Treatment of Raynaud's phenomenon with the selective serotonin reuptake inhibitor fluoxetine von Coleiro, B., Marshall, S. E., Denton, C. P., Howell, K., Blann, A., Welsh, K. I., Black, C. M.

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Cytokine (TNF alpha, LT alpha and IL-10) polymorphisms in inflammatory bowel diseases and normal controls: differential effects on production and allele frequencies von Koss, K, Satsangi, J, Fanning, G C, Welsh, K I, Jewell, D P

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The molecular classification of the clinical manifestations of Crohn's disease von Ahmad, Tariq, Armuzzi, Alessandro, Bunce, Mike, Mulcahy-Hawes, Kim, Marshall, Sara E., Orchard, Timothy R., Crawshaw, Jonathan, Large, Oliver, De Silva, Arjuna, Cook, Julia T., Barnardo, Martin, Cullen, Sue, Welsh, Ken I., Jewell, Derek P.

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Genetic variation and response to morphine in cancer patients: catechol-O-methyltransferase and multidrug resistance-1 gene polymorphisms are associated with central side effects von Ross, Joy R, Riley, Julia, Taegetmeyer, Annie B, Sato, Hiroe, Gretton, Sophy, du Bois, Roland M, Welsh, Kenneth I

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Uveitis and erythema nodosum in inflammatory bowel disease: Clinical features and the role of HLA genes von Orchard, Timothy R., Chua, C.N., Ahmad, Tariq, Cheng, Hung, Welsh, Kenneth I., Jewell, Derek P.

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Vitamin D receptor gene polymorphism: association with Crohn's disease susceptibility von Simmons, J D, Mullighan, C, Welsh, K I, Jewell, D P

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MBL genotype and risk of invasive pneumococcal disease: a case-control study von Roy, Suchismita, Knox, Kyle, Segal, Shelley, Griffiths, David, Moore, Catrin E, Welsh, Kenneth I, Smarason, Alex, Day, Nicholas P, McPheat, William L, Crook, Derrick W, Hill, Adrian VS

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Genotype-phenotype analysis of the Crohn’s disease susceptibility haplotype on chromosome 5q31 von Armuzzi, A, Ahmad, T, Ling, K-L, de Silva, A, Cullen, S, van Heel, D, Orchard, T R, Welsh, K I, Marshall, S E, Jewell, D P

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A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer von WINSEY, Samantha L, HALDAR, Neil A, MARSH, Howard P, BUNCE, Mike, MARSHALL, Sara E, HARRIS, Adrian L, WOJNAROWSKA, Fenella, WELSH, Ken I

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A common haplotype of the C‐C chemokine receptor 2 gene and HLA‐DRB10301 are independent genetic risk factors for Löfgren’s syndrome von Spagnolo, P., Sato, H., Grunewald, J., Brynedal, B., Hillert, J., Mañá, J., Wells, A. U., Eklund, A., Welsh, K. I., Du Bois, R. M.

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KL-6 levels are elevated in plasma from patients with acute respiratory distress syndrome von Sato, H, Callister, M.E.J, Mumby, S, Quinlan, G.J, Welsh, K.I, duBois, R.M, Evans, T.W

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Haplotype-specific linkage disequilibrium patterns define the genetic topography of the human MHC von Ahmad, Tariq, Neville, Matt, Marshall, Sara E., Armuzzi, Alessandro, Mulcahy-Hawes, Kim, Crawshaw, Jonathan, Sato, Hiroe, Ling, Khoon-Lin, Barnardo, Martin, Goldthorpe, Sue, Walton, Robert, Bunce, Mike, Jewell, Derek P., Welsh, Ken I.

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Clinical phenotype is related to HLA genotype in the peripheral arthropathies of inflammatory bowel disease von Orchard, Timothy R., Thiyagaraja, S., Welsh, Kenneth I., Wordsworth, B.Paul, Gaston, J.S.Hill, Jewell, Derek P.

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Clinical Pharmacology and Pharmacotherapy of Opioid Switching in Cancer Patients von Ross, Joy R., Riley, Julia, Quigley, Columba, Welsh, Ken I.

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HLA-DQB10201: A Marker for Good Prognosis in British and Dutch Patients with Sarcoidosis von Sato, Hiroe, Grutters, Jan C, Pantelidis, Panagiotis, Mizzon, A. Neil, Ahmad, Tariq, van Houte, Arend-Jan, Lammers, Jan-Willem J, van den Bosch, Jules M.M, Welsh, Kenneth I, du Bois, Roland M

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HLA Alleles Determine Human T-lymphotropic Virus-I (HTLV-I) Proviral Load and the Risk of HTLV-I-Associated Myelopathy von Katie J. M. Jeffery, Usuku, Koichiro, Hall, Sarah E., Matsumoto, Wataru, Taylor, Graham P., Procter, Jeanette, Bunce, Mike, Ogg, Graham S., Welsh, Kenneth I., Weber, Jonathan N., Lloyd, Alun L., Nowak, Martin A., Nagai, Masahiro, Kodama, Daisuke, Izumo, Shuji, Osame, Mitsuhiro, Charles R. M. Bangham

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The Influence of HLA Class I Alleles and Heterozygosity on the Outcome of Human T Cell Lymphotropic Virus Type I Infection von Jeffery, Katie J. M, Siddiqui, Asna A, Bunce, Mike, Lloyd, Alun L, Vine, Alison M, Witkover, Aviva D, Izumo, Shuji, Usuku, Koichiro, Welsh, Kenneth I, Osame, Mitsuhiro, Bangham, Charles R. M

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Analysis of tumor necrosis factor-α, lymphotoxin-α, tumor necrosis factor receptor II, and interleukin-6 polymorphisms in patients with idiopathic pulmonary fibrosis von PANTELIDIS, Panagiotis, FANNING, Gregory C, WELLS, Athol U, WELSH, Kenneth I, DU BOIS, Roland M

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Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease von Satsangl, J, Farrant, J.M, Jewell, D.P, Bell, J.I, Welsh, K.I, Bunce, M, Julier, C

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Increased Frequency of the Uncommon Tumor Necrosis Factor -857T Allele in British and Dutch Patients with Sarcoidosis von Grutters, Jan C, Sato, Hiroe, Pantelidis, Panagiotis, Lagan, Anna L, McGrath, Deirdre S, Lammers, Jan-Willem J, van den Bosch, Jules M. M, Wells, Athol U, du Bois, Roland M, Welsh, Kenneth I

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