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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.Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, 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.American Journal of Human Genetics|September 28, 2021
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed programAnna V Mikhaylova, Caitlin P McHugh, Linda M Polfus, et al.Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.Blood|February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levelsPaul S de Vries, Paula Reventun, Michael R Brown, 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 Genetics|January 26, 2023
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposingFang Chen, Xingyan Wang, Seon-Kyeong Jang, et al.Pageof 39