Lower regional and temporal ultraviolet exposure is associated with increased rates and severity of inflammatory bowel disease hospitalisation von Limketkai, B. N., Bayless, T. M., Brant, S. R., Hutfless, S. M.

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Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis von Festen, E A M, Goyette, P, Scott, R, Annese, V, Zhernakova, A, Lian, J, Lefèbvre, C, Brant, S R, Cho, J H, Silverberg, M S, Taylor, K D, de Jong, D J, Stokkers, P C, Mcgovern, D, Palmieri, O, Achkar, J-P, Xavier, R J, Daly, M J, Duerr, R H, Wijmenga, C, Weersma, R K, Rioux, J D

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The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases von De Jager, P L, Franchimont, D, Waliszewska, A, Bitton, A, Cohen, A, Langelier, D, Belaiche, J, Vermeire, S, Farwell, L, Goris, A, Libioulle, C, Jani, N, Dassopoulos, T, Bromfield, G P, Dubois, B, Cho, J H, Brant, S R, Duerr, R H, Yang, H, Rotter, J I, Silverberg, M S, Steinhart, A H, Daly, M J, Podolsky, D K, Louis, E, Hafler, D A, Rioux, J D

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Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis von Goyette, P, Lefebvre, C, Ng, A, Brant, S R, Cho, J H, Duerr, R H, Silverberg, M S, Taylor, K D, Latiano, A, Aumais, G, Deslandres, C, Jobin, G, Annese, V, Daly, M J, Xavier, R J, Rioux, J D

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The utilization of parenteral nutrition during the in‐patient management of inflammatory bowel disease in the United States: a national survey von NGUYEN, G. C., LAVEIST, T. A., BRANT, S. R.

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Cloning and sequencing of a rabbit cDNA encoding an intestinal and kidney-specific Na+/H+ exchanger isoform (NHE-3) von CHUNG-MING TSE, BRANT, S. R, WALKER, M. S, PUYSSEGUR, J, DONOWITZ, M

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American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12 von Brant, Steven R., Fu, Yifan, Fields, Carter T., Baltazar, Romulo, Ravenhill, Geoffrey, Pickles, Michael R., Rohal, Patrick M., Mann, Jasdeep, Kirschner, Barbara S., Jabs, Ethylin Wang, Bayless, Theodore M., Hanauer, Stephen B., Cho, Judy H.

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease von Ogura, Yasunori, Bonen, Denise K., Inohara, Naohiro, Nicolae, Dan L., Chen, Felicia F., Ramos, Richard, Britton, Heidi, Moran, Thomas, Karaliuskas, Reda, Duerr, Richard H., Achkar, Jean-Paul, Brant, Steven R., Bayless, Theodore M., Kirschner, Barbara S., Hanauer, Stephen B., Nuñez, Gabriel, Cho, Judy H.

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Functional Characteristics of a Cloned Epithelial Na+/H+Exchanger (NHE3): Resistance to Amiloride and Inhibition by Protein Kinase C von CHUNG-MING TSE, LEVINE, S. A, YUN, C. H. C, BRANT, S. R, POUYSSEGUR, J, MONTROSE, M. H, DONOWITZ, M

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Extended haplotype association study in Crohn’s disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3 von Zhang, W, Hui, K Y, Gusev, A, Warner, N, Ng, S M E, Ferguson, J, Choi, M, Burberry, A, Abraham, C, Mayer, L, Desnick, R J, Cardinale, C J, Hakonarson, H, Waterman, M, Chowers, Y, Karban, A, Brant, S R, Silverberg, M S, Gregersen, P K, Katz, S, Lifton, R P, Zhao, H, Nuñez, G, Pe'er, I, Peter, I, Cho, J H

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An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29 von Shugart, Y Y, Silverberg, M S, Duerr, R H, Taylor, K D, Wang, M-H, Zarfas, K, Schumm, L P, Bromfield, G, Steinhart, A H, Griffiths, A M, Kane, S V, Barmada, M M, Rotter, J I, Mei, L, Bernstein, C N, Bayless, T M, Langelier, D, Cohen, A, Bitton, A, Rioux, J D, Cho, J H, Brant, S R

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CTLA4 −1661A/G and 3′UTR long repeat polymorphisms are associated with ulcerative colitis and influence CTLA4 mRNA and protein expression von Chen, Z, Brant, S R, Li, C, Shrestha, U K, Jiang, T, Zhou, F, Jiang, Y, Shi, X, Zhao, Y, Li, J, Xia, B

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Glucocorticoid stimulation of ileal Na+ absorptive cell brush border Na+/H+ exchange and association with an increase in message for NHE-3, an epithelial Na+/H+ exchanger isoform von C H Yun, S Gurubhagavatula, S A Levine, J L Montgomery, S R Brant, M E Cohen, E J Cragoe, Jr, J Pouyssegur, C M Tse, M Donowitz

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Identification of Novel Susceptibility Loci for Inflammatory Bowel Disease on Chromosomes 1p, 3q, and 4q: Evidence for Epistasis between 1p and IBD1 von Cho, Judy H., Nicolae, Dan L., Gold, Leslee H., Fields, Carter T., LaBuda, Michele C., Rohal, Patrick M., Pickles, Michael R., Qin, Li, Fu, Yifan, Mann, Jasdeep S., Kirschner, Barbara S., Jabs, Ethylin Wang, Weber, James, Hanauer, Stephen B., Bayless, Theodore M., Brant, Steven R.

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Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohnʼs disease risk in a population-based case-control study: Evidence of gene-gene interactions von Okazaki, T, Wang, M H, Rawsthorne, P, Sargent, M, Datta, L W, Shugart, Y Y, Bernstein, C N, Brant, S R

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MAST3: a novel IBD risk factor that modulates TLR4 signaling von Labbé, C, Goyette, P, Lefebvre, C, Stevens, C, Green, T, Tello-Ruiz, M K, Cao, Z, Landry, A L, Stempak, J, Annese, V, Latiano, A, Brant, S R, Duerr, R H, Taylor, K D, Cho, J H, Steinhart, A H, Daly, M J, Silverberg, M S, Xavier, R J, Rioux, J D

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Mammalian Na+/H+ exchanger gene family: structure and function studies von Yun, C. H., Tse, C. M., Nath, S. K., Levine, S. A., Brant, S. R., Donowitz, M.

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Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease von Cho, J H, Nicolae, D L, Ramos, R, Fields, C T, Rabenau, K, Corradino, S, Brant, S R, Espinosa, R, LeBeau, M, Hanauer, S B, Bodzin, J, Bonen, D K

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Evaluation of IBD candidate genes and the case of NRAMP2 von Brant, S R

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Cloning, tissue distribution, and functional analysis of the human Na+/N+ exchanger isoform, NHE3 von Brant, S. R, Yun, C. H, Donowitz, M, Tse, C. M

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