopkins Bloomberg School of Public Health.

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Maria Teresa Landi'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

Genome partitioning of genetic variation for complex traits using common SNPs (2011) (869)
Gene Expression Signature of Cigarette Smoking and Its Role in Lung Adenocarcinoma Development and Survival (2008) (605)
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
Detectable clonal mosaicism from birth to old age and its relationship to cancer (2012) (514)
Detectable clonal mosaicism and its relationship to aging and cancer (2012) (512)
Genome-wide association study identifies three loci associated with melanoma risk (2009) (444)
Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study (2017) (425)
Quality control and quality assurance in genotypic data for genome‐wide association studies (2010) (425)
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci (2010) (423)
Cigarette smoking and lung cancer—relative risk estimates for the major histological types from a pooled analysis of case–control studies (2012) (416)
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. (2006) (401)
Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD (2010) (400)
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents (2006) (384)
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes (2017) (353)
MicroRNA Expression Differentiates Histology and Predicts Survival of Lung Cancer (2010) (324)
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2014) (322)
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia (2012) (277)
Genetically based N-acetyltransferase metabolic polymorphism and low-level environmental exposure to carcinogens (1994) (275)
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (2014) (275)
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer (2014) (273)
Cancer Incidence in a Population Accidentally Exposed to 2,3,7,8‐Tetrachlorodibenzo-para‐dioxin (1993) (270)
Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors (2009) (262)
Genome-wide association study identifies three new melanoma susceptibility loci (2011) (252)
Characterizing human lung tissue microbiota and its relationship to epidemiological and clinical features (2016) (223)
The 5p15.33 Locus Is Associated with Risk of Lung Adenocarcinoma in Never-Smoking Females in Asia (2010) (210)
Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption (2011) (204)
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma (2015) (199)
MC1R Germline Variants Confer Risk for BRAF-Mutant Melanoma (2006) (197)
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls (2012) (196)
BRAF mutations in cutaneous melanoma are independently associated with age, anatomic site of the primary tumor, and the degree of solar elastosis at the primary tumor site (2011) (194)
Expression polymorphism of the blood-brain barrier component P-glycoprotein (MDR1) in relation to Parkinson's disease. (2002) (183)
Genome-wide Association Study Identifies Two Susceptibility Loci for Osteosarcoma (2013) (181)
Handling of dioxin measurement data in the presence of non-detectable values: overview of available methods and their application in the Seveso chloracne study. (2005) (174)
Exposure to diesel motor exhaust and lung cancer risk in a pooled analysis from case-control studies in Europe and Canada. (2011) (169)
MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population. (2005) (161)
MC1R germline variants confer risk for BRAF-mutant melanoma. (2006) (158)
Chronic Obstructive Pulmonary Disease and Altered Risk of Lung Cancer in a Population-Based Case-Control Study (2009) (156)
Relevance of metabolic polymorphisms to human carcinogenesis: evaluation of epidemiologic evidence. (1991) (149)
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 (2011) (146)
Mutations in the Tyrosine Kinase Domain of the Epidermal Growth Factor Receptor in Non–Small Cell Lung Cancer (2005) (145)
Genome-wide association study identifies multiple loci associated with bladder cancer risk. (2014) (136)
Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis. (2012) (134)
Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. (2015) (133)
Immunologic effects of dioxin: new results from Seveso and comparison with other studies. (2002) (130)
Strengths and Limitations of Laboratory Procedures for MicroRNA Detection (2010) (127)
Environment And Genetics in Lung cancer Etiology (EAGLE) study: An integrative population-based case-control study of lung cancer (2008) (124)
Neonatal Thyroid Function in Seveso 25 Years after Maternal Exposure to Dioxin (2008) (122)
Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study (2016) (120)
A variant in FTO shows association with melanoma risk not due to BMI (2013) (120)
Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue (2014) (119)
Dioxin Exposure and Cancer Risk: A 15‐Year Mortality Study after the “Seveso Accident” (1997) (119)
Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study (2015) (119)
Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression (2009) (117)
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study (2010) (113)
International Lung Cancer Consortium: Pooled Analysis of Sequence Variants in DNA Repair and Cell Cycle Pathways (2008) (110)
Genome‐wide association studies of pigmentation and skin cancer: a review and meta‐analysis (2010) (108)
Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer. (2013) (104)
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length (2014) (103)
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. (2020) (101)
Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations. (2005) (100)
Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence (2017) (100)
DNA repair, dysplastic nevi, and sunlight sensitivity in the development of cutaneous malignant melanoma. (2002) (98)
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3. (2011) (97)
TERT promoter mutations in melanoma survival (2016) (97)
