| human | Q5 |
| P2381 | Academic Tree ID | 361887 |
| P4955 | MR Author ID | 924194 |
| P496 | ORCID iD | 0000-0002-4472-8103 |
| P1153 | Scopus author ID | 57210773481 |
| P184 | doctoral advisor | Duncan C Thomas | Q88599544 |
| P69 | educated at | University of Southern California | Q4614 |
| P108 | employer | Harvard T.H. Chan School of Public Health | Q5676556 |
| P734 | family name | Kraft | Q10548439 |
| Kraft | Q10548439 | ||
| Kraft | Q10548439 | ||
| P735 | given name | Peter | Q2793400 |
| Peter | Q2793400 | ||
| Lawrence | Q15635788 | ||
| Lawrence | Q15635788 | ||
| Phillip | Q19816553 | ||
| Phillip | Q19816553 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q31154835 | A Bayesian latent class analysis for whole-genome association analyses: an illustration using the GAW15 simulated rheumatoid arthritis dense scan data |
| Q39477976 | A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium |
| Q28384141 | A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer |
| Q55210146 | A Large Study of Androgen Receptor Germline Variants and Their Relation to Sex Hormone Levels and Prostate Cancer Risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium. |
| Q92224274 | A Mendelian randomization analysis of circulating lipid traits and breast cancer risk |
| Q92858823 | A Prospective Analysis of Circulating Plasma Metabolites Associated with Ovarian Cancer Risk |
| Q92515702 | A Transcriptome-Wide Association Study (TWAS) Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer |
| Q57306192 | A candidate gene approach to searching for low-penetrance breast and prostate cancer genes |
| Q46378338 | A common 8q24 variant in prostate and breast cancer from a large nested case-control study |
| Q35755874 | A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer |
| Q33980349 | A comprehensive analysis of common IGF1, IGFBP1 and IGFBP3 genetic variation with prospective IGF-I and IGFBP-3 blood levels and prostate cancer risk among Caucasians |
| Q45305326 | A comprehensive analysis of polymorphic variants in steroid hormone and insulin-like growth factor-1 metabolism and risk of in situ breast cancer: Results from the Breast and Prostate Cancer Cohort Consortium. |
| Q35605845 | A comprehensive analysis of the androgen receptor gene and risk of breast cancer: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q36310685 | A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts |
| Q35093501 | A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer |
| Q34350941 | A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation |
| Q28740367 | A genome-wide association search for type 2 diabetes genes in African Americans |
| Q28303909 | A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer |
| Q33335147 | A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation |
| Q24597370 | A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33 |
| Q91694193 | A genome-wide association study of bitter and sweet beverage consumption |
| Q28943434 | A genome-wide association study of depressive symptoms |
| Q36682471 | A genome-wide association study of early menopause and the combined impact of identified variants |
| Q58803790 | A genome-wide association study of energy intake and expenditure |
| Q34881099 | A genome-wide association study of marginal zone lymphoma shows association to the HLA region |
| Q33780746 | A genome-wide association study of prognosis in breast cancer |
| Q37192589 | A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication |
| Q113906180 | A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome |
| Q35177444 | A genome-wide pleiotropy scan for prostate cancer risk |
| Q33566592 | A large prospective study of SEP15 genetic variation, interaction with plasma selenium levels, and prostate cancer risk and survival |
| Q34113217 | A large study of androgen receptor germline variants and their relation to sex hormone levels and prostate cancer risk. Results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium |
| Q24619411 | A large-scale candidate gene association study of age at menarche and age at natural menopause |
| Q91119899 | A large-scale exome array analysis of venous thromboembolism |
| Q99554778 | A lipid-related metabolomic pattern of diet quality |
| Q35248192 | A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer |
| Q36435849 | A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. |
| Q36477652 | A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease |
| Q34085748 | A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). |
| Q92711687 | A network analysis to identify mediators of germline-driven differences in breast cancer prognosis |
| Q33577138 | A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies |
| Q33870435 | A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes |
| Q36535684 | A prospective study of plasma adiponectin and pancreatic cancer risk in five US cohorts |
| Q37318709 | A prospective study of relative telomere length and postmenopausal breast cancer risk |
| Q91960210 | A response to "Personalised medicine and population health: breast and ovarian cancer" |
| Q50103145 | A test for gene-environment interaction in the presence of measurement error in the environmental variable. |
| Q57305942 | A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer |
| Q36083454 | ABO blood group alleles and prostate cancer risk: Results from the breast and prostate cancer cohort consortium (BPC3). |
| Q36848913 | ABO blood group and breast cancer incidence and survival |
| Q34949621 | ABO blood group and risk of colorectal cancer |
| Q37131928 | ABO blood group and the risk of pancreatic cancer |
| Q30370833 | APOE ε variants increase risk of warfarin-related intracerebral hemorrhage. |
