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Circulation|December 21, 2021
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing StudyAndrew M Glazer, Giovanni Davogustto, Christian M Shaffer, et al.
Circulation. Genomic and Precision Medicine|July 28, 2021
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry AnalysisSeung Hoan Choi, Sean J Jurgens, Christopher M Haggerty, et al.
Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.
Nature Communications|August 23, 2022
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetesParsa Akbari, Olukayode A Sosina, Jonas Bovijn, et al.
Nature Genetics|March 4, 2022
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe diseaseJulie E Horowitz, Jack A Kosmicki, Amy Damask, et al.
Science (New York, N.Y.)|July 2, 2021
Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesityParsa Akbari, Ankit Gilani, Olukayode Sosina, et al.
Nature|March 7, 2022
Whole-genome sequencing reveals host factors underlying critical COVID-19Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik, et al.
American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.
Nature Communications|June 15, 2018
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetesViktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, et al.
Research Square|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillationSean Jurgens, Nobuyuki Enzan, Ian Dinsmore, et al.
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