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Hypertension (Dallas, Tex. : 1979)|June 7, 2006
Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension StudyPatricia B Munroe, Chris Wallace, Ming-Zhan Xue, et al.
Scientific Reports|October 13, 2016
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-AnalysisChristina Loley, Maris Alver, Themistocles L Assimes, et al.
The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|July 11, 2006
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertensionChris Wallace, Ming-Zhan Xue, Stephen J Newhouse, et al.
International Journal of Epidemiology|May 17, 2015
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysisEveline Nüesch, Caroline Dale, Tom M Palmer, et al.
Hypertension (Dallas, Tex. : 1979)|November 15, 2012
Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertensionSamantha Alvarez-Madrazo, Scott M Mackenzie, Eleanor Davies, et al.
Plos One|January 5, 2012
Large scale association analysis identifies three susceptibility loci for coronary artery diseaseStephanie Saade, Jean-Baptiste Cazier, Michella Ghassibe-Sabbagh, et al.
Plos One|August 6, 2014
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery diseaseMaria Sabater-Lleal, Anders Mälarstig, Lasse Folkersen, et al.
Scientific Reports|March 25, 2025
An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamtenLisa Leinhos, Paul Robinson, Giulia Poloni, et al.
Circulation. Cardiovascular Genetics|September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular NoncompactionRobert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
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