Comprehensive evaluation of allele frequency differences of MC1R variants across populations. (2006) (96)
Lung cancer and socioeconomic status in a pooled analysis of case-control studies (2018) (92)
Is previous respiratory disease a risk factor for lung cancer? (2014) (91)
Assessment of Human Papillomavirus in Lung Tumor Tissue (2011) (91)
Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
MC1R variants increase risk of melanomas harboring BRAF mutations. (2008) (90)
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. (2016) (87)
Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (87)
MC1R variants increased the risk of sporadic cutaneous melanoma in darker‐pigmented Caucasians: A pooled‐analysis from the M‐SKIP project (2014) (86)
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21 (2016) (83)
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data (2016) (83)
Intakes of red meat, processed meat, and meat mutagens increase lung cancer risk. (2009) (82)
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers (2017) (81)
Informed Conditioning on Clinical Covariates Increases Power in Case-Control Association Studies (2012) (81)
XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk (2004) (81)
Combined risk factors for melanoma in a Mediterranean population (2001) (78)
Identification of 14-3-3θ as an antigen that induces a humoral response in lung cancer (2007) (78)
Lung Cancer and Occupation in a Population-based Case-Control Study (2010) (77)
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence (2015) (76)
Integrating Clinical and Multiple Omics Data for Prognostic Assessment across Human Cancers (2017) (76)
Genetic Variation and Willingness to Participate in Epidemiologic Research: Data from Three Studies (2005) (75)
Aryl-hydrocarbon receptor-dependent pathway and toxic effects of TCDD in humans: a population-based study in Seveso, Italy. (2003) (73)
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
Cytochrome P4501A2: enzyme induction and genetic control in determining 4-aminobiphenyl-hemoglobin adduct levels. (1996) (72)
Are women who smoke at higher risk for lung cancer than men who smoke? (2013) (71)
Comprehensive evaluation of allele frequency differences of MC1R variants across populations (2007) (70)
Lung cancer prognosis before and after recurrence in a population-based setting. (2015) (70)
Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers. (2014) (69)
Sample collection, processing and storage. (1997) (69)
CYP1A1 and CYP1B1 genotypes, haplotypes, and TCDD-induced gene expression in subjects from Seveso, Italy. (2005) (69)
Influence of Quercetin-Rich Food Intake on microRNA Expression in Lung Cancer Tissues (2012) (69)
A Gene Expression Signature from Peripheral Whole Blood for Stage I Lung Adenocarcinoma (2011) (67)
Shared heritability and functional enrichment across six solid cancers (2018) (67)
Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk. (2010) (66)
Impact of occupational carcinogens on lung cancer risk in a general population. (2013) (66)
Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never‐smoking women in Asia: a report from the female lung cancer consortium in Asia (2015) (64)
Cigarette smoking behaviour and blood metabolomics. (2016) (63)
International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants. (2010) (62)
HPV-associated lung cancers: an international pooled analysis. (2014) (60)
Uncovering novel mutational signatures by de novo extraction with SigProfilerExtractor (2020) (58)
TCDD-mediated alterations in the AhR-dependent pathway in Seveso, Italy, 20 years after the accident. (2003) (58)
Genetic and epigenetic intratumor heterogeneity impacts prognosis of lung adenocarcinoma (2019) (58)
Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer. (2015) (57)
A novel point mutation in a 3' splice site of the NADH-cytochrome b5 reductase gene results in immunologically undetectable enzyme and impaired NADH-dependent ascorbate regeneration in cultured fibroblasts of a patient with type II hereditary methemoglobinemia. (1995) (56)
Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma. (2012) (56)
Outdoor particulate matter (PM10) exposure and lung cancer risk in the EAGLE study (2018) (56)
Hormone use and risk for lung cancer: a pooled analysis from the International Lung Cancer Consortium (ILCCO) (2013) (56)
Exposure–Response Analyses of Asbestos and Lung Cancer Subtypes in a Pooled Analysis of Case–Control Studies (2017) (56)
Alcohol consumption and lung cancer risk in the Environment and Genetics in Lung Cancer Etiology (EAGLE) study. (2010) (55)
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers (2019) (55)
Identification of 14-3-3 theta as an antigen that induces a humoral response in lung cancer. (2007) (53)
Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations (2016) (53)
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits (2020) (53)
Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer (2009) (52)
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk. (2016) (52)
Occupational exposure to organic dust increases lung cancer risk in the general population (2011) (52)
Inherited polymorphisms in the RNA-mediated interference machinery affect microRNA expression and lung cancer survival (2010) (51)
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (51)
Welding and lung cancer in a pooled analysis of case-control studies. (2013) (51)
Microarray analysis of gene expression in peripheral blood mononuclear cells from dioxin-exposed human subjects. (2007) (48)
MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project (2018) (48)
Genome-wide interaction study of smoking and bladder cancer risk. (2014) (46)
Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies (2018) (46)
Genetic susceptibility in familial melanoma from northeastern Italy (2004) (45)
Menstrual and reproductive factors and lung cancer risk: A pooled analysis from the international lung cancer consortium (2017) (44)
Reproductive and hormonal factors and the risk of lung cancer: The EAGLE study (2013) (44)
