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Annals of Internal Medicine|April 30, 2019
Precision Medicine in Internal MedicineKrzysztof Kiryluk, David B Goldstein, John W Rowe, et al.
Plos Biology|November 9, 2005
Ancient and recent positive selection transformed opioid cis-regulation in humansMatthew V Rockman, Matthew W Hahn, Nicole Soranzo, et al.
Human Molecular Genetics|February 18, 2025
The impact of TRPV4 pathogenic mutations on barrier integrityGabriela Sampaio, Taylor Ismaili, Ali Torkamani, et al.
Nature Reviews. Genetics|June 12, 2013
Sequencing studies in human genetics: design and interpretationDavid B Goldstein, Andrew Allen, Jonathan Keebler, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 10, 2018
Association of CYP2B6 Single-Nucleotide Polymorphisms Altering Efavirenz Metabolism With Hepatitis C Virus (HCV) Treatment Relapse Among Human Immunodeficiency Virus/HCV-Coinfected African Americans Receiving Ledipasvir/Sofosbuvir in the ION-4 TrialSarah E Kleinstein, Patrick R Shea, Luisa M Stamm, et al.
American Journal of Human Genetics|May 4, 2010
Interpretation of association signals and identification of causal variants from genome-wide association studiesKai Wang, Samuel P Dickson, Catherine A Stolle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2015
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 triosXiaolin Zhu, Slavé Petrovski, Pingxing Xie, et al.
Hippocampus|September 25, 2010
Brain-derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasksNancy A Dennis, Roberto Cabeza, Anna C Need, et al.
Genomics|March 7, 2003
High-throughput analysis of informative CYP2D6 compound haplotypesBenjamin Fletcher, David B Goldstein, Amanda L R Bradman, et al.
Molecular Genetics & Genomic Medicine|November 10, 2019
Sudden unexpected death in asymptomatic infants due to PPA2 variantsColin K L Phoon, Matthew Halvorsen, David B Goldstein, et al.
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