Professor Bill Ollier 

2011

• Carrol, E., Payton, A., Payne, D., Miyajima, F., Chaponda, M., Mankhambo, L., Banda, D., Molyneux, E., Cox, H., Jacobson, G., Carr, D., Molyneux, M., Stewart, J., Quinn, J., Hart, C. & Ollier, W (2011). The IL1RN promoter rs4251961 correlates with IL-1 receptor antagonist concentrations in human infection and is differentially regulated by GATA-1. J Immunol, 186(4), 2329-35. eScholarID:125779 | PMID:21248262 | DOI:10.4049/jimmunol.1002402
• Chinoy, H., Adimulam, S., Marriage, F., New, P., Vincze, M., Zilahi, E., Kapitány, A., Gyetvai, A., Ekholm, L., Novota, P., Remakova, M., Charles, P., McHugh, N., Padyukov, L., Alfredsson, L., Vencovsky, J., Lundberg, I., Danko, K., Ollier, W. & Cooper, R (2011). Interaction of HLA-DRB1*03 and smoking for the development of anti-Jo-1 antibodies in adult idiopathic inflammatory myopathies: a European-wide case study. Ann Rheum Dis, Epub ahead of print, eScholarID:144086 | PMID:22186711 | DOI:10.1136/annrheumdis-2011-200182
• Chinoy, H., Lamb, J., Ollier, W. & Cooper, R (2011). Recent advances in the immunogenetics of idiopathic inflammatory myopathy. Arthritis Res Ther, 13(3), 216 (Epub ahead of print). eScholarID:125777 | PMID:21658295 | DOI:10.1186/ar3327
• Chinoy, H., Li, C., Platt, H., Fertig, N., Varsani, H., Gunawardena, H., Betteridge, Z., Oddis, C., McHugh, N., Wedderburn, L., Ollier, W. & Cooper, R (2011). Genetic association study of NF-κB genes in UK Caucasian adult and juvenile onset idiopathic inflammatory myopathy. Rheumatology (Oxford), Epub ahead of print, eScholarID:144087 | PMID:22210660 | DOI:10.1093/rheumatology/ker379
• Clements, D., Kennedy, L., Short, A., Barnes, A., Ferguson, J. & Ollier, W (2011). Risk of canine cranial cruciate ligament rupture is not associated with the major histocompatibility complex. Vet Comp Orthop Traumatol, 24(4), Epub ahead of print. eScholarID:125778 | PMID:21597649 | DOI:10.3415/VCOT-11-03-0048
• Davies G, Tenesa A, Payton A, Yang J, Harris SE, Liewald D, Ke X, Le Hellard S, Christoforou A, Luciano M, McGhee K, Lopez L, Gow AJ, Corley J, Redmond P, Fox HC, Haggarty P, Whalley LJ, McNeill G, Goddard ME, Espeseth T, Lundervold AJ, Reinvang I, Pickles A, Steen VM, Ollier W, Porteous DJ, Horan M, Starr JM, Pendleton N, Visscher PM, Deary IJ. (2011). Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Mol Psychiatry, Epub ahead of print, eScholarID:128070 | DOI:10.1038/mp.2011.85
• Day-Williams, et al (2011). A Variant in MCF2L Is Associated with Osteoarthritis. Am J Hum Genet, 89(3), 446-50. eScholarID:129672 | PMID:21871595 | DOI:10.1016/j.ajhg.2011.08.001
• Evangelou, et al (2011). Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. Ann Rheum Dis, 70(2), 349-355. eScholarID:96110 | PMID:21068099 | DOI:10.1136/ard.2010.132787
• Fox-Clipsham, L., Carter, S., Goodhead, I., Hall, N., Knottenbelt, D., May, P., Ollier, W. & Swinburne, J (2011). Identification of a mutation associated with fatal foal immunodeficiency syndrome in the fell and dales pony. PLoS Genet, 7(7), e1002133. eScholarID:127221 | PMID:21750681 | DOI:10.1371/journal.pgen.1002133
• International et al. (2011). Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature, 476(7359), 214-219. eScholarID:128071 | DOI:10.1038/nature10251
• Jayasekeran, V., Pendleton, N., Holland, G., Payton, A., Jefferson, S., Michou, E., Vasant, D., Ollier, B., Horan, M., Rothwell, J. & Hamdy, S (2011). Val66Met in Brain-Derived Neurotrophic Factor Affects Stimulus-Induced Plasticity in the Human Pharyngeal Motor Cortex. Gastroenterology, Epub ahead of print, eScholarID:125806 | PMID:21699787 | DOI:10.1053/j.gastro.2011.05.047
• Karasneh, J., Ababneh, K., Taha, A., Al-Abbadi, M. & Ollier, W (2011). Investigation of the interleukin-1 gene cluster polymorphisms in Jordanian patients with chronic and aggressive periodontitis. Arch Oral Biol, 56(3), 269-76. eScholarID:96109 | PMID:21035110 | DOI:10.1016/j.archoralbio.2010.10.001
• Kennedy, L., Randall, D., Knobel, D., Brown, J., Fooks, A., Argaw, K., Shiferaw, F., Ollier, W., Sillero-Zubiri, C., Macdonald, D. & Laurenson, M (2011). Major histocompatibility complex diversity in the endangered Ethiopian wolf (Canis simensis). Tissue Antigens, 77(2), 118-125. eScholarID:106676 | PMID:21214524 | DOI:10.1111/j.1399-0039.2010.01591.x
• Lopez, L., Harris, S., Luciano, M., Liewald, D., Davies, G., Gow, A., Tenesa, A., Payton, A., Ke, X., Whalley, L., Fox, H., Haggerty, P., Ollier, W., Pickles, A., Porteous, D., Horan, M., Pendleton, N., Starr, J. & Deary, I (2011). Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts. Eur J Hum Genet, Epub ahead of print, eScholarID:135835 | PMID:22045296 | DOI:10.1038/ejhg.2011.201
• Mekli, K., Payton, A., Miyajima, F., Platt, H., Thomas, E., Downey, D., Lloyd-Williams, K., Chase, D., Toth, Z., Elliott, R., Ollier, W., Anderson, I., Deakin, J., Bagdy, G. & Juhasz, G (2011). The HTR1A and HTR1B receptor genes influence stress-related information processing. Eur Neuropsychopharmacol, 21(1), 129-39. eScholarID:106675 | PMID:20638825 | DOI:10.1016/j.euroneuro.2010.06.013
• Newman, W., Payne, K., Tricker, K., Roberts, S., Fargher, E., Pushpakom, S., Alder, J., Sidgwick, G., Payne, D., Elliott, R., Heise, M., Elles, R., Ramsden, S., Andrews, J., Houston, J., Qasim, F., Shaffer, J., Griffiths, C., Ray, D., Bruce, I. & Ollier, W (2011). A pragmatic randomized controlled trial of thiopurine methyltransferase genotyping prior to azathioprine treatment: the TARGET study. Pharmacogenomics, 12(6), 815-26. eScholarID:125773 | PMID:21692613 | DOI:10.2217/pgs.11.32
• Panoutsopoulou, et al (2011). Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study. Ann Rheum Dis, 70(5), 864-7. eScholarID:125776 | PMID:21177295 | DOI:10.1136/ard.2010.141473
• Quilez, J., Short, A., Martinez, V., Kennedy, L., Ollier, W., Sanchez, A., Altet, L. & Francino, O (2011). A selective sweep of >8 Mb on chromosome 26 in the Boxer genome. BMC Genomics, 12(1), 339 (Epub ahead of print). eScholarID:126103 | PMID:21722374 | DOI:10.1186/1471-2164-12-339
• Selvarajah, J., Smith, C., Hulme, S., Georgiou, R., Sherrington, C., Staniland, J., Illingworth, K., Jury, F., Payton, A., Ollier, W., Vail, A., Rothwell, N., Hopkins, S. & Tyrrell, P (2011). Does inflammation predispose to recurrent vascular events after recent transient ischaemic attack and minor stroke? The North West of England transient ischaemic attack and minor stroke (NORTHSTAR) study. Int J Stroke, 6(3), 187-94. eScholarID:125775 | PMID:21557802 | DOI:10.1111/j.1747-4949.2010.00561.x
• Short, A., Dunne, A., Lohi, H., Boulton, S., Carter, S., Timofte, D. & Ollier, W (2011). Characteristics of epileptic episodes in UK dog breeds: an epidemiological approach. Vet Rec, Epub ahead of print, eScholarID:125774 | PMID:21709047 | DOI:10.1136/vr.d1901
• Southam, L., Panoutsopoulou, K., Rayner, N., Chapman, K., Durrant, C., Ferreira, T., Arden, N., Carr, A., Deloukas, P., Doherty, M., Loughlin, J., McCaskie, A., Ollier, W., Ralston, S., Spector, T., Valdes, A., Wallis, G., Wilkinson, J., consortium, a., Marchini, J. & Zeggini, E (2011). The effect of genome-wide association scan quality control on imputation outcome for common variants. Eur J Hum Genet, 19(5), 610-4. eScholarID:125780 | PMID:21267008 | DOI:10.1038/ejhg.2010.242
• Vaysse, A., Ratnakumar, A., Derrien, T., Axelsson, E., Rosengren Pielberg, G., Sigurdsson, S., Fall, T., Seppälä, E., Hansen, M., Lawley, C., Karlsson, E., LUPA Consortium, P., Bannasch, D., Vilà, C., Lohi, H., Galibert, F., Fredholm, M., Häggström, J., Hedhammar, A., André, C., Lindblad-Toh, K., Hitte, C. & Webster, M (2011). Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping. PLoS Genet, 7(10), e1002316. eScholarID:144088 | PMID:22022279 | DOI:10.1371/journal.pgen.1002316