| Q58074718 | Abstract 4593: Genome-wide association study identifies novel loci associated with osteosarcoma |
| Q58047207 | Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk |
| Q61948762 | Abstract LB-448: Genome-wide association study identifies new prostate cancer susceptibility loci |
| Q51980808 | Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques. |
| Q57748350 | Addition of a polygenic risk score, mammographic density, and endogenous hormones to existing breast cancer risk prediction models: A nested case-control study |
| Q34472668 | Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium |
| Q35059386 | Adjusting for heritable covariates can bias effect estimates in genome-wide association studies |
| Q29248820 | Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample |
| Q64989893 | Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer. |
| Q44030444 | Ala12 variant of the peroxisome proliferator-activated receptor-gamma gene (PPARG) is associated with higher polyunsaturated fat in adipose tissue and attenuates the protective effect of polyunsaturated fat intake on the risk of myocardial infarctio |
| Q34993331 | Alcohol intake and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (PanScan) |
| Q38752732 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans |
| Q37170192 | An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general population |
| Q80120952 | Analyses of genome-wide association scans for additional outcomes |
| Q36055011 | Analysis of case-control association studies with known risk variants |
| Q38045344 | Analysis of epidemiologic studies of genetic effects and gene-environment interactions |
| Q24170413 | Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types |
| Q40044635 | Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry |
| Q34287725 | Androgen receptor CAG repeat polymorphism and risk of TMPRSS2:ERG-positive prostate cancer |
| Q53267259 | Androgen receptor polymorphisms and endometrial cancer risk. |
| Q34059780 | Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan). |
| Q34390505 | Aspirin use, 8q24 single nucleotide polymorphism rs6983267, and colorectal cancer according to CTNNB1 alterations |
| Q37292397 | Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses |
| Q90666760 | Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium |
| Q97070156 | Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers |
| Q57305944 | Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci |
| Q45979098 | Association analysis identifies 65 new breast cancer risk loci. |
| Q36123803 | Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses |
| Q37608701 | Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss |
| Q35020463 | Association of KLK3 (PSA) genetic variants with prostate cancer risk and PSA levels |
| Q37276250 | Association of adiposity genetic variants with menarche timing in 92,105 women of European descent |
| Q36191018 | Association of breast cancer risk loci with breast cancer survival |
| Q37268494 | Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry |
| Q114182713 | Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment |
| Q34314362 | Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the Breast and Prostate Cancer Cohort Consortium |
| Q61822090 | Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use |
| Q91045562 | Associations of autozygosity with a broad range of human phenotypes |
| Q91495299 | Associations of dairy intake with risk of mortality in women and men: three prospective cohort studies |
| Q57056093 | Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis |
| Q36792641 | Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation |
| Q63966080 | Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci |
| Q64118820 | Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci |
| Q55399654 | Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. |
| Q60907509 | Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry |
| Q85036540 | Averaged or stratified measures of risk profile discrimination: horses for courses |
| Q58047301 | Beyond odds ratios — communicating disease risk based on genetic profiles |
| Q33808553 | Biomarker correlation network in colorectal carcinoma by tumor anatomic location |
| Q35852637 | Body Mass Index Genetic Risk Score and Endometrial Cancer Risk |
| Q46115524 | Body mass index and breast cancer survival: a Mendelian randomization analysis |
| Q39734134 | Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States |
| Q36955118 | Breast cancer susceptibility loci and mammographic density |
| Q26999715 | CHRNA5 risk variant predicts delayed smoking cessation and earlier lung cancer diagnosis--a meta-analysis |
| Q36998293 | COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration |
| Q44449983 | CYP17 genetic variation and risk of breast and prostate cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q45222299 | CYP19 (aromatase) haplotypes and endometrial cancer risk |
| Q33616702 | CYP19A1 genetic variation in relation to prostate cancer risk and circulating sex hormone concentrations in men from the Breast and Prostate Cancer Cohort Consortium |
| Q36916332 | Challenges and opportunities in genome-wide environmental interaction (GWEI) studies |
| Q36030354 | Characterization of gene-environment interactions for colorectal cancer susceptibility loci |
| Q24169697 | Characterization of large structural genetic mosaicism in human autosome |
| Q33842251 | Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3. |
| Q40266936 | Cigarette Smoking and Pancreatic Cancer Survival |
| Q37323444 | Cigarette smoking and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium |
| Q28387050 | Circadian genes and breast cancer susceptibility in rotating shift workers |
| Q90588115 | Circulating Lysophosphatidylcholines, Phosphatidylcholines, Ceramides, and Sphingomyelins and Ovarian Cancer Risk: a 23-year Prospective Study |