Genomic and evolutionary classification of lung cancer in never smokers (2021) (43)
t(14;18) translocations in lymphocytes of healthy dioxin-exposed individuals from Seveso, Italy. (2006) (42)
Large-Scale Pathway-Based Analysis of Bladder Cancer Genome-Wide Association Data from Five Studies of European Background (2012) (42)
Effect modification of the association of cumulative exposure and cancer risk by intensity of exposure and time since exposure cessation: a flexible method applied to cigarette smoking and lung cancer in the SYNERGY Study. (2014) (41)
Circulating levels of immune and inflammatory markers and long versus short survival in early-stage lung cancer. (2013) (41)
Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium. (2015) (40)
Genome-wide association study of familial lung cancer (2018) (40)
A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer (2016) (39)
Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma (2018) (39)
Higher‐than‐expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history (2017) (39)
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. (2016) (38)
Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci. (2016) (38)
MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project (2015) (38)
Time to smoke first morning cigarette and lung cancer in a case-control study. (2014) (38)
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity (2018) (37)
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL). (2008) (37)
Combining common genetic variants and non‐genetic risk factors to predict risk of cutaneous melanoma (2018) (37)
Causal relationships between body mass index, smoking and lung cancer: Univariable and multivariable Mendelian randomization (2020) (37)
Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 (2017) (37)
Nucleotide diversity and population differentiation of the Melanocortin 1 Receptor gene, MC1R (2008) (36)
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (36)
Telomere structure and maintenance gene variants and risk of five cancer types (2016) (34)
Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA (2022) (34)
Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (34)
Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia (2014) (33)
Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking (2013) (33)
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. (2016) (33)
Alcohol and lung cancer risk among never smokers: A pooled analysis from the international lung cancer consortium and the SYNERGY study (2017) (33)
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions (2014) (32)
Genetic variation in innate immunity and inflammation pathways associated with lung cancer risk (2012) (32)
Multistage Analysis of Variants in the Inflammation Pathway and Lung Cancer Risk in Smokers (2012) (31)
Publisher correction: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 (2018) (31)
Antibody response to Helicobacter pylori CagA and heat-shock proteins in determining the risk of gastric cancer development. (2000) (30)
Lung cancer among coal miners, ore miners and quarrymen: smoking-adjusted risk estimates from the synergy pooled analysis of case-control studies. (2015) (30)
MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations. (2016) (28)
HLA-G expression in trophoblast cells is independent of embryonic development. (2000) (28)
An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs. (2011) (27)
Lung cancer risk among bricklayers in a pooled analysis of case–control studies (2014) (26)
Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model (2021) (26)
POT1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma families (2019) (26)
MicrobiomeGWAS: A Tool for Identifying Host Genetic Variants Associated with Microbiome Composition (2015) (25)
Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners (2018) (25)
Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia (2017) (24)
Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types (2015) (24)
Characterization of melanoma susceptibility genes in high-risk patients from Central Italy (2017) (24)
Genetic determinants for promoter hypermethylation in the lungs of smokers: a candidate gene-based study. (2012) (24)
A Flexible Bayesian Model for Studying Gene–Environment Interaction (2012) (23)
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations (2016) (23)
Evaluation of normalization methods for two-channel microRNA microarrays (2010) (22)
Respirable Crystalline Silica Exposure, Smoking, and Lung Cancer Subtype Risks: A Pooled Analysis of Case-control Studies. (2020) (22)
An efficient stochastic search for Bayesian variable selection with high-dimensional correlated predictors (2011) (22)
A Novel Pathway-Based Approach Improves Lung Cancer Risk Prediction Using Germline Genetic Variations (2016) (22)
Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels (2018) (22)
Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers. (2018) (21)
Epstein–Barr virus microRNAs and lung cancer (2011) (21)
Deciphering associations for lung cancer risk through imputation and analysis of 12 316 cases and 16 831 controls (2015) (21)
The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease. (2014) (21)
A regression model for risk difference estimation in population-based case–control studies clarifies gender differences in lung cancer risk of smokers and never smokers (2013) (20)
On combining family and case‐control studies (2008) (20)
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (20)
Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer: A Mendelian Randomization Analysis (2019) (20)
Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. (2019) (19)
Occupational prestige, social mobility and the association with lung cancer in men (2016) (19)
Transcriptome‐wide association study reveals candidate causal genes for lung cancer (2018) (19)
Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data (2016) (18)
