Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease von Nijmeijer, Rian M, Gadaleta, Raffaella M, van Mil, Saskia W C, van Bodegraven, Adriaan A, Crusius, J Bart A, Dijkstra, Gerard, Hommes, Daan W, de Jong, Dirk J, Stokkers, Pieter C F, Verspaget, Hein W, Weersma, Rinse K, van der Woude, C Janneke, Stapelbroek, Janneke M, Schipper, Marguerite E I, Wijmenga, Cisca, van Erpecum, Karel J, Oldenburg, Bas

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Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP von Zhernakova, Alexandra, Festen, Eleanora M., Franke, Lude, Trynka, Gosia, van Diemen, Cleo C., Monsuur, Alienke J., Bevova, Marianna, Nijmeijer, Rian M., van ‘t Slot, Ruben, Heijmans, Roel, Boezen, H. Marike, van Heel, David A., van Bodegraven, Adriaan A., Stokkers, Pieter C.F., Wijmenga, Cisca, Crusius, J. Bart A., Weersma, Rinse K.

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Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms von Monsuur, Alienke J, de Bakker, Paul I W, Zhernakova, Alexandra, Pinto, Dalila, Verduijn, Willem, Romanos, Jihane, Auricchio, Renata, Lopez, Ana, van Heel, David A, Crusius, J Bart A, Wijmenga, Cisca

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Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project von Cleynen, Isabelle, González, Juan R, Figueroa, Carolina, Franke, Andre, McGovern, Dermot, Bortlík, Martin, Crusius, Bart J A, Vecchi, Maurizio, Artieda, Marta, Szczypiorska, Magdalena, Bethge, Johannes, Arteta, David, Ayala, Edgar, Danese, Silvio, van Hogezand, Ruud A, Panés, Julian, Peña, Salvador Amado, Lukas, Milan, Jewell, Derek P, Schreiber, Stefan, Vermeire, Severine, Sans, Miquel

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Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1 von Cortes, Adrian, Pulit, Sara L., Leo, Paul J., Pointon, Jenny J., Robinson, Philip C., Weisman, Michael H., Ward, Michael, Gensler, Lianne S., Zhou, Xiaodong, Garchon, Henri-Jean, Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A., Førre, Øystein, Tuomilehto, Jaakko, Laiho, Kari, Bradbury, Linda A., Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Haroon, Nigil, Mulero, Juan, Blanco, Francisco J., Gonzalez-Gay, Miguel A., Lopez-Larrea, C, Bowness, Paul, Gaffney, Karl, Gaston, Hill, Gladman, Dafna D., Rahman, Proton, Maksymowych, Walter P., Crusius, J. Bart A., van der Horst-Bruinsma, Irene E., Valle-Oñate, Raphael, Romero-Sánchez, Consuelo, Hansen, Inger Myrnes, Pimentel-Santos, Fernando M., Inman, Robert D., Martin, Javier, Breban, Maxime, Wordsworth, Bryan Paul, Reveille, John D., Evans, David M., de Bakker, Paul I.W., Brown, Matthew A.

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Genetic association analysis of the functional c.714T>G polymorphism and mucosal expression of dectin-1 in inflammatory bowel disease von de Vries, Hilbert S, Plantinga, Theo S, van Krieken, J Han, Stienstra, Rinke, van Bodegraven, Ad A, Festen, Eleonora A M, Weersma, Rinse K, Crusius, J Bart A, Linskens, Ronald K, Joosten, Leo A B, Netea, Mihai G, de Jong, Dirk J

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Prospective Human Leukocyte Antigen, Endomysium Immunoglobulin A Antibodies, and Transglutaminase Antibodies Testing for Celiac Disease in Children with Down Syndrome von Wouters, Jeroen, Weijerman, Michel E., MD, van Furth, A. Marceline, PhD, Schreurs, Marco W.J., PhD, Crusius, J. Bart A., PhD, von Blomberg, B. Mary E., PhD, de Baaij, Laura R, Broers, Chantal J.M., MD, Gemke, Reinoud J.B.J., PhD

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Effect of B vitamin supplementation on plasma homocysteine levels in celiac disease von Hadithi, Muhammed, Mulder, Chris J J, Stam, Frank, Azizi, Joshan, Crusius, J Bart A, Peña, Amado Salvador, Stehouwer, Coen D A, Smulders, Yvo M

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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci von Cortes, Adrian, Hadler, Johanna, Pointon, Jenny P, Robinson, Philip C, Karaderi, Tugce, Leo, Paul, Cremin, Katie, Pryce, Karena, Harris, Jessica, Lee, Seunghun, Joo, Kyung Bin, Shim, Seung-Cheol, Weisman, Michael, Ward, Michael, Zhou, Xiaodong, Garchon, Henri-Jean, Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A, Førre, Øystein, Tuomilehto, Jaakko, Laiho, Kari, Jiang, Lei, Liu, Yu, Wu, Xin, Bradbury, Linda A, Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Kenna, Tony J, Haroon, Nigil, Ferreira, Manuel A, Yang, Jian, Mulero, Juan, Fernandez-Sueiro, Jose Luis, Gonzalez-Gay, Miguel A, Lopez-Larrea, Carlos, Deloukas, Panos, Donnelly, Peter, Bowness, Paul, Gafney, Karl, Gaston, Hill, Gladman, Dafna D, Rahman, Proton, Maksymowych, Walter P, Xu, Huji, Crusius, J Bart A, van der Horst-Bruinsma, Irene E, Chou, Chung-Tei, Valle-Oñate, Raphael, Romero-Sánchez, Consuelo, Hansen, Inger Myrnes, Pimentel-Santos, Fernando M, Inman, Robert D, Videm, Vibeke, Martin, Javier, Breban, Maxime, Reveille, John D, Evans, David M, Kim, Tae-Hwan, Wordsworth, Bryan Paul, Brown, Matthew A

