Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci von Reveille, John D, Sims, Anne-Marie, Danoy, Patrick, Evans, David M, Leo, Paul, Pointon, Jennifer J, Jin, Rui, Zhou, Xiaodong, Bradbury, Linda A, Appleton, Louise H, Davis, John C, Diekman, Laura, Doan, Tracey, Dowling, Alison, Duan, Ran, Duncan, Emma L, Farrar, Claire, Hadler, Johanna, Harvey, David, Karaderi, Tugce, Mogg, Rebecca, Pomeroy, Emma, Pryce, Karena, Taylor, Jacqueline, Savage, Laurie, Deloukas, Panos, Kumanduri, Vasudev, Peltonen, Leena, Ring, Sue M, Whittaker, Pamela, Glazov, Evgeny, Thomas, Gethin P, Maksymowych, Walter P, Inman, Robert D, Ward, Michael M, Stone, Millicent A, Weisman, Michael H, Wordsworth, B Paul, Brown, Matthew A

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Investigating the genetic association between ERAP1 and ankylosing spondylitis von Harvey, David, Pointon, Jennifer J., Evans, David M., Karaderi, Tugce, Farrar, Claire, Appleton, Louise H., Sturrock, Roger D., Stone, Millicent A., Oppermann, Udo, Brown, Matthew A., Wordsworth, B. Paul

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Genetic Dissection of Acute Anterior Uveitis Reveals Similarities and Differences in Associations Observed With Ankylosing Spondylitis von Robinson, Philip C., Claushuis, Theodora A. M., Cortes, Adrian, Martin, Tammy M., Evans, David M., Leo, Paul, Mukhopadhyay, Pamela, Bradbury, Linda A., Cremin, Katie, Harris, Jessica, Maksymowych, Walter P., Inman, Robert D., Rahman, Proton, Haroon, Nigil, Gensler, Lianne, Powell, Joseph E., Horst‐Bruinsma, Irene E., Hewitt, Alex W., Craig, Jamie E., Lim, Lyndell L., Wakefield, Denis, McCluskey, Peter, Voigt, Valentina, Fleming, Peter, Degli‐Esposti, Mariapia, Pointon, Jennifer J., Weisman, Michael H., Wordsworth, B. Paul, Reveille, John D., Rosenbaum, James T., Brown, Matthew A.

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Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease von Danoy, Patrick, Pryce, Karena, Hadler, Johanna, Bradbury, Linda A, Farrar, Claire, Pointon, Jennifer, Ward, Michael, Weisman, Michael, Reveille, John D, Wordsworth, B Paul, Stone, Millicent A, Maksymowych, Walter P, Rahman, Proton, Gladman, Dafna, Inman, Robert D, Brown, Matthew A

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Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case–control study and meta-analysis of published series von Karaderi, Tugce, Harvey, David, Farrar, Claire, Appleton, Louise H., Stone, Millicent A., Sturrock, Roger D., Brown, Matthew A., Wordsworth, Paul, Pointon, Jennifer J.

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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis von Merryweather-Clarke, Alison T., Cadet, Estelle, Bomford, Adrian, Capron, Dominique, Viprakasit, Vip, Miller, Anne, McHugh, Paddy J., Chapman, Roger W., Pointon, Jennifer J., Wimhurst, Victoria L.C., Livesey, Karen J., Tanphaichitr, Voravarn, Rochette, Jacques, Robson, Kathryn J.H.

