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Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca2+ regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.Nature Genetics|August 27, 2024
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequencesOliver S Burren, Ryan S Dhindsa, Sri V V Deevi, et al.Bone|November 7, 2021
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosisAdi Cohen, Joseph Hostyk, Evan H Baugh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2022
Diagnostic sequencing to support genetically stratified medicine in a tertiary care settingNatalie Lippa, Louise Bier, Anya Revah-Politi, et al.The Journal of Infectious Diseases|March 9, 2010
Host determinants of HIV-1 control in African AmericansKimberly Pelak, David B Goldstein, Nicole M Walley, et al.Current Biology : CB|June 5, 2003
A Y chromosome census of the British IslesCristian Capelli, Nicola Redhead, Julia K Abernethy, et al.Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.Nature Genetics|February 13, 2025
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesisSean Wen, Pablo Kuri-Morales, Fengyuan Hu, et al.Nature|October 4, 2023
Rare variant associations with plasma protein levels in the UK BiobankRyan S Dhindsa, Oliver S Burren, Benjamin B Sun, et al.Pageof 34