Diesel Engine Exhaust Exposure, Smoking, and Lung Cancer Subtype Risks: A Pooled Exposure-response Analysis of 14 Case-control Studies. (2020) (18)
On the Interplay of Telomeres, Nevi and the Risk of Melanoma (2012) (18)
Instrumental measurements of skin color and skin ultraviolet light sensitivity and risk of cutaneous malignant melanoma: a case-control study in an Italian population. (2002) (18)
Nut Consumption and Lung Cancer Risk: Results from Two Large Observational Studies (2017) (18)
Dermoscopic features of cutaneous melanoma are associated with clinical characteristics of patients and tumours and with MC1R genotype (2014) (18)
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families. (2017) (18)
Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association study. (2011) (17)
Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus (2017) (17)
Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (17)
Risk factors for keratinocyte skin cancer in patients diagnosed with melanoma, a large retrospective study. (2016) (17)
Peritoneal mesothelioma and asbestos exposure: a population-based case–control study in Lombardy, Italy (2019) (17)
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT. (2019) (16)
Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project. (2016) (16)
A Penalized Regression Framework for Building Polygenic Risk Models Based on Summary Statistics From Genome-Wide Association Studies and Incorporating External Information (2020) (16)
Lung Cancer Among Firefighters: Smoking-Adjusted Risk Estimates in a Pooled Analysis of Case-Control Studies (2016) (16)
GPC5 rs2352028 variant and risk of lung cancer in never smokers. (2010) (16)
The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15. (2015) (16)
Identification of shared and unique susceptibility pathways among cancers of the lung, breast, and prostate from genome-wide association studies and tissue-specific protein interactions. (2015) (16)
Gene-environment interaction in parkinson's disease. The case of CYP2D6 gene polymorphism. (1996) (16)
Lower Risk of Lung Cancer after Multiple Pneumonia Diagnoses (2010) (16)
Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility (2019) (16)
Pleiotropic Analysis of Lung Cancer and Blood Triglycerides. (2016) (15)
Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma‐prone family (2012) (15)
Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium. (2016) (15)
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC 14 A 1 , a urea transporter gene on chromosome 18 q 12 . 3 (2011) (15)
Blood DNA methylation, nevi number, and the risk of melanoma (2014) (15)
Heme‐related gene expression signatures of meat intakes in lung cancer tissues (2014) (14)
Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies (2012) (14)
Alcohol consumption and lung cancer risk: A pooled analysis from the International Lung Cancer Consortium and the SYNERGY study. (2019) (14)
Mortality of a young population after accidental exposure to 2,3,7,8-tetrachlorodibenzodioxin. (1992) (14)
GSTM1 and GSTT1 copy numbers and mRNA expression in lung cancer (2012) (13)
Functional variants in DCAF4 associated with lung cancer risk in European populations (2017) (13)
FMelanoma from bench to bedside: meeting report from the 6th international melanoma congress. Pigment Cell Melanoma Res. 23, 14-26 (2010) (13)
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers (2021) (12)
A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindreds. (2011) (12)
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families. (2016) (12)
Lung cancer risk among bakers, pastry cooks and confectionary makers: the SYNERGY study (2013) (12)
The genomic and epigenomic evolutionary history of papillary renal cell carcinomas (2018) (12)
A multifactorial score including autophagy for prognosis and care of COVID-19 patients (2020) (12)
Lung Cancer Risk Among Cooks When Accounting for Tobacco Smoking: A Pooled Analysis of Case–Control Studies From Europe, Canada, New Zealand, and China (2015) (11)
Association of MC 1 R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN 2 A Mutations (2005) (11)
Lung cancer risk among hairdressers: a pooled analysis of case-control studies conducted between 1985 and 2010. (2013) (11)
An exposure‐weighted score test for genetic associations integrating environmental risk factors (2015) (11)
Cancer morbidity in the Seveso area, 1976–1986 (1992) (11)
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (11)
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. (2015) (11)
Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia (2021) (10)
DNA Methylation in Lung Cancer: Mechanisms and Associations with Histological Subtypes, Molecular Alterations, and Major Epidemiological Factors (2022) (10)
Mood Disorders and Risk of Lung Cancer in the EAGLE Case-Control Study and in the U.S. Veterans Affairs Inpatient Cohort (2012) (10)
MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort. (2019) (10)
Glucocorticoid use and melanoma risk (2001) (10)
Association of MC1R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN2A Mutations (2005) (10)
Pathway‐analysis of published genome‐wide association studies of lung cancer: A potential role for the CYP4F3 locus (2017) (10)
Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families (2013) (10)
Lung cancer risk in painters: results from the SYNERGY pooled case–control study consortium (2020) (9)
Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs (2017) (9)
Plasma levels of dioxins, furans, non-ortho-PCBs, and TEQs in the Seveso population 17 years after the accident. (2012) (9)
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes. (2019) (9)
Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer (2018) (9)
Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium (2017) (9)
Clinical characteristics of 20 Italian melanoma-prone families. (1999) (9)
Familial melanoma aggregation in north-eastern Italy. (2000) (9)
Genome‐wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk (2020) (8)
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma (2020) (8)
