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Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.

A. Antoniou, P. Pharoah, S. Narod, et al.. (2003). American journal of human genetics. Cited 3,763 times. https://doi.org/10.1086/375033

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

Karoline B. Kuchenbaecker, J. Hopper, D. Barnes, et al.. (2017). JAMA. Cited 2,421 times. https://doi.org/10.1001/jama.2017.7112

Genome-wide association study identifies novel breast cancer susceptibility loci

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Association analysis identifies 65 new breast cancer risk loci

K. Michailidou, S. Lindström, J. Dennis, et al.. (2017). Nature. Cited 1,288 times. https://doi.org/10.1038/nature24284

Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease

T. Möller, Hampus Olsson, J. Ranstam. (2002). The Lancet. Cited 1,250 times. https://doi.org/10.1016/S0140-6736(02)09454-0

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

K. Michailidou, P. Hall, A. González-Neira, et al.. (2013). Nature Genetics. Cited 1,123 times. https://doi.org/10.1038/ng.2563

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease

P. Brandt, R. Goldbohm. (2001). The Lancet. Cited 1,099 times. https://doi.org/10.1016/S0140-6736(01)06524-2

Alcohol, tobacco and breast cancer – collaborative reanalysis of individual data from 53 epidemiological studies, including 58 515 women with breast cancer and 95 067 women without the disease

Nobuyuki Hamajima, K. Hirose, K. Tajima, et al.. (2002). British Journal of Cancer. Cited 923 times. https://doi.org/10.1038/sj.bjc.6600596

Gene-panel sequencing and the prediction of breast-cancer risk.

D. Easton, Paul D. P. Pharoah, A. Antoniou, et al.. (2015). The New England journal of medicine. Cited 846 times. https://doi.org/10.1056/NEJMsr1501341

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies.

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A common coding variant in CASP8 is associated with breast cancer risk

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A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)

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Detectable clonal mosaicism and its relationship to aging and cancer

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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

S. Bojesen, K. Pooley, S. Johnatty, et al.. (2013). Nature Genetics. Cited 561 times. https://doi.org/10.1038/ng.2566

MicroRNA Related Polymorphisms and Breast Cancer Risk

Sofia Khan, Dario Greco, K. Michailidou, et al.. (2014). PLoS ONE. Cited 560 times. https://doi.org/10.1371/journal.pone.0109973

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

N. Mavaddat, D. Barrowdale, I. Andrulis, et al.. (2011). Cancer Epidemiology, Biomarkers & Prevention. Cited 556 times. https://doi.org/10.1158/1055-9965.EPI-11-0775

Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer: a multicenter, prospective study.

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Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2

Shahana Ahmed, G. Thomas, M. Ghoussaini, et al.. (2009). Nature Genetics. Cited 514 times. https://doi.org/10.1038/ng.354

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

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CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.

D. Easton, L. McGuffog, D. Thompson, et al.. (2004). American journal of human genetics. Cited 473 times. https://doi.org/10.1086/421251

Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.

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Genome-wide association studies identify four ER negative–specific breast cancer risk loci

M. García-Closas, F. Couch, S. Lindstrom, et al.. (2013). Nature Genetics. Cited 435 times. https://doi.org/10.1038/ng.2561

Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.

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Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

F. Couch, Xianshu Wang, L. McGuffog, et al.. (2013). PLoS Genetics. Cited 411 times. https://doi.org/10.1371/journal.pgen.1003212

Circulating sex hormones and breast cancer risk factors in postmenopausal women: reanalysis of 13 studies

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Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics

M. García-Closas, P. Hall, H. Nevanlinna, et al.. (2008). PLoS Genetics. Cited 392 times. https://doi.org/10.1371/journal.pgen.1000054

RAD51B in Familial Breast Cancer

Liisa M. Pelttari, Sofia Khan, Mikko Vuorela, et al.. (2016). PLoS ONE. Cited 368 times. https://doi.org/10.1371/journal.pone.0153788

Multiple loci with different cancer specificities within the 8q24 gene desert.

