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Lancet (London, England)|February 14, 2012
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosomeFadi J Charchar, Lisa Ds Bloomer, Timothy A Barnes, et al.European Journal of Heart Failure|January 11, 2020
Genetic risk and atrial fibrillation in patients with heart failureMariëlle Kloosterman, Bernadet T Santema, Carolina Roselli, et al.Circulation. Cardiovascular Genetics|November 10, 2012
Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChipTom R Gaunt, Sonia Shah, Christopher P Nelson, et al.Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.Blood|September 14, 2010
Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet functionAlison H Goodall, Philippa Burns, Isabelle Salles, et al.Journal of Internal Medicine|May 7, 2020
Tumour biomarkers: association with heart failure outcomesC Shi, H H van der Wal, H H W Silljé, et al.European Journal of Heart Failure|December 19, 2020
Is acute heart failure a distinctive disorder? An analysis from BIOSTAT-CHFBeth A Davison, Stefanie Senger, Iziah E Sama, et al.Circulation Research|October 22, 2015
Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk FactorsMarissa LeBlanc, Verena Zuber, Bettina Kulle Andreassen, et al.Oncotarget|December 10, 2015
Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma riskKyle M Walsh, Veryan Codd, Terri Rice, et al.Plos One|December 14, 2011
RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studiesChristian Herder, Wouter Peeters, Thomas Illig, et al.Pageof 67