2010

• Brown JJ, Ollier WE, Arscott G, Bayat A. (2010). Association of HLA-DRB1* and keloid disease in an Afro-Caribbean population. Clin Exp Dermatol, 35(3), 305-310. eScholarID:81679 | DOI:10.1111/j.1365-2230.2009.03506.x
• Clements, D., Short, A., Barnes, A., Kennedy, L., Ferguson, J., Butterworth, S., Fitzpatrick, N., Pead, M., Bennett, D., Innes, J., Carter, S. & Ollier, W (2010). A candidate gene study of canine joint diseases. J Hered, 101(1), 54-60. eScholarID:81703 | PMID:19965910 | DOI:10.1093/jhered/esp088
• Hakooz, N., Arafat, T., Payne, D., Ollier, W., Pushpakom, S., Andrews, J. & Newman, W (2010). Genetic analysis of thiopurine methyltransferase polymorphism in the Jordanian population. Eur J Clin Pharmacol, 66, 999-1003. eScholarID:86643 | PMID:20521035 | DOI:10.1007/s00228-010-0826-1
• Ke, X., Kennedy, L., Short, A., Seppälä, E., Barnes, A., Clements, D., Wood, S., Carter, S., Happ, G., Lohi, H. & Ollier, W (2010). Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies. Anim Genet, Epub ahead of print, eScholarID:96108 | PMID:21070295 | DOI:10.1111/j.1365-2052.2010.02132.x
• Mekli, K., Payton, A., Miyajima, F., Platt, H., Thomas, E., Downey, D., Lloyd-Williams, K., Chase, D., Toth, Z., Elliott, R., Ollier, W., Anderson, I., Deakin, J., Bagdy, G. & Juhasz, G (2010). The HTR1A and HTR1B receptor genes influence stress-related information processing. Eur Neuropsychopharmacol, Epub ahead of print, eScholarID:86640 | PMID:20638825 | DOI:10.1016/j.euroneuro.2010.06.013
• Payton A, Miyajima F, Ollier WER, Rabbitt P, Pickles A, Weiss V, Pendleton N, Horan M A. (2010). Investigation of a functional quinine oxidoreductase (NQO2) polymorphism and cognitive decline. Neurobiol Aging, 31(2)(Epub 2008), 351-352. eScholarID:1d17390 | DOI:10.1016/j.neurobiolaging.2008.04.014
• Remmers, E., Cosan, F., Kirino, Y., Ombrello, M., Abaci, N., Satorius, C., Le, J., Yang, B., Korman, B., Cakiris, A., Aglar, O., Emrence, Z., Azakli, H., Ustek, D., Tugal-Tutkun, I., Akman-Demir, G., Chen, W., Amos, C., Dizon, M., Kose, A., Azizlerli, G., Erer, B., Brand, O., Kaklamani, V., Kaklamanis, P., Ben-Chetrit, E., Stanford, M., Fortune, F., Ghabra, M., Ollier, W., Cho, Y., Bang, D., O'Shea, J., Wallace, G., Gadina, M., Kastner, D. & Gül, A (2010). Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. Nat Genet, Epub ahead of print, eScholarID:86641 | PMID:20622878 | DOI:10.1038/ng.625
• Short, A., Mellersh, C., Platt, H., Carter, S., Timofte, D., Lohi, H. & Ollier, W (2010). Exonic mutations in the L2HGDH gene in Staffordshire bull terriers. Vet Rec, 167(12), 455-7. eScholarID:96111 | PMID:20852250 | DOI:10.1136/vr.c4476
• Short, A., Saleh, N., Catchpole, B., Kennedy, L., Barnes, A., Jones, C., Fretwell, N. & Ollier, W (2010). CTLA4 promoter polymorphisms are associated with canine diabetes mellitus. Tissue Antigens, 75(3), 242-52. eScholarID:81702 | PMID:20196832 | DOI:10.1111/j.1399-0039.2009.01434.x
• Steinbach, F., Müller, K., Aasted, B., Amadori, M., Büttner, M., Carter, S., Charley, B., Dominguez, J., Fossum, C., Fischer, U., Goddeeris, B., Hopkins, J., Kaspers, B., Marti, E., Ollier, W., Rutten, V., Saalmüller, A., Storset, A., Toman, M., Werling, D., Weber, C. & Mauel, S (2010). Summary of the third European Veterinary Immunology Workshop (EVIW), September 2009, Berlin, Germany. Vet Immunol Immunopathol, Epub ahead of print, eScholarID:86642 | PMID:20615554 | DOI:10.1016/j.vetimm.2010.06.008
• Wood, S., Ollier, W., Nuttall, T., McEwan, N. & Carter, S (2010). Despite identifying some shared gene associations with human atopic dermatitis the use of multiple dog breeds from various locations limits detection of gene associations in canine atopic dermatitis. Vet Immunol Immunopathol, 138(3), 193-7. eScholarID:96112 | PMID:20728225 | DOI:10.1016/j.vetimm.2010.07.020
• Yuille M, Dixon K, Platt A, Pullum S, Lewis D, Hall A, Ollier W. (2010). The UK DNA banking network: a "fair access" biobank. Cell Tissue Bank, 11(3), 241-251. eScholarID:53554 | DOI:10.1007/s10561-009-9150-3

