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The Pharmacogenomics Journal|July 15, 2015
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced coughJ D Mosley, C M Shaffer, S L Van Driest, et al.
Clinical Pharmacology and Therapeutics|February 10, 2016
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE networkW S Bush, D R Crosslin, A Owusu-Obeng, et al.
Clinical Pharmacology and Therapeutics|June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systemsL J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Genome Biology|June 26, 2015
Comparison of RNA-seq and microarray-based models for clinical endpoint predictionWenqian Zhang, Ying Yu, Falk Hertwig, et al.
Nature Genetics|January 12, 2016
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucomaJessica N Cooke Bailey, Stephanie J Loomis, Jae H Kang, et al.
The Lancet. Diabetes & Endocrinology|December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyAmand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
BMC Cardiovascular Disorders|October 31, 2019
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9Amand F Schmidt, Michael V Holmes, David Preiss, et al.
Nature Genetics|December 23, 2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variantsLars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, et al.
Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Nature Genetics|June 5, 2019
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesityValérie Turcot, Yingchang Lu, Heather M Highland, et al.
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