Increased lung cancer risk among bricklayers in an Italian population-based case-control study. (2012) (8)
MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortium (2018) (8)
P1.04: Defining the Genetic Architecture of Lung Cancer Etiology: Track: Prevention, Early Detection, Epidemiology and Tobacco Control. (2016) (8)
Tracing Lung Cancer Risk Factors Through Mutational Signatures in Never-Smokers. (2020) (8)
A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians (2022) (7)
Susceptibility loci of CNOT6 in the general mRNA degradation pathway and lung cancer risk—A re‐analysis of eight GWASs (2017) (7)
Abstract 2931: Inherited variation at chromosome 12p13.33 includingRAD52influences squamous cell lung carcinoma risk (2012) (7)
[Metabolic polymorphisms and the cancer risk: the evaluation of epidemiological studies]. (1992) (7)
Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium (2015) (7)
Smoking cessation (SC) and lung cancer (LC) outcomes: A survival benefit for recent-quitters? A pooled analysis of 34,649 International Lung Cancer Consortium (ILCCO) patients. (2020) (6)
Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population (2019) (6)
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer (2022) (6)
Abstract 4719: Genome-wide association studies of pigmentation and skin cancer: A meta-analysis (2010) (6)
Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls. (2016) (6)
Sub-multiplicative interaction between polygenic risk score and household coal use in relation to lung adenocarcinoma among never-smoking women in Asia. (2020) (6)
Common TDP1 Polymorphisms in Relation to Survival among Small Cell Lung Cancer Patients: A Multicenter Study from the International Lung Cancer Consortium (2017) (6)
Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies (2019) (6)
Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and informs melanocyte gene regulatory mechanisms (2021) (6)
Characterizing the tumor microenvironment in rare renal cancer histological types (2021) (5)
MEGSA: A powerful and flexible framework for analyzing mutual exclusivity of tumor mutations (2015) (5)
Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals (2021) (5)
Integration of multiomic annotation data to prioritize and characterize inflammation and immune‐related risk variants in squamous cell lung cancer (2020) (5)
Identifying Host Genetic Variants Associated with Microbiome Composition by Testing Multiple Beta Diversity Matrices (2017) (5)
Using imputed genotype data in the joint score tests for genetic association and gene–environment interactions in case‐control studies (2018) (5)
[Risk factors of malignant skin melanoma in Italian population: review of results of a case-control study]. (2002) (4)
Publisher Correction: Shared heritability and functional enrichment across six solid cancers (2019) (4)
Corrigendum: Impact of occupational carcinogens on lung cancer risk in a general population [Int J Epidemiol., 41 (2012), 711-721] DOI:10.1093/ije/dys042 (2013) (4)
Clinical Implications of Inter- and Intra-Tumor Heterogeneity of Immune Cell Markers in Lung Cancer. (2021) (4)
Education and lung cancer among never smokers. (2014) (4)
Abstract 942: Imputation from The 1000 Genomes Project identifies rare large effect variants of BRCA2-K3326X and CHEK2-I157T as risk factors for lung cancer; a study from the TRICL consortium (2014) (4)
Molecular epidemiology: a new perspective for the study of toxic exposures in man. A consideration of the influence of genetic susceptibility factors on risk in different lung cancer histologies. (1994) (4)
Occupational exposure to nickel and hexavalent chromium and the risk of lung cancer in a pooled analysis of case‐control studies (SYNERGY) (2022) (4)
Autophagopathies: from autophagy gene polymorphisms to precision medicine for human diseases (2022) (4)
A Likelihood Ratio Test for Gene-Environment Interaction Based on the Trend Effect of Genotype Under an Additive Risk Model Using the Gene-Environment Independence Assumption. (2020) (4)
Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (4)
Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and Spain. (2020) (4)
Identification of Genetic Risk Factors for Familial Urinary Bladder Cancer: An Exome Sequencing Study (2021) (4)
MC1R variants and cutaneous melanoma risk according to histological type, body site, and Breslow thickness: a pooled analysis from the M-SKIP project (2020) (4)
A COPULA-MODEL BASED SEMIPARAMETRIC INTERACTION TEST UNDER THE CASE-CONTROL DESIGN. (2013) (3)
Multi-trait genetic analysis identifies auto-immune loci associated with cutaneous melanoma. (2021) (3)
Separation of trophoblastic and vascular cell lineages and vascular maturation in early human placental development. (2004) (3)
Association Analysis of Driver Gene–Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls (2020) (3)
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility (2020) (3)
No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families (2008) (3)
Correspondence re: K. Toide et al., Aryl hydrocarbon hydroxylase represents CYP1B1, and not CYP1A1, in human freshly isolated white cells: trimodal distribution of Japanese population according to induction of CYP1B1 mRNA by environmental dioxins. 12: 219-222, 2003. (2003) (3)
Assessment of HER2 Protein Overexpression and Gene Amplification in Renal Collecting Duct Carcinoma: Therapeutic Implication (2020) (2)
Occupational Exposure to Polycyclic Aromatic Hydrocarbons and Lung Cancer Risk: Results from a Pooled Analysis of Case–Control Studies (SYNERGY) (2022) (2)
Investigating the genetic relationship between Alzheimer’s disease and cancer using GWAS summary statistics (2017) (2)
VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions (2014) (2)
MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M‐SKIP project (2020) (2)
Rare germline deleterious variants increase susceptibility for lung cancer. (2022) (2)
Characterization of nonacral melanoma patients without typical risk factors (2012) (2)
