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BMC Medical Genomics|June 21, 2017
Pharmacogenetic testing through the direct-to-consumer genetic testing company 23andMeMengfei Lu, Cathryn M Lewis, Matthew TraylorEuropean Journal of Human Genetics : EJHG|October 2, 2014
Homogeneous case subgroups increase power in genetic association studiesMatthew Traylor, Hugh Markus, Cathryn M LewisPlos One|June 1, 2019
ukbtools: An R package to manage and query UK Biobank dataKen B Hanscombe, Jonathan R I Coleman, Matthew Traylor, et al.Stroke|August 6, 2015
Genetic Architecture of Lacunar StrokeMatthew Traylor, Steve Bevan, Jean-Claude Baron, et al.Annals of Neurology|February 26, 2016
Shared genetic contribution to Ischaemic Stroke and Alzheimer's DiseaseMatthew Traylor, Poneh Adib-Samii, Denise Harold, et al.Nature Communications|May 3, 2020
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participantsElodie Persyn, Ken B Hanscombe, Joanna M M Howson, et al.Genetic Epidemiology|May 16, 2013
Using phenotypic heterogeneity to increase the power of genome-wide association studies: application to age at onset of ischaemic stroke subphenotypesMatthew Traylor, Steve Bevan, Peter M Rothwell, et al.Genome Medicine|November 10, 2021
The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcareKen B Hanscombe, Elodie Persyn, Matthew Traylor, et al.Neurology. Genetics|March 29, 2017
Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke StudyMatthew Traylor, Loes Rutten-Jacobs, Charles Curtis, et al.Briefings in Bioinformatics|July 26, 2002
Genetic association studies: design, analysis and interpretationCathryn M LewisPageof 39