Simple and Accurate PCR-Based System for Typing Vacuolating Cytotoxin Alleles of Helicobacter pylori von ATHERTON, J. C, COVER, T. L, TWELLS, R. J, MORALES, M. R, HAWKEY, C. J, BLASER, M. J

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Determinants of Non-toxicity in the Gastric Pathogen Helicobacter pylori von Letley, Darren P., Rhead, Joanne L., Twells, Rachel J., Dove, Brian, Atherton, John C.

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Haplotype tagging for the identification of common disease genes von Todd, John A, Johnson, Gillian C.L, Esposito, Laura, Barratt, Bryan J, Smith, Annabel N, Heward, Joanne, Di Genova, Gianfranco, Ueda, Hironori, Cordell, Heather J, Eaves, Iain A, Dudbridge, Frank, Twells, Rebecca C.J, Payne, Felicity, Hughes, Wil, Nutland, Sarah, Stevens, Helen, Carr, Phillipa, Tuomilehto-Wolf, Eva, Tuomilehto, Jaakko, Gough, Stephen C.L, Clayton, David G

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Cost-effective analysis of candidate genes using htSNPs: a staged approach von Lowe, C E, Cooper, J D, Chapman, J M, Barratt, B J, Twells, R C J, Green, E A, Savage, D A, Guja, C, Ionescu-Tîrgovişte, C, Tuomilehto-Wolf, E, Tuomilehto, J, Todd, J A, Clayton, D G

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Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1 von Gispert, S, Twells, R, Orozco, G, Brice, A, Weber, J, Heredero, L, Scheufler, K, Riley, B, Allotey, R, Nothers, C, Hillermann, R, Lunkes, A, Khati, C, Stevanin, G, Hernandez, A, Magariño, C, Klockgether, T, Durr, A, Chneiweiss, H, Enczmann, J, Farrall, M, Beckmann, J, Mullan, M, Wernet, P, Agid, Y, Freund, H.-J, Williamson, R, Auburger, G, Chamberlain, S

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Expression of the Type I Diabetes-associated Gene LRP5 in Macrophages, Vitamin A System Cells, and the Islets of Langerhans Suggests Multiple Potential Roles in Diabetes von Figueroa, David J, Hess, J. Fred, Ky, Bonnie, Brown, Sheryl D, Sandig, Volker, Hermanowski-Vosatka, Anne, Twells, Rebecca C. J, Todd, John A, Austin, Christopher P

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GOBLET: the Global Organisation for Bioinformatics Learning, Education and Training von Attwood, Teresa K, Atwood, Teresa K, Bongcam-Rudloff, Erik, Brazas, Michelle E, Corpas, Manuel, Gaudet, Pascale, Lewitter, Fran, Mulder, Nicola, Palagi, Patricia M, Schneider, Maria Victoria, van Gelder, Celia W G

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Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene von Maier, L M, Twells, R C J, Howson, J M M, Lam, A C, Clayton, D G, Smyth, D J, Savage, D, Carson, D, Patterson, C C, Smink, L J, Walker, N M, Burren, O S, Nutland, S, Rance, H, Tuomilehto-Wolf, E, Tuomilehto, J, Guja, C, Ionescu-Tirgoviste, C, Undlien, D E, Rønningen, K S, Cucca, F, Todd, J A

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Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis von CHUNG, E, CURTIS, D, GONG CHEN, MARSDEN, P. A, TWELLS, R, WEIMING XU, GARDINER, M

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Fine Mapping of the Diabetes-Susceptibility Locus, IDDM4, on Chromosome 11q13 von Nakagawa, Yusuke, Kawaguchi, Yoshihiko, Twells, Rebecca C.J., Muxworthy, Claire, Hunter, Kara M.D., Wilson, Amanda, Merriman, Marilyn E., Cox, Roger D., Merriman, Tony, Cucca, Francesco, McKinney, Patricia A., Shield, Julian P.H., Tuomilehto, Jaakko, Tuomilehto-Wolf, Eva, Ionesco-Tirgoviste, Constantin, Nisticò, Lorenza, Buzzetti, Raffaella, Pozzilli, Paolo, San-Raffaele Family Study, Joner, Geir, Thorsby, Eric, Undlien, Dag E., Pociot, Flemming, Nerup, Jörn, Rönningen, Kjersti S., Bart's-Oxford Family Study Group, Bain, Stephen C., Todd, John A.

