Penetrance of male breast cancer susceptibility genes: a systematic review.
Chamseddine RS, Wang C, Yin K, Wang J, Singh P, Zhou J, Robson ME, Braun D, Hughes KS.
Breast Cancer Res Treat. 2021 Oct 13. PMID: 34642874
Education and Training
PhD, Biostatistics
Harvard T.H. Chan School of Public Health
Bibliography
Search Behavior Regarding Cancer Susceptibility Genes Using a Clinical Decision Support Tool for Gene-Specific Penetrance: Content Analysis.
Yin K, Zhou J, Singh P, Wang J, Braun D, Hughes KS.
JMIR Cancer. 2021 Jul 13. 7(3):e28527. PMID: 34255640
Disease spectrum of gastric cancer susceptibility genes.
McKinley SK, Singh P, Yin K, Wang J, Zhou J, Bao Y, Wu M, Pathak K, Mullen JT, Braun D, Hughes KS.
Med Oncol. 2021 Mar 24. 38(5):46. PMID: 33760988
Familial pancreatic cancer: who should be considered for genetic testing?
Kartal K, Guan Z, Tang R, Griffin M, Wang Y, Braun D, Klein AP, Hughes KS.
Ir J Med Sci. 2021 Mar 17. PMID: 33733397
Nationwide Study of Short-term Exposure to Fine Particulate Matter and Cardiovascular Hospitalizations Among Medicaid Enrollees.
deSouza P, Braun D, Parks RM, Schwartz J, Dominici F, Kioumourtzoglou MA.
Epidemiology. 2021 01. 32(1):6-13. PMID: 33009251
A likelihood-based approach to assessing frequency of pathogenicity among variants of unknown significance in susceptibility genes.
Yang Y, Hong C, Liang JW, Gruber S, Parmigiani G, Idos G, Braun D.
Stat Med. 2021 02 10. 40(3):593-606. PMID: 33120437
Long-term effects of PM2·5 on neurological disorders in the American Medicare population: a longitudinal cohort study.
Shi L, Wu X, Danesh Yazdi M, Braun D, Abu Awad Y, Wei Y, Liu P, Di Q, Wang Y, Schwartz J, Dominici F, Kioumourtzoglou MA, Zanobetti A.
Lancet Planet Health. 2020 12. 4(12):e557-e565. PMID: 33091388
Variation in cancer risk among families with genetic susceptibility.
Huang T, Braun D, Lynch HT, Parmigiani G.
Genet Epidemiol. 2021 03. 45(2):209-221. PMID: 33030277
Statistical approaches for meta-analysis of genetic mutation prevalence.
Hujoel MLA, Parmigiani G, Braun D.
Genet Epidemiol. 2021 03. 45(2):154-170. PMID: 33000511
A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome.
Gao F, Pan X, Dodd-Eaton EB, Recio CV, Montierth MD, Bojadzieva J, Mai PL, Zelley K, Johnson VE, Braun D, Nichols KE, Garber JE, Savage SA, Strong LC, Wang W.
Genome Res. 2020 08. 30(8):1170-1180. PMID: 32817165