2009

• Alfirevic, A, Vilar, F, Alsbou, M, Jawaid, A, Thomson, W, Ollier, WER, Bowman, C, Delrieu, O, Park, B, Pirmohamed, M. (2009). TNF, LTA, HSPA1L and HLA-DR gene polymorphisms in HIV-positive patients with hypersensitivity to cotrimoxazole. Pharmacogenomics, 10(4), 531-40. eScholarID:1d19081 | DOI:10.2217/pgs.09.6
• Barnes, A, O'Neill, T, Kennedy, LJ, Short, AD, Catchpole, B, House, A, Binns, M, Fretwell, N, Day, M, Ollier, WER. (2009). Association of canine anal furunculosis with TNFA is secondary to linkage disequilibrium with DLA-DRB1*. Tissue Antigens, 73( 3), 218-24. eScholarID:1d18958 | DOI:10.1111/j.1399-0039.2008.01188.x
• Betteridge ZE, Gunawardena H, Chinoy H, North J, Ollier WER, Cooper RG, McHugh NJ. (2009). Clinical and HLA-class II haplotype associations of autoantibodies to small ubiquitin-like modifier enzyme, a dermatomyositis-specific autoantigen target, in UK adult-onset Caucasian myositis. Ann Rheum Dis, 68(10), 1621-1625. eScholarID:1d17954 | DOI:10.1136/ard.2008.097162
• Brown, J., Donev, A., Aslanidis, C., Bracegirdle, P., Dixon, K., Foedinger, M., Gwilliam, R., Hardy, M., Illig, T., Ke, X., Krinka, D., Lagerberg, C., Laiho, P., Lewis, D., McArdle, W., Patton, S., Ring, S., Schmitz, G., Stevens, H., Tybring, G., Wichmann, H., Ollier, W. & Yuille, M (2009). Observational study on variability between biobanks in the estimation of DNA concentration. BMC Res Notes, 2(Epub), 8. eScholarID:68196 | PMID:19825187 | DOI:10.1186/1756-0500-2-208
• Chinoy, H., Lamb, J., Ollier, W. & Cooper, R (2009). An update on the immunogenetics of idiopathic inflammatory myopathies: major histocompatibility complex and beyond. Curr Opin Rheumatol, 21(6), 588-593. eScholarID:68198 | PMID:19730377 | DOI:10.1097/BOR.0b013e3283315a22
• Chinoy, H., Payne, D., Poulton, K., Fertig, N., Betteridge, Z., Gunawardena, H., Davidson, J., Oddis, C., McHugh, N., Wedderburn, L., Ollier, W. & Cooper, R (2009). HLA-DPB1 associations differ between DRB1*03 positive anti-Jo-1 and anti-PM-Scl antibody positive idiopathic inflammatory myopathy. Rheumatology (Oxford), 48(10), 1213-1217. eScholarID:68199 | PMID:19690132 | DOI:10.1093/rheumatology/kep248
• Gunawardena, H, Wedderburn, L, Chinoy, H, Betteridge, Z, North, J, Ollier, WER, Cooper, RG, Oddis, C, Ramanan, A, Davidson, J, McHugh, N, NULL. (2009). Autoantibodies to a 140-kd protein in juvenile dermatomyositis are associated with calcinosis. Arthritis Rheum, 60(6)(6), 1807-14. eScholarID:1d19262 | DOI:10.1002/art.24547
• Karasneh JA, Baszrafshani R, Thornhill M, Ollier WER. (2009). Endothelial nitric oxide synthase gene polymorphisms are not associated with recurrent aphthous stomatitis. Arch Oral Biol, 54(6), 583-587. eScholarID:1d19096 | DOI:10.1016/j.archoralbio.2009.03.008
• Lind, P, Luciano, M, Horan, M A, Marioni, R, Wright, M, Bates, T, Rabbitt, P, Harris, S, Davidson, YS, Deary, I, Gibbons, LC, Pickles, A, Ollier, WER, Pendleton, N, Price, J, Payton, A, Martin, N. (2009). No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples. Behav Genet, 39(5), 513-523. eScholarID:1d19095 | DOI:10.1007/s10519-009-9274-z
• Luciano, M, Miyajima, F, Lind, P, Bates, T, Horan, M, Harris, S, Wright, M, Ollier, WER, Hayward, C, Pendleton, N, Gow, A, Visscher, P, Starr, J, Deary, I, Martin, N, Payton, A. (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes Brain Behav, 8(2), 218-227. eScholarID:1d18675 | DOI:10.1111/j.1601-183X.2008.00462.x
• Mohammadi, M., Bazrafshani, M., Day, P. & Ollier, W (2009). Vascular Endothelial Growth Factor Production is Regulated by Gene Polymorphisms. Iran J Immunol, 6(3), 119-29. eScholarID:68197 | PMID:19801785
• Payton A, Payne D, Mankhambo L, Banda D, Hart C, Ollier WER, Carrol E. (2009). Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease. BMC Med Genet, 10, eScholarID:1d18956 | DOI:10.1186/1471-2350-10-28
• Pease CT, Haugeberg G, Montague B, Hensor EM, Bhakta BB, Thomson W, Ollier WER, Morgan AW. (2009). Polymyalgia rheumatica can be distinguished from late onset rheumatoid arthritis at baseline: results of a 5-yr prospective study. Rheumatology (Oxford), 48 (2), 1213-127. eScholarID:1d18236 | DOI:10.1093/rheumatology/ken343
• Short AD, Catchpole B, Kennedy LJ, Barnes A, Lee AC, Jones CA, Fretwell N, Ollier WER. (2009). T cell cytokine gene polymorphisms in canine diabetes mellitus. Vet Immunol Immunopathol, 128, 137-146. eScholarID:1d18677 | DOI:10.1016/j.vetimm.2008.10.301
• Wood SH, Clements D, Ollier WER, Nuttall T, McEwan NA, Carter SD. (2009). Gene expression in canine atopic dermatitis and correlation with clinical severity scores. J Dermatol Sci, 55(1), 27-33. eScholarID:1d19098 | DOI:10.1016/j.jdermsci.2009.03.005
• Wood, S., Ke, X., Nuttall, T., McEwan, N., Ollier, W. & Carter, S (2009). Genome-wide association analysis of canine atopic dermatitis and identification of disease related SNPs. Immunogenetics, Epub ahead of print, eScholarID:68195 | PMID:19838693 | DOI:10.1007/s00251-009-0402-y
• Amoli MM, Miranda-Filloy JA, Vazquez-Rodriguez TR, Ollier WE, Gonzalez-Gay MA. (2009). Regulated upon activation normal T-cell expressed and secreted (RANTES) and epithelial cell-derived neutrophil-activating peptide (ENA-78) gene polymorphisms in patients with biopsy-proven erythema nodosum. Clin Exp Rheumatol, 1(Suppl 52), S142-S143. eScholarID:81673
• Chinoy H, Salway F, Fertig N, Oddis CV, Ollier WER, Cooper RG. (2009). Clinical, serological and HLA profiles in non-Caucasian UK idiopathic inflammatory myopathy. Rheumatology (Oxford), 48(5), 591-592. eScholarID:17d964 | DOI:10.1093/rheumatology/kep035