M. Ghoussaini, Honglin Song, T. Koessler, et al.. (2008). Journal of the National Cancer Institute. Cited 361 times. https://doi.org/10.1093/jnci/djn190

A 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

A. Antoniou, Xianshu Wang, Z. Fredericksen, et al.. (2010). Nature Genetics. Cited 358 times. https://doi.org/10.1038/ng.669

The landscape of recombination in African Americans

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Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups.

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DNA methylation in white blood cells

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Obesity and Outcomes in Premenopausal and Postmenopausal Breast Cancer

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Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25–q27

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A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer

C. Edlund, A. Ekici, Peter A. Fasching, et al.. (2011). Nature Genetics. Cited 320 times. https://doi.org/10.1038/ng.985

Mammographic density phenotypes and risk of breast cancer: a meta-analysis.

A. Pettersson, R. Graff, G. Ursin, et al.. (2014). Journal of the National Cancer Institute. Cited 313 times. https://doi.org/10.1093/jnci/dju078

The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer

E. John, J. Hopper, J. Beck, et al.. (2004). Breast Cancer Research. Cited 309 times. https://doi.org/10.1186/bcr801

Genome-wide association analysis identifies three new breast cancer susceptibility loci

M. Ghoussaini, O. Fletcher, K. Michailidou, et al.. (2012). Nature genetics. Cited 303 times. https://doi.org/10.1038/ng.1049

Regulation of BRCC, a holoenzyme complex containing BRCA1 and BRCA2, by a signalosome-like subunit and its role in DNA repair.

Yuanshu Dong, Mohamed-Ali Hakimi, Xiaowei Chen, et al.. (2003). Molecular cell. Cited 301 times. https://doi.org/10.1016/S1097-2765(03)00424-6

Key concepts in genetic epidemiology

P. Burton, M. Tobin, J. Hopper. (2005). The Lancet. Cited 294 times. https://doi.org/10.1016/S0140-6736(05)67322-9

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

T. Rebbeck, T. Friebel, E. Friedman, et al.. (2018). Human Mutation. Cited 277 times. https://doi.org/10.1002/humu.23406

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Karoline B. Kuchenbaecker, L. McGuffog, D. Barrowdale, et al.. (2017). JNCI Journal of the National Cancer Institute. Cited 277 times. https://doi.org/10.1093/jnci/djw302

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

A. Antoniou, A. Spurdle, O. Sinilnikova, et al.. (2008). American journal of human genetics. Cited 277 times. https://doi.org/10.1016/j.ajhg.2008.02.008

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.

A. Antoniou, O. Sinilnikova, J. Simard, et al.. (2007). American journal of human genetics. Cited 269 times. https://doi.org/10.1086/522611

Dominant negative ATM mutations in breast cancer families.

G. Chenevix-Trench, A. Spurdle, M. Gatei, et al.. (2002). Journal of the National Cancer Institute. Cited 265 times. https://doi.org/10.1093/JNCI/94.3.205

The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations

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A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

K. Monda, K. Monda, Gary K. Chen, et al.. (2013). Nature genetics. Cited 255 times. https://doi.org/10.1038/ng.2608

Distinct molecular pathogeneses of early-onset breast cancers in BRCA1 and BRCA2 mutation carriers: a population-based study.

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Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

E. Bancroft, E. Page, E. Castro, et al.. (2014). European Urology. Cited 243 times. https://doi.org/10.1016/j.eururo.2014.01.003

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.

J. French, M. Ghoussaini, S. Edwards, et al.. (2013). American journal of human genetics. Cited 235 times. https://doi.org/10.1016/j.ajhg.2013.01.002

Classification of rare missense substitutions, using risk surfaces, with genetic‐ and molecular‐epidemiology applications

S. Tavtigian, G. Byrnes, D. Goldgar, et al.. (2008). Human Mutation. Cited 234 times. https://doi.org/10.1002/humu.20896

Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients

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Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

Yan Guo, Shaneda Warren Andersen, X. Shu, et al.. (2016). PLoS Medicine. Cited 229 times. https://doi.org/10.1371/journal.pmed.1002105

Rare variants in the ATM gene and risk of breast cancer

D. Goldgar, S. Healey, J. Dowty, et al.. (2011). Breast Cancer Research : BCR. Cited 227 times. https://doi.org/10.1186/bcr2919

Activation of Notch signaling in human colon adenocarcinoma.