| Q36848069 | Circulating Metabolites and Survival Among Patients With Pancreatic Cancer |
| Q102380856 | Circulating carotenoids and breast cancer among high-risk individuals |
| Q37155349 | Circulating prediagnostic interleukin-6 and C-reactive protein and prostate cancer incidence and mortality |
| Q63352590 | Circulating vitamin D concentrations and risk of breast and prostate cancer: a Mendelian randomization study |
| Q27336054 | Circulating vitamin D, vitamin D-related genetic variation, and risk of fatal prostate cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium |
| Q91639125 | Colorectal cancer susceptibility variants and risk of conventional adenomas and serrated polyps: results from three cohort studies |
| Q94486442 | Combined associations of a polygenic risk score and classical risk factors with breast cancer risk |
| Q24806302 | Common ataxia telangiectasia mutated haplotypes and risk of breast cancer: a nested case-control study |
| Q35062523 | Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease |
| Q35868793 | Common genetic variants in prostate cancer risk prediction--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3) |
| Q35749326 | Common genetic variation in IGF1, IGFBP-1, and IGFBP-3 in relation to mammographic density: a cross-sectional study |
| Q36514160 | Common genetic variation of the calcium-sensing receptor and lethal prostate cancer risk |
| Q35794653 | Common germline polymorphisms associated with breast cancer-specific survival |
| Q34792833 | Common variants in ZNF365 are associated with both mammographic density and breast cancer risk |
| Q24641880 | Common variants near MC4R are associated with fat mass, weight and risk of obesity |
| Q37170656 | Common variants of FUT2 are associated with plasma vitamin B12 levels |
| Q24289171 | Complex Diseases, Complex Genes |
| Q24614574 | Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium |
| Q34380520 | Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal breast cancer risk |
| Q34181322 | Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer |
| Q91721688 | Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria |
| Q57565042 | Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54] |
| Q41006049 | Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses |
| Q56879642 | Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis |
| Q42697299 | Covariate selection for association screening in multiphenotype genetic studies |
| Q28396029 | Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer |
| Q45070922 | Cross-Cancer Analysis Reveals Novel Pleiotropic Associations-Response |
| Q28388475 | Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations |
| Q101216461 | Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers |
| Q34096825 | Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia |
| Q47251942 | Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases |
| Q37243708 | Curses--winner's and otherwise--in genetic epidemiology |
| Q37396372 | Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities |
| Q23916196 | Detectable clonal mosaicism and its relationship to aging and cancer |
| Q36487491 | Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium |
| Q98396140 | Diabetes, Weight Change, and Pancreatic Cancer Risk |
| Q57800567 | Diet quality and genetic association with body mass index: results from 3 observational studies |
| Q28646221 | Directional dominance on stature and cognition in diverse human populations |
| Q37626678 | Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking |
| Q37155238 | Does genetic variation in the Delta6-desaturase promoter modify the association between alpha-linolenic acid and the prevalence of metabolic syndrome? |
| Q47838945 | Drinking from the fire hose--statistical issues in genomewide association studies |
| Q45289624 | Effect of apolipoprotein E genotype and saturated fat intake on plasma lipids and myocardial infarction in the Central Valley of Costa Rica |
| Q61800379 | Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes |
| Q45303097 | Efficient two-stage genome-wide association designs based on false positive report probabilities |
| Q34338886 | Eighteen insulin-like growth factor pathway genes, circulating levels of IGF-I and its binding protein, and risk of prostate and breast cancer |
| Q34315320 | Elevation of circulating branched-chain amino acids is an early event in human pancreatic adenocarcinoma development |
| Q91694200 | Erratum: A genome-wide association study of bitter and sweet beverage consumption |
| Q56917552 | Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses |
| Q57202568 | Erratum: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk |
| Q56879641 | Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution |
| Q115038505 | Estimating the effective sample size in association studies of quantitative traits |
| Q37475917 | Estimation of absolute risk for prostate cancer using genetic markers and family history |
| Q37016927 | Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States |
| Q91549968 | Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk |
| Q33873837 | Evaluation of polygenic risk scores for predicting breast and prostate cancer risk |
| Q30275016 | Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. |
| Q38845261 | Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk |
| Q33584276 | Exome-wide association study of endometrial cancer in a multiethnic population |
| Q36524374 | Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction |
| Q56992638 | Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study |
| Q36572987 | Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes |
| Q36472841 | Exploring the genetic architecture of circulating 25-hydroxyvitamin D. |
