Christopher A. Haiman

researcher

Christopher A. Haiman is …
instance of (P31):
humanQ5

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P496ORCID iD0000-0002-0097-9971
P2038ResearchGate profile IDChris_Haiman
P214VIAF ID948150323752009970436
P7859WorldCat Identities ID (superseded)lccn-n2017186642

P734family nameHaimanQ36979220
HaimanQ36979220
HaimanQ36979220
P735given nameChristopherQ1084472
ChristopherQ1084472
P106occupationresearcherQ1650915
P21sex or gendermaleQ6581097

Reverse relations

author (P50)
Q9033986312 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population
Q338488952q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
Q350647478q24 risk alleles and prostate cancer in African-Barbadian men.
Q60460674A Collaborative Analysis of Individual Participant Data from 19 Prospective Studies Assesses Circulating Vitamin D and Prostate Cancer Risk
Q94683498A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry
Q55210146A 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.
Q35327105A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer
Q40071308A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes
Q40597341A Meta-analysis of Multiple Myeloma Risk Regions in African and European Ancestry Populations Identifies Putatively Functional Loci
Q36927005A case-control analysis of smoking and breast cancer in African American women: findings from the AMBER Consortium
Q46378338A common 8q24 variant in prostate and breast cancer from a large nested case-control study
Q36667989A common genetic risk factor for colorectal and prostate cancer
Q34585661A common prostate cancer risk variant 5' of microseminoprotein-beta (MSMB) is a strong predictor of circulating beta-microseminoprotein (MSP) levels in multiple populations
Q35755874A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Q33980349A 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
Q33308309A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the multiethnic cohort
Q45305326A 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.
Q35605845A 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).
Q35957063A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density
Q34211808A comprehensive examination of breast cancer risk loci in African American women
Q44307819A comprehensive haplotype analysis of CYP19 and breast cancer risk: the Multiethnic Cohort
Q33731355A functionally significant SNP in TP53 and breast cancer risk in African-American women
Q35093501A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer
Q37109758A genome-wide association study of breast cancer in women of African ancestry
Q37705188A genome-wide association study of prostate cancer in West African men
Q35177444A genome-wide pleiotropy scan for prostate cancer risk
Q34628377A genomewide admixture map for Latino populations
Q33306108A high-density admixture scan in 1,670 African Americans with hypertension
Q35925225A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Q34113217A 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
Q37619303A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium
Q30416161A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Q35248192A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Q36435849A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
Q36477652A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
Q92711687A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Q43612263A polymorphism in CYP17 and endometrial cancer risk
Q43528266A priori-defined diet quality indices, biomarkers and risk for type 2 diabetes in five ethnic groups: the Multiethnic Cohort
Q46083367A promoter polymorphism in the CASP8 gene is not associated with cancer risk
Q37981608A review of cancer in U.S. Hispanic populations
Q51541955A sequence repeat in the insulin-like growth factor-1 gene and risk of breast cancer.
Q55470614A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women.
Q35870195A systematic approach to understand the functional consequences of non-protein coding risk regions
Q46226734A systematic assessment of common genetic variation in CYP11A and risk of breast cancer
Q57750722A tetranucleotide repeat polymorphism inCYP19 and breast cancer risk
Q57305942A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Q43985011A variant in the cytochrome p450 oxidoreductase gene is associated with breast cancer risk in African Americans
Q62583660AA9int: SNP interaction pattern search using non-hierarchical additive model set
Q36083454ABO blood group alleles and prostate cancer risk: Results from the breast and prostate cancer cohort consortium (BPC3).
Q57785674Abstract LB-282: Transethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A
Q61948762Abstract LB-448: Genome-wide association study identifies new prostate cancer susceptibility loci
Q34472668Additive 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
Q37271961Admixture Mapping of African-American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
Q35080445Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men.
Q35856257Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas
Q33450573Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.
Q34206098African ancestry and its correlation to type 2 diabetes in African Americans: a genetic admixture analysis in three U.S. population cohorts
Q28386602Age-related clonal hematopoiesis associated with adverse outcomes
Q64989893Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.