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (2)
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. (2021) (2)
Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) (2015) (2)
Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting (2022) (2)
p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome (2012) (2)
Abstract 286: Epigenome-wide association study of normal lung tissues identifies hypomethylation of multiple CpG sites associated with cigarette smoking (2014) (1)
Iam hiQ—a novel pair of accuracy indices for imputed genotypes (2022) (1)
[Occupational epidemiology and new challenges in occupational medicine]. (1999) (1)
A hybrid parametric and empirical likelihood model for evaluating interactions in case-control Studies. (2016) (1)
Erratum to “Increased lung cancer risk among bricklayers in an italian population-based case–control study” (2013) (1)
Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility (2020) (1)
Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. (2022) (1)
Abstract #LB-139: A comprehensive genome-wide association study of lung cancer (2009) (1)
A blood-based gene expression signature of early-stage non-small cell lung cancer. (2012) (1)
Fine-mapping of chromosome 5p15.33 based on a targeted deep sequencing identifies novel lung cancer susceptibility loci Running Title (40 characters): Novel 5p15.33 lung cancer susceptibility loci (2016) (1)
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family (2021) (1)
Abstract 2157: Causal effects of delaying smoking initiation on subsequent lung cancer risk (2014) (1)
Gaining insights into the DICER1 syndrome: An early report from the Italian DICER1 registry. (2019) (1)
RESPONSE: Re: MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population (2006) (1)
Genetic Relationship Between Endometriosis and Melanoma (2021) (1)
Occupational exposure to organic dust increases lung cancer risk in the general population (2011) (1)
Identi fi cation of shared and unique susceptibility pathways among cancers of the lung , breast , and prostate from genome-wide association studies and tissue-speci fi c protein interactions (2015) (1)
Identi ﬁ cation of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (1)
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers (2020) (1)
Authors' response to: qualitative job-exposure matrix--a tool for the quantification of population-attributable fractions for occupational lung carcinogens? (2013) (1)
Abstract SY26-02: Sherlock-Lung: Tracing lung cancer mutational processes in never smokers (2019) (1)
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk (2021) (1)
MA06.10 Germline Mutation in ATM Affect Lung Cancer Risk with High Effect (2018) (1)
Authors' response to: comment upon the article: impact of occupational carcinogens on lung cancer risk in a general population. (2013) (1)
P025 Lung cancer risk among firefighters when accounting for tobacco smoking – preliminary results from a pooled analysis of case-control studies from europe, canada, new zealand and china (2016) (1)
Occupational risks for lung cancer in the population-based case-control "EAGLE study" (2008) (1)
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers (2020) (1)
Characterizing human lung tissue microbiota and its relationship to epidemiological and clinical features (2016) (0)
Prevalence of Cytomegalovirus infections in ulcerative rettocolitis patients, using PCR in whole blood and biopsies (2013) (0)
Reactivation of intestinal CMV in a renal transplant patient after 10 years from the transplant (2013) (0)
Markers of susceptibility and environmental cancer risk: experiences in Italy. (1995) (0)
Cutaneous Malignant Melanoma in five patients with HIV disease.: ABSTRACT 68 (2000) (0)
Accounting for EGFR mutations in epidemiological analyses of non-small cell lung cancers: Examples based on the International Lung Cancer Consortium data. (2022) (0)
Gene–gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer (2022) (0)
session E : melanoma , sarcoma , rare cancer , brain tumours (2009) (0)
Impact of Histology and Tumor Grade on Clinical Outcomes Beyond 5 Years of Follow-Up in a Large Cohort of Renal Cell Carcinomas. (2021) (0)
Abstract 2748: Gene expression signatures of meat intake in lung cancer tissues (2011) (0)
Lung cancer risk among cooks and kitchen workers in a pooled analysis of case-control studies in Europe and Canada (2011) (0)
A NovelPointMutation ina3'Splice SiteoftheNADH- Cytochrome b5Reductase GeneResults inImmunologically Undetectable EnzymeandImpaired NADH-Dependent Ascorbate Regeneration inCultured Fibroblasts ofaPatient withType11Hereditary Methemoglobinemia (1995) (0)
Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium (2017) (0)
0259 Interaction between genetic and occupational factors in lung cancer aetiology. A population-based case-control study0259 Interaction between genetic and occupational factors in lung cancer aetiology. A population-based case-control study (2014) (0)
Abstract 2248: CommonTDP1polymorphisms in relation to survival among small cell lung cancer patients in a multicenter study from the International Lung Cancer Consortium (2017) (0)
Mosaic chromosomal alterations is associated with increased lung cancer risk: insight from the INTEGRAL-ILCCO cohort analysis (2023) (0)
A UVB-responsive common variant at chr7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor gene (AHR) (2021) (0)
Abstract 2185: Multiple region whole-genome sequencing reveals intratumor heterogeneity and branching clonal architecture of non-clear-cell renal cell carcinoma (2018) (0)
Abstract 1187: Comparison of intra-tumor heterogeneity and clonal evolution across lung cancer subtypes by multi-region whole genome sequencing (2018) (0)
’ Response to : Comment upon the article : Impact of occupational carcinogens on lung cancer risk in a general population From (2014) (0)
Gene-gene Interaction of AhR With and Within the Wnt Cascade Affects Susceptibility to Lung Cancer (2021) (0)
