No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study

No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study

Bibliografiska uppgifter
Huvudupphovsmän:	Newhouse, S, Dobson, R, Wallace, C, Pembroke, J, Garcia, E, Mein, C, Clayton, D, Samani, N, Dominiczak, A, Brown, M, Webster, J, Lathrop, G, Farrall, M, Connell, J, Caulfield, M, Munroe, P
Materialtyp:	Conference item
Publicerad:	2004

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Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis
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Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
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Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes
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Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study
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Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
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Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.
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Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.
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Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study.
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Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study
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Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study.
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Genome-wide mapping of human loci for essential hypertension.
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Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
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