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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.
American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2021
A catalog of associations between rare coding variants and COVID-19 outcomesJ A Kosmicki, J E Horowitz, N Banerjee, et al.
Nature Genetics|October 16, 2023
Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic targetTanmoy Roychowdhury, Derek Klarin, Michael G Levin, et al.
Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Nature Genetics|February 20, 2019
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distributionAnne E Justice, Tugce Karaderi, Heather M Highland, et al.
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