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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.Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, 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.Circulation. Genomic and Precision Medicine|November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.European Journal of Social Psychology|October 1, 2020
Subjective status and perceived legitimacy across countriesMark J Brandt, Toon Kuppens, Russell Spears, 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.Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.American Journal of Human Genetics|January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.Circulation|December 28, 2018
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma LevelsMaria Sabater-Lleal, Jennifer E Huffman, Paul S de Vries, et al.BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.Pageof 251