Esther M. John

researcher ORCID ID = 0000-0003-3259-8003

Esther M. John is …
instance of (P31):
humanQ5

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P496ORCID iD0000-0003-3259-8003

P108employerStanford University School of MedicineQ4115969
P734family nameJohnQ5281981
JohnQ5281981
JohnQ5281981
P735given nameEstherQ837839
EstherQ837839
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q6411528410-year performance of four models of breast cancer risk: a validation study
Q3601638611q13 is a susceptibility locus for hormone receptor positive breast cancer
Q3587156719p13.1 is a triple-negative-specific breast cancer susceptibility locus
Q434258435-lipoxygenase and 5-lipoxygenase-activating protein gene polymorphisms, dietary linoleic acid, and risk for breast cancer
Q371698739q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium
Q94683498A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry
Q40597341A Meta-analysis of Multiple Myeloma Risk Regions in African and European Ancestry Populations Identifies Putatively Functional Loci
Q35755874A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Q34211808A comprehensive examination of breast cancer risk loci in African American women
Q33731355A functionally significant SNP in TP53 and breast cancer risk in African-American women
Q37109758A genome-wide association study of breast cancer in women of African ancestry
Q29417036A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
Q92937384A genome-wide association study of prostate cancer in Latinos
Q35889669A genome-wide linkage study of mammographic density, a risk factor for breast cancer
Q34611972A genome-wide scan for breast cancer risk haplotypes among African American women
Q35089479A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
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
Q36152991A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers
Q47919650A pilot study on the utility of reduced urine collection frequency protocols for the assessment of reproductive hormones in adolescent girls
Q39982410A qualitative study evaluating parental attitudes towards the creation of a female youth cohort (LEGACY) in the Breast Cancer Family Registry
Q37981608A review of cancer in U.S. Hispanic populations
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
Q36043159ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry
Q92102602Accuracy of Risk Estimates from the iPrevent Breast Cancer Risk Assessment and Management Tool
Q36173722Active and passive cigarette smoking and mortality among Hispanic and non-Hispanic white women diagnosed with invasive breast cancer
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.
Q34447543Adult body size, hormone receptor status, and premenopausal breast cancer risk in a multiethnic population: the San Francisco Bay Area breast cancer study
Q99545000African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer
Q39437211Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
Q58613780Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC)
Q91618412Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium
Q40195005Alcohol consumption and cigarette smoking in combination: A predictor of contralateral breast cancer risk in the WECARE study
Q30779634Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases
Q37437960An admixture scan in 1,484 African American women with breast cancer
Q46063050An inverse association between ovarian cysts and breast cancer in the breast cancer family registry
Q45930391Androgen receptor and prostate-specific antigen gene polymorphisms and breast cancer in African-American women.
Q37315498Angiogenesis genes, dietary oxidative balance and breast cancer risk and progression: the Breast Cancer Health Disparities Study
Q35242849Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers
Q34613673Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study
Q64940233Assessing patient readiness for personalized genomic medicine.
Q57305944Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q45979098Association analysis identifies 65 new breast cancer risk loci.
Q38776757Association of Common Genetic Variants With Contralateral Breast Cancer Risk in the WECARE Study
Q91271723Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness
Q64112402Association of Prepubertal and Adolescent Androgen Concentrations With Timing of Breast Development and Family History of Breast Cancer
Q36178189Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
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
Q35957703Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
Q46409708Associations between ALDH1A1 polymorphisms, alcohol consumption, and mortality among Hispanic and non-Hispanic white women diagnosed with breast cancer: the Breast Cancer Health Disparities Study
Q35527962Associations between ALOX, COX, and CRP polymorphisms and breast cancer among Hispanic and non-Hispanic white women: The breast cancer health disparities study
Q35619090Associations between CYP19A1 polymorphisms, Native American ancestry, and breast cancer risk and mortality: the Breast Cancer Health Disparities Study
Q36870645Associations between TCF7L2 polymorphisms and risk of breast cancer among Hispanic and non-Hispanic white women: the Breast Cancer Health Disparities Study
Q33869600Associations between genetic variants in the TGF-β signaling pathway and breast cancer risk among Hispanic and non-Hispanic white women
Q35022847Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
Q35532898Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium
Q57056093Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Q37386163Associations with growth factor genes (FGF1, FGF2, PDGFB, FGFR2, NRG2, EGF, ERBB2) with breast cancer risk and survival: the Breast Cancer Health Disparities Study
Q36792641Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation
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
Q33927874Availability and accuracy of medical record information on language usage of cancer patients from a multi-ethnic population
Q37416050BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research
Q34571646BRCA1 and BRCA2 mutation carriers, oral contraceptive use, and breast cancer before age 50.
