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Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.Nature Genetics|August 14, 2019
Mutations in RABL3 alter KRAS prenylation and are associated with hereditary pancreatic cancerSahar Nissim, Ignaty Leshchiner, Joseph D Mancias, et al.Nature|October 14, 2011
Genome sequencing reveals insights into physiology and longevity of the naked mole ratEun Bae Kim, Xiaodong Fang, Alexey A Fushan, et al.Biorxiv : the Preprint Server for Biology|March 18, 2024
Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathiesSumaiya Nazeen, Xinyuan Wang, Dina Zielinski, et al.American Journal of Respiratory and Critical Care Medicine|March 16, 2016
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino AmericansBrian E Cade, Han Chen, Adrienne M Stilp, et al.Nature Genetics|August 11, 2015
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseasesTobias L Lenz, Aaron J Deutsch, Buhm Han, et al.Human Molecular Genetics|November 8, 2018
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino AmericansHeming Wang, Brian E Cade, Tamar Sofer, et al.NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.Plos Genetics|April 17, 2019
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepBrian E Cade, Han Chen, Adrienne M Stilp, et al.Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discoveryJeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.Pageof 11