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Genetic Epidemiology|October 10, 2018
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotypeIan B Stanaway, Taryn O Hall, Elisabeth A Rosenthal, et al.HGG Advances|November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorderLot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.The Journal of Experimental Medicine|May 5, 2021
Constrained chromatin accessibility in PU.1-mutated agammaglobulinemia patientsCarole Le Coz, David N Nguyen, Chun Su, et al.Nature Communications|November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failureMichael G Levin, Noah L Tsao, Pankhuri Singhal, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 26, 2022
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 NetworkKathleen A Leppig, Alanna Kulchak Rahm, Paul Appelbaum, et al.Journal of the American Academy of Child and Adolescent Psychiatry|August 25, 2010
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorderBenjamin M Neale, Sarah E Medland, Stephan Ripke, et al.The Journal of Allergy and Clinical Immunology|November 14, 2009
A genome-wide association study on African-ancestry populations for asthmaRasika A Mathias, Audrey V Grant, Nicholas Rafaels, et al.JAMA|January 10, 2016
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical RecordsSara L Van Driest, Quinn S Wells, Sarah Stallings, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 21, 2020
Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variantsJoanna Kennedy, David Goudie, Edward Blair, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 5, 2015
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's diseaseChristina M Lill, Aina Rengmark, Lasse Pihlstrøm, et al.Pageof 91