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Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.Plos Pathogens|August 13, 2013
Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controlsPaul J McLaren, Cédric Coulonges, Stephan Ripke, et al.Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.Annals of Internal Medicine|November 27, 2018
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome SequencingHila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, et al.The Journal of Infectious Diseases|October 5, 2010
Determinants of protection among HIV‐exposed seronegative persons: an overviewMichael M Lederman, Galit Alter, Demetre C Daskalakis, et al.The Journal of Pharmacology and Experimental Therapeutics|October 27, 2009
CYP2C9*1B promoter polymorphisms, in linkage with CYP2C19*2, affect phenytoin autoinduction of clearance and maintenance doseAmarjit S Chaudhry, Thomas J Urban, Jatinder K Lamba, et al.Nature Genetics|December 21, 2004
A single-nucleotide polymorphism tagging set for human drug metabolism and transportKourosh R Ahmadi, Mike E Weale, Zhengyu Y Xue, et al.Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.American Journal of Human Genetics|September 4, 2012
Using ERDS to infer copy-number variants in high-coverage genomesMingfu Zhu, Anna C Need, Yujun Han, et al.Nature Medicine|November 8, 2016
Determinants of HIV-1 broadly neutralizing antibody inductionPeter Rusert, Roger D Kouyos, Claus Kadelka, et al.Pageof 51