2008

• Ollier WER, Worthington J, Hochberg MC; SilmanA.J.; Smolen JS; Weinblatt ME; Weisman MH. (2008). Investigation of the genetic basis of rheumatic diseases. Rheumatology. ( 13, pp. 123-131). London: Elsevier. eScholarID:3d658
• Amoli MM, Carthy D, Platt H, Ollier WER. (2008). EBV Immortalization of human B lymphocytes separated from small volumes of cryo-preserved whole blood. International Journal of Epidemiology, 37, suppl_1, i41-i45. eScholarID:1d17110
• Ashworth JJ, Smyth JV, Pendleton N, Horan M A, Payton A, Worthington J, Ollier WER, Ashcroft GG. (2008). Polymorphisms spanning the 0N exon and promoter of the estrogen receptor-beta (ERbeta) gene ESR2 are associated with venous ulceration. Clin Genet, 73 (1), 55-61. eScholarID:1d16791
• Brown J, Ollier WER, Thomson W, Bayat A. (2008). Positive association of HLA-DRB1*15 with Dupuytren's disease in Caucasians. Tissue Antigens, 72 (2), 166-70. eScholarID:1d17735 | DOI:10.1111/j.1399-0039.2008.01082.x
• Brown JJ, Ollier WER, Thomson W, Bayat A. (2008). Positive association of HLA-DRB1*15 with keloid disease in Caucasians. Int J Immunogenet, 35 (4-5), 303-7. eScholarID:1d18235 | DOI:10.1111/j.1744-313X.2008.00780.x
• Catchpole B, Kennedy LJ, Davison L.J, Ollier WER. (2008). Canine diabetes mellitus: from phenotype to genotype. J. Small Anim Pract, 49, 1, eScholarID:1d16140
• Chinoy H., Platt H., Lamb J.A., Betteridge Z., Gunawardena H., Fertig N., Varsani H., Davidson J., Oddis C.V., McHugh N.J., Wedderburn L.R., Ollier W.E.R., Cooper R.G. (2008). The PTPN22 gene is associated with juvenile and adult idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype in British Caucasian patients. Arthritis Rheum, 58(10), 3247-3254. eScholarID:79202 | DOI:10.1002/art.23900
• Clements D, CarterS.D, InnesJ.F, Ollier WER, Day PJR. (2008). Gene expression profiling of normal and ruptured canine anterior cruciate ligaments. Osteoarthritis Cartilage, 16, 2, 195-203. eScholarID:1d16137
• Clements D, Wood SH, CarterS.D, Ollier WER. (2008). Assessment of the quality and quantity of genomic DNA recovered from canine blood samples by three different extraction methods. Res. Vet. Sci, 85(1), 74-79. eScholarID:1d16998
• Kennedy LJ, Brown JJ, Barnes A, Ollier WER, KnyazevS. (2008). Major histocompatibility complex typing of dogs from Russia shows further dog leukocyte antigen diversity. Tissue Antigens, 71(2), 151-156. eScholarID:1d17000
• Kennedy, LJ, O'Neill,T., House,A., Barnes, A, Kyostila,K., Innes,J., Fretwell,N., Day,M.J., Catchpole,B., Lohi,H., Ollier, WER. (2008). Risk of anal furunculosis in German Shepherd dogs is associated with the major histocompatibility complex. Tissue Antigens, 71, 1, 51-56. eScholarID:1d17009 | DOI:10.1111/j.1399-0039.2007.00964.x
• Merryman-Simpson,A.E., Wood, SH, Fretwell,N., Jones,P.G., McLaren,W.M., McEwan,N.A., Clements,D.N., Carter,S.D., Ollier, WER, Nuttall,T. (2008). Gene (mRNA) expression in canine atopic dermatitis: microarray analysis. Veterinary Dermatology, 19, 2, 59-66. eScholarID:1d17059 | DOI:10.1111/j.1365-3164.2008.00653.x
• Miyajima F, Ollier WER, Mayes AR, Jackson A-, Thacker NA, Rabbitt P-, Pendleton N, Horan M A, Payton A. (2008). Brain-derived neurotrophic factor polymorphism Val66Met influences cognitive abilities in the elderly. Genes Brain Behav, 7(4), 411-417. eScholarID:1d16825
• Miyajima F, Quinn JP, Horan M A, Pickles A, Ollier WER, Pendleton N, Payton A. (2008). Additive effect of BDNF and REST polymorphisms is associated with improved general cognitive ability. Genes Brain Behav, 7(7), 714-719. eScholarID:1d17392 | DOI:10.1111/j.1601-183X.2008.00409.x
• RehmanS, Salway F, StanleyJ.K, Ollier WER, Day PJR, BayatA. (2008). Molecular Phenotypic Descriptors of Dupuytren's Disease Defined Using Informatics Analysis of the Transcriptome. Journal of Hand Surgery (Am), 33, 3, 359-372. eScholarID:1d17057 | DOI:10.1016/j.jhsa.2007.11.010
• Salway F, Day PJR, Ollier WER, Peakman TTC. (2008). Levels of 5' RNA tags in plasma and buffy coat from EDTA blood increase with time. International Journal of Epidemiology, 37, suppl_1, i11-i15. eScholarID:1d17112
• ThomM.D, StockleyP, Jury F, Ollier WER, BeynonR.J, HurstJ.L. (2008). The direct assessment of genetic heterozygosity through scent in the mouse. Current Biology, 18, 8, eScholarID:1d17716 | DOI:10.1016/j.cub.2008.03.056
• WiersmaA.C, StabejP, LeegwaterP.A, Van OostB.A, Ollier WER, Dukes-McEwanJ. (2008). Evaluation of 15 Candidate Genes for Dilated Cardiomyopathy in the Newfoundland Dog. Journal of Heredity, 99(1), 73-80. eScholarID:1d17007 | DOI:10.1093/jhered/esm090
• Amoli M, Miranda-Filloy J, Fernandez-Diaz M, Martin J, Ollier WER, Gonzalez-Gay M. (2008). Interleukin-6 promoter polymorphism at position -174 in biopsy-proven patients with erythema nodosum from a defined population. Clin Exp Rheumatol, 26(3 Suppl 49), S155-6. eScholarID:17d702
• Gonzalez-GayM.A, Gonzalez-JuanateyC, LlorcaJ, Ollier WER, MartinJ. (2008). Contribution of HLA-DRB1 shared epitope alleles and chronic inflammation to the increased incidence of cardiovascular disease in rheumatoid arthritis: Comment on the article by Farragher et al. Arthritis and Rheumatism, 58, 8, 2584. eScholarID:17d516

2007

• AlzoubiF.Q, Ollier WER, RamsdenR.T, SaeedS.R. (2007). No evidence of linkage between 7q33-36 locus (OTSC2) and otosclerosis in seven British Caucasian pedigrees. Journal of Laryngology and Otology, 121, 12, eScholarID:1d16991
• Amoli MM, Lopez-AgredaH, Suarez-AmorO, MartinJ, Ollier WER, Gonzalez-GayM.A. (2007). Endothelial nitric oxide synthase polymorphisms in biopsy-proven erythema nodosum from a defined population. Clinical and Experimental Rheumatology, 25, 4, eScholarID:1d16993
• Amoli MM, Martin J, Miranda-Filloy J, Garcia-Porrua C, Ollier WER, Gonzalez-Gay M. (2007). Lack of association between interleukin-6 promoter polymorphism at position -174 and Henoch-Schonlein purpura. Clin Exp Rheumatol, 25( 1 Suppl 44), 6-8. eScholarID:1d15759
• CarrolE.D, Salway F, PepperS.D, SaundersE, MankhamboL.A, Ollier WER, HartC.A, Day PJR. (2007). Successful downstream application of the Paxgene Blood RNA system from small blood samples in paediatric patients for quantitative PCR analysis. BMC.Immunol, 8, eScholarID:1d16994
• CheethamS.A, ThomM.D, Jury F, Ollier WER, BeynonR.J, HurstJ.L. (2007). The genetic basis of individual-recognition signals in the mouse. Current Biology, 17, 20, 1771-1777. eScholarID:1d16996
• Chinoy H, Fertig N, Oddis CV, Ollier WER, Cooper RG. (2007). The diagnostic utility of myositis autoantibody testing for predicting the risk of cancer-associated myositis. Ann Rheum Dis, 66(10), 1345-1349. eScholarID:1d15762 | DOI:10.1136/ard.2006.068502
• Chinoy H, Salway F, Fertig N, Tait BD, Oddis CV, Ollier WER, Cooper RG. (2007). Monocyte chemotactic protein-1 single nucleotide polymorphisms do not confer susceptibility for the development of adult onset polymyositis/dermatomyositis in UK Caucasians. Rheumatology (Oxford), 46(4), 604-607. eScholarID:1d14018 | DOI:10.1093/rheumatology/kel359
• Chinoy H, Salway F, John S, Fertig N, Tait BD, Oddis CV, Ollier WER, Cooper RG. (2007). Interferon-Gamma and Interleukin-4 Gene polymorphisms in UK caucasian idiopathic inflammatory myopathy patients. Ann Rheum Dis, 66(7), 970-973. eScholarID:1d15761 | DOI:10.1136/ard.2006.068858
• Chinoy H, Salway F, John S, FertigN, Tait BD, Oddis CV, Ollier WER, Cooper RG. (2007). Tumour necrosis factor-{alpha} single nucleotide polymorphisms are not independent of HLA class I in UK Caucasians with adult onset idiopathic inflammatory myopathies. Rheumatology (Oxford), 46(9), 1411-1416. eScholarID:1d27866 | DOI:10.1093/rheumatology/kem145
• Gonzalez-Gay M, Gonzalez-Juanatey C, Lopez-Diaz M, Pineiro A, Garcia-Porrua C, Miranda-Filloy J, Ollier WER, Martin J, Llorca J. (2007). HLA-DRB1 and persistent chronic inflammation contribute to cardiovascular events and cardiovascular mortality in patients with rheumatoid arthritis. Arthritis Rheum, 57(1), eScholarID:1d15752
• Kennedy LJ, AnglesJ.M, Barnes A, CarmichaelL.E, RadfordA.D, Ollier WER, HappG.M. (2007). DLA-DRB1, DQA1, and DQB1 Alleles and Haplotypes in North American Gray Wolves. Journal of Heredity, 98, 5, eScholarID:1d16144
• Kennedy LJ, Barnes A, Short AD, Brown JJ, Lester S, Seddon J, Happ G, Ollier WER. (2007). Canine DLA diversity: 2. Family studies. Tissue Antigens, 69 Suppl 1, 289-91. eScholarID:1d15756
• Kennedy LJ, Lunt M, Barnes A, McElhinneyL, FooksA.R, BaxterD.N, Ollier WER. (2007). Factors influencing the antibody response of dogs vaccinated against rabies. Vaccine, 25, 51, 8500 - 8507. eScholarID:1d17002
• Kennedy, LJ, Barnes, A, Short, AD, Brown, JJ, Lester, S, Seddon, J, Fleeman, L, Francino, O, Brkljacic, M, Knyazev, S, Happ, G, Ollier, WER. (2007). Canine DLA diversity: 1. New alleles and haplotypes. Tissue Antigens, 69 Suppl 1, 272-88. eScholarID:1d15757
• Kennedy, LJ, Barnes, A, Short, AD, Brown, JJ, Seddon, J, Fleeman, L, Brkljacic, M, Happ, G, Catchpole, B, Ollier, WER. (2007). Canine DLA diversity: 3. Disease studies. Tissue Antigens, 69 Suppl 1, 292-6. eScholarID:1d15755
• Llorca J, Lopez-Diaz MJ, Gonzalez-Juanatey C, Ollier WER, Martin J, Gonzalez-Gay MA. (2007). Persistent Chronic Inflammation Contributes to the Development of Cancer in Patients with Rheumatoid Arthritis from a Defined Population of Northwestern Spain. Semin Arthritis Rheum, 37, 31-38. eScholarID:1d15764
• Malik MA, Bayat A, Jury F, Kay P, Ollier WER. (2007). Genetic susceptibility to total hip arthroplasty failure-positive association with mannose-binding lectin. J Arthroplasty, 22(2), 265-70. eScholarID:1d15753
• Malik MA, Jury F, Bayat A, Ollier WER, Kay PR. (2007). Genetic susceptibility to total hip replacement failure- Preliminary study on the influence of matrix metalloproteinase-1, interleukin-6 and vitamin D receptor polymorphisms. Ann Rheum Dis, 66, 1116-1120. eScholarID:1d15763
• Mattey, D, Thomson, W, Ollier, WER, Batley, M, Davies, P, Gough, A, Devlin, J, Prouse, P, James, D, Williams, P, Dixey, J, Winfield, J, Cox, N, Koduri, G, Young, A. (2007). Association of DRB1 shared epitope genotypes with early mortality in rheumatoid arthritis: Results of eighteen years of followup from the early rheumatoid arthritis study. Arthritis Rheum, 56(5), 1408-1416. eScholarID:1d15754
• Payne K, Newman WG, Fargher EA, Tricker K, Bruce IN, Ollier WER. (2007). TPMT testing in rheumatology: any better than routine monitoring? Rheumatology, 46, 727-729. eScholarID:1d15522
• Rafatpanah H, PravicaV, FaridhosseiniR, TabatabaeiA, Ollier WER, PoultonK, Thomson W, HutchinsonI. (2007). Association between HLA-DRB1*01 and HLA-Cw*08 and Outcome Following HTLV-I Infection. Iran J.Immunol, 4, 2, 94 - 100. eScholarID:1d16139
• Salonen, J, Uimari, P, Aalto, J, Pirskanen, M, Kaikkonen, J, Todorova, B, Hypponen, J, Korhonen, V, Asikainen, J, Devine, C, Tuomainen, T, Luedemann, J, Nauck, M, Kerner, W, Stephens, RH, New, JP, Ollier, WER, Gibson, JM, Payton, A, Horan, M A, Pendleton, N, Mahoney, W, Meyre, D, Delplanque, J, Froguel, P, Luzzatto, O, Yakir, B, Darvasi, A. (2007). Type 2 Diabetes Whole-Genome Association Study in Four Populations: The DiaGen Consortium. Am J Hum Genet, 81(2), 338-45. eScholarID:1d16155 | DOI:10.1086/520599
• SherborneA.L, ThomM.D, PatersonS, Jury F, Ollier WER, StockleyP, BeynonR.J, HurstJ.L. (2007). The genetic basis of inbreeding avoidance in house mice. Current Biology, 17, 23, 2061-2066. eScholarID:1d17004
• Short AD, CatchpoleB, Kennedy LJ, Barnes A, FretwellN, JonesC, Thomson W, Ollier WER. (2007). Analysis of candidate susceptibility genes in canine diabetes. Journal of Heredity, 98, 5, 518 - 525. eScholarID:1d16142
• Short AD, Kennedy LJ, Barnes A, FretwellN, JonesC, Thomson W, Ollier WER. (2007). Hardy-Weinberg Expectations in Canine Breeds: Implications for genetic studies. Journal of Heredity, 98(5), 445-451. eScholarID:1d15875
• Wedderburn,L.R., McHugh,N.J., Chinoy, H, Cooper, RG, Salway, F, Ollier, WER, McCann,L.J., Varsani,H., Dunphy,J., North,J., Davidson,J.E. (2007). HLA class II haplotype and autoantibody associations in children with juvenile dermatomyositis and juvenile dermatomyositis-scleroderma overlap. Rheumatology (Oxford), 46(12), 1786-1791. eScholarID:1d28132 | DOI:10.1093/rheumatology/kem265
• WiersmaA.C, LeegwaterP.A, Van OostB.A, Ollier WER, Dukes-McEwanJ. (2007). Canine Candidate Genes for Dilated Cardiomyopathy: Annotation of and polymorphic markers for 14 genes. BMC.Vet.Res, 3(1), eScholarID:1d17006
• Amoli MM, Ollier WER, Gonzalez-Gay M. (2007). Lack of association of epithelial cell-derived neurophil-activating peptide (ENA)-78 gene polymorphism with susceptibility to biopsy-proven giant cell arteritis. Clin Exp Rheumatol, 25( 1 Suppl 44), 40. eScholarID:17d956