SYNERGY epidemiological database and some results on smoking by major histological subtypes of lung cancer (2011) (0)
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia (2012) (0)
Association of germline variants in telomere maintenance genes (POT1, TERF2IP, ACD, and TERT) with spitzoid morphology in familial melanoma: A multi-center case series (2023) (0)
Zeros of complex random polynomials spanned by Bergman polynomials (2020) (0)
Abstract SY26-02:Sherlock-Lung: Tracing lung cancer mutational processes in never smokers (2019) (0)
Abstract 4824: Little evidence of human papillomavirus in lung tumor tissue (2010) (0)
Correction: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (0)
SAGES 2015. Symposium of Advances in Genomics, Epidemiology and Statistics 2015: Abstracts (2017) (0)
Abstract 4597: A novel variant in DNA repair gene GTF2H4 is associated with lung cancer risk: A reanalysis of GWAS datasets from the TRICL consortium (2015) (0)
Correction: Red and Processed Meats, Meat Mutagens, and Lung Cancer (2009) (0)
[Molecular epidemiology for the study of the environment-genome interaction]. (2003) (0)
P1.08-A Sherlock Lung Tracing Lung Cancer Mutational Processes in Never-smokers (2019) (0)
Prevalence and genotyping of HPV, by cervical brushing, in Irpinia area of Campania region (2012) (0)
Abstract 1601: Genetic and epigenetic intratumor heterogeneity of lung adenocarcinoma (2019) (0)
Cell-type-specific meQTL extends melanoma GWAS annotation beyond eQTL and 1 informs melanocyte gene regulatory mechanisms 2 (2021) (0)
Genome-wide association study identifies novel loci associated with osteosarcoma (2013) (0)
P1.05: An International Epidemiological Analysis of Young Patients Diagnosed With NSCLC (ADUJOV-CLICaP): Track: Prevention, Early Detection, Epidemiology and Tobacco Control (2016) (0)
Proceedings of the fifth international Molecular Pathological Epidemiology (MPE) meeting (2019) (0)
Exomic Sequencing to Identify Germline Variants in Familial Melanoma. (2013) (0)
Abstract 4610: Functional characterization of a multicancer risk locus on chr5p15.33 reveals regulation ofTERTby ZNF148 (2015) (0)
Abstract 630: Tobacco smoking women are not at higher risk than men for lung cancer (2012) (0)
Abstract 865: Genomic and evolutionary classification of lung cancer in never smokers from the Sherlock-Lungstudy (2021) (0)
Abstract 1877: Lung cancer risk in painters: Results from the SYNERGY pooled analysis (2011) (0)
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity (2018) (0)
Comparison of quantitative HCMV DNAemia in whole blood and leukocytes, and Real-Time PCR in a BMT patient (2012) (0)
Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (0)
A Robust Test for Additive Gene-Environment Interaction Under the Trend Effect of Genotype Using an Empirical Bayes-Type Shrinkage Estimator. (2021) (0)
Family history of cancer and family history of smoking in lung cancer risk by histology (2008) (0)
Association of Nut Consumption and Lung Cancer Risk in a Large Population‐based Case‐control Study (2015) (0)
I’am hiQ – A Novel Accuracy Index for Imputed Genotypes (2021) (0)
Bone metabolism in adults witth serious neurological lesions: a preliminary study (1992) (0)
Genome-Wide Analyses Characterize Shared Heritability Among Cancers and Identify Novel Cancer Susceptibility Regions. (2023) (0)
Epidemiology and genetics: New results in melanoma etiology and their application to melanoma prevention. (2006) (0)
A Novel Point Mutation in a 3' Splice Site of the NADH-Cytochrome b5 Reductase Gene Results in Immunologically Undetectable Enzyme and Impaired NADH-Dependent Ascorbate Regeneration in Cultured Fibroblasts of a Patient with Type 11 Hereditary Methemoglobinemia (2007) (0)
Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels (2018) (0)
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family (2021) (0)
Abstract 2244: The M-SKIP Project: an international pooled-analysis on melanocortin-1 receptor (MC1 R) variants and skin carcinogenesis (2011) (0)
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2018) (0)
Abstract 817: Mendelian randomization and mediation analysis of 5p15.33, telomere length and lung cancer risk (2016) (0)
Correction to: Overlapping genetic architecture between Parkinson disease and melanoma (2020) (0)
Iam hiQ—a novel pair of accuracy indices for imputed genotypes (2022) (0)
Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22 (2015) (0)
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations (2016) (0)
Quantification of BKV in urine and plasma in renal transplant recipients at PVAN (Polyomavirus-associated nephropathy) risk (2013) (0)
Abstract 4710: A candidate gene expression signature of early stage lung adenocarcinoma from peripheral whole blood (2010) (0)
Molecular Epidemiology of Dioxin Illness in Seveso (2006) (0)
Abstract 234: Understanding melanoma susceptibility through GWAS of risk phenotypes (2018) (0)
Shared heritability and functional enrichment across six solid cancers (2019) (0)
Abstract 3445: C-reactive protein and lung cancer risk: a Mendelian randomization analysis (2016) (0)
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (0)
Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting (2022) (0)
Abstract 2292: Lung function and lung cancer risk: a Mendelian randomization study of UK Biobank cohort and the International Lung Cancer Consortium (2017) (0)
Public health impact of exposure to occupational carcinogens on lung cancer risk (2011) (0)
Abstract 5909: Characterization of the lung cancer microbiome using whole genome sequencing (2023) (0)
Title: Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility (2020) (0)
Table 2 . ORs and 95 % CIs for associations of lung cancer with pneumonia and tuberculosis diagnosed at least 1 y prior to entry into the EAGLE case-control study , both overall and stratified by smoking status (2010) (0)
Tumor Mutational Burden by Whole-Genome Sequencing in Resected NSCLC of Never Smokers (2022) (0)
Abstract 1874: Public health impact of occupational carcinogens exposure and lung cancer (2011) (0)