Q37002955BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Q42506232BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays
Q30423088Body mass index and risk of second primary breast cancer: the WECARE Study
Q37430003Body mass index, weight change, and risk of second primary breast cancer in the WECARE study: influence of estrogen receptor status of the first breast cancer
Q34972027Body size throughout adult life influences postmenopausal breast cancer risk among hispanic women: the breast cancer health disparities study
Q36913430Body size, modifying factors, and postmenopausal breast cancer risk in a multiethnic population: the San Francisco Bay Area Breast Cancer Study
Q50046604Breast Cancer Family History and Allele-Specific DNA Methylation in the Legacy Girls Study.
Q57420847Breast Cancer Family History and Contralateral Breast Cancer Risk in Young Women: An Update From the Women's Environmental Cancer and Radiation Epidemiology Study
Q57265621Breast Cancer Prognosis inBRCA1andBRCA2Mutation Carriers: An International Prospective Breast Cancer Family Registry Population-Based Cohort Study
Q46167081Breast and ovarian cancer in relatives of cancer patients, with and without BRCA mutations
Q33955302Breast cancer incidence patterns among California Hispanic women: differences by nativity and residence in an enclave
Q35609710Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: findings from the Breast Cancer Family Registry
Q37410693Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab
Q35940158Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Q36449203CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer
Q59789681CYP2D6 phenotype, tamoxifen, and risk of contralateral breast cancer in the WECARE Study
Q35603160Calcium intake and prostate cancer among African Americans: effect modification by vitamin D receptor calcium absorption genotype
Q39002074Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry
Q36683188Cigarette Smoking and Breast Cancer Risk in Hispanic and Non-Hispanic White Women: The Breast Cancer Health Disparities Study
Q37219731Cohort Profile: The Breast Cancer Prospective Family Study Cohort (ProF-SC)
Q94486442Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Q36839777Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
Q34394665Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction
Q35889575Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.
Q33742096Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Q36393232Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
Q35870067Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Q37434133Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Q104263819Comparing Five-Year and Lifetime Risks of Breast Cancer in the Prospective Family Study Cohort
Q31082788Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q37047463Comparison of Clinical, Maternal, and Self Pubertal Assessments: Implications for Health Studies
Q52579925Comparison of methods to assess onset of breast development in the LEGACY Girls Study: methodological considerations for studies of breast cancer.
Q34181322Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer
Q35029565Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry
Q36395280Contribution of the neighborhood environment and obesity to breast cancer survival: the California Breast Cancer Survivorship Consortium
Q57266620Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
Q57278898Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q34084261Correlation of DNA methylation levels in blood and saliva DNA in young girls of the LEGACY Girls study
Q21144874DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers
Q35911581Diabetes and other comorbidities in breast cancer survival by race/ethnicity: the California Breast Cancer Survivorship Consortium (CBCSC)
Q33588213Diagnostic chest X-rays and breast cancer risk before age 50 years for BRCA1 and BRCA2 mutation carriers
Q34145554Diet and lifestyle factors interact with MAPK genes to influence survival: the Breast Cancer Health Disparities Study
Q34359953Diet and lifestyle factors modify immune/inflammation response genes to alter breast cancer risk and prognosis: the Breast Cancer Health Disparities Study
Q36341190Diet quality of cancer survivors and noncancer individuals: Results from a national survey
Q46515439Dietary fat, cooking fat, and breast cancer risk in a multiethnic population
Q38927282Dietary isoflavone intake and all-cause mortality in breast cancer survivors: The Breast Cancer Family Registry
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.
Q40060771Discovery of mutations in homologous recombination genes in African-American women with breast cancer
Q36288541Early-life factors and breast cancer risk in Hispanic women: the role of adolescent body size
Q53770189Energy homeostasis genes and breast cancer risk: The influence of ancestry, body size, and menopausal status, the breast cancer health disparities study.
Q36803979Energy homeostasis genes and survival after breast cancer diagnosis: the Breast Cancer Health Disparities Study
Q30432415Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
Q64114291Enrollment and biospecimen collection in a multiethnic family cohort: the Northern California site of the Breast Cancer Family Registry
Q37367221Epidermal growth factor receptor (EGFR) polymorphisms and breast cancer among Hispanic and non-Hispanic white women: the Breast Cancer Health Disparities Study
Q40781176Ethnic differences in the relationships between diabetes, early age adiposity and mortality among breast cancer survivors: the Breast Cancer Health Disparities Study
Q33780831European ancestry is positively associated with breast cancer risk in Mexican women
Q37307773Evaluating breast cancer risk projections for Hispanic women
Q35883587Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry
Q33614244Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Q36720821Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors
Q33863235Exploring the link between MORF4L1 and risk of breast cancer
Q37308563Family history of breast cancer and all-cause mortality after breast cancer diagnosis in the Breast Cancer Family Registry
Q36971965Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers
Q36087170Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
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.