2006

• Amoli MM, Martin J, Miranda-Filloy J.A, Garcia-Porrua C, Ollier WER, Gonzalez-Gay M.A. (2006). Lack of association between macrophage migration inhibitory factor gene (-173 G/C) polymorphism and cutaneous vasculitis. Clin Exp Rheumatol, 24(5), 576-59. eScholarID:1d14521
• Brown JJ, Ollier WER, Thomson W, Matthews J, Carter S, Binns M, Pinchbeck G, Clegg P. (2006). TNF-alpha SNP haplotype frequencies in equidae. Tissue Antigens, 67( 5), 377-82. eScholarID:1d13219
• Burwick, R, Ramsay, P, Haines, J, Hauser, S, Oksenberg, J, Pericak-Vance, M, Schmidt, S, Compston, A, Sawcer, S, Cittadella, R, Savettieri, G, Quattrone, A, Polman, C, Uitdehaag, B, Zwemmer, J, Hawkins, C, Ollier, WER, Weatherby, S, Enzinger, C, Fazekas, F, Schmidt, H, Schmidt, R, Hillert, J, Masterman, T, Hogh, P, Niino, M, Kikuchi, S, Maciel, P, Santos, M, Rio, M, Kwiecinski, H, Zakrzewska-Pniewska, B, Evangelou, N, Palace, J, Barcellos, L. (2006). APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers. Neurology, 66( 9), 1373-83. eScholarID:1d13218
• Chinoy, H, Salway, F, N Fertig, Shephard, N, B D Tait, Thomson, W, D A Isenberg, C V Oddis, Silman, AJ, Ollier, WER, Cooper, RG, UK Adult Onset Myositis Immunogenetic Collaboration (AOMIC). (2006). In adult onset myositis, the presence of interstitial lung disease and myositis specific/associated antibodies are governed by HLA class II haplotype, rather than by myositis subtype. Arthritis Research & Therapy, 8(R13), eScholarID:1d12161 | DOI:10.1186/ar1862
• Clements D, Carter S, Innes J, Ollier WER. (2006). Genetic basis of secondary osteoarthritis in dogs with joint dysplasia. Am J Vet Res, 67( 5), 909-18. eScholarID:1d13220
• Clements D, Carter SD, Innes JF, Ollier WER, Day PJR. (2006). Analysis of normal and osteoarthritic canine cartilage mRNA expression by quantitative-PCR. Arthritis Res Ther, 8(6), eScholarID:1d14019
• Clements D, Vaughan-Thomas A, Peansukmanee S, Carter S, Innes J, Ollier WER, Clegg P. (2006). Assessment of the use of RNA quality metrics for the screening of articular cartilage specimens from clinically normal dogs and dogs with osteoarthritis. Am J Vet Res, 67(8), 1438-44. eScholarID:1d14020
• F Jury, Al-Mahrous, M Apostolou, Sandiford SSK, A Fox, Ollier WER, Upton M. (2006). Rapid, cost-effective sub-typing of methicillin resistant Staphylococcus aureus by denaturing high pressure liquid chromatography. Journal of Medical Microbiology, 55(PT8), 1043-1051. eScholarID:1d13064 | DOI:10.1099/jmm.0.46409-0
• Farzaneh F, Roberts SA, Mandal D, Ollier WER, Winters U, Kitchener HC, Brabin L. (2006). The IL-1082G polymorphism is associated with clearance of HPV infection. British Journal Of Obstetrics And Gynaecology, 113(8), 961-964. eScholarID:1d27020
• Greig, C, Spreckley, KB, Aspinwall, R, Gillaspy, E, Gillaspy, EE, Grant, M, Ollier, WER, John, S, Doherty, M, Wallis, GA. (2006). Linkage to nodal osteoarthritis: Quantitative and qualitative analyses of data from a whole genome screen identifies trait dependent susceptibility loci. Ann Rheum Dis, 65(9), 1131-1138. eScholarID:1d13084 | DOI:10.1136/ard.2005.048165
• Jury F, Al-Mahrous M, Apostolou M, Sandiford S, Fox A, Ollier WER, Upton M. (2006). Rapid cost-effective subtyping of meticillin-resistant Staphylococcus aureus by denaturing HPLC. J Med Microbiol, 55( Pt 8), 1053-60. eScholarID:1d13821
• Kennedy LJ, Barnes A, Ollier WER, MJ Day. (2006). Association of a common dog leucocyte antigen class II haplotype with canine primary immune-mediated haemolytic anaemia. Tissue Antigens, 68(6), 502-8. eScholarID:1d14242
• Kennedy LJ, LJ Davison, Barnes A, Short AD, N Fretwell, CA Jones, AC Lee, Ollier WER, B Catchpole. (2006). Identification of susceptibility and protective major histocompatibility complex haplotypes in canine diabetes mellitus. Tissue Antigens, 68(6), 467-76. eScholarID:1d14254
• Kennedy, LJ, Quarmby, SL, Happ, GM, Barnes, A, Ramsey, IK, Dixon, RM, Catchpole, B, Rusbridge, C, Graham, PA, Roethel, C, Dodds, WJ, Carmichael, N, Ollier, WER. (2006). Association of canine Hypothyroidism with a common Major Histocompatibility Complex DLA class II allele. Tissue Antigens, 68(1), 82-6. eScholarID:1d13148
• Malik MA, Bayat A, Jury F, Ollier WER, Kay PR, Kay P. (2006). Genetic susceptibility to hip arthroplasty failure-association with the RANK/OPG pathway. Int Orthop, 30(3), 177-181. eScholarID:1d13221
• Morgan AW, Robinson JI, Barrett JH, Martin J, Walker A, Babbage SJ, Ollier WER, Gonzalez-Gay MA, Isaacs JD. (2006). Association of FCGR2A and FCGR2A-FCGR3A haplotypes with susceptibility to giant cell arteritis. Arthritis Res Ther, 8( 4), eScholarID:1d14021
• Payton A, Horan M A, Davidson YS, Gibbons LC, Ollier WER, Rabbitt P-, Worthington J, Pendleton N, Pendleton N. (2006). Influence and interactions of cathepsin D, HLA-DRB1 and APOE on cognitive abilities in an older non-demented population. Genes Brain and Behavior, 5, Suppl 1, 23-31. eScholarID:1d11375 | DOI:10.1111/j.1601-183X.2006.00191.x
• Simpson A, John S, Jury F, Niven R, Niven RR M, Woodcock AA, Ollier WER, Custovic A. (2006). Endotoxin Exposure, CD14 and Allergic Disease: An Interaction between Genes and the Environment. Am J Respir Crit Care Med, 174(4), 386-392. eScholarID:1d13021 | DOI:10.1164/rccm.200509-1380OC