Q37417691Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study
Q37437960An admixture scan in 1,484 African American women with breast cancer
Q39706039An exome-wide analysis of low frequency and rare variants in relation to risk of breast cancer in African American Women: the AMBER Consortium
Q36073563An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
Q36865904Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation
Q36055011Analysis of case-control association studies with known risk variants
Q24170413Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types
Q37118791Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels
Q97070156Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers
Q57305944Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q45979098Association analysis identifies 65 new breast cancer risk loci.
Q36123803Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses
Q37205569Association between breast cancer susceptibility loci and mammographic density: the Multiethnic Cohort
Q38686091Association of Coffee Consumption With Total and Cause-Specific Mortality Among Nonwhite Populations
Q37292963Association of ESR1 gene tagging SNPs with breast cancer risk
Q35764730Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort
Q35588251Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population
Q36191018Association of breast cancer risk loci with breast cancer survival
Q37684672Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Q34457646Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study
Q37306082Association of diabetes with prostate cancer risk in the multiethnic cohort
Q43636885Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels.
Q37268494Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry
Q114182713Association 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
Q37127877Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE study
Q34314362Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the Breast and Prostate Cancer Cohort Consortium
Q36722084Associations Between Genetic Ancestries and Nicotine Metabolism Biomarkers in the Multiethnic Cohort Study
Q91045562Associations of autozygosity with a broad range of human phenotypes
Q35022847Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
Q57056093Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Q36792641Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation
Q35652541Atopic allergic conditions and colorectal cancer risk in the Multiethnic Cohort Study
Q63966080Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q64118820Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q60907509Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Q60917567Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
Q38914005BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
Q37002955BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Q35951033Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort
Q37045556Blood lipids and prostate cancer: a Mendelian randomization analysis
Q35852637Body Mass Index Genetic Risk Score and Endometrial Cancer Risk
Q46115524Body mass index and breast cancer survival: a Mendelian randomization analysis
Q39734134Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States
Q35940158Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Q36558326CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants
Q44449983CYP17 genetic variation and risk of breast and prostate cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).
Q33616702CYP19A1 genetic variation in relation to prostate cancer risk and circulating sex hormone concentrations in men from the Breast and Prostate Cancer Cohort Consortium
Q34515023Caution in generalizing known genetic risk markers for breast cancer across all ethnic/racial populations
Q24169697Characterization of large structural genetic mosaicism in human autosome
Q37163691Characterization of the colorectal cancer-associated enhancer MYC-335 at 8q24: the role of rs67491583
Q39002074Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry
Q33842251Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.
Q33921139Characterizing genetic risk at known prostate cancer susceptibility loci in African Americans
Q46083526Characterizing the neighborhood obesogenic environment in the Multiethnic Cohort: a multi-level infrastructure for cancer health disparities research
Q30815307Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study
Q47267193Circulating Folate, Vitamin B6, and Methionine in Relation to Lung Cancer Risk in the Lung Cancer Cohort Consortium (LC3).
Q56089366Circulating Vitamin D and Colorectal Cancer Risk: An International Pooling Project of 17 Cohorts
Q56089362Circulating cotinine concentrations and lung cancer risk in the Lung Cancer Cohort Consortium (LC3)
Q91647649Circulating markers of cellular immune activation in prediagnostic blood sample and lung cancer risk in the Lung Cancer Cohort Consortium (LC3)
Q47242967Circulating sex hormones in relation to anthropometric, sociodemographic and behavioural factors in an international dataset of 12,300 men.