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
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
Q43427398Fish intake, cooking practices, and risk of prostate cancer: results from a multi-ethnic case-control study
Q36124728Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Q34716723Generalizability of established prostate cancer risk variants in men of African ancestry
Q37277056Genetic ancestry and risk factors for breast cancer among Latinas in the San Francisco Bay Area
Q37173291Genetic ancestry and risk of breast cancer among U.S. Latinas
Q37436758Genetic ancestry and risk of mortality among U.S. Latinas with breast cancer
Q37065332Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women
Q35999323Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study
Q37739048Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Q52561250Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.
Q35815439Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry
Q37610843Genetic variants and non-genetic factors predict circulating vitamin D levels in Hispanic and non-Hispanic White women: the Breast Cancer Health Disparities Study
Q33811527Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation
Q34009975Genetic variants in interleukin genes are associated with breast cancer risk and survival in a genetically admixed population: the Breast Cancer Health Disparities Study
Q39373193Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry
Q35022825Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Q35524233Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent
Q36841890Genetic variation in bone morphogenetic proteins and breast cancer risk in hispanic and non-hispanic white women: The breast cancer health disparities study
Q36402013Genetic variation in genes involved in hormones, inflammation and energetic factors and breast cancer risk in an admixed population
Q34204163Genetic variation in the JAK/STAT/SOCS signaling pathway influences breast cancer-specific mortality through interaction with cigarette smoking and use of aspirin/NSAIDs: the Breast Cancer Health Disparities Study
Q30000080Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Q36842233Genome-wide association analysis identifies three new breast cancer susceptibility loci
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
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
Q95329367Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Q27008356Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
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.
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.
Q28655044Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture
Q59756250Germline Variation and Breast Cancer Incidence: A Gene-Based Association Study and Whole-Genome Prediction of Early-Onset Breast Cancer
Q36278329Germline mutations in PALB2 in African-American breast cancer cases
Q34643959Global DNA methylation levels in girls with and without a family history of breast cancer
Q36640906Global patterns of prostate cancer incidence, aggressiveness, and mortality in men of african descent
Q35382206Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
Q36276540Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Q33709421Heterogeneity of breast cancer subtypes and survival among Hispanic women with invasive breast cancer in California
Q35713044History of Recreational Physical Activity and Survival After Breast Cancer: The California Breast Cancer Survivorship Consortium
Q33919320Hormone receptor status of a first primary breast cancer predicts contralateral breast cancer risk in the WECARE study population
Q34522623Human subjects protection: an event monitoring committee for research studies of girls from breast cancer families
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
Q39321320Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site
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
Q90091185Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Q61448654Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas
Q29417022Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
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
Q53708209Impact of individual and neighborhood factors on disparities in prostate cancer survival.
Q33599178Impact of neighborhood and individual socioeconomic status on survival after breast cancer varies by race/ethnicity: the Neighborhood and Breast Cancer Study
Q36384545Impact of neighborhoods and body size on survival after breast cancer diagnosis
Q114184688Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Q37410472Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
Q53698864Intake of bean fiber, beans, and grains and reduced risk of hormone receptor-negative breast cancer: the San Francisco Bay Area Breast Cancer Study.
Q36065460Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions
Q36249029Interaction between common breast cancer susceptibility variants, genetic ancestry, and nongenetic risk factors in Hispanic women
Q34081324Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
Q36235844Intersection of Race/Ethnicity and Socioeconomic Status in Mortality After Breast Cancer
Q36897623Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry
Q46504474Lifetime physical activity and breast cancer risk in a multiethnic population: the San Francisco Bay area breast cancer study.
Q35576848Lifetime physical activity and risk of endometrial cancer
Q43843244Limited influence of germline genetic variation on all-cause mortality in women with early onset breast cancer: evidence from gene-based tests, single-marker regression, and whole-genome prediction
Q35670157MAPK genes interact with diet and lifestyle factors to alter risk of breast cancer: the Breast Cancer Health Disparities Study
Q31043651Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.
Q36998162Mammographic density and breast cancer: a comparison of related and unrelated controls in the Breast Cancer Family Registry
Q34733697Matrix metalloproteinase genes are associated with breast cancer risk and survival: the Breast Cancer Health Disparities Study
Q52691048Measuring serum melatonin in postmenopausal women: Implications for epidemiologic studies and breast cancer studies.