2005

• Stephens, RH, McElduff, P, Worthington, J, Ollier, WER, New, JP, Payton, A, Pendleton, N, Horan, M A, Cruickshank, (K, Gibson, JM. (2005). Single-nucleotide polymorphisms (SNPs) in the IGFBP1 gene are associated with diabetes risk and nephropathy in a cohort of type 2 diabetes mellitus patients. eScholarID:2d2022
• Amoli M, Garcia-Porrua C, Ollier WER, Gonzalez-Gay M. (2005). Lack of association between macrophage migration inhibitory factor gene polymorphism and giant cell arteritis. J Rheumatol, 32( 1), 74-6. eScholarID:1d11725
• Amoli MM, Larijani B, Thomson W, Ollier WER, Gonzalez-Gay M. (2005). Two polymorphisms in the epithelial cell-derived neutrophil-activating peptide (ENA-78) gene. Dis Markers, 21( 2), 75-7. eScholarID:1d11720
• Amoli MM, Salway F, Zeggini E, Ollier WER, Gonzalez-Gay M. (2005). MCP-1 gene haplotype association in biopsy proven giant cell arteritis. J Rheumatol, 32( 3), 507-10. eScholarID:1d11722
• Ashworth J J, Smyth J Vincent, Pendleton N, Horan M A, Payton A, Worthington J, Ollier WER, Ashcroft GG. (2005). The dinucleotide (CA)repeat polymorphism of estrogen receptor beta but not the dinulclotide (TA)repeat polymorphism of estrogen receptor alpha is associated with venous ulceration. J Steroid Biochem Mol Biol, 97(3), 266-70. eScholarID:1d11193
• Bayat A, Arscott G, Ollier WER, McGrouther D, Ferguson M. (2005). Keloid disease: clinical relevance of single versus multiple site scars. Br J Plast Surg, 58( 1), 28-37. eScholarID:1d11726
• Bayat A, Walter J, Bock O, Mrowietz U, Ollier WER, Ferguson M. (2005). Genetic susceptibility to keloid disease: mutation screening of the TGFbeta(3) gene. Br J Plast Surg, 58( 7), 914-21. eScholarID:1d11714
• Bayat A, Walter J, Lamb H, Marino M, Ferguson M, Ollier WER. (2005). Mitochondrial mutation detection using enhanced multiplex denaturing high-performance liquid chromatography. Int J Immunogenet, 32( 3), 199-205. eScholarID:1d11718
• Bayat A, Walter J, Lambe H, Watson J, Stanley JK, Marino M, Ferguson M, Ollier WER. (2005). Identification of a novel mitochondrial mutation in Dupuytren's disease using multiplex DHPLC. Plast Reconstr Surg, 115( 1), 134-41. eScholarID:1d11728
• Debenham S, Hart E, Ashurst J, Howe K, Quail M, Ollier WER, Binns M. (2005). Genomic sequence of the class II region of the canine MHC: comparison with the MHC of other mammalian species. Genomics, 85( 1), 48-59. eScholarID:1d9887
• Gonzalez-Gay MA, Oliver J, Sanchez E, Garcia-Porrua C, Paco L, Lopez-Nevot MA, Ollier WER, Martin J. (2005). Association of a Functional Inducible Nitric Oxide Synthase Promoter Variant with Susceptibility to Biopsy-Proven Giant Cell Arteritis. J Rheumatol, 32( 11), 2178-2182. eScholarID:1d11885
• Karasneh J, Gul A, Ollier WER, Silman AJ, Worthington J. (2005). Whole-genome screening for susceptibility genes in multicase families with Behcet's disease. Arthritis Rheum, 52( 6), 1836-42. eScholarID:1d11717
• Karasneh J, Hajeer A, Silman AJ, Worthington J, Ollier WER, Gul A. (2005). Polymorphisms in the endothelial nitric oxide synthase gene are associated with Behcet's disease. Rheumatology (Oxford), 44( 5), 614-7. eScholarID:1d11724
• Kennedy LJ, Quarmby S, Fretwell N, Martin AJ, Jones PG, Jones CA, Ollier WER. (2005). High-Resolution Characterization of the Canine DLA-DRB1 Locus Using Reference Strand-Mediated Conformational Analysis. J Hered, 96(7), 836-842. eScholarID:1d11711
• Martin J, Paco L, Ruiz M, Lopez-Nevot M, Garcia-Porrua C, Amoli M, Calvino M, Ollier WER, Gonzalez-Gay M. (2005). Inducible nitric oxide synthase polymorphism is associated with susceptibility to Henoch-Schonlein purpura in northwestern Spain. J Rheumatol, 32( 6), 1081-5. eScholarID:1d11715
• Ollier WER, Sprosen T, Peakman T. (2005). UK Biobank: from concept to reality. Pharmacogenomics, 6( 6), 639-46. eScholarID:1d11713
• Payton A, Gibbons LC, Davidson YS, Ollier WER, Rabbitt P-, Worthington J, Pickles A, Pendleton N, Horan M A. (2005). Influence of serotonin transporter gene polymorphisms on cognitive decline and cognitive abilities in a nondemented elderly population. Molecular Psychiatry, 10(12), 1133-1139. eScholarID:1d11213 | DOI:10.1038/sj.mp.4001733
• Short AD, Kennedy LJ, Forman O, Barnes A, Fretwell N, Wiggall R, Thomson W, Ollier WER. (2005). Canine DNA Subjected to Whole Genome Amplification is Suitable for a Wide Range of Molecular Applications. J Hered, 96(7), 829-835. eScholarID:1d11884
• Simpson, A, Maniatis, N, Jury, F, Cakebread, J, Lowe, L, Holgate, S, Woodcock, AA, Ollier, WER, Collins, A, Custovic, A, Holloway, J, John, S. (2005). Polymorphisms in a disintegrin and metalloprotease 33 (ADAM33)predict impaired early-life lung function. Am J Respir Crit Care Med, 172(1), 55-60. eScholarID:1d10460 | DOI:10.1164/rccm.200412-1708OC
• Stephens RH, McElduff P, Heald A, New JP, Worthington J, Ollier WER, Gibson JM. (2005). Polymorphisms in insulin-like growth factor-binding protein 1 are associated with impaired renal function in Type-2 diabetes mellitus. Diabetes, 54(12), 3547-53. eScholarID:1d11934 | DOI:10.2337/diabetes.54.12.3547
• Stevenson J, Langley K, Pay H, Payton A, Worthington J, Ollier WER, Thapar A. (2005). Attention deficit hyperactivity disorder with reading disabilities: preliminary genetic findings on the involvement of the ADRA2A gene. J Child Psychol Psychiatry, 46(10), 1081-8. eScholarID:1d11712
• ZegginiE, Barton A, Eyre SS, WardD, Ollier WER, Worthington J, John S. (2005). Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition. BMC Genet, 6, 1, eScholarID:1d11173