| Q34430369 | Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types |
| Q34080597 | Family history of cancer and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan). |
| Q92341884 | Family history of cancer, Ashkenazi Jewish ancestry, and pancreatic cancer risk |
| Q36943801 | Fat mass-and obesity-associated (FTO) gene variant is associated with obesity: longitudinal analyses in two cohort studies and functional test |
| Q27908479 | Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome |
| Q88013247 | Fine Tuning the Risk of Hereditary Cancer Using Genome-Wide Association Studies |
| Q37164415 | Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility |
| Q34158088 | Fine mapping of 14q24.1 breast cancer susceptibility locus |
| Q35056055 | Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer |
| Q28384269 | Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci |
| Q36856343 | Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression |
| Q55380382 | Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. |
| Q61230414 | Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes |
| Q92480972 | Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes |
| Q55311842 | Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants. |
| Q35097143 | Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer |
| Q34979715 | Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium |
| Q39839071 | Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies |
| Q114182808 | Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element |
| Q33629880 | Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 |
| Q36742577 | Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers |
| Q45830306 | GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. |
| Q38408978 | GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer |
| Q24289531 | Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report |
| Q35681271 | Gene-environment interactions in genome-wide association studies: a comparative study of tests applied to empirical studies of type 2 diabetes |
| Q92242283 | Genetic Correlations Between Diabetes and Glaucoma: An Analysis of Continuous and Dichotomous Phenotypes |
| Q39200248 | Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma |
| Q115209620 | Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus |
| Q93161394 | Genetic and Circulating Biomarker Data Improve Risk Prediction for Pancreatic Cancer in the General Population |
| Q38602403 | Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis |
| Q35999323 | Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study |
| Q57661758 | Genetic evidence of assortative mating in humans |
| Q34501150 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci |
| Q108609948 | Genetic insights into biological mechanisms governing human ovarian ageing |
| Q29417068 | Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study |
| Q92588645 | Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes |
| Q37281843 | Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer |
| Q34328685 | Genetic predisposition to higher body mass index or type 2 diabetes and leukocyte telomere length in the Nurses' Health Study |
| Q35806601 | Genetic risk variants associated with in situ breast cancer |
| Q30276970 | Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses |
| Q33904459 | Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes |
| Q33773702 | Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes |
| Q30275688 | Genetic variants in CETP increase risk of intracerebral hemorrhage |
| Q24642114 | Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians |
| Q24811147 | Genetic variation in the HSD17B1 gene and risk of prostate cancer |
| Q35218136 | Genetic variation in the toll-like receptor 4 and prostate cancer incidence and mortality |
| Q36741744 | Genetic variation in the vitamin d pathway in relation to risk of prostate cancer--results from the breast and prostate cancer cohort consortium |
| Q30000080 | Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent |
| Q92387949 | Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European Descent |
| Q28393571 | Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes |
| Q58618794 | Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders |
| Q35948055 | Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium |
| Q28388497 | Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types |
| Q30313778 | Genome-wide analysis identifies 12 loci influencing human reproductive behavior |
| Q21092142 | Genome-wide and candidate gene association study of cigarette smoking behaviors |
| Q24620065 | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations |
| Q28943312 | Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions |
| Q36515582 | Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma |
| Q37637724 | Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia |
| Q35996692 | Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer |
| Q63681757 | Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer |
| Q24622610 | Genome-wide association studies identify four ER negative-specific breast cancer risk loci |
| Q24632585 | Genome-wide association studies identify loci associated with age at menarche and age at natural menopause |
| Q95329367 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses |
| Q100316395 | Genome-wide association study identifies 48 common genetic variants associated with handedness |
| Q35200169 | Genome-wide association study identifies common variants associated with circulating vitamin E levels |
| Q34288685 | Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region |
| Q28659283 | Genome-wide association study identifies multiple loci associated with bladder cancer risk |
