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Atherosclerosis|August 17, 2010
Genetic variation in complement factor H and risk of coronary heart disease: eight new studies and a meta-analysis of around 48,000 individualsReecha Sofat, Juan P Casas, Meena Kumari, et al.Journal of Molecular Medicine (Berlin, Germany)|August 1, 2007
Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and womenSteve E Humphries, David Gable, Jackie A Cooper, et al.Lancet (London, England)|May 11, 2010
Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies, Nadeem Sarwar, Manjinder S Sandhu, et al.Plos One|December 19, 2013
Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart diseaseCécilia G Maubaret, Klelia D Salpea, Casey E Romanoski, et al.Diabetologia|April 2, 2011
Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studiesP J Talmud, J A Cooper, T Gaunt, et al.American Journal of Human Genetics|April 2, 2013
The benefits of using genetic information to design prevention trialsYouna Hu, Li Li, Margaret G Ehm, et al.Nature Genetics|October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordomaNischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.Thrombosis and Haemostasis|November 2, 2013
Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChipTom R Gaunt, Delilah Zabaneh, Sonia Shah, et al.Lancet (London, England)|February 26, 2013
Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control studyPhilippa J Talmud, Sonia Shah, Ros Whittall, et al.Circulation. Cardiovascular Genetics|January 14, 2015
PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease RiskMontse Guardiola, Holly J Exeter, Claire Perret, et al.Pageof 23