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Nature Communications|June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disordersXinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
American Journal of Respiratory and Critical Care Medicine|September 10, 2016
Identification of Four Novel Loci in Asthma in European American and African American PopulationsBerta Almoguera, Lyam Vazquez, Frank Mentch, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 14, 2019
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE networkXinyuan Zhang, Yogasudha Veturi, Shefali Verma, et al.
JAMIA Open|May 14, 2023
A metadata framework for computational phenotypesMatthew Spotnitz, Nripendra Acharya, James J Cimino, et al.
Scientific Reports|April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE networkJacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
The Journal of Pediatrics|September 3, 2011
Replication of a genome-wide association study of birth weight in preterm neonatesKelli K Ryckman, Bjarke Feenstra, John R Shaffer, et al.
Clinical and Translational Science|October 17, 2012
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOELaura J Rasmussen-Torvik, Jennifer A Pacheco, Russell A Wilke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2019
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panelTheodore Chiang, Xiuping Liu, Tsung-Jung Wu, et al.
American Journal of Human Genetics|October 27, 2020
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research StudiesLaura M Amendola, Kathleen Muenzen, Leslie G Biesecker, et al.
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