Mark Lathrop
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Canadian scientist
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Biology
Mark Lathrop's Degrees
- Masters Biochemistry McGill University
- Bachelors Biology University of British Columbia
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Why Is Mark Lathrop Influential?
(Suggest an Edit or Addition)According to Wikipedia, Mark Lathrop is a Canadian Biostatistician. He headed the Center for the Study of Human Polymorphisms, but returned to Canada as Scientific Director at McGill University and Genome Quebec's Innovation Centre in 2011.
Mark Lathrop'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-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2013) (3484)
- A comprehensive genetic map of the human genome based on 5,264 microsatellites (1996) (3041)
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) (2621)
- Strategies for multilocus linkage analysis in humans. (1984) (2612)
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) (2511)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
- The 1993–94 Généthon human genetic linkage map (1994) (1944)
- Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- Genetics of rheumatoid arthritis contributes to biology and drug discovery (2013) (1877)
- International network of cancer genome projects (2010) (1839)
- SLCO1B1 variants and statin-induced myopathy--a genomewide study. (2008) (1819)
- A second-generation linkage map of the human genome (1992) (1791)
- A large-scale, consortium-based genomewide association study of asthma. (2010) (1779)
- Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
- Newly identified loci that influence lipid concentrations and risk of coronary artery disease (2008) (1626)
- Easy calculations of lod scores and genetic risks on small computers. (1984) (1597)
- Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) (1996) (1567)
- Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma (2007) (1493)
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease (2009) (1476)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
- Common variants at 30 loci contribute to polygenic dyslipidemia (2009) (1380)
- A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 (2008) (1264)
- Genetic variants associated with Lp(a) lipoprotein level and coronary disease. (2009) (1242)
- Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease (2014) (1230)
- Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
- Genome-wide analysis of genetic loci associated with Alzheimer disease. (2010) (1177)
- Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis (2013) (1170)
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
- Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. (1985) (1099)
- Genomewide Scan Reveals Association of Psoriasis with IL-23 and NF-κB Pathways (2008) (1070)
- A genome-wide association study of global gene expression (2007) (1021)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- Mapping complex disease traits with global gene expression (2009) (851)
- EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome (2000) (809)
- A genome-wide search for quantitative trait loci underlying asthma (1996) (808)
- Genome-wide association study identifies five susceptibility loci for glioma (2009) (781)
- A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
- Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12 (1996) (740)
- Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease (1999) (689)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13 (2001) (675)
- Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 (1988) (648)
- A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) (638)
- Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats (1991) (614)
- Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (2013) (606)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
- Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4 (2007) (589)
- Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
- Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. (1990) (583)
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 (1993) (568)
- Lung cancer susceptibility locus at 5p15.33 (2008) (562)
- Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
- The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption (2005) (548)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
- Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis. (1997) (531)
- Genetic analysis of autoimmune type 1 diabetes mellitus in mice (1991) (526)
- Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
- The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology (2010) (524)
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
- A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 (2007) (498)
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
- Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. (2005) (463)
- A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma (2011) (459)
- Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome. (2001) (453)
- Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments (2014) (452)
- Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. (2008) (450)
- Genome-wide association study identifies three loci associated with melanoma risk (2009) (444)
- Genetic Structure of Europeans: A View from the North–East (2009) (437)
- Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus (1992) (434)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy (2007) (421)
- Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq (1994) (407)
- Adolescent impulsivity phenotypes characterized by distinct brain networks (2012) (396)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility (1991) (386)
- Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q (1990) (384)
- Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls (1999) (381)
- Effect of 17q21 variants and smoking exposure in early-onset asthma. (2008) (379)
- A gene for familial hemiplegic migraine maps to chromosome 19 (1993) (377)
- Patterns of somatic structural variation in human cancer genomes (2020) (377)
- Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders (2012) (371)
- The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery (2016) (360)
- Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. (2008) (357)
- Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus (1992) (355)
- Rat gene mapping using PCR-analyzed microsatellites. (1992) (347)
- Maternal inheritance of atopic IgE responsiveness on chromosome 11 q (1992) (345)
- Positional cloning of a novel gene influencing asthma from Chromosome 2q14 (2003) (342)
- Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements. (2013) (341)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
- SLC2A9 Is a High-Capacity Urate Transporter in Humans (2008) (334)
- Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. (2010) (330)
- Human polymorphism at microRNAs and microRNA target sites. (2013) (330)
- Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat (1996) (324)
- A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. (2001) (323)
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2014) (322)
- Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults (2007) (319)
- A variant in the CD209 promoter is associated with severity of dengue disease (2005) (317)
- CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs (2011) (314)
- Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology (2013) (308)
- Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. (2009) (304)
- Polygenic control of autoimmune diabetes in nonobese diabetic mice (1993) (302)
- Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population (2012) (299)
- Genome-wide association analysis identifies three new breast cancer susceptibility loci (2012) (291)
- Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR (1993) (286)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (2011) (286)
- A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate. (2009) (285)
- SHANK1 Deletions in Males with Autism Spectrum Disorder. (2012) (284)
- A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium (2011) (278)
- Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16. (1997) (278)
- Localisation of atopy and β subunit of high-affinity IgE receptor (Fc∈RI) on chromosome 11q (1993) (277)
- Family-based designs for genome-wide association studies (2011) (277)
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (2014) (275)
- Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. (2003) (272)
- Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. (2012) (267)
- Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein. (2002) (265)
- Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. (2011) (263)
- Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression (2007) (262)
- Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy (2006) (261)
- Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy (2002) (254)
- Genome screen for asthma and related phenotypes in the French EGEA study. (2000) (253)
- SRPX2 mutations in disorders of language cortex and cognition. (2006) (253)
- Polygenic disease: methods for mapping complex disease traits. (1995) (252)
- Genome-wide association study identifies three new melanoma susceptibility loci (2011) (252)
- Genome-wide association study of major recurrent depression in the U.K. population. (2010) (251)
- Perilipin deficiency and autosomal dominant partial lipodystrophy. (2011) (250)
- A radiation hybrid map of the rat genome containing 5,255 markers (1999) (250)
- Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. (2002) (247)
- A NOVEL ALZHEIMER DISEASE LOCUS LOCATED NEAR THE GENE ENCODING TAU PROTEIN (2015) (246)
- Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 (2011) (246)
- Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. (2003) (245)
- Control of fetal hemoglobin: new insights emerging from genomics and clinical implications. (2009) (245)
- A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome (1996) (243)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age (2014) (238)
- Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene. (1994) (233)
- Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
- Genome-wide association study of glioma and meta-analysis (2012) (225)
- Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14 (1990) (222)
- Measured haplotype analysis of the angiotensin-I converting enzyme gene. (1998) (221)
- A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q (1995) (216)
- HLA has strongest association with IgA nephropathy in genome-wide analysis. (2010) (216)
- Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis (1986) (215)
- Genome-wide mapping of human loci for essential hypertension (2003) (214)
- Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors (2017) (213)
- Lower ventral striatal activation during reward anticipation in adolescent smokers. (2011) (210)
- PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans (2012) (208)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- SNP and haplotype mapping for genetic analysis in the rat (2008) (200)
- Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma (2015) (199)
- Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. (1988) (198)
- Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
- Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis (2009) (197)
- Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls (2012) (196)
- A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals (2011) (193)
- Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. (1997) (191)
- HLA heterozygosity contributes to susceptibility to rheumatoid arthritis. (1992) (191)
- Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. (2006) (186)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- Mutations in the gene encoding SLURP-1 in Mal de Meleda. (2001) (185)
- Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity. (2004) (183)
- Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease (2011) (182)
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. (2012) (182)
- Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias (2012) (180)
- A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis (2013) (179)
- An Epigenome-Wide Association Study of Total Serum Immunoglobulin E Concentration (2014) (179)
- Investigation of the fine structure of European populations with applications to disease association studies (2008) (178)
- Blood pressure loci identified with a gene-centric array. (2011) (177)
- Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach (1996) (177)
- Combined sequence-based and genetic mapping analysis of complex traits in outbred rats (2013) (176)
- Genome‐wide linkage analysis for human longevity: Genetics of Healthy Aging Study (2013) (174)
- Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection (2014) (173)
- Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
- Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2018) (171)
- Genetic Influences on the End-Stage Effector Phase of Arthritis (2001) (170)
- Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis. (2004) (169)
- The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. (1988) (168)
- A missense mutation in the glucagon receptor gene is associated with non–insulin–dependent diabetes mellitus (1995) (168)
- Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation. (1997) (168)
- Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. (2011) (167)
- A linkage map of the rat genome derived from three F2 crosses. (1997) (166)
- A radiation hybrid map of 506 STS markers spanning human chromosome 11 (1994) (163)
- Chromosome 7p11.2 (EGFR) variation influences glioma risk. (2011) (161)
- A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines (2013) (158)
- Epidemiological study of the genetics and environment of asthma, bronchial hyperresponsiveness, and atopy: phenotype issues. (1997) (158)
- Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions (2012) (157)
- The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. (2010) (157)
- Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3). (1997) (157)
- Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'. (2006) (156)
- Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22 (2002) (155)
- Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13. (1992) (155)