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Transmission of Haplotypes of Microsatellite Markers Rather Than Single Marker Alleles in the Mapping of a Putative Type 1 Diabetes Susceptibility Gene (IDDM6) von Merriman, Tony R., Eaves, Iain A., Twells, Rebecca C. J., Merriman, Marilyn E., Danoy, Patrick A. C., Muxworthy, Claire E., Hunter, Kara M. D., Cox, Roger D., Cucca, Francesco, McKinney, Patricia A., Shield, Julian P. H., Baum, J. David, Tuomilehto, Jaakko, Tuomilehto-Wolf, Eva, Ionesco-Tirgoviste, C., Joner, Geir, Thorsby, Erik, Undlien, Dag E., Pociot, Flemming, Nerup, Jørn, Rønningen, Kjersti S., Bain, Steve C., Todd, John A.

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Cloning of a novel member of the low-density lipoprotein receptor family von Hey, Patricia J., Twells, Rebecca C.J., Phillips, Michael S., Yusuke Nakagawa, Brown, Sheryl D., Kawaguchi, Yoshihiko, Cox, Roger, Guochun Xie, Dugan, Valarie, Hammond, Holly, Metzker, Michael L., Todd, John A., Hess, J.Fred

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Isolation and characterization of LRP6, a novel member of the low density lipoprotein receptor gene family von Brown, S D, Twells, R C, Hey, P J, Cox, R D, Levy, E R, Soderman, A R, Metzker, M L, Caskey, C T, Todd, J A, Hess, J F

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A Sequence-Ready Physical Map of a Region of 12q24.1 von Renault, Beatrice, Hovnanian, Alain, Bryce, Steven, Chang, Joan-Jung, Lau, Stephanie, Sakuntabhai, Anavaj, Monk, Sarah, Carter, Simon, Ross, Colin J.D., Pang, Joanna, Twells, Rebecca, Chamberlain, Susan, Monaco, Anthony P., Strachan, Tom, Kucherlapati, Raju

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The spinocerebellar ataxia 2 locus is located within a 3-cM interval on chromosome 12q23-24.1 von Allotey, R, Twells, R, Cemal, C, Norte, B S, Weissenbach, J, Pook, M, Williamson, R, Chamberlain, S

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The Sequence and Gene Characterization of a 400-kb Candidate Region for IDDM4 on Chromosome 11q13 von Twells, Rebecca C.J., Metzker, Michael L., Brown, Sheryl D., Cox, Roger, Garey, Caroline, Hammond, Holly, Hey, Patricia J., Levy, Elaine, Nakagawa, Yusuke, Philips, Michael S., Todd, John A., Hess, J.Fred

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Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21 von Merriman, Tony, Twells, Rebecca, Merriman, Marilyn, Eaves, Iain, Cox, Roger, Cucca, Francesco, McKinney, Patricia, Shield, Julian, Baum, David, Bosi, Emanuele, Pozzilli, Paolo, Nisticò, Lorenza, Buzzetti, Raffaella, Joner, Geir, Rønningen, Kjersti S., Thorsby, Erik, Undlien, Dag, Pociot, Flemming, Nerup, Jørn, Bain, Stephen, Barnett, Anthony, Todd, John

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Evidence by Allelic Association-Dependent Methods for a Type 1 Diabetes Polygene (IDDM6) on Chromosome 18q21 von Merriman, Tony, Twells, Rebecca, Merriman, Marilyn, Eaves, Iain, Cox, Roger, Cucca, Francesco, McKinney, Patricia, Shield, Julian, Baum, David, Bosi, Emanuele, Pozzilli, Paolo, Nisticò, Lorenza, Buzzetti, Raffaella, Joner, Geir, Rønningen, Kjersti, Thorsby, Erik, Undlien, Dag, Pociot, Flemming, Nerup, Jørn, Bain, Stephen, Barnett, Anthony, Todd, John

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Erratum: Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes von Smyth, D J, Howson, J M M, Lowe, C E, Walker, N M, Lam, A C, Nutland, S, Hutchings, J, Tuomilehto-Wolf, E, Tuomilehto, J, Guja, C, Ionescu-Tîrgovi te, C, Undlien, D E, Rønningen, K S, Savage, D, Dunger, D B, Twells, R C J, McArdle, W L, Strachan, D P, Todd, J A

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Exclusion of the neuronal nitric oxide synthase gene and the human achaete-scute homologue I gene as candidate loci for spinal cerebellar ataxia 2 von Twells, R, Xu, W, Ball, D, Allotey, R, Williamson, R, Chamberlain, S

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