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Author Details

David E Goldgar
University of Utah
1980
350
94
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36623243Contralateral Breast Cancer Risk Among Carriers of Germline Pathogenic Variants in <i>ATM</i>, <i>BRCA1</i>, <i>BRCA2</i>, <i>CHEK2</i>, and <i>PALB2</i>.J Clin Oncol2023
36623243Contralateral Breast Cancer Risk Among Carriers of Germline Pathogenic Variants in <i>ATM</i>, <i>BRCA1</i>, <i>BRCA2</i>, <i>CHEK2</i>, and <i>PALB2</i>.J Clin Oncol2023
35048954Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits.J Natl Cancer Inst2022
35665744An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance.NPJ Genom Med2022
35659930Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions.Am J Hum Genet2022
35048954Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits.J Natl Cancer Inst2022
34906479Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.Genet Med2022
35665744An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance.NPJ Genom Med2022
35659930Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions.Am J Hum Genet2022
34906479Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.Genet Med2022
33471974A Population-Based Study of Genes Previously Implicated in Breast Cancer.N Engl J Med2021
34292776Risk of Late-Onset Breast Cancer in Genetically Predisposed Women.J Clin Oncol2021
33471974A Population-Based Study of Genes Previously Implicated in Breast Cancer.N Engl J Med2021
34273903An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategy.Hum Mutat2021
34101481Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score.J Clin Oncol2021
34042955Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States.JAMA Oncol2021
33990587Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.Nat Commun2021
34199804Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&amp;I).J Pers Med2021
33609447Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance.Am J Hum Genet2021
34341517Mendelian randomisation study of smoking exposure in relation to breast cancer risk.Br J Cancer2021
33146377Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer.J Natl Cancer Inst2021
33087888Integration of functional assay data results provides strong evidence for classification of hundreds of BRCA1 variants of uncertain significance.Genet Med2021
33301022Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort.J Natl Cancer Inst2021
34672684Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.J Clin Oncol2021
33609447Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance.Am J Hum Genet2021
34672684Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.J Clin Oncol2021
34273903An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategy.Hum Mutat2021
34042955Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United States.JAMA Oncol2021
33990587Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.Nat Commun2021
34101481Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score.J Clin Oncol2021
34292776Risk of Late-Onset Breast Cancer in Genetically Predisposed Women.J Clin Oncol2021
34341517Mendelian randomisation study of smoking exposure in relation to breast cancer risk.Br J Cancer2021
34199804Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&amp;I).J Pers Med2021
33146377Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer.J Natl Cancer Inst2021
33087888Integration of functional assay data results provides strong evidence for classification of hundreds of BRCA1 variants of uncertain significance.Genet Med2021
33301022Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort.J Natl Cancer Inst2021
31406321A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.Genet Med2020
31853058Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort.Genet Med2020
32427313Contribution of Germline Predisposition Gene Mutations to Breast Cancer Risk in African American Women.J Natl Cancer Inst2020
31584660Considerations When Using Breast Cancer Risk Models for Women with Negative BRCA1/BRCA2 Mutation Results.J Natl Cancer Inst2020
32119081Radiation Treatment, ATM, BRCA1/2, and CHEK2*1100delC Pathogenic Variants and Risk of Contralateral Breast Cancer.J Natl Cancer Inst2020
32091585The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort.J Natl Cancer Inst2020
32442341Mutation prevalence tables for hereditary cancer derived from multigene panel testing.Hum Mutat2020
33022221Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.Am J Hum Genet2020
32773770Considerations in assessing germline variant pathogenicity using cosegregation analysis.Genet Med2020
31406321A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.Genet Med2020
31853058Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort.Genet Med2020
32091585The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort.J Natl Cancer Inst2020
32773770Considerations in assessing germline variant pathogenicity using cosegregation analysis.Genet Med2020
33022221Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.Am J Hum Genet2020
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The Institute of Cancer Research
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Fondazione IRCCS Istituto Nazionale dei Tumori
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Co-authored papers 42
Pomeranian Medical University
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German Cancer Research Center (DKFZ)
Co-authored papers 39
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David Geffen School of Medicine, University of California los angeles
Co-authored papers 35
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Guy's and St Thomas' NHS Foundation Trust
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Center for Cancer Equity and Engagement, Dana-Farber/Harvard Cancer Center
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International Hereditary Cancer Center, Pomeranian Medical University
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