| Q35061252 | Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk |
| Q28943339 | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia |
| Q33804470 | Genome-wide association study identifies multiple risk loci for renal cell carcinoma |
| Q28248768 | Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma |
| Q34314018 | Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer |
| Q28924380 | Genome-wide association study identifies new prostate cancer susceptibility loci |
| Q35030839 | Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk |
| Q28943349 | Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma |
| Q33773696 | Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels |
| Q28659642 | Genome-wide association study identifies two susceptibility loci for osteosarcoma |
| Q33740363 | Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels |
| Q28390712 | Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort |
| Q24626464 | Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer |
| Q47557957 | Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels |
| Q101565595 | Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women |
| Q61847493 | Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan |
| Q34375940 | Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. |
| Q34295620 | Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women |
| Q35532911 | Genome-wide association study of circulating retinol levels |
| Q33904451 | Genome-wide association study of circulating vitamin D levels |
| Q28660394 | Genome-wide association study of endometrial cancer in E2C2 |
| Q64040390 | Genome-wide association study of germline variants and breast cancer-specific mortality |
| Q38970751 | Genome-wide association study of prostate cancer-specific survival |
| Q33900326 | Genome-wide association study of relative telomere length |
| Q27301096 | Genome-wide association study of selenium concentrations |
| Q28943489 | Genome-wide association study of survival in patients with pancreatic adenocarcinoma |
| Q37380035 | Genome-wide association study of tanning phenotype in a population of European ancestry |
| Q96431376 | Genome-wide gene-diabetes and gene-obesity interaction scan in 8,255 cases and 11,900 controls from the PanScan and PanC4 Consortia |
| Q28943359 | Genome-wide interaction study of smoking and bladder cancer risk |
| Q49816011 | Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. |
| Q21144958 | Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption |
| Q30303149 | Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption |
| Q36541143 | Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels |
| Q35002165 | Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway |
| Q29417007 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility |
| Q37235560 | Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits |
| Q59566871 | Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility |
| Q38823212 | Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk |
| Q92667373 | Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism |
| Q52858262 | Genomics, Telomere Length, Epigenetics, and Metabolomics in the Nurses' Health Studies. |
| Q96432094 | Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk |
| Q114182677 | Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis |
| Q58611475 | Germline variation at 8q24 and prostate cancer risk in men of European ancestry |
| Q44667184 | Group 6: Pleiotropy and multivariate analysis |
| Q54465029 | HLA class I and II diversity contributes to the etiologic heterogeneity of non-Hodgkin lymphoma subtypes. |
| Q24797370 | Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer |
| Q46952791 | Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies |
| Q37484235 | Haplotypes of the estrogen receptor beta gene and breast cancer risk |
| Q36276540 | Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization |
| Q94588922 | Height, nevus count, and risk of cutaneous malignant melanoma: results from two large cohorts of US women |
| Q33330850 | Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics |
| Q36547888 | Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers |
| Q24630979 | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Q37021217 | Hyperglycemia, insulin resistance, impaired pancreatic β-cell function, and risk of pancreatic cancer. |
| Q34754791 | Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma |
| Q33348545 | IGF-1, IGFBP-1, and IGFBP-3 polymorphisms predict circulating IGF levels but not breast cancer risk: findings from the Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q29417155 | Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array |
| Q36069872 | Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer |
| Q29417013 | Identification of a melanoma susceptibility locus and somatic mutation in TET2. |
| Q36198138 | Identification of a new prostate cancer susceptibility locus on chromosome 8q24. |
| Q36062033 | Identification of a novel percent mammographic density locus at 12q24. |
| Q36754771 | 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 |
| Q36859142 | Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer |
| Q36968428 | Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders |
| Q36086247 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus |
| Q57170142 | Identification of nine new susceptibility loci for endometrial cancer |
| Q36014067 | Identification of novel genetic markers of breast cancer survival |
| Q28275237 | Identification of ten loci associated with height highlights new biological pathways in human growth |
| Q46103372 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer |
| Q47150982 | Identifying the metabolomic fingerprint of high and low flavonoid consumers. |
| Q36918149 | Impact of Pre-analytic Blood Sample Collection Factors on Metabolomics |
