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Nature|August 11, 2015
Mutations in DCHS1 cause mitral valve prolapseRonen Durst, Kimberly Sauls, David S Peal, et al.The American Surgeon|August 7, 2024
Tranexamic Acid and Pulmonary Complications: A Secondary Analysis of an EAST Multicenter TrialShariq S Raza, Danielle Tatum, Kristen D Nordham, et al.Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.Nature Medicine|September 23, 2024
Posthospitalization COVID-19 cognitive deficits at 1 year are global and associated with elevated brain injury markers and gray matter volume reductionGreta K Wood, Brendan F Sargent, Zain-Ul-Abideen Ahmad, et al.Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.Genome Medicine|March 22, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.Human Molecular Genetics|September 23, 2021
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiativeAmarise Little, Yao Hu, Quan Sun, et al.Pageof 137