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Nature Communications|August 28, 2019
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran ProgramJacklyn N Hellwege, Digna R Velez Edwards, Ayush Giri, et al.
Medrxiv : the Preprint Server for Health Sciences|October 13, 2021
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran ProgramAnurag Verma, Noah Tsao, Lauren Thomann, et al.
Scientific Reports|January 3, 2024
Clinical correlates of CT imaging-derived phenotypes among lean and overweight patients with hepatic steatosisIsabel Song, Elizabeth W Thompson, Anurag Verma, et al.
Human Molecular Genetics|June 16, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartX Rosa Ma, Stephanie D Conley, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Plos Genetics|April 6, 2021
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver diseaseConnor A Emdin, Mary E Haas, Amit V Khera, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Circulation|July 25, 2019
Association of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran ProgramAlexander G Bick, Elvis Akwo, Cassianne Robinson-Cohen, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
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