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Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
Nature Genetics|September 5, 2017
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart diseaseWei Zhao, Asif Rasheed, Emmi Tikkanen, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Research Square|February 13, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Diabetes|June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramNingyuan Wang, Daniel A DiCorpo, Yixin Zhang, et al.
Nature Communications|April 13, 2021
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indicesPradeep Natarajan, Akhil Pampana, Sarah E Graham, et al.
Nature|June 6, 2020
Identification of type 2 diabetes loci in 433,540 East Asian individualsCassandra N Spracklen, Momoko Horikoshi, Young Jin Kim, et al.
Nature Genetics|June 8, 2023
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptakeAlice Williamson, Dougall M Norris, Xianyong Yin, et al.
American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
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