| Q36865877 | Improved ancestry inference using weights from external reference panels |
| Q23924183 | Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 |
| Q34225990 | Inclusion of endogenous hormone levels in risk prediction models of postmenopausal breast cancer |
| Q47864609 | Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions |
| Q36350246 | Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers |
| Q36831927 | Inflammatory plasma markers and pancreatic cancer risk: a prospective study of five U.S. cohorts |
| Q36384402 | Informed conditioning on clinical covariates increases power in case-control association studies |
| Q55693698 | Insulin-like Growth Factor Pathway Genetic Polymorphisms, Circulating IGF1 and IGFBP3, and Prostate Cancer Survival. |
| Q36849912 | Insulin-like growth factor pathway genes and blood concentrations, dietary protein and risk of prostate cancer in the NCI Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q33845203 | Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival |
| Q37140897 | Insulin-like growth factor-1- and interleukin-6-related gene variation and risk of multiple myeloma |
| Q36065460 | Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions |
| Q38842066 | Interactions Between Genome-Wide Significant Genetic Variants and Circulating Concentrations of 25-Hydroxyvitamin D in Relation to Prostate Cancer Risk in the National Cancer Institute BPC3. |
| Q40071035 | Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consortium |
| Q35166701 | Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium |
| Q36077025 | Interactions between genome-wide significant genetic variants and circulating concentrations of insulin-like growth factor 1, sex hormones, and binding proteins in relation to prostate cancer risk in the National Cancer Institute Breast and Prostate |
| Q53080453 | Interactions of established risk factors and a GWAS-based genetic risk score on the risk of venous thromboembolism. |
| Q37100113 | Interleukin and interleukin receptor gene polymorphisms and susceptibility to melanoma |
| Q97556532 | Involvement of fine particulate matter exposure with gene expression pathways in breast tumor and adjacent-normal breast tissue |
| Q90711101 | Joint Analysis of Multiple Interaction Parameters in Genetic Association Studies |
| Q28396727 | Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations |
| Q64279327 | Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk |
| Q35132050 | Joint effects of colorectal cancer susceptibility loci, circulating 25-hydroxyvitamin D and risk of colorectal cancer |
| Q37301357 | Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry |
| Q57191573 | Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair |
| Q28272915 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes |
| Q34899553 | Large-scale exploration of gene-gene interactions in prostate cancer using a multistage genome-wide association study |
| Q35119669 | Large-scale fine mapping of the HNF1B locus and prostate cancer risk |
| Q60222265 | Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions |
| Q60300821 | Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria |
| Q28267893 | Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair |
| Q47915070 | Lessons Learned From Past Gene-Environment Interaction Successes |
| Q40503345 | Leucocyte telomere length, genetic variants at the TERT gene region and risk of pancreatic cancer |
| Q51124795 | Leveraging family history in population-based case-control association studies. |
| Q98157789 | Low dose environmental radon exposure and breast tumor gene expression |
| Q46737936 | Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma |
| Q42495860 | Melanocortin 1 receptor variants and skin cancer risk |
| Q114182490 | Mendelian randomisation study of smoking exposure in relation to breast cancer risk |
| Q98772941 | Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer |
| Q99616191 | Mendelian randomization analysis of n-6 polyunsaturated fatty acid levels and pancreatic cancer risk |
| Q30276350 | Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer. |
| Q37143043 | Meta-Analysis of Rare Variant Association Tests in Multiethnic Populations |
| Q34248904 | Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways |
| Q34142739 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution |
| Q35266365 | Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism |
| Q36675182 | Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia |
| Q30410308 | Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage |
| Q35670184 | Meta-analysis of new genome-wide association studies of colorectal cancer risk |
| Q64922604 | Metabolites Associated With the Risk of Incident Venous Thromboembolism: A Metabolomic Analysis. |
| Q92306908 | Metabolome-Wide Association Study of the Relationship Between Habitual Physical Activity and Plasma Metabolite Levels |
| Q48522700 | Metabolomic analysis of 92 pulmonary embolism patients from a nested case-control study identifies metabolites associated with adverse clinical outcomes. |
| Q91974034 | Mixed-model admixture mapping identifies smoking-dependent loci of lung function in African Americans |
| Q57760214 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores |
| Q36133352 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores |
| Q42930725 | Multiple comparisons in studies of gene x gene and gene x environment interaction |
| Q28290169 | Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. |
| Q28943507 | Multiple loci identified in a genome-wide association study of prostate cancer |
| Q112608653 | Multitrait GWAS to connect disease variants and biological mechanisms |
| Q115032642 | Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations |
| Q37356243 | Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. |
| Q34029677 | Next generation analytic tools for large scale genetic epidemiology studies of complex diseases |
| Q45144461 | No association between GPX1 Pro198Leu and breast cancer risk |
| Q43714077 | Nonsynonymous polymorphisms in genes in the one-carbon metabolism pathway and associations with colorectal cancer |
| Q35752042 | Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures |
| Q34221038 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals |
| Q59137307 | Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways |
| Q61840927 | Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways |
| Q37381214 | Obesity susceptibility loci and uncontrolled eating, emotional eating and cognitive restraint behaviors in men and women |
| Q33778268 | Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study |
| Q37654985 | One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study |
| Q28584533 | PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS |
| Q37137091 | PIK3CA mutation is associated with poor prognosis among patients with curatively resected colon cancer |
| Q33705238 | PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q40515239 | Pancreatic Cancer Risk Associated with Prediagnostic Plasma Levels of Leptin and Leptin Receptor Genetic Polymorphisms |
| Q34094983 | Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium |
| Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
| Q37464310 | Pathway analysis by adaptive combination of P-values |
| Q34008159 | Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade |
| Q34241383 | Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer |
| Q34064069 | Performance of common genetic variants in breast-cancer risk models |
| Q98775279 | Personalizing Breast Cancer Screening Based on Polygenic Risk and Family History |
| Q37649794 | Physical activity and risk of endometrial adenocarcinoma in the Nurses' Health Study |
| Q35767152 | Physical activity, sedentary behavior, and leukocyte telomere length in women |
| Q35661250 | Plasma 25-hydroxyvitamin D and risk of pancreatic cancer |
| Q36831883 | Plasma carotenoid- and retinol-weighted multi-SNP scores and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium |
| Q37570238 | Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia |
| Q62583133 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes |
| Q57172887 | Polygenic risk score of shorter telomere length and risk of depression and anxiety in women |
| Q34708672 | Polymorphisms in genes hydroxysteroid-dehydrogenase-17b type 2 and type 4 and endometrial cancer risk |
| Q34024839 | Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4. |
| Q61565600 | Polymorphisms in the CC-chemokine receptor-2 (CCR2) and -5 (CCR5) genes and risk of coronary heart disease among US women |
| Q33733210 | Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer |
| Q53082870 | Population stratification bias: more widespread than previously thought. |
| Q34155371 | Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women |
| Q34544433 | Powerful SNP-set analysis for case-control genome-wide association studies |
| Q64090151 | Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic |
| Q90832887 | Pre-diagnostic 25-hydroxyvitamin D concentrations in relation to tumor molecular alterations and risk of breast cancer recurrence |
| Q89120347 | Precision Prevention and Early Detection of Cancer: Fundamental Principles |
| Q52688122 | Prediagnosis Use of Statins Associates With Increased Survival Times of Patients With Pancreatic Cancer. |
| Q92707869 | Prediagnostic Leukocyte Telomere Length and Pancreatic Cancer Survival |
| Q37234780 | Prediagnostic Plasma 25-Hydroxyvitamin D and Pancreatic Cancer Survival |
| Q34656804 | Prediagnostic body mass index and pancreatic cancer survival |
| Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
| Q37223335 | Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status |
| Q35624758 | Premenopausal plasma carotenoids, fluorescent oxidation products, and subsequent breast cancer risk in the nurses' health studies |
| Q37633508 | Premenopausal plasma ferritin levels, HFE polymorphisms, and risk of breast cancer in the nurses' health study II. |
| Q37716304 | Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study |
| Q85118673 | Prospective study of ABO blood type and the risk of pulmonary embolism in two large cohort studies |
| Q36546861 | Prospective study of effect modification by Toll-like receptor 4 variation on the association between Trichomonas vaginalis serostatus and prostate cancer |
| Q37735483 | Prostate cancer (PCa) risk variants and risk of fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium |
| Q60909421 | Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways |
| Q90242034 | Publisher Correction: Shared heritability and functional enrichment across six solid cancers |
| Q88214332 | Publisher correction: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 |
| Q92184278 | Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis |
| Q38668303 | Quantifying the Genetic Correlation between Multiple Cancer Types |
| Q24656179 | Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3) |
| Q114182625 | Rare germline copy number variants (CNVs) and breast cancer risk |
| Q90821315 | Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry |
| Q34964012 | Red meat intake, NAT2, and risk of colorectal cancer: a pooled analysis of 11 studies |
| Q33835331 | Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2. |
| Q47788165 | Regular Use of Aspirin or Non-Aspirin Nonsteroidal Anti-Inflammatory Drugs Is Not Associated With Risk of Incident Pancreatic Cancer in Two Large Cohort Studies. |
| Q24288830 | Replication in Genome-Wide Association Studies |
