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Human Molecular Genetics|January 13, 2021
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidomeKathryn A McGurk, Simon G Williams, Hui Guo, et al.
Stroke|September 24, 2005
Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysisBongani M Mayosi, Peter J Avery, Michelle Baker, et al.
Diabetes|July 28, 2005
Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family studyMichelle Baker, Nicole Gaukrodger, Bongani M Mayosi, et al.
Hypertension (Dallas, Tex. : 1979)|October 15, 2008
Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genesJulian Palomino-Doza, Thahira J Rahman, Peter J Avery, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2004
Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretionBernard Keavney, Bongani Mayosi, Nicole Gaukrodger, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 26, 2018
Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk VariantsJoshua T Chai, Neil Ruparelia, Anuj Goel, et al.
International Journal of Epidemiology|November 14, 2007
The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: a possible explanation for heterogeneity in genetic association studies of AGT and hypertensionMichelle Baker, Thahira Rahman, Darroch Hall, et al.
Blood|August 23, 2007
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humansStephan Menzel, Jie Jiang, Nicholas Silver, et al.
Scientific Reports|October 4, 2017
A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11Mahmood F Bhutta, Jane Lambie, Lindsey Hobson, et al.
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
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