2004

• Addie D, Kennedy LJ, Ryvar R, Willoughby K, Gaskell R, Ollier WER, Nart P, Radford A. (2004). Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis. J Feline Med Surg, 6( 2), 59-62. eScholarID:1d8107
• Alansari A, Gul A, Inanc M, Ordi J, Teh L, Ollier WER, Gonzalez-Gay M, Hajeer A. (2004). Fc receptor gamma subunit polymorphisms and systemic lupus erythematosus. Saudi Med J, 25( 10), 1445-8. eScholarID:1d9730
• Amoli M, Calvino M, Garcia-Porrua C, Llorca J, Ollier WER, Gonzalez-Gay M. (2004). Interleukin 1beta gene polymorphism association with severe renal manifestations and renal sequelae in Henoch-Schonlein purpura. J Rheumatol, 31( 2), 295-8. eScholarID:1d8112
• Amoli MM, Garcia-Porrua C, Calvino M, Ollier WER, Gonzalez-Gay M. (2004). Lack of association between endothelial nitric oxide synthase polymorphisms and Henoch-Schonlein purpura. J Rheumatol, 31( 2), 299-301. eScholarID:1d8109
• Amoli MM, Gonzalez-Gay M, Zeggini E, Salway F, Garcia-Porrua C, Ollier WER. (2004). Epistatic interactions between HLA-DRB1 and interleukin 4, but not interferon-gamma, increase susceptibility to giant cell arteritis. J Rheumatol, 31( 12), 2413-7. eScholarID:1d9732
• Amoli MM, Llorca J, Gomez-Gigirey A, Garcia-Porrua C, Lueiro M, El-Magadmi M, Fernandez M, Ollier WER, Gonzalez-Gay M. (2004). E-selectin polymorphism in erythema nodosum secondary to sarcoidosis. Clin Exp Rheumatol, 22( 2), 230-2. eScholarID:1d8111
• Barton, A, Barton, A, Platt, H, Salway, F, Symmons, D, Barrett, EM, Bukhari, MAS, Lunt, M, Zeggini, E, Eyre, SS, Hinks, AM, Tellam, DJ, Brintnell, W, Ollier, WER, Worthington, J, Silman, AJ. (2004). Polymorphisms in the tumour necrosis factor gene are not associated with severity of inflammatory polyarthritis. Ann Rheum Dis, 63, 3, 280-284. eScholarID:1d9454
• Barton, A, Woolmore,J.A., Ward,D., Eyre, SS, Hinks, AM, Ollier, WER, Strange,R.C., Fryer,A.A., John, S, Hawkins,C.P., Worthington, J. (2004). Association of protein kinase C alpha (PRKCA) gene with multiple sclerosis in a UK population. Brain, 127, 8, 1717-1722. eScholarID:1d8159
• Bayat A, Arscott G, Ollier WER, Ferguson M, McGrouther D. (2004). Description of site-specific morphology of keloid phenotypes in an Afrocaribbean population. Br J Plast Surg, 57( 2), 122-33. eScholarID:1d8124
• Bayat A, Barton A, Ollier WER. (2004). Dissection of complex genetic disease: implications for orthopaedics. Clin Orthop, ( 419), 297-305. eScholarID:1d8134
• Bayat A, Bock O, Mrowietz U, Ollier WER, Ferguson M. (2004). Genetic susceptibility to keloid disease: transforming growth factor beta receptor gene polymorphisms are not associated with keloid disease. Exp Dermatol, 13( 2), 120-4. eScholarID:1d8123
• Brown JJ, Thomson W, Clegg P, Eyre SS, Kennedy LJ, Matthews J, Carter S, Ollier WER. (2004). Polymorphisms of the equine major histocompatibility complex class II DRA locus. Tissue Antigens, 64( 2), 173-9. eScholarID:1d8259
• Chinoy H, Ollier WER, Cooper RG. (2004). Have recent immunogenetic investigations increased our understanding of disease mechanisms in the idiopathic inflammatory myopathies? Curr Opin Rheumatol, 16(6), 707-713. eScholarID:1d9745 | DOI:10.1097/01.bor.0000142339.24380.b7
• Drake G, Kennedy LJ, Auty H, Ryvar R, Ollier WER, Kitchener A, Freeman A, Radford A. (2004). The use of reference strand-mediated conformational analysis for the study of cheetah (Acinonyx jubatus) feline leucocyte antigen class II DRB polymorphisms. Mol Ecol, 13( 1), 221-9. eScholarID:1d8125
• Eyre, SS, Barton, A, Shephard, N, Hinks, AM, Brintnell, W, MacKay,K., Silman, AJ, Ollier, WER, Wordsworth,P., John, S, Worthington, J. (2004). Investigation of susceptibility loci identified in the UK rheumatoid arthritis whole-genome scan in a further series of 217 UK affected sibling pairs. Arthritis and Rheumatism, 50, 3, 729-735. eScholarID:1d8165 | DOI:10.1002/art.20039
• Gonzalez-Gay M, Gonzalez-Juanatey C, Ollier WER. (2004). Endothelial dysfunction in rheumatoid arthritis: influence of HLA-DRB1 alleles. Autoimmun Rev, 3( 4), 301-4. eScholarID:1d8260
• Gonzalez-Gay M, Hajeer A, Dababneh A, Garcia-Porrua C, Amoli MM, Llorca J, Ollier WER. (2004). Interferon-gamma gene microsatellite polymorphisms in patients with biopsy-proven giant cell arteritis and isolated polymyalgia rheumatica. Clin Exp Rheumatol, 22( 6 Suppl 36), S18-20. eScholarID:1d15751
• Gonzalez-Gay MA, Llorca J, Sanchez E, Lopez-Nevot MA, Amoli MM, Garcia-Porrua C, Ollier WER, Martin J. (2004). Inducible but not endothelial nitric oxide synthase polymorphism is associated with susceptibility to rheumatoid arthritis in northwest Spain. Rheumatology (Oxford), 43(9), 1182-85. eScholarID:1d8127
• Gonzalez-Juanatey C, Testa A, Garcia-Castelo A, Garcia-Porrua C, Llorca J, Ollier WER, Gonzalez-Gay M. (2004). Echocardiographic and Doppler findings in long-term treated rheumatoid arthritis patients without clinically evident cardiovascular disease. Semin Arthritis Rheum, 33( 4), 231-8. eScholarID:1d8128
• James D, Young A, Kulinskaya E, Knight E, Thomson W, Ollier WER, Dixey J. (2004). Orthopaedic intervention in early rheumatoid arthritis. Occurrence and predictive factors in an inception cohort of 1064 patients followed for 5 years. Rheumatology (Oxford), 43( 3), 369-76. eScholarID:1d8129
• John, S, Shephard, N, Liu, G, Zeggini, E, Cao, M, Chen, W, Vasavda, N, Barton, A, Hinks, AM, Eyre, SS, Jones, K, Ollier, WER, Silman, AJ, Gibson, N, Worthington, J, Kennedy, G. (2004). Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites. Am J Hum Genet, 75( 1), 54-64. eScholarID:1d8131
• Mattey D, Nixon N, Dawes P, Ollier WER, Hajeer A. (2004). Association of matrix metalloproteinase 3 promoter genotype with disease outcome in rheumatoid arthritis. Genes Immun, 5( 2), 147-9. eScholarID:1d8132
• Ollier WER. (2004). Cytokine genes and disease susceptibility. Cytokine, 28( 4-5), 174-8. eScholarID:1d11729
• Partridge, J, Weatherby, S, Woolmore, J, Highland, D, Fryer, A, Mann, C, Boggild, M, Ollier, WER, Strange, R, Hawkins, C. (2004). Susceptibility and outcome in MS: associations with polymorphisms in pigmentation-related genes. Neurology, 62( 12), 2323-5. eScholarID:1d8133
• Shah P, Griffith S, Shadforth M, Fisher J, Dawes P, Poulton K, Thomson W, Ollier WER, Mattey D. (2004). Can gold therapy be used more safely in rheumatoid arthritis? Adverse drug reactions are more likely in patients with nodular disease, independent of HLA-DR3 status. J Rheumatol, 31( 10), 1903-5. eScholarID:1d9746
• Amoli MM, Ollier WER, Lueiro M, Fernandez M, Garcia-Porrua C, Gonzalez-Gay M. (2004). Lack of association between ICAM-1 gene polymorphisms and biopsy-proven erythema nodosum. J Rheumatol, 31( 2), 403-5. eScholarID:17d170

