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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.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.Neurology|February 27, 2001
A randomized, controlled trial of remacemide for motor fluctuations in Parkinson's diseaseI Shoulson, J Penney, M McDermott, et al.American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, 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.Nature Communications|December 10, 2021
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locusAdrienne Tin, Pascal Schlosser, Pamela R Matias-Garcia, 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 Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, 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|April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesisJoshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.Pageof 156