Q94486442Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Q36600605Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk
Q36856357Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls
Q35868793Common genetic variants in prostate cancer risk prediction--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)
Q45135637Common genetic variation at PTEN and risk of sporadic breast and prostate cancer
Q35749326Common genetic variation in IGF1, IGFBP-1, and IGFBP-3 in relation to mammographic density: a cross-sectional study
Q46140030Common genetic variation in the sex steroid hormone-binding globulin (SHBG) gene and circulating shbg levels among postmenopausal women: the Multiethnic Cohort
Q35794653Common germline polymorphisms associated with breast cancer-specific survival
Q34379032Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Q39389957Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese
Q57251792Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
Q34631785Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
Q24614574Comprehensive 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
Q34622559Comprehensive analysis of hormone and genetic variation in 36 genes related to steroid hormone metabolism in pre- and postmenopausal women from the breast and prostate cancer cohort consortium (BPC3).
Q45960056Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations.
Q37533894Comprehensive functional annotation of 77 prostate cancer risk loci
Q34744860Comprehensive functional annotation of seventy-one breast cancer risk Loci
Q33701819Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups
Q28384670Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) Consortium
Q46112906Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium
Q45912452Correction: African Ancestry and Its Correlation to Type 2 Diabetes in African Americans: A Genetic Admixture Analysis in Three U.S. Population Cohorts.
Q42348998Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
Q28396029Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer
Q45070922Cross-Cancer Analysis Reveals Novel Pleiotropic Associations-Response
Q28388475Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Q34096825Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia
Q33768593Cyclin D1 splice variants: polymorphism, risk, and isoform-specific regulation in prostate cancer
Q34478869Cyclin D1b variant influences prostate cancer growth through aberrant androgen receptor regulation
Q37396372Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities
Q34441746Defining the role of common variation in the genomic and biological architecture of adult human height
Q23916196Detectable clonal mosaicism and its relationship to aging and cancer
Q28385149Detectable clonal mosaicism from birth to old age and its relationship to cancer
Q51716837Diabetes and urothelial cancer risk: the Multiethnic Cohort study.
Q38719262Dietary Red and Processed Meat Intake and Markers of Adiposity and Inflammation: The Multiethnic Cohort Study
Q30252516Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
Q34545744Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study
Q34338886Eighteen insulin-like growth factor pathway genes, circulating levels of IGF-I and its binding protein, and risk of prostate and breast cancer
Q30432415Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
Q35741878Established risk factors account for most of the racial differences in cardiovascular disease mortality
Q46138958Ethnic and racial differences in the smoking-related risk of lung cancer
Q36643784Ethnic differences in ovulatory function in nulliparous women
Q36388749Evaluating genetic risk for prostate cancer among Japanese and Latinos
Q54989897Evaluation of 71 Coronary Artery Disease Risk Variants in a Multiethnic Cohort.
Q31060192Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study
Q35064451Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
Q37342144Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
Q60297002Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use
Q64108431Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Q33584276Exome-wide association study of endometrial cancer in a multiethnic population
Q40527295Exploring Differences in the Aspirin-Colorectal Cancer Association by Sex and Race/Ethnicity: The Multiethnic Cohort Study
Q34430369Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types
Q37594336FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Q37323340FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation
Q27908479Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
Q37217089Fine Mapping and Identification of BMI Loci in African Americans
Q30275202Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations
Q35056055Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer
Q33947843Fine mapping of the association with obesity at the FTO locus in African-derived populations
Q37236216Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).
Q33878276Fine scale mapping of the breast cancer 16q12 locus
Q36111237Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus
Q30371049Fine-mapping IGF1 and prostate cancer risk in African Americans: the multiethnic cohort study.
Q34388513Fine-mapping and initial characterization of QT interval loci in African Americans
Q36856343Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression
Q55380382Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.
Q35524465Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Q61230414Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes
Q92480972Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Q35389444Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans
Q37332218Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans
Q30252583Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci
Q55311842Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.
Q35097143Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer
Q39844032Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Q36248936Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk
Q34903062Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Q37367871Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Q34979715Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium
Q36124728Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Q36742577Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
Q38408978GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer
Q35952814Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array
Q50041886Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Q36961082Gene-based analysis of the fibroblast growth factor receptor signaling pathway in relation to breast cancer in African American women: the AMBER consortium
Q34848573Generalizability and epidemiologic characterization of eleven colorectal cancer GWAS hits in multiple populations
Q34050485Generalizability of associations from prostate cancer genome-wide association studies in multiple populations
Q34716723Generalizability of established prostate cancer risk variants in men of African ancestry
Q34998144Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study
Q37629802Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations
Q57316036Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits
Q30301097Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium
Q115209620Genetic 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
Q37436758Genetic ancestry and risk of mortality among U.S. Latinas with breast cancer
Q34960835Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts
Q63457086Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex
Q45962404Genetic determinants of circulating insulin-like growth factor (IGF)-I, IGF binding protein (BP)-1, and IGFBP-3 levels in a multiethnic population.