ELEVATED DIOXIN LEVELS IN CHLORACNE CASES TWENTY YEARS AFTER THE SEVESO, ITALY ACCIDENT (2004) (0)
Abstract 1274: Alcohol and lung cancer risk: a pooled analysis using International Lung Cancer Consortium studies (2014) (0)
[Cytological screening of uterine cervical cancer by samples in liquid medium (CytoRich). Preliminary study of a series of 111 292 patients]. (1999) (0)
Abstract B52: Time to smoke first cigarette after morning awakening differentiates lung cancer risk beyond standard smoking measures (2013) (0)
Systematic Reviews and Meta-and Pooled Analyses Welding and Lung Cancer in a Pooled Analysis of Case-Control Studies (2013) (0)
Lung cancer risk among hairdressers in SYNERGY – pooled analysis from case-control studies in Europe and Canada (2011) (0)
Abstract 5722: The mutational signatures of 100,477 targeted sequenced tumors (2023) (0)
Occupational prestige, social mobility and the association with lung cancer in men (2016) (0)
Proceedings of the fifth international Molecular Pathological Epidemiology (MPE) meeting (2022) (0)
Identi fi cation of susceptibility pathways for the role of chromosome 15 q 25 . 1 in modifying lung cancer risk (2018) (0)
The genomic and epigenomic evolutionary history of papillary renal cell carcinomas (2020) (0)
EP16.03-020 High Tumor Mutational Burden by Whole-Genome Sequencing in Resected NSCLC in Never Smokers is Associated with Worse Prognosis (2022) (0)
Deciphering associations between three RNA splicing-related genetic variants and lung cancer risk (2022) (0)
Melanoma from bench to bedside: Meeting report from the 6th international melanoma congress (Pigment Cell and Melanoma Research (2010) 23, (14-26 )) (2010) (0)
Lung cancer risk in painters: results from the SYNERGY pooled analysis (2011) (0)
families from three continents mutations: a GenoMEL study of melanoma-prone Features associated with germline CDKN2A (2007) (0)
cancer risk among hairdressers: a pooled analysis of case-control studies conducted between and 2010. cancer risk among a pooled (0)
Genetic and epigenetic intratumor heterogeneity impacts prognosis of lung adenocarcinoma (2020) (0)
Application of two job indices for general occupational demands in a pooled analysis of case–control studies on lung cancer (2021) (0)
Pigmentation, DNA Repair, and Candidate Genes (2006) (0)
Abstract 228: Association analysis across different populations identifies 26 new cutaneous melanoma risk loci (2018) (0)
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (0)
MC1R variants in childhood and adolescent melanoma: A pooled-analysis from a large worldwide multicenter cohort of patients (2019) (0)
Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue (2014) (0)
Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies (2016) (0)
A stool antigen test (HpSA) for the detection of H. pylori infection (2000) (0)
Comment on: DNA repair, dysplastic nevi, and sunlight sensitivity in the development of cutaneous malignant melanoma. Authors' reply (2002) (0)
Abstract 1875: Lung cancer risk among hairdressers in SYNERGY – pooled analysis from case-control studies in Europe and Canada with detailed smoking data (2011) (0)
Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer. (2022) (0)
POT1 and TERT promoter molecular screening in Spanish melanoma families (2019) (0)
SUITOR: Selecting the number of mutational signatures through cross-validation (2020) (0)
University of Groningen Exposure-Response Analyses of Asbestos and Lung Cancer Subtypes in a Pooled Analysis of Case-Control Studies (2017) (0)
Function and Aggressive Disease The 19 q 12 Bladder Cancer GWAS Signal : Association with Cyclin E Updated (2014) (0)
Time to first cigarette and its impact on lung tumorigenesis (2022) (0)
Combining two genome wide association scans for seven smoking related phenotypes replicates published associations in the CHRNA3/5 region (2008) (0)
From copy number alterations to structural variants: the evolutionary cascade of papillary renal cell carcinomas (2018) (0)
Abstract 941: Exome sequencing identifiedPOT1, a telomere shelterin gene, as a major susceptibility gene for familial cutaneous malignant melanoma (2014) (0)
RESPONSE: Re: DNA Repair, Dysplastic Nevi, and Sunlight Sensitivity in the Development of Cutaneous Malignant Melanoma (2002) (0)
Abstract A34: Association of nut consumption and lung cancer risk in a large population-based case-control study (2015) (0)
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (0)
Dietary consumption of processed meat increases risk of lung cancer (2007) (0)
Suspected chromosomally integrated human herpes virus 6 in hematopoietic stem cell transplantation (2016) (0)
Abstract 2251: nrf2-keap1 axis molecular profile in small cell lung cancer cell lines (2014) (0)
Italy accident in 1976 : T(14;18) translocations in lymphocytes of healthy dioxin-exposed individuals (2006) (0)
Abstract 2569: A genome wide association study of lung cancer identifies 11 novel susceptibility loci (2016) (0)
Erratum: Article on red and processed meats, meat mutagens, and lung cancer (Cancer Res (2009) 69 (932:939)) (2009) (0)
Abstract LB-337: Synergistic effects of twelve common genetic polymorphisms and smoking habits on absolute risk of bladder cancer (2012) (0)
Abstract 889: An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for theXRCC4SNPs (2011) (0)
Abstract A105: Dietary quercetin, quercetin‐gene interaction, metabolic gene expression in lung tissue, and lung cancer risk (2010) (0)
Integrating Clinical and Multiple Omics Data for Prognostic Assessment across Human Cancers (2017) (0)
Abstract A38: Role of MC1R variants in childhood and adolescent melanoma (2015) (0)
Abstract 1166: APOBEC deaminases compete with tobacco smoking mutagenesis and affect age at onset of lung cancer (2023) (0)
Pleiotropic Associations of r isk Variants identified for Other c ancers With l ung c ancer r isk: t he PAG e and tricl c onsortia (2014) (0)

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