| Q35661241 | Replication of five prostate cancer loci identified in an Asian population--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3). |
| Q55397876 | Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'. |
| Q37265647 | Reproducibility of metabolomic profiles among men and women in 2 large cohort studies |
| Q37442687 | Reproductive factors and postmenopausal hormone use in relation to endometrial cancer risk in the Nurses' Health Study cohort 1976-2004. |
| Q42559180 | Response to Day et al. |
| Q58033520 | Sequence Variants of Toll-Like Receptor 4 and Susceptibility to Prostate Cancer |
| Q33723482 | Sequence variants in the TLR4 and TLR6-1-10 genes and prostate cancer risk. Results based on pooled analysis from three independent studies |
| Q33986279 | Sequence variants of elaC homolog 2 (Escherichia coli) (ELAC2) gene and susceptibility to prostate cancer in the Health Professionals Follow-Up Study |
| Q29417074 | Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study |
| Q92969786 | Sex specific associations in genome wide association analysis of renal cell carcinoma |
| Q61118451 | Shared heritability and functional enrichment across six solid cancers |
| Q64004349 | Shared heritability and functional enrichment across six solid cancers |
| Q24646434 | Six new loci associated with body mass index highlight a neuronal influence on body weight regulation |
| Q43881436 | Strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS): explanation and elaboration |
| Q24289354 | Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration. |
| Q24289476 | Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration |
| Q56632047 | Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration |
| Q34716541 | Survival among patients with pancreatic cancer and long-standing or recent-onset diabetes mellitus |
| Q37154761 | TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US women |
| Q28386653 | TERT gene harbors multiple variants associated with pancreatic cancer susceptibility |
| Q28397509 | Telomere structure and maintenance gene variants and risk of five cancer types |
| Q34678258 | Testing calibration of risk models at extremes of disease risk |
| Q47564384 | Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets |
| Q34372389 | The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease |
| Q92608385 | The Association of Modifiable Breast Cancer Risk Factors and Somatic Genomic Alterations in Breast Tumors: The Cancer Genome Atlas Network |
| Q91178389 | The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer |
| Q37578078 | The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers |
| Q34101736 | The association of telomere length and genetic variation in telomere biology genes |
| Q37151220 | The causal relevance of body mass index in different histological types of lung cancer: A Mendelian randomization study |
| Q36948291 | The common obesity variant near MC4R gene is associated with higher intakes of total energy and dietary fat, weight change and diabetes risk in women |
| Q93054131 | The genetic interplay between body mass index, breast size and breast cancer risk: a Mendelian randomization analysis |
| Q35807814 | The impact of direct-to-consumer personal genomic testing on perceived risk of breast, prostate, colorectal, and lung cancer: findings from the PGen study |
| Q33434473 | The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk |
| Q34151528 | Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies |
| Q114677146 | Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction |
| Q89961489 | Transcriptome-wide association study of breast cancer risk by estrogen-receptor status |
| Q24609915 | Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis |
| Q56763236 | Twenty-four non-synonymous polymorphisms in the one-carbon metabolic pathway and risk of colorectal adenoma in the Nurses' Health Study |
| Q57285472 | Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia |
| Q35575585 | Two susceptibility loci identified for prostate cancer aggressiveness |
| Q92994868 | Two truncating variants in FANCC and breast cancer risk |
| Q50084544 | Use of deep whole genome sequencing data to identify structure risk variants in breast cancer susceptibility genes. |
| Q89087134 | Using a Mendelian randomization approach to explore a causal relationship between vitamin D and nonmelanoma skin cancer |
| Q36756285 | Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium |
| Q33708556 | Using principal components of genetic variation for robust and powerful detection of gene-gene interactions in case-control and case-only studies |
| Q38814549 | VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis |
| Q34422433 | Variant ABO blood group alleles, secretor status, and risk of pancreatic cancer: results from the pancreatic cancer cohort consortium |
| Q42725643 | Variation in KLK genes, prostate-specific antigen and risk of prostate cancer |
| Q37370221 | Variation in predictive ability of common genetic variants by established strata: the example of breast cancer and age. |
| Q40012482 | Vitamin D receptor polymorphisms and breast cancer risk: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium |
| Q35164176 | Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3). |
| Q35925515 | Vitamin D-related genetic variation, plasma vitamin D, and risk of lethal prostate cancer: a prospective nested case-control study |
| Q33235328 | XPA, haplotypes, and risk of basal and squamous cell carcinoma |
| Q36398341 | β-Carotene 15,15'-monooxygenase 1 single nucleotide polymorphisms in relation to plasma carotenoid and retinol concentrations in women of European descent |
| Q88599544 | Duncan C Thomas | doctoral student | P185 |
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