SLCO1B1 variants and statin-induced myopathy--a genomewide study. by Link, E, Parish, S, Armitage, J, Bowman, L, Heath, S, Matsuda, F, Gut, I, Lathrop, M, Collins, R

A large-scale, consortium-based genomewide association study of asthma. by Moffatt, M, Gut, I, Demenais, F, Strachan, D, Bouzigon, E, Heath, S, von Mutius, E, Farrall, M, Lathrop, M, Cookson, W

DNA methylation in human gastric epithelial cells defines regional identity without restricting lineage plasticity by Fritsche, K, Boccellato, F, Schlaermann, P, Koeppel, M, Denecke, C, Link, A, Malfertheiner, P, Gut, I, Meyer, TF, Berger, H

Tumour necrosis factor haplotypes associated with sensory neuropathy in Asian and Caucasian human immunodeficiency virus patients by Chew, C.S.N., Cherry, C.L., Imran, D., Yunihastuti, E., Kamarulzaman, A., Varna, S., Ismail, R., Phipps, M., Aghafar, Z., Gut, I., Price, P.

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. by Menzel, S, Garner, C, Gut, I, Matsuda, F, Yamaguchi, M, Heath, S, Foglio, M, Zelenika, D, Boland, A, Rooks, H, Best, S, Spector, T, Farrall, M, Lathrop, M, Thein, S

A genome-wide association study of global gene expression. by Dixon, A, Liang, L, Moffatt, M, Chen, W, Heath, S, Wong, K, Taylor, J, Burnett, E, Gut, I, Farrall, M, Lathrop, G, Abecasis, G, Cookson, W

A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15 by Menzel, S, Garner, C, Gut, I, Matsuda, F, Yamaguchi, M, Heath, S, Foglio, M, Zelenka, D, Boland, A, Rooks, H, Best, S, Spector, T, Farrall, M, Lathrop, M, Thein, S

EURAGEDIC; European consortium for the genetics of diabetic nephropathy: strategy and first results. by Vionnet, N, Gut, I, Matsuda, F, Marre, M, Hadjadj, S, Parving, H, Tarnow, L, Groop, P, Forsblom, C, Gauguier, D, Cox, R, Kazeem, G, Farrall, M, Lathrop, M, Cambien, F

Genetic studies of diabetic nephropathy in three European populations (EURAGEDIC consortium): analyses of 14 candidate genes on chromosome 3q by Vionnet, N, Tregouet, D, Groop, P, Gut, I, Tarnow, L, Parving, H, Hadjadj, S, Forsblom, C, Kazeem, G, Farrall, M, Matsuda, F, Rousseau, R, Cambien, F, Marre, M, Lathrop, M

EURAGEDIC study: analyses of 144 candidate genes for diabetic nephropathy by Vionnet, N, Kazeem, G, Gut, I, Groop, P, Forsblom, C, Tarnow, L, Parving, H, Hadjadj, S, Marre, M, Gauguier, D, Cox, R, Farrall, M, Tregouet, D, Cambien, F, Lathrop, MG

HLA has strongest association with IgA nephropathy in genome-wide analysis. by Feehally, J, Farrall, M, Boland, A, Gale, D, Gut, I, Heath, S, Kumar, A, Peden, J, Maxwell, P, Morris, D, Padmanabhan, S, Vyse, T, Zawadzka, A, Rees, A, Lathrop, M, Ratcliffe, P

EURAGEDIC study: identification of new candidate genes for diabetic nephropathy by Hager-Vionnet, N, Tregouet, D, Tarnow, L, Parving, H, Groop, P, Forsblom, C, Hadjadj, S, Marre, M, Gut, I, Cox, R, Gauguier, D, Kazeem, G, Farrall, M, Cambien, F, Lathrop, M

Resistome analyses of sputum from COPD and healthy subjects reveals bacterial load-related prevalence of target genes by Ramsheh, MY, Haldar, K, Bafadhel, M, George, L, Free, RC, John, C, Reeve, NF, Ziegler-Heitbrock, L, Gut, I, Singh, D, Mistry, V, Tobin, MD, Oggioni, MR, Brightling, C, Barer, MR

European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy. by Tarnow, L, Groop, P, Hadjadj, S, Kazeem, G, Cambien, F, Marre, M, Forsblom, C, Parving, H, Trégouët, D, Thévard, A, Farrall, M, Gut, I, Gauguier, D, Cox, R, Matsuda, F, Lathrop, M, Vionnet, N

Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations. by Hadjadj, S, Tarnow, L, Forsblom, C, Kazeem, G, Marre, M, Groop, P, Parving, H, Cambien, F, Tregouet, D, Gut, I, Théva, A, Gauguier, D, Farrall, M, Cox, R, Matsuda, F, Lathrop, M, Hager-Vionnet, N

Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the ad... by Vionnet, N, Tregouët, D, Kazeem, G, Gut, I, Groop, P, Tarnow, L, Parving, H, Hadjadj, S, Forsblom, C, Farrall, M, Gauguier, D, Cox, R, Matsuda, F, Heath, S, Thévard, A, Rousseau, R, Cambien, F, Marre, M, Lathrop, M

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 by Libioulle, C, Louis, E, Hansoul, S, Sandor, C, Farnir, F, Franchimont, D, Vermeire, S, Dewit, O, de Vos, M, Dixon, A, Demarche, B, Gut, I, Heath, S, Foglio, M, Liang, L, Laukens, D, Mni, M, Zelenika, D, Gossum, A, Rutgeerts, P, Belaiche, J, Lathrop, M, Georges, M

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. by Moffatt, M, Kabesch, M, Liang, L, Dixon, A, Strachan, D, Heath, S, Depner, M, von Berg, A, Bufe, A, Rietschel, E, Heinzmann, A, Simma, B, Frischer, T, Willis-Owen, SA, Wong, K, Illig, T, Vogelberg, C, Weiland, S, von Mutius, E, Abecasis, G, Farrall, M, Gut, I, Lathrop, G, Cookson, W

SNP and haplotype mapping for genetic analysis in the rat. by Saar, K, Beck, A, Bihoreau, M, Birney, E, Brocklebank, D, Chen, Y, Cuppen, E, Demonchy, S, Dopazo, J, Flicek, P, Foglio, M, Fujiyama, A, Gut, I, Gauguier, D, Guigo, R, Guryev, V, Heinig, M, Hummel, O, Jahn, N, Klages, S, Kren, V, Kube, M, Kuhl, H, Kuramoto, T, Kuroki, Y

G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes. by Trégouet, D, Groop, P, McGinn, S, Forsblom, C, Hadjadj, S, Marre, M, Parving, H, Tarnow, L, Telgmann, R, Godefroy, T, Nicaud, V, Rousseau, R, Parkkonen, M, Hoverfält, A, Gut, I, Heath, S, Matsuda, F, Cox, R, Kazeem, G, Farrall, M, Gauguier, D, Brand-Herrmann, S, Cambien, F, Lathrop, M, Vionnet, N