Q33954461Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study
Q24807377Genetic determinants of mammographic density
Q35999323Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study
Q59544908Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners
Q33488319Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).
Q35925620Genetic predisposition to ductal carcinoma in situ of the breast
Q35151684Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Q28390241Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study
Q48197879Genetic risk of prostate cancer in ugandan men.
Q35806601Genetic risk variants associated with in situ breast cancer
Q22305005Genetic studies of body mass index yield new insights for obesity biology
Q62583135Genetic susceptibility to radiation-induced breast cancer after Hodgkin lymphoma
Q28392218Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study
Q50020878Genetic variants in immune-related pathways and breast cancer risk in African American women in the AMBER consortium.
Q39373193Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry
Q37220236Genetic variants in the mTOR pathway and breast cancer risk in African American women
Q34592585Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study
Q35179897Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
Q46750307Genetic variation at the CYP19A1 locus predicts circulating estrogen levels but not breast cancer risk in postmenopausal women
Q37219153Genetic variation in DNA repair pathway genes and premenopausal breast cancer risk
Q46552527Genetic variation in angiotensin I-converting enzyme (ACE) and breast cancer risk: the multiethnic cohort
Q34378972Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Q24811147Genetic variation in the HSD17B1 gene and risk of prostate cancer
Q36422109Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium
Q37482022Genetic variation in the insulin, insulin-like growth factor, growth hormone, and leptin pathways in relation to breast cancer in African-American women: the AMBER consortium
Q34042346Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach
Q36741744Genetic variation in the vitamin d pathway in relation to risk of prostate cancer--results from the breast and prostate cancer cohort consortium
Q40638709Genetic variations in the Hippo signaling pathway and breast cancer risk in African American women in the AMBER Consortium
Q37381735Genetic variations in vitamin D-related pathways and breast cancer risk in African American women in the AMBER consortium
Q30000080Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Q28388497Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Q35996692Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Q63681757Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Q96683580Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer
Q30417624Genome-wide association of body fat distribution in African ancestry populations suggests new loci
Q24622610Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Q40346126Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer
Q38668307Genome-wide association studies of cancer in diverse populations
Q28383750Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population
Q95329367Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Q35565707Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Q28659283Genome-wide association study identifies multiple loci associated with bladder cancer risk
Q34314018Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Q28924380Genome-wide association study identifies new prostate cancer susceptibility loci
Q24645441Genome-wide association study identifies novel breast cancer susceptibility loci
Q28924377Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
Q37045108Genome-wide association study of age at menarche in African-American women
Q34375940Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.
Q36927009Genome-wide association study of colorectal cancer in Hispanics
Q28943291Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
Q28660394Genome-wide association study of endometrial cancer in E2C2
Q64040390Genome-wide association study of germline variants and breast cancer-specific mortality
Q35009643Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.
Q38970751Genome-wide association study of prostate cancer-specific survival
Q28943359Genome-wide interaction study of smoking and bladder cancer risk
Q47248078Genome-wide meta-analyses identifies novel taxane-induced peripheral neuropathy-associated loci
Q36001590Genome-wide meta-analyses of smoking behaviors in African Americans
Q49816011Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer.