- True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. (1997) (153)
- Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. (2013) (149)
- A mapped set of DNA markers for human chromosome 17. (1988) (148)
- Gene-environment interaction for childhood asthma and exposure to farming in Central Europe. (2011) (148)
- Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. (1986) (148)
- Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals. (2010) (147)
- The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence. (1991) (147)
- Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study (2011) (144)
- Genetic and Haplotypic Structure in 14 European and African Cattle Breeds (2007) (142)
- Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease (2011) (142)
- Variation in genomic landscape of clear cell renal cell carcinoma across Europe (2014) (142)
- Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups. (2012) (142)
- IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes (2018) (139)
- Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults – The GOYA Study (2011) (137)
- Determinants of Early Alcohol Use In Healthy Adolescents: The Differential Contribution of Neuroimaging and Psychological Factors (2012) (136)
- Serial translocation by means of circular intermediates underlies colour sidedness in cattle (2012) (135)
- Impaired anti-pneumococcal antibody response in patients with AIDS-related persistent generalized lymphadenopathy. (1987) (135)
- Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene. (1992) (135)
- Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysis. (2010) (134)
- Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis (2000) (134)
- Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. (2011) (133)
- Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats (1993) (130)
- Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome. (2001) (129)
- Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene (2014) (128)
- CD14 and toll-like receptor gene polymorphisms, country living, and asthma in adults. (2009) (124)
- Gene–environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study (2010) (124)
- Efficient computations in multilocus linkage analysis. (1988) (123)
- L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1. (2004) (122)
- Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior. (2008) (122)
- Common variants at 12q15 and 12q24 are associated with infant head circumference (2012) (121)
- Risk taking and the adolescent reward system: a potential common link to substance abuse. (2012) (121)
- A variant in FTO shows association with melanoma risk not due to BMI (2013) (120)
- Antibiotic treatment of venereal disease and Reiter's syndrome in a Greenland population. (1992) (119)
- Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. (1987) (119)
- Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 (2013) (119)
- Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies (2016) (118)
- Incidence of breast cancer and its subtypes in relation to individual and multiple low-penetrance genetic susceptibility loci. (2010) (117)
- The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility (2017) (113)
- Genome-wide association study of lung function decline in adults with and without asthma. (2012) (113)
- Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking. (2011) (113)
- A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project. (2005) (112)
- Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. (2005) (112)
- Regulation of insulin gene expression by the IDDM associated, insulin locus haplotype. (1995) (110)
- Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci. (1995) (109)
- Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE). (2001) (108)
- Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11. (1990) (108)
- Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. (2002) (107)
- Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls (2017) (107)
- Genome-wide association study identifies multiple susceptibility loci for glioma (2015) (107)
- A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. (2002) (107)
- A Genome‐Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium (2013) (106)
- Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (2012) (106)
- Combined linkage and segregation analysis using regressive models. (1988) (106)
- Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis (2011) (104)
- Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project (2010) (104)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
- Estimating genotype relative risks. (2008) (104)
- Unifying Candidate Gene and GWAS Approaches in Asthma (2010) (104)
- Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration (2011) (104)
- The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length (2014) (103)
- A primary genetic linkage map for human chromosome 12. (1987) (101)
- Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene (1991) (101)
- Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations (2011) (101)
- Nicotine consumption is regulated by a human polymorphism in dopamine neurons (2014) (100)
- Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. (1989) (99)
- Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls (2011) (99)
- Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension (2013) (99)
- Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (2018) (98)
- The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells. (2009) (98)
- Robustness and power of the unified model in the analysis of quantitative measurements. (1986) (98)
- Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study (2012) (97)
- A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. (2012) (97)
- Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis. (1984) (96)
- Multiple loci for multiple sclerosis (1996) (96)
- 17q21 variants modify the association between early respiratory infections and asthma (2009) (95)
- Transient receptor potential genes, smoking, occupational exposures and cough in adults (2012) (95)
- Erratum: Corrigendum: The European dimension for the mouse genome mutagenesis program (2004) (95)
- EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics. (1999) (95)
- Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6. (1997) (94)
- Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans (2013) (94)
- A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure. (1993) (93)
- Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome. (2004) (93)
- Genome-wide scan reveals association of psoriasis with IL-23 and NFB pathways (2016) (93)
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- Lipoxygenase-3 ( ALOXE 3 ) and 12 ( R )-lipoxygenase ( ALOX 12 B ) are mutated in non-bullous congenital ichthyosiform erythroderma ( NCIE ) linked to chromosome 17 p 13 . 1 (2001) (46)
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- Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. (2007) (45)
- A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. (2007) (44)
- DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34 (2002) (44)
- Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa. (1998) (44)
