Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemia. by Dixon-McIver, A, East, P, Mein, C, Cazier, J, Molloy, G, Chaplin, T, Andrew Lister, T, Young, B, Debernardi, S

A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children. by Korbonits, M, Gueorguiev, M, O'Grady, E, Lecoeur, C, Swan, D, Mein, C, Weill, J, Grossman, AB, Froguel, P

Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen. by Martins, V, Vyas, J, Chen, M, Purdie, K, Mein, C, South, A, Storey, A, McGrath, J, O'Toole, E

A genetic study of the ghrelin and growth hormone secretagogue receptor (GHSR) genes and stature. by Gueorguiev, M, Lecoeur, C, Benzinou, M, Mein, C, Meyre, D, Vatin, V, Weill, J, Heude, B, Grossman, AB, Froguel, P, Korbonits, M

Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesity. by Gueorguiev, M, Lecoeur, C, Meyre, D, Benzinou, M, Mein, C, Hinney, A, Vatin, V, Weill, J, Heude, B, Hebebrand, J, Grossman, AB, Korbonits, M, Froguel, P

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. by Newhouse, S, Wallace, C, Dobson, R, Mein, C, Pembroke, J, Farrall, M, Clayton, D, Brown, M, Samani, N, Dominiczak, A, Connell, J, Webster, J, Lathrop, G, Caulfield, M, Munroe, P

Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes. by Gueorguiev, M, Wiltshire, S, Garcia, E, Mein, C, Lecoeur, C, Kristen, B, Allotey, R, Hattersley, A, Walker, M, O'rahilly, S, Froguel, P, Grossman, AB, McCarthy, M, Hitman, G, Korbonits, M

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension. by Bell, J, Wallace, C, Dobson, R, Wiltshire, S, Mein, C, Pembroke, J, Brown, M, Clayton, D, Samani, N, Dominiczak, A, Webster, J, Lathrop, G, Connell, J, Munroe, P, Caulfield, M, Farrall, M

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

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension by Tzenova Bell, J, Wallace, C, Dobson, R, Wiltshire, S, Mein, C, Pembroke, J, Brown, M, Clayton, D, Samani, N, Dominiczak, A, Webster, J, Lathrop, G, Connell, J, Munroe, P, Caulfield, M, Farrall, M

Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes by 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. by 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 by 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 by 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. by 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. by 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 by 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

Genome-wide association study of survival from sepsis due to pneumonia: An observational cohort study by Rautanen, A, Mills, T, Gordon, A, Hutton, P, Steffens, M, Nuamah, R, Chiche, J, Parks, T, Chapman, S, Davenport, E, Elliott, K, Bion, J, Lichtner, P, Meitinger, T, Meitinger, T, Wienker, T, Caulfield, M, Mein, C, Bloos, F, Bobek, I, Cotogni, P, Sramek, V, Sarapuu, S, Kobilay, M, Ranieri, V

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study. by Rautanen, A, Mills, T, Gordon, A, Hutton, P, Steffens, M, Nuamah, R, Chiche, J, Parks, T, Chapman, S, Davenport, E, Elliott, K, Bion, J, Lichtner, P, Meitinger, T, Wienker, T, Caulfield, M, Mein, C, Bloos, F, Bobek, I, Cotogni, P, Sramek, V, Sarapuu, S, Kobilay, M, Ranieri, V, Rello, J

Blood pressure loci identified with a gene-centric array by 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