M. Reedijk, S. Odorcic, Hui Zhang, et al.. (2008). International journal of oncology. Cited 224 times. https://doi.org/10.3892/IJO_00000112

Genetic evidence and integration of various data sources for classifying uncertain variants into a single model

D. Goldgar, D. Easton, G. Byrnes, et al.. (2008). Human Mutation. Cited 203 times. https://doi.org/10.1002/humu.20897

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

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Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers

A. Eisen, J. Lubiński, J. Gronwald, et al.. (2008). JNCI Journal of the National Cancer Institute. Cited 198 times. https://doi.org/10.1093/jnci/djn313

Identification of Novel Genetic Markers of Breast Cancer Survival

Qi Guo, M. Schmidt, P. Kraft, et al.. (2015). JNCI Journal of the National Cancer Institute. Cited 195 times. https://doi.org/10.1093/jnci/djv081

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

G. Wishart, C. Bajdik, E. Dicks, et al.. (2012). British Journal of Cancer. Cited 192 times. https://doi.org/10.1038/bjc.2012.338

Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.

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Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.

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CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer.

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A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

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Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

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Familial risks, early-onset breast cancer, and BRCA1 and BRCA2 germline mutations.

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Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers.

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Rare mutations in XRCC2 increase the risk of breast cancer.

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Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer.

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Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.

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Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.

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An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

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Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium.

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Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors

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Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.

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BRCA2 Mutation-associated Breast Cancers Exhibit a Distinguishing Phenotype Based on Morphology and Molecular Profiles From Tissue Microarrays

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Misclassification of race/ethnicity in a Population-based Cancer Registry (United States)

S. Gomez, S. Glaser. (2006). Cancer Causes & Control. Cited 171 times. https://doi.org/10.1007/s10552-006-0013-y

Expression of the circadian clock genes Per1 and Per2 in sporadic and familial breast tumors.

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SNP-SNP interactions in breast cancer susceptibility

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Constitutional Methylation of the BRCA1 Promoter Is Specifically Associated with BRCA1 Mutation-Associated Pathology in Early-Onset Breast Cancer

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A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers.

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Breast cancer prognosis in BRCA1 and BRCA2 mutation carriers: an International Prospective Breast Cancer Family Registry population-based cohort study.

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Environmental exposures during windows of susceptibility for breast cancer: a framework for prevention research

M. B. Terry, Karin B. Michels, J. Brody, et al.. (2019). Breast Cancer Research : BCR. Cited 162 times. https://doi.org/10.1186/s13058-019-1168-2

Population-based family studies in genetic epidemiology

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Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

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Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

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Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.

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Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

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Germline Mutation in BRCA1 or BRCA2 and Ten-Year Survival for Women Diagnosed with Epithelial Ovarian Cancer

F. Candido-dos-Reis, Honglin Song, E. Goode, et al.. (2014). Clinical Cancer Research. Cited 151 times. https://doi.org/10.1158/1078-0432.CCR-14-2497

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

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Short telomere length and breast cancer risk: a study in sister sets.

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Prevalence 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.

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A genome wide linkage search for breast cancer susceptibility genes

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Reproductive and Hormonal Factors, and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers: Results from the International BRCA1/2 Carrier Cohort Study

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The CYP3A4*1B polymorphism has no functional significance and is not associated with risk of breast or ovarian cancer.

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A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.

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Communication of BRCA1 and BRCA2 results to at‐risk relatives: A cancer risk assessment program's experience

J. Costalas, M. Itzen, J. Malick, et al.. (2003). American Journal of Medical Genetics Part C: Seminars in Medical Genetics. Cited 139 times. https://doi.org/10.1002/ajmg.c.10003

Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study

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Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium

B. Pasaniuc, B. Pasaniuc, Noah Zaitlen, et al.. (2011). PLoS Genetics. Cited 138 times. https://doi.org/10.1371/journal.pgen.1001371

Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25

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Oral Contraceptive Use and Risk of Early-Onset Breast Cancer in Carriers and Noncarriers of BRCA1 and BRCA2 Mutations

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Expression of constitutively activated EGFRvlll in non‐small cell lung cancer

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10-year performance of four models of breast cancer risk: a validation study.

