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Communications Biology|December 14, 2020
Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variantsXinyi Jiang, Nefeli Dellepiane, Erola Pairo-Castineira, et al.
European Journal of Epidemiology|July 11, 2024
A phenome-wide association and factorial Mendelian randomization study on the repurposing of uric acid-lowering drugs for cardiovascular outcomesLijuan Wang, Ines Mesa-Eguiagaray, Harry Campbell, et al.
American Journal of Human Genetics|March 26, 2005
Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study designVeronique Vitart, Andrew D Carothers, Caroline Hayward, et al.
Wellcome Open Research|October 25, 2017
Electronic health record and genome-wide genetic data in Generation Scotland participantsShona M Kerr, Archie Campbell, Jonathan Marten, et al.
Disease Models & Mechanisms|August 9, 2021
A mouse model of brittle cornea syndrome caused by mutation in Zfp469Chloe M Stanton, Amy S Findlay, Camilla Drake, et al.
Human Molecular Genetics|December 10, 2019
Insights into the genetic basis of retinal detachmentThibaud S Boutin, David G Charteris, Aman Chandra, et al.
Nature Communications|October 8, 2017
Regional variation in health is predominantly driven by lifestyle rather than geneticsCarmen Amador, Charley Xia, Réka Nagy, et al.
BMC Genomics|June 7, 2015
Recent genomic heritage in ScotlandCarmen Amador, Jennifer Huffman, Holly Trochet, et al.
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