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A CCR6 variant strongly associated with rheumatoid arthritis in two populations is not associated with ankylosing spondylitis von Cohen, Carla J., Karaderi, Tugce, Pointon, Jennifer J., Wordsworth, B. Paul

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The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD) von Pointon, Jennifer J, Harvey, David, Karaderi, Tugce, Appleton, Louise H, Farrar, Claire, Stone, Millicent A, Sturrock, Roger D, Reveille, John D, Weisman, Michael H, Ward, Michael M, Brown, Matthew A, Wordsworth, B Paul

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A common functional variant of endoplasmic reticulum aminopeptidase 2 (ERAP2) that reduces major histocompatibility complex class I expression is not associated with ankylosing spo... von HARVEY, David, POINTON, Jennifer J, KARADERI, Tugce, APPLETON, Louise H, FARRAR, Claire, WORDSWORTH, B. Paul

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Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility von Brown, Matthew A, Donnelly, Peter, Evans, David M, Spencer, Chris C A, Pointon, Jennifer J, Su, Zhan, Harvey, David, Kochan, Grazyna, Opperman, Udo, Dilthey, Alexander, Pirinen, Matti, Stone, Millicent A, Appleton, Louise, Moutsianis, Loukas, Leslie, Stephen, Wordsworth, Tom, Kenna, Tony J, Karaderi, Tugce, Thomas, Gethin P, Ward, Michael M, Weisman, Michael H, Farrar, Claire, Bradbury, Linda A, Danoy, Patrick, Inman, Robert D, Maksymowych, Walter, Gladman, Dafna, Rahman, Proton, Morgan, Ann, Marzo-Ortega, Helena, Bowness, Paul, Gaffney, Karl, Gaston, J S Hill, Smith, Malcolm, Bruges-Armas, Jacome, Couto, Ana-Rita, Sorrentino, Rosa, Paladini, Fabiana, Ferreira, Manuel A, Xu, Huji, Liu, Yu, Jiang, Lei, Lopez-Larrea, Carlos, Díaz-Peña, Roberto, López-Vázquez, Antonio, Zayats, Tetyana, Band, Gavin, Bellenguez, Céline, Blackburn, Hannah, Blackwell, Jenefer M, Bramon, Elvira, Bumpstead, Suzannah J, Casas, Juan P, Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Duncanson, Audrey, Edkins, Sarah, Freeman, Colin, Gillman, Matthew, Gray, Emma, Gwilliam, Rhian, Hammond, Naomi, Hunt, Sarah E, Jankowski, Janusz, Jayakumar, Alagurevathi, Langford, Cordelia, Liddle, Jennifer, Markus, Hugh S, Mathew, Christopher G, McCann, Owen T, McCarthy, Mark I, Palmer, Colin N A, Peltonen, Leena, Plomin, Robert, Potter, Simon C, Rautanen, Anna, Ravindrarajah, Radhi, Ricketts, Michelle, Samani, Nilesh, Sawcer, Stephen J, Strange, Amy, Trembath, Richard C, Viswanathan, Ananth C, Waller, Matthew, Weston, Paul, Whittaker, Pamela, Widaa, Sara, Wood, Nicholas W, McVean, Gilean, Reveille, John D, Wordsworth, B Paul

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ERAP1 and ankylosing spondylitis von Keidel, Sarah, Chen, Liye, Pointon, Jennifer, Wordsworth, Paul

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A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient von Pointon, Jennifer J., Lok, Chun Yu, Shearman, Jeremy D., Suckling, Richard J., Rochette, Jacques, Merryweather-Clarke, Alison T., Robson, Kathryn J.H.