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- Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls (2013) (37)
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- Loss of chromosome Y leads to down regulation of KDM5D and KDM6C epigenetic modifiers in clear cell renal cell carcinoma (2017) (35)
- PNPLA 1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans (2014) (35)
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- A high-resolution linkage map for the Z chromosome in chicken reveals hot spots for recombination (2007) (33)
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- Multipoint mapping under genetic interference. (1993) (33)
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- Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects (2019) (32)
- Fine mapping of eight psoriasis susceptibility loci (2014) (32)
- A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients (2007) (32)
- Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions (2014) (32)
- Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families (2007) (32)
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- Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease (2005) (30)
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- A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis (2013) (29)
- Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits (2012) (28)
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- Genome-Wide Association Analysis of Young Onset Stroke Identifies a Locus on Chromosome 10 q 25 Near HABP 2 (2015) (28)
- Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study (2006) (28)
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- MeQA: a pipeline for MeDIP-seq data quality assessment and analysis (2012) (26)
- Quantitative Variation in Plasma Angiotensin‐I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus (2013) (26)
- Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells (2016) (26)
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- Evidence for linkage of a new region (11p14) to eczema and allergic diseases (2007) (26)
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- Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotype. (2003) (24)
- Identification of a new locus at 16q12 associated with time to asthma onset. (2016) (24)
- A Locus on Chromosome 2 Influences Levels of Tissue Factor Pathway Inhibitor: Results From the GAIT study (2005) (23)
- Linkage relationships among 20 genetic markers in cattle. Evidence for linkage between two pairs of blood group systems: B-Z and S-F/V respectively. (1990) (23)
- Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children (2008) (23)
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- Isolation and mapping of a polymorphic DNA sequence for human muscle glycogen phosphorylase (pMCMP1) on chromosome 11 [PYGM] (1988) (13)
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- Isolation and mapping of a polymorphic DNA sequence (pYNM18.1) on chromosome 15 [D15S35]. (1988) (2)
- Genome-Wide Analysis Identifies Strong Association Between HLA and IgA Nephropathy (2010) (2)
- Dysregulation at multiple points of the kynurenine pathway is a ubiquitous feature of renal cancer: implications for tumour immune evasion (2020) (2)
- Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations. (2020) (2)
- Isolation and mapping of a polymorphic DNA sequence (pTHIZ53) on chromosome 12 [D12S18]. (1988) (2)
- Leveling the Playing Field in Homozygosity Mapping Using Map Distances (2015) (2)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence pHHH122 on chromosome 2 (D2S54) (1987) (2)
- Isolation and mapping of a polymorphic DNA sequence (pEFD53.2) on chromosome 1 [D1S73]. (1988) (2)
- Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer’s disease (2021) (2)
- Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential (2007) (2)
- A new tool for checks of data precision within the MRC British genetics of hypertension study (2000) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH171) on chromosome 6p [D6S38]. (1988) (2)
- Correction: Global Genetic Variations Predict Brain Response to Faces (2014) (2)
- Data Analysis for Linkage Studies (1991) (2)
- 25.10.3 Linkage maps of human chromosomes (1989) (2)
- A7: Search for susceptibility loci to hypertension in a region on human chromosome 20Q, the homologous region to rat chromosome 3 (1997) (2)
- Isolation of mapping of a polymorphic DNA sequence pEFZ10 on chromosome 18 [D18S22]. (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p [D1S62]. (1988) (2)
- Localization, cDNA sequence and genomic organization of the rat seipin gene (Bscl2) and sequence analysis in inbred rat models of Type 2 diabetes mellitus (2003) (2)
- Association of a single nucleotide polymorphism in ubxn6 gene with long term non progression phenotype in hiv-positive individuals. (2019) (2)
- The canosinase gene (CNDP1) is not a protection factor of diabetic nephropathy in type 1 diabetics (2006) (2)
- Human variable number of tandem repeat probes as a source of polymorphic markers in experimental animals. (1991) (2)
- Isolation and mapping of a polymorphic DNA sequence pTHH54 on chromosome 10 [D10S13] (1988) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH119) on chromosome 1 [D1S59]. (1988) (2)
- Genetic mapping through the use of synthetic tandem repeats in the mouse genome (2004) (2)
- The Microbial Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function (2018) (2)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40]. (1988) (2)
- Susceptibility to lethal cerebral malaria is regulated by epistatic interaction between chromosome 4 (Berr6) and chromosome 1 (Berr7) loci in mice (2013) (2)
- Linkage analysis ofneurofibromatosis (1987) (2)
- MA23.10 Low Number of Mutations and Frequent Co-Deletions of CDKN2A and IFN Type I Characterize Malignant Pleural Mesothelioma (2019) (2)
- Estimation of recombination and genetic risks using several markers. (1984) (2)
- Isolation and mapping of a polymorphic DNA sequence (pHHH106) on chromosome 1 [D1S67]. (1988) (2)
- Mapping of 20 polymorphic DNA markers in the rat by somatic hybrid and linkage analysis (2009) (2)
- Detection of CNVs throughout the genome of a porcine melanoma model. (2011) (2)
- Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (2019) (2)
- Isolation and mapping of a polymorphic DNA sequence (pRMU7.4) on chromosome 7p [D7S370]. (1988) (2)
- Multiple therapeutic pathways in malignant mesothelioma identified by genomic mapping (2020) (2)
- Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma (2015) (2)
- Mapping approaches to gene identification in humans. (1987) (2)
- Isolation and mapping of a polymorphic DNA sequence for human muscle glycogen phosphorylase (pMCMP1) on chromosome II [PYGM]. (1988) (2)
- Aberration hubs in protein interaction networks highlight actionable targets in cancer (2018) (2)
- Genome-wide association scans identify novel loci that influence lipid levels and risk of coronary artery disease (2007) (2)
- Correction: Genetic Structure of Europeans: A View from the North–East (2010) (2)
- Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2019) (2)
- Isolation and mapping of a polymorphic DNA sequence pEKZ105 on chromosome 2 (D2S55). (1987) (2)
