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Author Details

Anthony Marcketta
2016
14
11
PMIDPaper TitleJournal TitlePublished Year
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
33619501Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.medRxiv2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
34184762Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.Genet Epidemiol2021
35047837Genome-wide survey of parent-of-origin-specific associations across clinical traits derived from electronic health records.HGG Adv2021
33087929Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Nature2020
31118516Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.Nature2019
29773658Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq.Genome Res2018
29899519Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.Nat Commun2018
29290336Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.Am J Hum Genet2018
28008009Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.Science2016
27111036Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.Nat Genet2016
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Corporal Michael J Crescenz VA Medical Center Philadelphia
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