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Arthritis & Rheumatology (Hoboken, N.J.)|April 25, 2023
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian RandomizationJie Zheng, Eleanor Wheeler, Maik Pietzner, et al.Plos Genetics|September 28, 2018
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back painPradeep Suri, Melody R Palmer, Yakov A Tsepilov, et al.Plos Genetics|October 5, 2016
Novel Genetic Variants for Cartilage Thickness and Hip OsteoarthritisMartha C Castaño-Betancourt, Dan S Evans, Yolande F M Ramos, et al.American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.Annals of Neurology|April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insightsEmily C Oates, Kristi J Jones, Sandra Donkervoort, et al.Nature|April 9, 2025
Translational genomics of osteoarthritis in 1,962,069 individualsKonstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefansdottir, et al.Pageof 8