- Differentiation power of SNPs for assessing the phylogenetic structure of populations (2014) (2)
- Isolation and mapping of a polymorphic DNA sequence pTBAB5.7 on chromosome 2 (D2S47). (1987) (1)
- Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants (2015) (1)
- Isolation and mapping of a polymorphic DNA sequence pYNZ90.1 on chromosome 15 [D15S28]. (1988) (1)
- A genome scan for allergic asthma and related phenotypes in an Italian population sample (2002) (1)
- Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54]. (2018) (1)
- Isolation and mapping of a polymorphic DNA sequence pMCT136 on chromosome 9q (D9S10). (1987) (1)
- Program and abstracts of the 6th Transgenic Technology Meeting (TT2005) (2005) (1)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.193) on chromosome 11 [D11S384]. (1989) (1)
- Abstract 19115: Genome-Wide Association Study and Replication Identifies a Novel Genetic Locus for Aortic Stenosis (2017) (1)
- Identification of a new locus at 16 q 12 associated with time-to-asthma onset 1 2 (2016) (1)
- Brief report KNG1 Ile581Thr and susceptibility to venous thrombosis (2011) (1)
- No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study. (2001) (1)
- Erratum: USP15 regulates type I interferon response and is required for pathogenesis of neuroinflammation (2016) (1)
- Association between C 677 T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease : Meta-Analysis of 7 , 697 Cases and 13 , 125 Controls Running title : Mamasoula : MTHFR C 677 T polymorphism and congenital heart disease (2013) (1)
- [Fiessinger-Leroy-Reiter syndrome in Greenland. Clinical and epidemiological aspects]. (1987) (1)
- Association between a genetic trait and a marker: Discrimination between epistasis and gametic disequilibrium (2004) (1)
- Pubertal development and prostate cancer risk (2018) (1)
- Individuals with a genetic shift in haematological indices (2008) (1)
- Isolation and mapping of a polymorphic DNA sequence (cYNA4) on chromosome 2 [D2S50]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pKKA35) on chromosome 17 [D17S75]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3. (1988) (1)
- Susceptibility to type 1 diabetes mellitus and the insulin locus (1992) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMCOC12) on chromosome 14 [D14S20] (1988) (1)
- No Association of the Wnk1 Gene With Essential Hypertension in the Mrc Bright Study (2004) (1)
- Isolation and mapping of a polymorphic DNA sequence (pTHH55) on chromosome 15 [D15S27]. (1988) (1)
- JEAN B DAUSSET, 19 OCTOBER 1916–6 JUNE 2009 (2009) (1)
- Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot (2018) (1)
- Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9). (1987) (1)
- Isolation and mapping of a polymorphic DNA sequence pEKZ104.1 on chromosome 15 [D15S30]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pMCT46.2 on chromosome 15 [D15S26]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence pHBI40 on chromosome 1 (D1S66). (1987) (1)
- Genetic linkage mapping of susceptibility loci in rheumatoid arthritis. (1996) (1)
- HLA antigens andseronegative rheumatoid arthritis (1985) (1)
- Genomic studies across the lifespan point to early mechanisms determining subcortical volumes. (2021) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD6) chromosome 6 [D6S41]. (1988) (1)
- Genetics of multifactorial disease (1998) (1)
- Nicotinic Acetylcholine Receptor Polymorphism, Smoking History and Lung Function Decline. (2009) (1)
- Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
- P. Meera Khan (1998) (1)
- Isolation and mapping of a polymorphic DNA sequence (pCMM66) on chromosome 14 [D14S22] (1988) (1)
- Efficiency of recombination estimates using two-and three-point linkage data. (1985) (1)
- ENHANCED SUPPORT FOR LINKAGE TO CHROMOSOME 5Q13.1 AND HYPERTENSION IN THE BRITISH GENETICS OF HYPERTENSION (BRIGHT) STUDY.: 5.1 (2005) (1)
- In search of genetic precision. Authors' reply (2003) (1)
- Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma (2023) (1)
- Title : Polymorphisms in the WNK 1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion (2009) (1)
- Isolation and mapping of a polymorphic DNA sequence (cKKA39) on chromosome 14 [D14S23]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ94) on chromosome 17 [D17S80]. (1988) (1)
- DNA methylation and lung function: an epigenome-wide association study (2017) (1)
- Isolation and mapping of a polymorphic DNA sequence pYNZ9.1 on chromosome 2 (D2S46). (1987) (1)
- Intergenic variants of HBSIL-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing HbF levels in adults. (2006) (1)
- High glucose and low lactate: a metabolic signature of hypertension in human serum? (2008) (1)
- THE LOCALIZATION OF 2 SUSCEPTIBILITY GENES FOR INSULIN-DEPENDENT DIABETES IN THE NONOBESE DIABETIC MOUSE (1991) (1)
- The clock gene Period 2 influences the glutamatergic system and thereby modulates alcohol consumption (2005) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNZ15) on chromosome 2 [D2S50]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMCOC14) on chromosome 4p [D4S124] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15 [DLSS44] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD85.7) on chromosome 15 [D15S37] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.1) on chromosome 16 [D16S152]. (1989) (1)
- In search of genetic precision (2003) (1)
- Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancer (2021) (1)
- Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study. (2015) (1)
- Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18)) (2012) (1)
- Isolation and mapping of a polymorphic DNA sequence (HBI18P1) on chromosome 11 [D11S147]. (1989) (1)
- Abstract #LB-139: A comprehensive genome-wide association study of lung cancer (2009) (1)
- Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D13S36] (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ21) on chromosome 9q [D9S30]. (1988) (1)
- Isolation and mapping of a polymorphic DNA sequence (pHHH208) on chromosome 14 [D14S19]. (1988) (1)
- Regions associated at P<5×10−5 with early-onset BD in meta-analysis. (2014) (0)
- Loci on Chromosomes 5p and 20q are Linked to Multiple Hypertension Phenotypes in the BRItish Genetics of HyperTension (BRIGHT) Study: LB13 (2005) (0)
- Isolation and mapping of a polymorphic DNA sequence pMHZ9 on chromosome 14 [D14S18] (1988) (0)
- Abstract 17386: LPA Variants and Aortic Stenosis - a Large-Scale Case-Control Study Using Electronic Health Records (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM17.1) on chromosome 10 [D10S16]. (1988) (0)
- Genome-wide association study identifies common variation associated with congenital heart disease (2013) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- P2.03-10 Comprehensive Molecular Profiling and Comparison of Common and Rarer Subtypes of Lung Cancer (2019) (0)
- 1 Interaction between DNAH 9 gene and early smoke exposure on bronchial hyper-responsiveness (2016) (0)
- Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. (2023) (0)
- HLA-B27 SUBTYPING BY SINGLE-STRAND CONFORMATION POLYMORPHISMS (SSCP) IN CAUCASOIDS, NEGROIDS AND INUITS FROM GREENLAND (1992) (0)
