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Plos One|November 17, 2015
Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)Ana Maria Fernandez-Pujals, Mark James Adams, Pippa Thomson, et al.
Hypertension (Dallas, Tex. : 1979)|November 1, 2006
Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiencyMarianne Barr, Scott M MacKenzie, Elaine C Friel, et al.
International Journal of Epidemiology|July 13, 2012
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illnessBlair H Smith, Archie Campbell, Pamela Linksted, et al.
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.
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.
Lancet (London, England)|June 27, 2003
Genome-wide mapping of human loci for essential hypertensionMark Caulfield, Patricia Munroe, Janine Pembroke, et al.
Journal of Hypertension|December 3, 2011
Association of central and peripheral pulse pressure with intermediate cardiovascular phenotypesUlf Neisius, Grzegorz Bilo, Chiara Taurino, et al.
Journal of the American Society of Nephrology : JASN|April 29, 2015
Renal Mechanisms of Association between Fibroblast Growth Factor 1 and Blood PressureMaciej Tomaszewski, James Eales, Matthew Denniff, et al.
Plos One|October 8, 2010
Urinary collagen fragments are significantly altered in diabetes: a link to pathophysiologyDavid M Maahs, Justyna Siwy, Angel Argilés, et al.
Nature Genetics|July 31, 2007
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosusMin Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, et al.
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