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Journal of the American Heart Association|August 9, 2017
Novel Urinary Peptidomic Classifier Predicts Incident Heart FailureZhen-Yu Zhang, Susana Ravassa, Esther Nkuipou-Kenfack, et al.
European Journal of Human Genetics : EJHG|March 23, 2023
A practical checklist for return of results from genomic research in the European contextDanya F Vears, Nina Hallowell, Heidi Beate Bentzen, et al.
Nature Communications|June 1, 2019
Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEPAnja Thormann, Mihail Halachev, William McLaren, et al.
BMC Medical Genetics|June 25, 2014
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based studyPenny J Norsworthy, Jana Vandrovcova, Ellen R A Thomas, et al.
Nature Communications|July 15, 2026
Genetic ancestry and monogenic disease risk in the Scottish Traveller founder populationAshwini Shanmugam, Benjamin S Fletcher, Maria Pala, et al.
American Journal of Human Genetics|March 15, 2025
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of resultsShona M Kerr, Lucija Klaric, Marisa D Muckian, et al.
Intelligence|June 20, 2014
Molecular genetic contributions to socioeconomic status and intelligenceRiccardo E Marioni, Gail Davies, Caroline Hayward, et al.
Scientific Reports|July 31, 2019
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohortShona M Kerr, Lucija Klaric, Mihail Halachev, et al.
Plos Genetics|November 26, 2019
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regionsMihail Halachev, Alison Meynert, Martin S Taylor, et al.
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