- Erratum: Genomic approach of AIDS pathogenesis: Exhaustive genotyping of the TNFR1 gene in a French AIDS cohort (Biomedicine and Pharmacotherapy 59:8 (476) DOI: 10.1016/j.biopha.2005.07.011) (2005) (0)
- Observational and Genetic Associations of Cardiovascular Risk Factors with Aortic Stenosis (2018) (0)
- MA23.11 Analysis of Immune Phenotype Composition in Malignant Pleural Mesothelioma (MPM) Using Bulk RNA Sequencing (2019) (0)
- Systems Genetics of Hepatic Metabolome Reveals Octopamine as a Target for Non-Alcoholic Fatty Liver Disease Treatment (2019) (0)
- Abstract 941: Exome sequencing identifiedPOT1, a telomere shelterin gene, as a major susceptibility gene for familial cutaneous malignant melanoma (2014) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.4) on chromosome 11 [D11S388]. (1989) (0)
- Localization of the rat stimulatory G-protein alpha subunit (GNPAS) gene to rat Chromosome 3 by linkage analysis (1996) (0)
- Linkage Analysis inSpinal Muscular Atrophy, bySixClosely Flanking Markers on Chromosome5 (1991) (0)
- Isolation and mapping of a polymorphic DNA sequence (2CJ52.208M2) on chromosome 11 [D11S351]. (1989) (0)
- Genome-wide association meta-analysis in 652,134 participants identifies 9 novel susceptibility loci for aortic stenosis (2020) (0)
- Abstract 2076: Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease (2009) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15. (1988) (0)
- This information is current as Typhoid-like Disease Mutants Confer Susceptibility to Acute Induced STAT 4 −-Nitrosourea N-Ethyl-N Transcriptional Expression Patterns in Mediated Immunity and − γ Altered IFN - (2013) (0)
- 183 The Sa gene locus cosegregates with increased blood pressure in the spontaneously hypertensive rat (1993) (0)
- A genomewide association meta-analysis of plasma beta-amyloid peptide concentrations in the elderly (2013) (0)
- Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation (2015) (0)
- COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: awaiting peer review] (2020) (0)
- Imputed classical HLA II alleles, occupational allergen exposure and adult-onset asthma (2012) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMI37) on chromosome 7 [D7S368]. (1988) (0)
- Attenuates Insulin Resistance in Obese Children Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and PIK3CB Association Analysis Indicates That a Variant GATA-Binding Site in the (2015) (0)
- Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH22) on chromosome 9 [D9S12]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.209M2) on chromosome 16 [D16S151]. (1989) (0)
- EURAGEDIC study: identification of new candidate genes for diabetic nephropathy (2007) (0)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks (2017) (0)
- Practicable approaches to targeted comparative mapping of rat chromosome regions: linkage mapping of five genes on rat chromosome 13 (1998) (0)
- [Viral epidemics and their relationship to the excess of males at birth: divergent data] (1983) (0)
- Stage 2 Genome-Wide Association Study of Candidate Low Penetrance Genes Implicated in Breast Cancer Risk (2009) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT106) on chromosome 2 [D2S61]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D15S36]. (1988) (0)
- DNA methylation and serum total immunoglobulin E (IgE) levels: a methylome-wide association study in adults with asthma (2018) (0)
- Confirmation ofgenetic linkage betweenatopic IgEresponsesandchromosome 11q13 (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOE32) on chromosome 2 [D2S53] (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.99M2) on chromosome 11 [D11S389]. (1989) (0)
- Influence of gene-by-early environmental tobacco smoke exposure interactions on time-to-asthma onset (2016) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOC46) on chromosome 13 [D13S54]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pKKA40) on chromosome 9q [D9S31]. (1988) (0)
- COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE (2010) (0)
- Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease (2009) (0)
- Detection and Estimation of Linkage, Especially Multipoint Mapping (1987) (0)
- Genetic analysis of autoimmune type 1 diabetes mellitus in mice. 1991. (2014) (0)
- Abstract 4730: Integrating pathway analysis and genetics of gene expression for genome-wide association study on basal cell carcinoma (2011) (0)
- Isolation and mapping of a polymorphic DNA sequence (p1CJ52.208M2) on chromosome 11 [D11S351]. (1989) (0)
- 6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA (2015) (0)
- Abstract LB113: Genomic classification to refine prognosis in clear cell renal cell carcinoma (2022) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.94T1) on chromosome 16 [D16S159]. (1989) (0)
- Sex specific associations in genome wide association analysis of renal cell carcinoma (2019) (0)
- Integrated genomics identify novel immunotherapy targets for malignant mesothelioma (2020) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD134.7) on chromosome 3 [D3S45]. (1988) (0)
- Abstract 3861: A genome-wide association study of upper aerodigestive tract cancers identifies 4q21, 4q23, and 12q24 as susceptibility loci (2010) (0)
- Isolation and mapping of a polymorphic DNA sequence (cYNA12) on chromosome 13 [D13S53]. (1988) (0)
- Copy number variations in malignant pleural mesothelioma reveal novel regions of genomic imbalances (2018) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.15) on chromosome 11 [D11S383]. (1989) (0)
- Efficiency of recombination estimates using two-and three-point linkage data. (1985) (0)
- Papillary thyroid cancer (PTC) among individuals exposed to radioactive iodine in their childhood or adolescence is a major internationally recognized health consequence of the Chernobyl accident. To identify genetic determinants affecting individual susceptibility to radiation-related PTC, we condu (2017) (0)
- Quantitative phenotype analysis for localization and identification of disease-related genes in a complex genetic background. (1996) (0)
- Annual Scientific Meeting of the British Hypertension Society, Cambridge, UK, 11–13 September 2000 (2000) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFZ38) on chromosome 2 [D2S60]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pYNH20) on chromosome 13 [D13S50]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.197) on chromosome 16 [D16S156]. (1989) (0)
- association studies cancer and the effect of control selection on genetic Genetic variation in protein specific antigen detected prostate (2014) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD49.3) on chromosome 15. (1988) (0)
- Abstract 17979: A Genome-Wide Association Study of Risk of Coronary Artery Disease in European and South Asian Populations (2010) (0)
- Abstracts from the 50th European Society of Human Genetics Conference: Oral Presentations (2018) (0)
- Abstract 13687: Global Rare Genic Copy Number Variants Contribute to Isolated Sporadic Tetralogy of Fallot (2011) (0)
- Isolation and mapping of a polymorphic DNA sequences (pTHH28) on chromosome 7p (1988) (0)
- 1q21.1 rearrangements in non-syndromic tetralogy of Fallot and other congenital heart defects (2011) (0)