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Tumoral Lymphocytic Infiltration and Expression of the Chemokine CXCL10 in Breast Cancers from the Ontario Familial Breast Cancer Registry

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Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

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A Genome-Wide “Pleiotropy Scan” Does Not Identify New Susceptibility Loci for Estrogen Receptor Negative Breast Cancer

D. Campa, Myrto Barrdahl, K. Tsilidis, et al.. (2014). PLoS ONE. Cited 8 times. https://doi.org/10.1371/journal.pone.0085955

EMSY and CCND1 amplification in familial breast cancer: from the Ontario site of the Breast Cancer Family Registry

A. Bane, A. Mulligan, Dushanthi Pinnaduwage, et al.. (2011). Breast Cancer Research and Treatment. Cited 8 times. https://doi.org/10.1007/s10549-011-1380-y

Availability and Accuracy of Medical Record Information on Language Usage of Cancer Patients from a Multi-Ethnic Population

L. McClure, S. Glaser, S. Shema, et al.. (2010). Journal of Immigrant and Minority Health. Cited 8 times. https://doi.org/10.1007/s10903-009-9282-3

Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development

Jianjun Liu, K. Desai, Yuqing Li, et al.. (2009). The HUGO Journal. Cited 8 times. https://doi.org/10.1007/s11568-010-9138-x

Re: On the use of familial aggregation in population-based case probands for calculating penetrance.

A. Whittemore, G. Gong. (2003). Journal of the National Cancer Institute. Cited 8 times. https://doi.org/10.1093/JNCI/95.1.76

Genetic association tests for family data with missing parental genotypes: A comparison

A. Whittemore, J. Halpern. (2003). Genetic Epidemiology. Cited 8 times. https://doi.org/10.1002/GEPI.10247

Re: "Presenting statistical uncertainty in trends and dose-response relations".

J. Hopper, G. Dite. (2002). American journal of epidemiology. Cited 8 times. https://doi.org/10.1093/AJE/155.10.977

ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry

Anne-Laure Renault, F. Lesueur, Yan Coulombe, et al.. (2016). PLoS ONE. Cited 7 times. https://doi.org/10.1371/journal.pone.0156820

Mammographic density and breast cancer: a comparison of related and unrelated controls in the Breast Cancer Family Registry

L. Linton, L. Martin, Qing Li, et al.. (2013). Breast Cancer Research : BCR. Cited 7 times. https://doi.org/10.1186/bcr3430

The postmenopausal hormone replacement therapy-related breast cancer risk is decreased in women carrying the CYP2C19*17 variant

C. Justenhoven, Ofure Obazee, S. Winter, et al.. (2011). Breast Cancer Research and Treatment. Cited 7 times. https://doi.org/10.1007/s10549-011-1827-1

Racial and Ethnic Differences in Adjuvant Hormonal Therapy Use

J. Livaudais, Christopher I. Li, Christopher I. Li, et al.. (2012). Journal of Women's Health. Cited 7 times. https://doi.org/10.1089/jwh.2011.3254

Adequacy of risk-reducing gynaecologic surgery in BRCA1 or BRCA2 mutation carriers and other women at high risk of pelvic serous cancer

B. Kiely, M. Friedlander, R. Milne, et al.. (2011). Familial Cancer. Cited 7 times. https://doi.org/10.1007/s10689-011-9435-0

The accuracy of cancer diagnoses as reported in families with head and neck cancer: a case-control study.

S. Jefferies, D. E. Goldgar, R. Eeles. (2008). Clinical oncology (Royal College of Radiologists (Great Britain)). Cited 7 times. https://doi.org/10.1016/j.clon.2008.01.008

Re: Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.

J. Hopper, J. Baron. (2003). Journal of the National Cancer Institute. Cited 7 times. https://doi.org/10.1093/JNCI/95.13.1010

New Ontario familial breast cancer registry to facilitate genetic and epidemiologic studies.