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Haplotype of prostaglandin synthase 2/cyclooxygenase 2 is involved in the susceptibility to inflammatory bowel disease von Cox, David-G, Crusius, J-Bart-A, Peeters, Petra-H-M, Bueno-de-Mesquita, H-Bas, Pena, A-Salvador, Canzian, Federico

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A candidate gene approach of immune mediators effecting the susceptibility to and severity of upper gastrointestinal tract diseases in relation to Helicobacter pylori and Epstein–B... von Ouburg, Sander, Bart A. Crusius, J, Klinkenberg-Knol, Elly C, Mulder, Chris J.J, Salvador Peña, A, Morré, Servaas A

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Common variants at CD40 and other loci confer risk of rheumatoid arthritis von Plenge, Robert M, Raychaudhuri, Soumya, Remmers, Elaine F, Lee, Annette T, Hackett, Rachel, Guiducci, Candace, Burtt, Noël P, Gianniny, Lauren, Korman, Benjamin D, Padyukov, Leonid, Kurreeman, Fina A S, Chang, Monica, Catanese, Joseph J, Ding, Bo, Wong, Sandra, van der Helm-van Mil, Annette H M, Neale, Benjamin M, Coblyn, Jonathan, Cui, Jing, Tak, Paul P, Wolbink, Gert Jan, Crusius, J Bart A, Horst-Bruinsma, Irene E van der, Criswell, Lindsey A, Amos, Christopher I, Seldin, Michael F, Kastner, Daniel L, Ardlie, Kristin G, Alfredsson, Lars, Costenbader, Karen H, Altshuler, David, Huizinga, Tom W J, Shadick, Nancy A, Weinblatt, Michael E, de Vries, Niek, Worthington, Jane, Seielstad, Mark, Toes, Rene E M, Karlson, Elizabeth W, Begovich, Ann B, Klareskog, Lars, Gregersen, Peter K, Daly, Mark J

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Distribution of peroxisome proliferator–activated receptor–gamma polymorphisms in Chinese and Dutch patients with inflammatory bowel disease von Shrestha, Umid Kumar, Karimi, Ouafae, Crusius, J. Bart A., Zhou, Feng, Wang, Zhongli, Chen, Zhitao, van Bodegraven, A. A., Xiao, Jun, Morré, Servaas A., Wang, Hongling, Li, Jin, Xia, Bing

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Analysis of multiple candidate genes in association with phenotypes of multiple sclerosis von Sombekke, Madeleine H, Arteta, David, van de Wiel, Mark A, Crusius, J Bart A, Tejedor, Diego, Killestein, Joep, Martínez, Antonio, Peña, A. Salvador, Polman, Chris H, Uitdehaag, Bernard MJ

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Serological Screening for Celiac Disease in Adult Chinese Patients With Diarrhea Predominant Irritable Bowel Syndrome von Wang, Hongling, Zhou, Guoying, Luo, Linjie, Crusius, J. Bart A., Yuan, Anlong, Kou, Jiguang, Yang, Guifang, Wang, Min, Wu, Jing, von Blomberg, B. Mary E., Morré, Servaas A., Peña, A. Salvador, Xia, Bing

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CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies von van der Linde, Klaas, Boor, Patrick P.C, Houwing-Duistermaat, Jeanine J, Crusius, Bart J.A, Wilson, Paul J.H, Kuipers, Ernst J, de Rooij, Felix W.M

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Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease von Fransen, Karin, Visschedijk, Marijn C., van Sommeren, Suzanne, Fu, Jinyuan Y., Franke, Lude, Festen, Eleonora A.M., Stokkers, Pieter C.F., van Bodegraven, Adriaan A., Crusius, J. Bart A., Hommes, Daniel W., Zanen, Pieter, de Jong, Dirk J., Wijmenga, Cisca, van Diemen, Cleo C., Weersma, Rinse K.

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Human Leukocyte Antigen–DQ2 Homozygosity and the Development of Refractory Celiac Disease and Enteropathy-Associated T-Cell Lymphoma von Al–Toma, Abdulbaqi, Goerres, Marije S., Meijer, Jos W.R., Peña, A. Salvador, Crusius, J. Bart A., Mulder, Chris J.J.

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Brief Report: The Role of Rare Protein‐Coding Variants in Anti–Tumor Necrosis Factor Treatment Response in Rheumatoid Arthritis von Cui, Jing, Diogo, Dorothee, Stahl, Eli A., Canhao, Helena, Mariette, Xavier, Greenberg, Jeffrey D., Okada, Yukinori, Pappas, Dimitrios A., Fulton, Robert S., Tak, Paul P., Nurmohamed, Michael T., Lee, Annette, Larson, David E., Kurreeman, Fina, Deluca, Tracie L., O'Laughlin, Michelle, Fronick, Catrina C., Fulton, Lucinda L., Mardis, Elaine R., van der Horst‐Bruinsma, Irene E., Wolbink, Gert‐Jan, Gregersen, Peter K., Kremer, Joel M., Crusius, J. Bart A., de Vries, Niek, Huizinga, Tom W. J., Fonseca, João Eurico, Miceli‐Richard, Corinne, Karlson, Elizabeth W., Coenen, Marieke J. H., Barton, Anne, Plenge, Robert M., Raychaudhuri, Soumya

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Association of tumor necrosis factor genetic polymorphism with chronic atrophic gastritis and gastric adenocarcinoma in Chinese Han population von Fei, Bao-Ying, Xia, Bing, Deng, Chang-Sheng, Xia, Xiao-Qing, Xie, Min, Crusius, J Bart A, Pena, A Salvador

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