Patterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancer von Abkevich, V, Timms, K M, Hennessy, B T, Potter, J, Carey, M S, Meyer, L A, Smith-McCune, K, Broaddus, R, Lu, K H, Chen, J, Tran, T V, Williams, D, Iliev, D, Jammulapati, S, FitzGerald, L M, Krivak, T, DeLoia, J A, Gutin, A, Mills, G B, Lanchbury, J S

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Prognostic value of a cell cycle progression signature for prostate cancer death in a conservatively managed needle biopsy cohort von Cuzick, J, Berney, D M, Fisher, G, Mesher, D, Møller, H, Reid, J E, Perry, M, Park, J, Younus, A, Gutin, A, Foster, C S, Scardino, P, Lanchbury, J S, Stone, S

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Prognostic value of PTEN loss in men with conservatively managed localised prostate cancer von Cuzick, J, Yang, Z H, Fisher, G, Tikishvili, E, Stone, S, Lanchbury, J S, Camacho, N, Merson, S, Brewer, D, Cooper, C S, Clark, J, Berney, D M, Møller, H, Scardino, P, Sangale, Z

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Single nucleotide polymorphisms and the future of genetic epidemiology von Schork, Nicholas J, Fallin, Daniele, Lanchbury, Jerry S

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Validation of an RNA cell cycle progression score for predicting death from prostate cancer in a conservatively managed needle biopsy cohort von Cuzick, J, Stone, S, Fisher, G, Yang, Z H, North, B V, Berney, D M, Beltran, L, Greenberg, D, Møller, H, Reid, J E, Gutin, A, Lanchbury, J S, Brawer, M, Scardino, P

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Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis von Steer, S, Abkevich, V, Gutin, A, Cordell, H J, Gendall, K L, Merriman, M E, Rodger, R A, Rowley, K A, Chapman, P, Gow, P, Harrison, A A, Highton, J, Jones, P B B, O'Donnell, J, Stamp, L, Fitzgerald, L, Iliev, D, Kouzmine, A, Tran, T, Skolnick, M H, Timms, K M, Lanchbury, J S, Merriman, T R

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Meta-analysis of genome searches von WISE, L. H., LANCHBURY, J. S., LEWIS, C. M.

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The Human Endoplasmic Reticulum Molecular Chaperone BiP Is an Autoantigen for Rheumatoid Arthritis and Prevents the Induction of Experimental Arthritis von Corrigall, Valerie M, Bodman-Smith, Mark D, Fife, Mark S, Canas, Benito, Myers, Linda K, Wooley, Paul H, Soh, Cecilia, Staines, Norman A, Pappin, Darryl J. C, Berlo, Suzanne E, van Eden, Willem, van der Zee, Ruurd, Lanchbury, Jerry S, Panayi, Gabriel S

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Genetic polymorphism of IL-12 p40 gene in immune-mediated disease von Hall, M A, McGlinn, E, Coakley, G, Fisher, S A, Boki, K, Middleton, D, Kaklamani, E, Moutsopoulos, H, Loughran, Jr, T P, Ollier, W E, Panayi, G S, Lanchbury, J S

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Allelic variation at the interleukin-1 receptor antagonist gene is associated with early postmenopausal bone loss at the spine von Keen, R.W, Woodford-Richens, K.L, Lanchbury, J.S, Spector, T.D

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Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations von Hall, M.A., Norman, P.J., Thiel, B., Tiwari, H., Peiffer, A., Vaughan, R.W., Prescott, S., Leppert, M., Schork, N.J., Lanchbury, J.S.

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HLA-DR4 Subtype Frequencies in Rheumatoid Arthritis Indicate that DRB1 is the Major Susceptibility Locus within the HLA Class II Region von Wordsworth, B. P., Lanchbury, J. S. S., Sakkas, L. I., Welsh, K. I., Panayi, G. S., Bell, J. I.

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HLA class II gene polymorphisms in antiphospholipid syndrome: haplotype analysis in 83 Caucasoid patients von Caliz, R., Atsumi, T., Kondeatis, E., Amengual, O., Khamashta, M. A., Vaughan, R. W., Lanchbury, J. S., Hughes, G. R. V.

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Novel association suggests multiple independent QTLs within chromosome 5q21-33 region control variation in total humans IgE levels von Ahmadi, K R, Lanchbury, J S, Reed, P, Chiano, M, Thompson, D, Galley, M, Line, A, Lank, E, Wong, H J, Strachan, D, Spector, T D

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A monoclonal antibody that detects a novel antigen on endothelial cells that is induced by tumor necrosis factor, IL-1, or lipopolysaccharide von Wellicome, SM, Thornhill, MH, Pitzalis, C, Thomas, DS, Lanchbury, JS, Panayi, GS, Haskard, DO

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Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15 von Steer, S., Fisher, S. A., Fife, M., Cuthbert, A., Newton, J., Wordsworth, P., Lewis, C. M., Mathew, C. G., Lanchbury, J. S.

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Plasma tumor necrosis factor α levels and the -238A promoter polymorphism in patients with antiphospholipid syndrome von BERTOLACCINI, M. L, ATSUMI, T, LANCHBURY, J. S, CALIZ, A. R, KATSUMATA, K, VAUGHAN, R. W, KONDEATIS, E, KHAMASHTA, M. A, KOIKE, T, HUGHES, G. R. V

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Genetic influence on peripheral blood T lymphocyte levels von Hall, M A, Ahmadi, K R, Norman, P, Snieder, H, MacGregor, A J, Vaughan, R W, Spector, T D, Lanchbury, J S

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Vitamin-D-receptor-gene polymorphism and bone loss von Keen, R.W., Major, P.J., Lanchbury, J.S., Spector, T.D., Koshiyama, Hiroyuki, Sone, Teruki, Nakao, Kazuwa

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A Fas promoter polymorphism at position −670 in the enhancer region does not confer susceptibility to Felty's and large granular lymphocyte syndromes von Coakley, G., Manolios, N., Loughran, T. P., Panayi, G. S., Lanchbury, J. S.

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