I. Andrulis, N. Boyd, H. Sutherland. (1997). Canadian family physician Medecin de famille canadien. Cited 7 times.

Body size at birth, early-life growth and the timing of the menopausal transition and natural menopause.

M. Goldberg, H. Tawfik, J. Kline, et al.. (2020). Reproductive toxicology. Cited 7 times. https://doi.org/10.1016/j.reprotox.2019.02.013

Hi-Plex targeted sequencing is effective using DNA derived from archival dried blood spots.

T. Nguyen-Dumont, M. Mahmoodi, F. Hammet, et al.. (2015). Analytical biochemistry. Cited 6 times. https://doi.org/10.1016/j.ab.2014.10.010

Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers

Kristen Stevens, Xianshu Wang, Z. Fredericksen, et al.. (2012). Breast Cancer Research and Treatment. Cited 6 times. https://doi.org/10.1007/s10549-012-2255-6

7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium

R. Milne, J. Lorenzo-Bermejo, B. Burwinkel, et al.. (2011). Journal of Medical Genetics. Cited 6 times. https://doi.org/10.1136/jmedgenet-2011-100303

Professional opportunities and responsibilities in the provision of genetic information to children relinquished for adoption

V. Venne, J. Botkin, S. Buys. (2003). American Journal of Medical Genetics Part A. Cited 6 times. https://doi.org/10.1002/ajmg.a.20071

Limited 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

Molly Scannell Bryan, Maria Argos, I. Andrulis, et al.. (2017). Breast Cancer Research and Treatment. Cited 5 times. https://doi.org/10.1007/s10549-017-4287-4

Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry

M. Walker, L. Mirea, K. Cooper, et al.. (2013). Familial Cancer. Cited 5 times. https://doi.org/10.1007/s10689-013-9689-9

Human subjects protection: an event monitoring committee for research studies of girls from breast cancer families.

Diana Harris, L. Patrick-Miller, Lisa A Schwartz, et al.. (2014). The Journal of adolescent health : official publication of the Society for Adolescent Medicine. Cited 5 times. https://doi.org/10.1016/j.jadohealth.2014.03.007

Are genetic and environmental components of variance in mammographic density measures that predict breast cancer risk independent of within-twin pair differences in body mass index?

G. Dite, J. Stone, A. Chiarelli, et al.. (2011). Breast Cancer Research and Treatment. Cited 5 times. https://doi.org/10.1007/s10549-011-1739-0

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

Kristen Stevens, M. García-Closas, Z. Fredericksen, et al.. (2011). British Journal of Cancer. Cited 5 times. https://doi.org/10.1038/bjc.2011.448

Family-based genetic association study of insulin-like growth factor I microsatellite markers and premenopausal breast cancer risk

G. Fehringer, N. Boyd, J. Knight, et al.. (2009). Breast Cancer Research and Treatment. Cited 5 times. https://doi.org/10.1007/s10549-009-0336-y

Re: On the use of familial aggregation in population-based case probands for calculating penetrance.

P. Pharoah, A. Antoniou, J. Hopper, et al.. (2003). Journal of the National Cancer Institute. Cited 5 times. https://doi.org/10.1093/JNCI/95.1.75

Early-life Growth and Benign Breast Disease.

M. Goldberg, B. Cohn, L. Houghton, et al.. (2019). American journal of epidemiology. Cited 5 times. https://doi.org/10.1093/aje/kwz126

Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer

G. Dite, R. MacInnis, A. Bickerstaffe, et al.. (2017). American Journal of Epidemiology. Cited 4 times. https://doi.org/10.1093/aje/kww241

A qualitative study evaluating parental attitudes towards the creation of a female youth cohort (LEGACY) in the Breast Cancer Family Registry

G. Glendon, Caren J. Frost, I. Andrulis, et al.. (2010). Psycho‐Oncology. Cited 4 times. https://doi.org/10.1002/pon.1543

Socio‐economic status and survival from breast cancer for young, Australian, urban women