- Shared genomic segment analysis with equivalence testing (2020) (0)
- Author Correction: EMPReSS: standardized phenotype screens for functional annotation of the mouse genome (2022) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]. (1988) (0)
- Consequences of VHL Loss on Global DNA Methylome (2018) (0)
- P-138 A comparison of the transcriptomic profiles of matched tissue from primary colorectal cancer and corresponding secondary lung metastases (2020) (0)
- Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma (2022) (0)
- Haplotype Signatures At HBS1L-MYB In Global Populations (2013) (0)
- Linkage Maps of Human Genes (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMC96.1 and pMCT96.2) on chromosome 9q (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNM17 on chromosome 9q (D9S6). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (DIS58). (1987) (0)
- OR4-4: The causal role of IGFs and IGFBPs in prostate cancer: a Mendelian randomization study (2014) (0)
- Gene-Environment (GxE) Interactions in Childhood Type 1 Diabetes (T1D): A Case-only Geographical Approach in the ISIS-Diab Cohort (2016) (0)
- Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells (2016) (0)
- HLA-B27 TYPING BY PCR OF A GREENLAND POPULATION (1992) (0)
- COVID-19 and Beyond: A Call for Action and Audacious Solidarity to All the Citizens and Nations, It Is Humanity’s Fight (2020) (0)
- The melanoblastoma-bearing Libechov minipig model: a tool for melanoma genetics (2009) (0)
- Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
- WNK1 - functional analyses of variants associated with blood pressure and essential hypertension (2008) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMCT96.1 and pMCT96.2) on chromosome 9q [D9S14]. (1988) (0)
- Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case–control study (2014) (0)
- Nucleic acid encoding cgl1 polypeptide and application of this nucleic acid and cgl1 polypeptide to diagnosis and therapeutics (2001) (0)
- Contents, Vol. 44, 1994 (1994) (0)
- Linkage Studies on Tuberous Sclerosis with Probes for Chromosome 11q (1991) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.5) on chromosome 11 [D11S386]. (1989) (0)
- Oppositional COMT Val158Met effects on resting state functional connectivity in adolescents and adults (2014) (0)
- 55: Somatic BAP1 and NF2 mutations in pleural malignant mesothelioma and their correlation with clinical phenotype (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH14) on chromosome 12p [D12S16]. (1988) (0)
- Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease (2007) (0)
- Correction: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (0)
- Quantitative phenotype analysis for localization and identification of disease-related genes in a complex genetic background. (1996) (0)
- Distinct pancreatic and neuronal Lung Carcinoid molecular subtypes revealed by integrative omic analysis (2021) (0)
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- Isolation and mapping of a polymorphic DNA sequence (pMCT32.1) on chromosome 3 [D3S31]. (1988) (0)
- 33rd European Mathematical Genetics Meeting, EMGM2005, Le Kremlin‐Bicêtre, France, April 1st‐2nd 2005 (2005) (0)
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- Subject Index, Vol. 33, 1983 (1983) (0)
- Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg 1859, 2018) (2020) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.27) on chromosome 16 [D16S149]. (1989) (0)
- T. Ohta — Evolution and variation of multigene families (1985) (0)
- Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome (2017) (0)
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- Isolation and mapping of a polymorphic DNA sequence (pMCT149.2) on chromosome 15. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFD122 on chromosome 2 (D2S48). (1987) (0)
- A small number of early introductions seeded widespread transmission of SARS-CoV-2 in Québec, Canada (2021) (0)
- ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP (2009) (0)
- Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
- Abstract / Session Information for Program Number 876 Print Close window Session Information Session Title : . Complex Traits and Polygenic Disorders Session Type : Poster Session (2009) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]. (1988) (0)
- Hypertension Summer School 1992 (1993) (0)
- Implication du gène SRPX2 dans des pathologies de l’aire rolandique (2007) (0)
- The BDA Warren Type 2 Diabetes Sibpair Repository: Susceptibility regions identified by genome scan of 439 European families (2000) (0)
- Interactive Effects ofNOS1andNOS3Genetic Variants and Asthma on FeNOLevel in the EGEA Study. (2009) (0)
- Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia (2016) (0)
- Copy number variation identified on chromosome 5p13. (2014) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ17) on chromosome 13 [D13S51]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM17.4) on chromosome 10 [D10S23]. (1988) (0)
- A Genome-Wide Association Study for Melanoma Predisposition in the MeLiM Biomedical Swine Model by using the PorcineSNP60 Beadchip (2010) (0)
- Chromosome 7p11.2(EGFR) and 7q36.1(XRCC2) variants influence glioma risk (2011) (0)
- Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15. (1988) (0)
- Comparison of the statistical power for three categories of prior odds for the null hypothesis when evaluating the noteworthiness of SNPs by BFDP. (2012) (0)
- Contents, Vol. 33, 1983 (1983) (0)
- Incidence and burden of major comorbidities among individuals with COPD: a comprehensive analysis using data from primary care (2009) (0)
- Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls Running title: Mamasoula: MTHFR C677T polymorphism and congenital heart disease (2017) (0)
- Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol (2019) (0)
- Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on genomics of renal cancer (2020) (0)
- BIOINFORMATICS APPLICATIONS MeQA: a pipeline for MeDIP-seq data quality assessment and analysis (2012) (0)
- DNA markers for the cystic fibrosis locus. (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (pMHZ13) on chromosome 9q [D9S13]. (1988) (0)
- Quantitative analysis of absence-epilepsy in the GAERS rat (2003) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMI40) on chromosome 13 [D13S49]. (1988) (0)
- Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2019) 178(1) (262), (S0092867419306798), (10.1016/j.cell.2019.06.016)) (2020) (0)
- Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature (2022) (0)
- FineStructure DNA Mapping Studies oftheChromosomal Region Harboring theGenetic Defect in Neurofibromatosis TypeI (1989) (0)
- Abstract 13234: 1q21.1 Microduplications are Strongly Associated with Tetralogy of Fallot and 1q21.1 Microdeletions are Associated with Other Congenital Heart Defects (2011) (0)
- [Reiter's syndrome in the Inuit population of Greenland. A clinical, immunogenetic and epidemiological study]. (1987) (0)
- Gene mapping. (1990) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH115.2 on chromosome 2 (D2S54). (1987) (0)
