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Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.Annals of Neurology|December 21, 2016
Genetic variation at 16q24.2 is associated with small vessel strokeMatthew Traylor, Rainer Malik, Mike A Nalls, et al.Neurology|September 11, 2020
Association of common genetic variants with brain microbleeds: A genome-wide association studyMaria J Knol, Dongwei Lu, Matthew Traylor, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 16, 2019
Vascular dysfunction-The disregarded partner of Alzheimer's diseaseMelanie D Sweeney, Axel Montagne, Abhay P Sagare, et al.Biological Psychiatry|July 23, 2013
A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation, , Elvira Bramon, et al.The Lancet. Neurology|October 9, 2012
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studiesMatthew Traylor, Martin Farrall, Elizabeth G Holliday, et al.Nature Genetics|October 19, 2010
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1, Amy Strange, Francesca Capon, et al.Journal of the American College of Cardiology|August 18, 2012
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolismAnna Helgadottir, Solveig Gretarsdottir, Gudmar Thorleifsson, et al.Nature Genetics|February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, , Céline Bellenguez, et al.Nature Genetics|July 12, 2011
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibilityDavid M Evans, Chris C A Spencer, Jennifer J Pointon, et al.Pageof 42