Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes por Newhouse, S, Wallace, C, Hoti, M, Burke, B, Marcano, A, Onipinla, A, Dobson, R, Mein, C, Clayton, D, Samani, N, Dominiczak, A, Brown, M, Webster, J, Lathrop, M, Farrall, M, Connell, J, Caulfield, M, Munroe, P

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension. por Wallace, C, Xue, M, Newhouse, S, Marcano, A, Onipinla, A, Burke, B, Gungadoo, J, Dobson, R, Brown, M, Connell, J, Dominiczak, A, Lathrop, G, Webster, J, Farrall, M, Mein, C, Samani, N, Caulfield, M, Clayton, D, Munroe, P

Systematic analysis of 123 candidate genes reveals two novel genes for hypertension por Brown, M, Newhouse, S, Wallace, C, Marcano, A, Shaw-Hawkins, S, Howard, P, Onipinla, A, Dobson, R, Mein, C, Lee, W, Delles, C, Padmanabhan, S, Dominiczak, A, Samani, N, Webster, J, Lathrop, M, Farrall, M, Connell, J, Caulfield, M, Monroe, P

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish Genetics of HyperTension (BRIGHT) study por Wallace, C, Xue, M, Dobson, R, Marcano, C, Gungadoo, J, Burke, B, Onipinla, A, Newhouse, S, Pembroke, J, Brown, M, Connell, J, Samani, N, Dominiczak, A, Lathrop, G, Webster, J, Farrall, M, Mein, C, Munroe, P, Clayton, D, Caulfield, M

Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension Study. por Munroe, P, Wallace, C, Xue, M, Marçano, A, Dobson, R, Onipinla, A, Burke, B, Gungadoo, J, Newhouse, S, Pembroke, J, Brown, M, Dominiczak, A, Samani, N, Lathrop, M, Connell, J, Webster, J, Clayton, D, Farrall, M, Mein, C, Caulfield, M

Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study. por Munroe, P, Wallace, C, Mein, C, Dobson, R, Xue, M, Marcano, C, Burke, B, Gungadoo, J, Onipinla, A, Newhouse, S, Pembroke, J, Connell, J, Brown, M, Samani, N, Dominczak, A, Webster, J, Lathrop, G, Clayton, D, Farrall, M, Caulfield, M

Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study por Wallace, C, Xue, M, Dobson, R, Marcano, C, Gungadoo, J, Burke, B, Onipinla, A, Newhouse, S, Pembroke, J, Brown, M, Connell, J, Samani, N, Dominiczak, A, Lathrop, G, Webster, J, Farrall, M, Mein, C, Munroe, P, Clayton, D, Caulfield, M

Blood pressure loci identified with a gene-centric array por Johnson, T, Gaunt, T, Newhouse, S, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R, Tzoulaki, I, O'Brien, E, Poulter, N, Sever, P, Shields, D, Thom, S, Wannamethee, S, Whincup, P, Brown, M, Connell, J, Dobson, R, Howard, P, Mein, C, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Smith, G, Day, I

Blood pressure loci identified with a gene-centric array. por Johnson, T, Gaunt, T, Newhouse, S, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R, Tzoulaki, I, O'Brien, E, Poulter, N, Sever, P, Shields, D, Thom, S, Wannamethee, S, Whincup, P, Brown, M, Connell, J, Dobson, R, Howard, P, Mein, C, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Davey Smith, G, Day, I

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. por Org, E, Eyheramendy, S, Juhanson, P, Gieger, C, Lichtner, P, Klopp, N, Veldre, G, Döring, A, Viigimaa, M, Sõber, S, Tomberg, K, Eckstein, G, Kelgo, P, Rebane, T, Shaw-Hawkins, S, Howard, P, Onipinla, A, Dobson, R, Newhouse, S, Brown, M, Dominiczak, A, Connell, J, Samani, N, Farrall, M, Caulfield, M

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. por Sober, S, Org, E, Kepp, K, Juhanson, P, Eyheramendy, S, Gieger, C, Lichtner, P, Klopp, N, Veldre, G, Viigimaa, M, Doring, A, Putku, M, Kelgo, P, Shaw-Hawkins, S, Howard, P, Onipinla, A, Dobson, R, Newhouse, S, Brown, M, Dominiczak, A, Connell, J, Samani, N, Farrall, M, Caulfield, M, Munroe, P, Illig, T, Wichmann, H, Meitinger, T, Laan, M

SLC2A9 is a high-capacity urate transporter in humans. por Caulfield, M, Munroe, P, O'Neill, D, Witkowska, K, Charchar, F, Doblado, M, Evans, S, Eyheramendy, S, Onipinla, A, Howard, P, Shaw-Hawkins, S, Dobson, R, Wallace, C, Newhouse, S, Brown, M, Connell, J, Dominiczak, A, Farrall, M, Lathrop, G, Samani, N, Kumari, M, Marmot, M, Brunner, E, Chambers, J, Elliott, P, Kooner, J, Laan, M, Org, E, Veldre, G, Viigimaa, M, Cappuccio, F, Ji, C, Iacone, R, Strazzullo, P, Moley, K, Cheeseman, C

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion. por Newhouse, S, Farrall, M, Wallace, C, Hoti, M, Burke, B, Howard, P, Onipinla, A, Lee, K, Shaw-Hawkins, S, Dobson, R, Brown, M, Samani, N, Dominiczak, A, Connell, J, Lathrop, G, Kooner, J, Chambers, J, Elliott, P, Clarke, R, Collins, R, Laan, M, Org, E, Juhanson, P, Veldre, G, Viigimaa, M, Eyheramendy, S, Cappuccio, F, Ji, C, Iacone, R, Strazzullo, P, Kumari, M, Marmot, M, Brunner, E, Caulfield, M, Munroe, P