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Circulation. Genomic and Precision Medicine|October 30, 2020
Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease PhenotypesAldo Córdova-Palomera, Catherine Tcheandjieu, Jason A Fries, et al.Diabetes Care|April 23, 2013
Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic studySonia S Anand, David Meyre, Guillaume Pare, et al.Proceedings of the National Academy of Sciences of the United States of America|December 28, 2019
Mouse genetics reveals Barttin as a genetic modifier of Joubert syndromeSimon A Ramsbottom, Peter E Thelwall, Katrina M Wood, et al.Hepatology Communications|April 7, 2023
Regulation of immune responses in primary biliary cholangitis: a transcriptomic analysis of peripheral immune cellsVictoria Mulcahy, Evaggelia Liaskou, Jose-Ezequiel Martin, et al.Translational Psychiatry|February 3, 2016
Exome sequencing in dementia with Lewy bodiesM J Keogh, M Kurzawa-Akanbi, H Griffin, et al.Plos Genetics|March 11, 2015
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritanceJorge Esparza-Gordillo, Anja Matanovic, Ingo Marenholz, et al.Nature Genetics|June 2, 2009
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillinAnn K Daly, Peter T Donaldson, Pallav Bhatnagar, et al.Genes and Immunity|August 24, 2007
Genes at human chromosome 5q31.1 regulate delayed-type hypersensitivity responses associated with Leishmania chagasi infectionS M B Jeronimo, A K B Holst, S E Jamieson, et al.Nature Microbiology|January 8, 2026
Gut microbial ethanol metabolism contributes to auto-brewery syndrome in an observational cohortCynthia L Hsu, Shikha Shukla, Linton Freund, et al.Clinical Genetics|October 23, 2022
Biallelic variants in CEP164 cause a motile ciliopathy-like syndromeLaura A Devlin, Janice Coles, Claire L Jackson, et al.Pageof 27