Q34180885Meat consumption, cooking practices, meat mutagens, and risk of prostate cancer
Q38463411Medical radiation exposure and breast cancer risk: findings from the Breast Cancer Family Registry
Q114182490Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Q89738967Menstrual and reproductive characteristics and breast cancer risk by hormone receptor status and ethnicity: The Breast Cancer Etiology in Minorities study
Q33649334Meta-analysis of loci associated with age at natural menopause in African-American women
Q55216953Metabolomic profiles in breast cancer:a pilot case-control study in the breast cancer family registry.
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
Q46040892Migration history, acculturation, and breast cancer risk in Hispanic women
Q35576887Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women
Q30491647Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium
Q42038345Multiple regions within 8q24 independently affect risk for prostate cancer
Q49024646Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations.
Q34325031Neighborhood influences on recreational physical activity and survival after breast cancer
Q37079859No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
Q44122211No increased risk of breast cancer associated with alcohol consumption among carriers of BRCA1 and BRCA2 mutations ages <50 years
Q37628084Non-invasive optical spectroscopic monitoring of breast development during puberty
Q37396186Obesity and mortality after breast cancer by race/ethnicity: The California Breast Cancer Survivorship Consortium
Q46492944Obesity before age 30 years and risk of advanced prostate cancer
Q52604554Obesity, Body Composition, and Breast Cancer: An Evolving Science.
Q34398269Oral contraceptive use and risk of early-onset breast cancer in carriers and noncarriers of BRCA1 and BRCA2 mutations
Q36280191Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
Q34964253Overall and abdominal adiposity and premenopausal breast cancer risk among hispanic women: the breast cancer health disparities study
Q34061135Past recreational physical activity, body size, and all-cause mortality following breast cancer diagnosis: results from the Breast Cancer Family Registry
Q35737888Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Q37252756Performance of prediction models for BRCA mutation carriage in three racial/ethnic groups: findings from the Northern California Breast Cancer Family Registry
Q44539407Phytoestrogen intake and endometrial cancer risk
Q62583133Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Q36401990Polymorphisms in carcinogen metabolism enzymes, fish intake, and risk of prostate cancer
Q40478488Pre-diagnostic breastfeeding, adiposity, and mortality among parous Hispanic and non-Hispanic white women with invasive breast cancer: the Breast Cancer Health Disparities Study.
Q37353677Prediagnosis reproductive factors and all-cause mortality for women with breast cancer in the breast cancer family registry
Q36356727Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q36494254Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network
Q45970196Prevalence of BRCA1 mutation carriers among U.S. non-Hispanic Whites.
Q46576514Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups
Q39076835Projecting Individualized Absolute Invasive Breast Cancer Risk in US Hispanic Women
Q37103045Prostate Cancer Susceptibility in Men of African Ancestry at 8q24
Q37149567Protective effects of low calcium intake and low calcium absorption vitamin D receptor genotype in the California Collaborative Prostate Cancer Study
Q37149228Psychosocial Adjustment in School-age Girls With a Family History of Breast Cancer
Q33781466Pubertal development in girls by breast cancer family history: the LEGACY girls cohort
Q90242034Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Q92831625Quantitative Ultrasound Spectroscopy for Differentiation of Hepatocellular Carcinoma from At-Risk and Normal Liver Parenchyma
Q34540638RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study
Q93130677Race/Ethnicity and Accuracy of Self-Reported Female First-Degree Family History of Breast and Other Cancers in the Northern California Breast Cancer Family Registry
Q36197983Racial and ethnic differences in adjuvant hormonal therapy use.
Q36273231Racial and ethnic disparities in the impact of obesity on breast cancer risk and survival: a global perspective
Q46068528Racial/Ethnic Differences in the Impact of Neighborhood Social and Built Environment on Breast Cancer Risk: The Neighborhoods and Breast Cancer Study
Q104564161Racial/ethnic disparities in survival after breast cancer diagnosis by estrogen and progesterone receptor status: A pooled analysis
Q28652308Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study
Q28652056Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers
Q35608690Rare variants in the ATM gene and risk of breast cancer
Q37373918Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer
Q28743906Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study
Q33693138Recent changes in breast cancer incidence and risk factor prevalence in San Francisco Bay area and California women: 1988 to 2004.
Q90439909Recreational Physical Activity Is Associated with Reduced Breast Cancer Risk in Adult Women at High Risk for Breast Cancer: A Cohort Study of Women Selected for Familial and Genetic Risk
Q24614203Red meat and poultry, cooking practices, genetic susceptibility and risk of prostate cancer: results from a multiethnic case-control study
Q36767427Red meat, poultry, and fish intake and breast cancer risk among Hispanic and Non-Hispanic white women: The Breast Cancer Health Disparities Study
Q35155449Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
Q64101959Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
Q45953705Reply to Dietary isoflavone intake and all-cause mortality in breast cancer survivors: The Breast Cancer Family Registry-methodological issues.