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Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes von Weedon, Michael N, Lindgren, Cecilia M, Timpson, Nicholas J, Freathy, Rachel M, Morris, Andrew P, Walker, Mark, Doney, Alex S.F, Clayton, David G, Craddock, Nick, Deloukas, Panos, Ouwehand, Willem H, Todd, John A, Evans, David, Leung, Hin-Tak, Attwood, Antony P, Boorman, James P, Everson, Ursula, Knight, Alexandra S, Stevens, Helen E, Walters, Graham R, Walker, Neil M, Winzer, Thilo, Ring, Susan M, Strachan, David P, Pembrey, Marcus, Fraser, Christine, Jones, Ian R, Kirov, George, Williamson, Richard, Young, Allan H, Ferrier, I. Nicol, Iles, Mark M, Maqbool, Azhar, Hall, Alistair S, Braund, Peter S, Stevens, Suzanne, Thompson, John R, Bredin, Francesca, Lees, Charles W, Forbes, Alastair, Lewis, Cathryn M, Prescott, Natalie J, Todhunter, Catherine E, Ahmad, Tariq, Cummings, Fraser R, Jewell, Derek P, Webster, John, Connell, John, Dominiczak, Anna, Gungadoo, Johannie, Lee, Kate L, Munroe, Patricia B, Onipinla, Abiodun, Caulfield, Mark, Farrall, Martin, Potter, Catherine, Silman, Alan J, Worthington, Jane, Newport, Melanie, Sirugo, Giorgio, Lyons, Emily, Farrar, Claire, Brown, Matthew A, Simmonds, Matthew J, Gough, Stephen C.L, Ban, Maria, Goris, An, Compston, Alastair, Hunt, Sarah E, Inouye, Michael, McGinnis, Ralph, Widden, Claire, Su, Zhan, Teo, Yik Ying, Ouwehand, Nilesh J, Samani, Michael R, Ardern-Jones, A, Brice, G, Castle, B, Donaldson, A, Eeles, R, Goodman, S, Gray, J, Greenhalgh, L, Hodgson, S.V, Izatt, L, Jeffers, L, Locke, I, Longmuir, M, Mackay, J, Magee, A, Miedzybrodzka, Z, Paterson, J, Porteous, M, Rowe, S, Shanley, S, Saggar, A, Side, L, Steel, M, Thomas, M

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Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A von Nejentsev, Sergey, Bailey, Rebecca, Hardy, Matthew, Cooper, Jason D, Howson, Joanna M. M, Walker, Neil M, Maier, Lisa M, Ribas, Gloria, King, Erna, Szeszko, Jeffrey, Field, Sarah F, Reynolds, Pamela, Smyth, Deborah, Todd, John A, Hulme, John, Clayton, David G, Masters, Jennifer, Stevens, Helen E, Campbell, R. Duncan

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Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene von Pointon, J J, Harvey, D, Karaderi, T, Appleton, L H, Farrar, C, Stone, M A, Sturrock, R D, Brown, M A, Wordsworth, B P

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A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations von Merryweather-Clarke, Alison T., Siimonsen, Henrik, Shearman, Jeremy D., Pointon, Jennifer J., Nørgaard-Pedersen, Bent, Robson, Kathryn J.H.

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Global prevalence of putative haemochromatosis mutations von Merryweather-Clarke, A T, Pointon, J J, Shearman, J D, Robson, K J

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Hemochromatosis gene ( HFE) mutations in South East Asia: a potential for iron overload von Pointon, Jennifer J, Viprakasit, Vip, Miles, Katie L, Livesey, Karen J, Steiner, Michael, O’Riordan, Sean, Hien, Tran T, Merryweather-Clarke, Alison T, Robson, Kathryn J.H

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Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results von Coppin, Hélène, Totaro, Angela, Gasparini, Paolo, Worwood, Mark, Darke, Chris, Rochette, Jacques, Shearman, Jeremy D, Mosser, Annick, Elsey, Terence S, Dooley, James S, David, Véronique, Vandwalle, Jean Luc, Ryan, Eleanor, Borot, Nicolas, Roetto, Antonella, Robson, Kathryn J.H, Crowe, John, Walker, Ann P, Cox, Timothy M, Clare, Michael, Kelly, Alison, Roth, Marie-Paule, Jouanolle, Anne Marie, Bomford, Adrian, Camaschella, Clara, Wallace, Daniel F, Le Gall, Jean-Yves, Pointon, Jennifer J, Halsall, David J, Merryweather-Clarke, Alison T, Saeb-Parsy, Kasra

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Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians von KARADERI, T, POINTON, J. J, WORDSWORTH, T. W. H, HARVEY, D, APPLETON, L. H, COHEN, C. J, FARRAR, C, HARIN, A, BROWN, M. A, WORDSWORTH, B. P

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