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JAMA|September 24, 2004
The "duty to warn" a patient's family members about hereditary disease risksKenneth Offit, Elizabeth Groeger, Sam Turner, et al.Mutation Research|December 17, 2008
cDNA analysis demonstrates that the BRCA2 intronic variant IVS4-12del5 is a deleterious mutationLiying Zhang, Ruben Bacares, Sherry Boyar, et al.Familial Cancer|May 2, 2020
Characterization of a germline splice site variant MLH1 c.678-3T>A in a Lynch syndrome familyCiyu Yang, Margaret Sheehan, Ester Borras, et al.Healthcare Policy = Politiques De Sante|December 24, 2017
What's Involved with Wanting to Be Involved? Comparing Expectations for Public Engagement in Health Policy across Research and Care ContextsCarolyn J Barg, Fiona A Miller, Robin Z Hayeems, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Effect of genetics clinical decision support tools on health-care providers' decision making: a mixed-methods systematic reviewAgnes Sebastian, June C Carroll, Leslie E Oldfield, et al.NPJ Genomic Medicine|February 14, 2024
Eliciting parental preferences and values for the return of additional findings from genomic sequencingIlias Goranitis, Yan Meng, Melissa Martyn, et al.Medical Care|February 12, 2022
The Prescription Drug User Fee Act: Much More Than User FeesAaron P Mitchell, Niti U Trivedi, Peter B BachJAMA|April 15, 2004
Lung cancer in US women: a contemporary epidemicJyoti D Patel, Peter B Bach, Mark G KrisChest|January 16, 2003
Screening for lung cancer: the guidelinesPeter B Bach, Dennis E Niewoehner, William C Black, et al.Health Affairs (Project Hope)|March 9, 2011
Episode-based payment for cancer care: a proposed pilot for MedicarePeter B Bach, Joshua N Mirkin, Jason J LukePageof 67