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Nature|September 15, 2015
The UK10K project identifies rare variants in health and disease, Klaudia Walter, Josine L Min, et al.European Journal of Endocrinology|April 7, 2025
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed pubertyRaíssa C Rezende, Wen He, Lena R Kaisinger, et al.Nature Communications|April 7, 2019
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviourSamuel E Jones, Vincent T van Hees, Diego R Mazzotti, et al.Nature Communications|March 9, 2019
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimatesHassan S Dashti, Samuel E Jones, Andrew R Wood, et al.American Journal of Human Genetics|September 2, 2022
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapiesCharli E Harlow, Josan Gandawijaya, Rosemary A Bamford, et al.Nature Genetics|April 23, 2021
Genetic analyses identify widespread sex-differential participation biasNicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, et al.Nature Communications|January 31, 2019
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythmsSamuel E Jones, Jacqueline M Lane, Andrew R Wood, et al.Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.Plos Medicine|November 30, 2016
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation AnalysisLuca A Lotta, Robert A Scott, Stephen J Sharp, et al.Diabetes|September 12, 2019
Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk StudyAlexia Cardona, Felix R Day, John R B Perry, et al.Pageof 44