Q30352681Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Q33610252Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
Q28655044Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture
Q34650062Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population
Q46573151Germ line variation at 8q24 and endometrial cancer risk
Q58611475Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Q36640906Global patterns of prostate cancer incidence, aggressiveness, and mortality in men of african descent
Q31047674HNF1B and endometrial cancer risk: results from the PAGE study
Q46952791Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies
Q43985413Haplotype-based association studies of IGFBP1 and IGFBP3 with prostate and breast cancer risk: the multiethnic cohort
Q37484235Haplotypes of the estrogen receptor beta gene and breast cancer risk
Q36276540Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Q33330850Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics
Q33739254High mortality due to sepsis in Native Hawaiians and African Americans: The Multiethnic Cohort
Q64234371High-Quality Diets Are Associated With Reduced Risk of Hepatocellular Carcinoma and Chronic Liver Disease: The Multiethnic Cohort
Q38827821High-Quality Diets Associate With Reduced Risk of Colorectal Cancer: Analyses of Diet Quality Indexes in the Multiethnic Cohort
Q37371491Hormone-related pathways and risk of breast cancer subtypes in African American women
Q33348545IGF-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).
Q34078803IGF1, IGFBP1, and IGFBP3 genes and mammographic density: the Multiethnic Cohort
Q33883948IGF2R missense single-nucleotide polymorphisms and breast cancer risk: the multiethnic cohort study
Q35102646Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Q30252854Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Q29417155Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Q36720814Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk
Q36069872Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer
Q28474694Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium
Q36198138Identification of a new prostate cancer susceptibility locus on chromosome 8q24.
Q36754771Identification 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
Q36859142Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Q36086247Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Q57170142Identification of nine new susceptibility loci for endometrial cancer
Q61448654Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas
Q36014067Identification of novel genetic markers of breast cancer survival
Q29417022Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Q36331604Identification of shared and unique susceptibility pathways among cancers of the lung, breast, and prostate from genome-wide association studies and tissue-specific protein interactions
Q46103372Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Q31036626Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
Q35747559Improved imputation of common and uncommon SNPs with a new reference set.
Q23924183Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33
Q30662194Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
Q114184688Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Q36384402Informed conditioning on clinical covariates increases power in case-control association studies
Q35104068Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
Q55693698Insulin-like Growth Factor Pathway Genetic Polymorphisms, Circulating IGF1 and IGFBP3, and Prostate Cancer Survival.
Q36849912Insulin-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).
Q33845203Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival
Q36065460Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions
Q35873064Interaction between Red Meat Intake and NAT2 Genotype in Increasing the Risk of Colorectal Cancer in Japanese and African Americans
Q40071035Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consortium
Q35166701Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium
Q40515571Investigating the possible causal role of coffee consumption with prostate cancer risk and progression using Mendelian randomization analysis
Q34698777Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study
Q63352570Is high vitamin B12 status a cause of lung cancer?
Q64279327Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk
Q57191573Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair
Q38730359Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
Q36250030Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer
Q35119669Large-scale fine mapping of the HNF1B locus and prostate cancer risk
Q28267893Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Q29416989Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Q57030056Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
Q36590875Levels of beta-microseminoprotein in blood and risk of prostate cancer in multiple populations
Q34572467Leveraging population admixture to characterize the heritability of complex traits
Q50050403Low diet quality and the risk of stroke mortality: the multiethnic cohort study.
Q35119701Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium
Q45187084MTHFR polymorphisms, diet, HRT, and breast cancer risk: the multiethnic cohort study
Q30276785Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity
Q114182490Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Q98772941Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer
Q35656389Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer
Q37143043Meta-Analysis of Rare Variant Association Tests in Multiethnic Populations
Q35785297Meta-analysis identifies common variants associated with body mass index in east Asians
Q33649334Meta-analysis of loci associated with age at natural menopause in African-American women
Q63352621Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Q36044839Metabolites of the Polycyclic Aromatic Hydrocarbon Phenanthrene in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer
Q30977635Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults
Q34497352MicroRNA related polymorphisms and breast cancer risk
Q35576887Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women
Q115238429Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Q33925293Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study
Q92912555Multiple functional variants in the IL1RL1 region are pretransplant markers for risk of GVHD and infection deaths
Q36897003Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Q35646703Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans
Q42038345Multiple regions within 8q24 independently affect risk for prostate cancer
Q35114362New genetic loci link adipose and insulin biology to body fat distribution
Q36963560No Association between the Mitochondrial Genome and Prostate Cancer Risk: The Multiethnic Cohort
Q34359901No association of risk variants for diabetes and obesity with breast cancer: the Multiethnic Cohort and PAGE studies
Q35220510No association of type 2 diabetes risk variants and prostate cancer risk: the multiethnic cohort and PAGE
Q30374367No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Q37491987No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population
Q37079859No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
Q35752042Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures
Q56359054Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Q40291645Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans
Q35634515Obesity, body fat distribution, and risk of breast cancer subtypes in African American women participating in the AMBER Consortium
Q37654985One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study
Q28584533PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Q47143943PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.