K. Morley, R. Milne, Graham G. Giles, et al.. (2010). Australian and New Zealand Journal of Public Health. Cited 4 times. https://doi.org/10.1111/j.1753-6405.2010.00507.x

No evidence of familial correlation in breast cancer metastasis

A. Whittemore, B. Stearman, V. Venne, et al.. (2009). Breast Cancer Research and Treatment. Cited 4 times. https://doi.org/10.1007/s10549-009-0368-3

Genome Wide Screening of CAG Trinucleotide Repeat Lengths in Breast Cancer

H. Jarjanazi, Hong Li, I. Andrulis, et al.. (2007). Disease Markers. Cited 3 times. https://doi.org/10.1155/2006/951857

Distribution of family history of a disease as a function of mode of inheritance, genetic relative hazard, allele frequency and disease status of the proband, with application to female breast cancer.

J. Cui, J. Hopper. (2001). Journal of epidemiology and biostatistics. Cited 3 times. https://doi.org/10.1080/13595220152601800

Performance of BCRAT in high-risk patients with breast cancer - Authors' reply.

M. Terry, Y. Liao, J. Hopper, et al.. (2019). The Lancet. Oncology. Cited 3 times. https://doi.org/10.1016/S1470-2045(19)30311-0

Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk

Conor Smyth, Iva Špakulová, Owen Cotton-Barratt, et al.. (2015). Molecular Genetics & Genomic Medicine. Cited 2 times. https://doi.org/10.1002/mgg3.129

Methodological 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

Fang Chen, Jing He, Jianqi Zhang, et al.. (2015). PLoS ONE. Cited 2 times. https://doi.org/10.1371/journal.pone.0131106

Is BRCA2 c.9079 G > A a predisposing variant for early onset breast cancer?

F. Hammet, J. George, A. Tesoriero, et al.. (2008). Breast Cancer Research and Treatment. Cited 2 times. https://doi.org/10.1007/s10549-007-9624-6

Response to ten Broeke et al.

M. Roberts, Nur Zeinomar, B. Solomon, et al.. (2018). Genetics in Medicine. Cited 2 times. https://doi.org/10.1038/s41436-018-0031-7

Response to Lee et al 2019: Essential to frame study implications within the context of prior findings from enriched cohorts for underlying familial risk of breast cancer

M. Terry, Nur Zeinomar. (2019). Occupational and Environmental Medicine. Cited 2 times. https://doi.org/10.1136/oemed-2019-105936

Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer.

R. MacInnis, M. Pike, J. Hopper. (2016). The New England journal of medicine. Cited 1 times. https://doi.org/10.1056/NEJMc1602861

Placental genes and breast cancer: can the offspring's or father's genotypes predict mother's risk?

H. Ahsan. (2003). Epidemiology. Cited 1 times. https://doi.org/10.1097/01.EDE.0000050696.19411.C0

Modified rapid expansion detection method to analyze Cag/CTG repeat expansions.

H. Jarjanazi, H. Ozçelik. (2002). BioTechniques. Cited 1 times. https://doi.org/10.2144/02325BM06

Response to Evans et al.

M. Roberts, Nur Zeinomar, B. Solomon, et al.. (2018). Genetics in Medicine. Cited 1 times. https://doi.org/10.1038/s41436-018-0400-2

Interpretation of genomic variation and disease association: the great missense mutation challenge!

T. Nguyen-Dumont, I. Winship, M. Southey. (2015). Breast Cancer Research and Treatment. https://doi.org/10.1007/s10549-015-3394-3

Genetic testing for BRCA1 and BRCA2: recommendations of the Stanford Program in Genomics, Ethics, and Society. Breast Cancer Working Group.

B. A. Koenig, H. T. Greely, L. M. McCONNELL, et al.. (1998). Journal of women's health.

Transient tumor marker surge following chemotherapy of testis tumors.

M. R. Shetty. (1987). Cancer treatment reports.

Response to Wang et al.

M. Roberts, Nur Zeinomar, B. Solomon, et al.. (2019). Genetics in Medicine. https://doi.org/10.1038/s41436-019-0469-2
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