Q36415317Reproductive factors, tumor estrogen receptor status and contralateral breast cancer risk: results from the WECARE study
Q48250088Reproductive history, breast-feeding and risk of triple negative breast cancer: The Breast Cancer Etiology in Minorities (BEM) study.
Q36089820Reproductive status at first diagnosis influences risk of radiation-induced second primary contralateral breast cancer in the WECARE study
Q46110960Residential sunlight exposure is associated with a decreased risk of prostate cancer
Q40396801Response to Conner et al. Re: "Cigarette Smoking and Breast Cancer Risk in Hispanic and Non-Hispanic White Women: The Breast Cancer Health Disparities Study".
Q35750765Risk factors for uncommon histologic subtypes of breast cancer using centralized pathology review in the Breast Cancer Family Registry
Q30415050Risk of asynchronous contralateral breast cancer in noncarriers of BRCA1 and BRCA2 mutations with a family history of breast cancer: a report from the Women's Environmental Cancer and Radiation Epidemiology Study
Q37085786Risk of pancreatic cancer in breast cancer families from the breast cancer family registry
Q38717239Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Q35053599SEPP1 influences breast cancer risk among women with greater native american ancestry: the breast cancer health disparities study
Q35983751Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry
Q37289611Second primary breast cancer occurrence according to hormone receptor status
Q38488106Segregation analysis of prostate cancer in 1,719 white, African-American and Asian-American families in the United States and Canada
Q29417074Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
Q61118451Shared heritability and functional enrichment across six solid cancers
Q64004349Shared heritability and functional enrichment across six solid cancers
Q37353501Socioeconomic status and prostate cancer incidence and mortality rates among the diverse population of California
Q46001274Sun exposure and prostate cancer risk: evidence for a protective effect of early-life exposure.
Q45951066Sun exposure, vitamin D receptor gene polymorphisms, and breast cancer risk in a multiethnic population.
Q34426763Sun exposure, vitamin D receptor gene polymorphisms, and risk of advanced prostate cancer
Q37085141Systemic therapy for breast cancer and risk of subsequent contralateral breast cancer in the WECARE Study
Q37122297Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
Q37252497Telomere length, telomere-related genes, and breast cancer risk: the breast cancer health disparities study
Q24806109The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer
Q44897750The CHEK2*1100delC allelic variant and risk of breast cancer: screening results from the Breast Cancer Family Registry
Q33716455The California Breast Cancer Survivorship Consortium (CBCSC): prognostic factors associated with racial/ethnic differences in breast cancer survival
Q37059764The Effect of Patient and Contextual Characteristics on Racial/Ethnic Disparity in Breast Cancer Mortality
Q91178389The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Q64116004The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With or Mutations
Q39117896The Interaction between Genetic Ancestry and Breast Cancer Risk Factors among Hispanic Women: The Breast Cancer Health Disparities Study
Q37686870The LEGACY Girls Study: Growth and Development in the Context of Breast Cancer Family History
Q52642368The association of mammographic density with risk of contralateral breast cancer and change in density with treatment in the WECARE study.
Q64998464The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium.
Q37624119The influence of genetic ancestry and ethnicity on breast cancer survival associated with genetic variation in the TGF-β-signaling pathway: The Breast Cancer Health Disparities 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
Q35476902The potential value of sibling controls compared with population controls for association studies of lifestyle-related risk factors: an example from the Breast Cancer Family Registry
Q36142060The role of genetic breast cancer susceptibility variants as prognostic factors
Q43110417Tobacco smoking, polymorphisms in carcinogen metabolism enzyme genes, and risk of localized and advanced prostate cancer: results from the California Collaborative Prostate Cancer Study
Q33654997Total energy intake and breast cancer risk in sisters: the Breast Cancer Family Registry
Q89961489Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Q92994868Two truncating variants in FANCC and breast cancer risk
Q35032730Validation of genome-wide prostate cancer associations in men of African descent
Q40075923Validation of self-reported comorbidity status of breast cancer patients with medical records: the California Breast Cancer Survivorship Consortium (CBCSC).
Q30416002Variation in genes related to obesity, weight, and weight change and risk of contralateral breast cancer in the WECARE Study population
Q33855441Whole-genome amplification enables accurate genotyping for microarray-based high-density single nucleotide polymorphism array

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