Q33705238PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).
Q34736954Parity, lactation, and breast cancer subtypes in African American women: results from the AMBER Consortium
Q34574903Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network
Q116031795Plant-based dietary patterns defined by a priori indices and colorectal cancer risk by sex and race/ethnicity: the Multiethnic Cohort Study
Q36831883Plasma carotenoid- and retinol-weighted multi-SNP scores and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
Q28383788Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia
Q37570238Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia
Q35112029Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium
Q62583133Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Q24791382Polymorphic repeat in AIB1 does not alter breast cancer risk
Q36066735Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
Q24810286Polymorphisms in genes involved in estrogen and progesterone metabolism and mammographic density changes in women randomized to postmenopausal hormone therapy: results from a pilot study
Q44325849Polymorphisms in steroid hormone pathway genes and mammographic density
Q39524941Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium
Q33733210Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer
Q34473598Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study
Q34155371Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women
Q37228261Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study
Q36871025Postmenopausal Female Hormone Use and Estrogen Receptor-Positive and -Negative Breast Cancer in African American Women
Q56516219Prediagnostic circulating markers of inflammation and risk of oesophageal adenocarcinoma: a study within the National Cancer Institute Cohort Consortium
Q92055460Prediction and clinical utility of a contralateral breast cancer risk model
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q37223335Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status
Q41584352Prediction of individual genetic risk to prostate cancer using a polygenic score
Q37103045Prostate Cancer Susceptibility in Men of African Ancestry at 8q24
Q36765569Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort
Q55508030Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Q90242034Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Q38668303Quantifying the Genetic Correlation between Multiple Cancer Types
Q24656179Quantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3)
Q36009422RAD51B in Familial Breast Cancer
Q108819063Race, ethnicity, community-level socioeconomic factors, and risk of COVID-19 in the United States and the United Kingdom
Q36054387Racial/ethnic differences in lifestyle-related factors and prostate cancer risk: the Multiethnic Cohort Study
Q46410535Racial/ethnic differences in postmenopausal endogenous hormones: the multiethnic cohort study
Q33539723Rapid assessment of genetic ancestry in populations of unknown origin by genome-wide genotyping of pooled samples
Q57177774Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease
Q38697838Reducing GWAS Complexity
Q35155449Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
Q33835331Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.
Q34870700Replication and functional genomic analyses of the breast cancer susceptibility locus at 6q25.1 generalize its importance in women of chinese, Japanese, and European ancestry
Q38623211Replication and validation of genetic polymorphisms associated with survival after allogeneic blood or marrow transplant
Q40498649Replication of associations between genetic polymorphisms and chronic graft-versus-host disease
Q35661241Replication of five prostate cancer loci identified in an Asian population--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3).
Q28383099Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study
Q34447165Reproducibility, performance, and clinical utility of a genetic risk prediction model for prostate cancer in Japanese
Q35815958Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci
Q38382935SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns
Q36545934SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival
Q24656096Screening and association testing of common coding variation in steroid hormone receptor co-activator and co-repressor genes in relation to breast cancer risk: the Multiethnic Cohort
Q34669917Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study
Q57271433Sequence Variants of Estrogen Receptor and Risk of Prostate Cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
Q24317364Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
Q29417074Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
Q46745482Sex and ethnic/racial-specific risk factors for gallbladder disease
Q61118451Shared heritability and functional enrichment across six solid cancers
Q64004349Shared heritability and functional enrichment across six solid cancers
Q47645244Sleep duration and incidence of type 2 diabetes: the Multiethnic Cohort
Q55667339Stepwise approach to SNP-set analysis illustrated with the Metabochip and colorectal cancer in Japanese Americans of the Multiethnic Cohort.
