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Current Atherosclerosis Reports|December 7, 2023
Should Familial Hypercholesterolaemia Be Included in the UK Newborn Whole Genome Sequencing Programme?Steve E Humphries, Uma Ramaswami, Neil HopperArteriosclerosis, Thrombosis, and Vascular Biology|July 6, 2023
Prevalence of FH-Causing Variants and Impact on LDL-C Concentration in European, South Asian, and African Ancestry Groups of the UK Biobank-Brief ReportJasmine Gratton, Steve E Humphries, Marta FutemaArchives of Disease in Childhood|March 8, 2016
The UK Paediatric Familial Hypercholesterolaemia Register: preliminary dataUma Ramaswami, Jackie Cooper, Steve E Humphries, et al.Atherosclerosis. Supplements|November 24, 2004
Mutation detection in patients with familial hypercholesterolaemia using heteroduplex and single strand conformation polymorphism analysis by capillary electrophoresisMert Sozen, Roslyn Whittall, Steve E HumphriesExpert Review of Molecular Diagnostics|August 18, 2017
How close are we to implementing a genetic risk score for coronary heart disease?Katherine Beaney, Fotios Drenos, Steve E HumphriesJournal of Evaluation in Clinical Practice|November 27, 2015
Improving detection of familial hypercholesterolaemia in primary care using electronic audit and nurse-led clinicsPeter Green, Dermot Neely, Steve E Humphries, et al.Cytokine & Growth Factor Reviews|November 29, 2008
Cytokine and cytokine receptor gene polymorphisms and their functionalityAndrew J P Smith, Steve E HumphriesCurrent Opinion in Lipidology|July 1, 2014
The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genesPhilippa J Talmud, Marta Futema, Steve E HumphriesHuman Heredity|May 9, 2013
The use of haplotypes in the identification of interaction between SNPsGie Ken-Dror, Steve E Humphries, Fotios DrenosCurrent Opinion in Lipidology|April 5, 2008
Cardiovascular disease risk prediction using genetic information (gene scores): is it really informative?Steve E Humphries, Nikos Yiannakouris, Philippa J TalmudPageof 42