- Targeted next-generation sequencing of malignant pleural mesothelioma identifies recurrent NRAS oncogene mutations (2018) (0)
- Isolation and mapping of a polymorphic DNA sequence (cMCOD13) on chromosome 3 [D3S44]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.10) on chromosome 16 [D16S153]. (1989) (0)
- Title: Sex Specific Associations in Genome Wide Association Analysis of Renal Cell Carcinoma (2019) (0)
- Correction to: Overlapping genetic architecture between Parkinson disease and melanoma (2020) (0)
- Symposium on variation in the human genome, held at the Ciba Foundation, London 13-15 June 1995 - Final discussion (1996) (0)
- Fast Accurate Heritability Screening Using Whole-genome Data (2014) (0)
- EURAGEDIC study: analyses of 144 candidate genes for diabetic nephropathy (2006) (0)
- Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements (2019) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH37) on chromosome 14 [D14S16]. (1988) (0)
- Abstract 1135: DRD2 is critical for pancreatic cancer and promises pharmacological therapy by already established antagonists (2017) (0)
- Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH220 on chromosome 9p (D9S27). (1987) (0)
- Contents Vol. 117, 2007 (2007) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.196M1) on chromosome 16 [D16S160]. (1989) (0)
- Abstract 1302: Genome-wide association study of glioma reveals specific differences in genetic susceptibility to glioblastoma and non-glioblastoma (2017) (0)
- 447. Respiratory diseases at at work: epidemiology, inflammation and challenge studies (2012) (0)
- The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource (2004) (0)
- Isolation and mapping of a polymorphic DNA sequence pRMU1 on chromosome 17q [D17S27]. (1988) (0)
- C Identification of the major genetic contributors to tetralogy of fallot (2019) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH133 on chromosome 2 (D2S45). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence pHHH152 on chromosome 17q [D17S32]. (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.95M1) on chromosome 16 [D16S148]. (1989) (0)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.105) on chromosome 16 [D16S154]. (1989) (0)
- Mold allergen sensitization in adult asthma according to ITGB 3 polymorphisms and TLR 2 / + 596 genotype (2012) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFZ18.2 on chromosome 14 [D14S17] (1988) (0)
- Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature (2022) (0)
- Taking into Account Gene-by-Early Environmental Tobacco Smoke Exposure Interactions to Detect Genetic Variants Influencing Time-to-Asthma Onset (2016) (0)
- Animal Cytogenetics and Comparative Mapping (2003) (0)
- Isolation and mapping of a polymorphic DNA sequence (2CJ52.208M2) on chromosome II [D11S351] (1989) (0)
- EURAGEDIC; European consortium for the genetics of diabetic nephropathy: strategy and first results. (2003) (0)
- Isolation and mapping of a polymorphic DNA sequence pYNZ156 on chromosome 10 [D10S18] (1988) (0)
- Isolation and mapping of a polymorphic DNA sequence (MCT117) on chromosome 11 [D11S145]. (1988) (0)
- Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome (2019) (0)
- Large-scale test of association between myocardial infarction, plasma lipid levels and apolipoprotein E e2/e3/e4 polymorphism in about 11,000 cases and controls (2000) (0)
- Running title: Genome-wide association study in long QT syndrome (2020) (0)
- HostSeq: a Canadian whole genome sequencing and clinical data resource (2022) (0)
- Nucleic Acids Research (2015) (0)
- IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes (2018) (0)
- HLA Class II Alleles, Occupational Exposures And Asthma: A Candidate Gene-Environment Interaction (2012) (0)
- Subject Index Vol. 44, 1994 (1994) (0)
- Multi-ancestry association study identifies new asthma risk loci that co-localize with 1 immune cell enhancer marks 2 (2017) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.209M1) on chromosome 16 [D16S151]. (1989) (0)
- Vitamin D levels and susceptibility to asthma, elevated IgE levels 3 and atopic dermatitis (2017) (0)
- A solution to the Crow-Omaha problem and its implications for future research into social organization (1978) (0)
- Abstract 13867: A Genome-wide Association Study of Nonsyndromic Mitral Valve Prolapse and Functional Studies of Risk Loci Provide Insight Into Underlying Biological Mechanisms (2014) (0)
- [Genetic effect on specific human immune responses to tetanus anatoxin]. (1983) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.161) on chromosome 16 [D16S150]. (1989) (0)
- Genes and Common Diseases: Genetics of hypertension (2007) (0)
- Abstract / Session Information for Program Number 765 Print Close window Session Information Session Title : . Complex Traits and Polygenic Disorders (2009) (0)
- Exploring rare and low-frequency variants in the Saguenay–Lac-Saint-Jean population identified genes associated with asthma and allergy traits (2018) (0)
- CombinedSegregation andLinkage Analysis ofGenetic Hemochromatosis UsingAffection Status, SerumIron, andHLA (1990) (0)
- Isolation and mapping of a polymorphic DNA sequence pEFD40.3 on chromosome 9 (D9S8). (1987) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.96) on chromosome 16 [D16S157]. (1989) (0)
- Familial Atherosclerotic Disease and Hypertension Localised To Chromosome 7p in the British Genetics of Hypertension Study: LB19 (2006) (0)
- GENETIC ANALYSIS OF CIRCADIAN RHYTHM GENES PER1 AND PER2 IN PATIENTS WITH ALCOHOL DEPENDENCE. (2004) (0)
- Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]. (1988) (0)
- Pillars Article: Genetic Analysis of Autoimmune Type 1 Diabetes Mellitus in Mice. Nature. 1991. 351: 542-547 (2014) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.75M1) on chromosome 11 [D11S385]. (1989) (0)
- A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15 (2008) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.199) on chromosome 16 [D16S155]. (1989) (0)
- Systematic analysis of 123 candidate genes reveals two novel genes for hypertension (2008) (0)
- COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: 3 approved with reservations] (2021) (0)
- University of Groningen Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation (2018) (0)
- ASSESSMENT OF T-CELL RECEPTOR-ALPHA/DELTA AND BETA-LOCI CONTRIBUTION TO RHEUMATOID-ARTHRITIS (RA) SUSCEPTIBILITY USING NEW POLYMORPHIC MARKERS (1992) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCJ52.102T1) on chromosome 11 [D11S387]. (1989) (0)
- Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
- Collective inference for Computational Discovery of Heart-Specific Cis-Regulatory Sites (2007) (0)
- A quantitative trait locus on chromosome 11 is the major genetic determinant of homocysteine plasma levels. Results from the GAIT Project (2003) (0)
- Isolation and mapping of a polymorphic DNA sequence (CJ52.112) on chromosome 16 [D16S158]. (1989) (0)
- A major quantitative trait locus on chromosome 6q23 for HbF levels - An update (2007) (0)
- Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study (2007) (0)
- Isolation and mapping of a polymorphic DNA sequence (pCMM62) on chromosome 14 [D14S21]. (1988) (0)
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