Q36223643Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array
Q36110159Susceptibility variants for obesity and colorectal cancer risk: the multiethnic cohort and PAGE studies
Q46136876T29C polymorphism in the transforming growth factor beta1 gene and postmenopausal breast cancer risk: the Multiethnic Cohort Study
Q28397509Telomere structure and maintenance gene variants and risk of five cancer types
Q55384494Testing the Predictive Validity of the Healthy Eating Index-2015 in the Multiethnic Cohort: Is the Score Associated with a Reduced Risk of All-Cause and Cause-Specific Mortality?
Q34372389The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease
Q37390854The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
Q49817640The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.
Q94552258The COronavirus Pandemic Epidemiology (COPE) Consortium: A Call to Action
Q40343659The Dietary Inflammatory Index Is Associated with Colorectal Cancer Risk in the Multiethnic Cohort
Q60923095The Dietary Inflammatory Index and All-Cause, Cardiovascular Disease, and Cancer Mortality in the Multiethnic Cohort Study
Q91178389The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Q28752426The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions
Q35223497The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study
Q37578078The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers
Q77678688The androgen receptor CAG repeat polymorphism and risk of breast cancer in the Nurses' Health Study
Q34000325The association of diabetes with colorectal cancer risk: the Multiethnic Cohort
Q63865847The associations of anthropometric, behavioural and sociodemographic factors with circulating concentrations of IGF‐I, IGF‐II, IGFBP‐1, IGFBP‐2 and IGFBP‐3 in a pooled analysis of 16,024 men from 22 studies
Q37151220The causal relevance of body mass index in different histological types of lung cancer: A Mendelian randomization study
Q34963910The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations
Q38856899The contribution of rare variation to prostate cancer heritability
Q36133295The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium
Q36326943The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.
Q57174781The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis
Q36796006The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study
Q30428393The landscape of recombination in African Americans
Q33686851The potential for enhancing the power of genetic association studies in African Americans through the reuse of existing genotype data
Q74592748The relationship between a polymorphism in CYP17 with plasma hormone levels and breast cancer
Q74147573The relationship between a polymorphism in CYP17 with plasma hormone levels and prostate cancer
Q46012348The relationship between twenty missense ATM variants and breast cancer risk: the Multiethnic Cohort.
Q46477592The role of established breast cancer susceptibility loci in mammographic density in young women
Q35049307The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery
Q29248193Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Q58722486Tobacco biomarkers and genetic/epigenetic analysis to investigate ethnic/racial differences in lung cancer risk among smokers
Q48142652Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.
Q38845982Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci
Q34649888Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained
Q37686157Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach
Q34270911Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.
Q89961489Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Q40041955Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium
Q79290429Transferability of tag SNPs in genetic association studies in multiple populations
Q37157438Two estrogen-related variants in CYP19A1 and endometrial cancer risk: a pooled analysis in the Epidemiology of Endometrial Cancer Consortium
Q35575585Two susceptibility loci identified for prostate cancer aggressiveness
Q92994868Two truncating variants in FANCC and breast cancer risk
Q50020860Type 2 Diabetes and Colorectal Cancer Survival: The Multiethnic Cohort.
Q35096343Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies
Q39021101Type II Diabetes, Obesity, and Breast Cancer Risk: The Multiethnic Cohort
Q33404621Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation
Q35032730Validation of genome-wide prostate cancer associations in men of African descent
Q33515702Variation in genetic admixture and population structure among Latinos: the Los Angeles Latino eye study (LALES).
Q40012482Vitamin D receptor polymorphisms and breast cancer risk: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
Q35164176Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3).
Q40050925Weight change in older adults and mortality: the Multiethnic Cohort Study
Q36895709Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk
Q37414133rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

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