2003

• Ollier WER. (2003). The genetic basis of rheumatic disease. In: Rheumatology (3rd edition). Eds. Hochberg MC, Silman AJ, Smolen JS, Weinblatt ME, Weisman MH. eScholarID:3d850
• Malik MA, Zeggini E, Ollier WER, Kay P. (2003). Candidate gene analysis of genetic susceptibility to aseptic loosening and deep infection of cemented total hip replacement. eScholarID:2d1573
• Ollier WER. (2003). Hypersensitivity vasculitis. eScholarID:2d1290
• Amoli MM, Garcia-PorruaC, CalvinoM.C, Ollier WER, Gonzalez-GayM.A. (2003). Lack of association between endothelial nitric oxide synthase polymorphisms and cutaneous vasculitis. Journal of Rheumatology, eScholarID:1d5758
• Amoli MM, Garcia-PorruaC, LlorcaJ, Ollier WER, Gonzalez-GayM.A. (2003). Endothelial nitric oxide synthase haplotype associations in biopsy-proven giant cell arteritis. Journal of Rheumatology, 30(9), 2019-2022. eScholarID:1d5752
• Ardy Bayat, Arscott G, Ollier WER, Ferguson M. W, McGrouther D. (2003). 'Aggressive keloid': a severe variant of familial keloid scarring. J R Soc Med, 96, 11, 554-555. eScholarID:1d7364
• Bayat A, BockO, MrowietzU, Ollier WER, FergusonM.W. (2003). Genetic susceptibility to keloid disease and hypertrophic scarring: transforming growth factor beta1 common polymorphisms and plasma levels. Plastic and Reconstructive Surgery, 111, 2, 535-543. eScholarID:1d5767
• Bayat A, Stanley JK, WatsonJ.S, FergusonM.W, Ollier WER. (2003). Genetic susceptibility to Dupuytren's disease: transforming growth factor beta receptor (TGFbetaR) gene polymorphisms and Dupuytren's disease. British Journal of Plastic Surgery, 56, 4, 328-333. eScholarID:1d5764
• Bayat A, Walter J, Lamb H, Ferguson M, Ollier WER. (2003). Rapid denaturing high-performance liquid chromatography (DHPLC) for mutation scanning of the transforming growth factor beta3 gene using a novel proof-reading polymerase. Eur J Immunogenet, 30( 5), 335-40. eScholarID:1d8103
• Bayat A, WatsonJ.S, Stanley JK, FergusonM.W, Ollier WER. (2003). Genetic susceptibility to dupuytren disease: association of zf9 transcription factor gene. Plastic and Reconstructive Surgery, 111, 7, 2133-2139. eScholarID:1d5766
• BazrafshaniM.R, HajeerA.H, Ollier WER, ThornhillM.H. (2003). Polymorphisms in the IL-10 and IL-12 gene cluster and risk of developing recurrent aphthous stomatitis. Oral Diseases, 9(6), 287-91. eScholarID:1d5770
• González-Gay M, Amoli MM, Garcia-Porrua C, Ollier WER. (2003). Genetic markers of disease susceptibility and severity in giant cell arteritis and polymyalgia rheumatica. Semin Arthritis Rheum, 33(1), 38-48. eScholarID:1d8106
• Gonzalez-GayM.A, HajeerA.H, Garcia-PorruaC, DababnehA, Amoli MM, BotanaM.A, Thomson W, LlorcaJ, Ollier WER. (2003). Corticotropin-releasing hormone promoter polymorphisms in patients with rheumatoid arthritis from northwest Spain. Journal of Rheumatology, 30, 5, 913-917. eScholarID:1d5836
• Gonzalez-Juanatey,C., Testa,A., Garcia-Castelo,A., Garcia-Porrua,C., Llorca,J., Vidan,J., Hajeer,A.H., Ollier, WER, Mattey,D.L., Gonzalez-Gay,M.A. (2003). HLA-DRB1 status affects endothelial function in treated patients with rheumatoid arthritis. American Journal of Medicine, 114, 8, 647-652. eScholarID:1d5779
• KarasnehJ, HajeerA.H, BarrettJ, Ollier WER, ThornhillM, GulA. (2003). Association of specific interleukin 1 gene cluster polymorphisms with increased susceptibility for Behcet's disease. Rheumatology (Oxford), 42, 7, 860-864. eScholarID:1d5781
• Kennedy LJ, Ryvar R, Brown JJ, Ollier WER, Radford AD. (2003). Resolution of complex feline leukocyte antigen DRB loci by reference strand-mediated conformational analysis (RSCA).Tissue Antigens. Tissue Antigens, 62(4), 313-23. eScholarID:1d25642
• Langley,K., Payton, A, Hamshere,M.L., Pay,H.M., Lawson,D.C., Turic,D., Ollier, WER, Worthington, J, Owen,M.J., O'Donovan,M.C., Thapar,A. (2003). No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder. Psychiatric Genetics, 13, 2, 107-110. eScholarID:1d5783
• Morgan,A.W., Keyte,V.H., Babbage,S.J., Robinson,J.I., Ponchel,F., Barrett,J.H., Bhakta,B.B., Bingham,S.J., Buch,M.H., Conaghan,P.G., Gough,A., Green,M., Lawson,C.A., Pease,C.T., Markham,A.F., Ollier, WER, Emery,P., Worthington, J, Isaacs,J.D. (2003). FcgammaRIIIA-158V and rheumatoid arthritis: a confirmation study. Rheumatology, 42, 4, 528-533. eScholarID:1d5792
• Payton, A, Holland,F., Diggle, P., Rabbitt, P-, Horan, M A, Davidson, YS, Gibbons, LC, Worthington, J, Ollier, WER, Pendleton, N. (2003). Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population. Molecular Psychiatry, 8, 1, 14-18. eScholarID:1d5796
• Payton, A, Turic, D, Langley, K, Mills, S, Lawson, D, Van den Bree, M, Owen, M, O'Donovan, M, Ollier, WER, Worthington, J, Thapar, A. (2003). No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder. Psychiatr Genet, 13( 3), 183-5. eScholarID:1d8104
• Quinnell,R.J., Kennedy, LJ, Barnes, A, Courtenay,O., Dye,C., Garcez,L.M., Shaw,M.A., Carter,S.D., Thomson, W, Ollier, WER. (2003). Susceptibility to visceral leishmaniasis in the domestic dog is associated with MHC class II polymorphism. Immunogenetics, 55, 1, 23-28. eScholarID:1d5800
• DavisonL.J, CatchpoleB, Kennedy LJ, Barnes A, Thomson W, Ollier WER. (2003). Research into canine diabetes mellitus. Vet Rec, 152, 5, 148. eScholarID:17d395
• Gonzalez-Gay M, Garcia-Porrua C, Ollier WER. (2003). Polymyalgia rheumatica and biopsy-proven giant cell arteritis exhibit different HLA-DRB1* associations. J Rheumatol, 30( 12), 2729. eScholarID:17d316
• StricklandP.L, John S, Payton A, Worthington J, Ollier WER, Deakin JFW. (2003). Do genetic polymorphisms of serotonin (5-HT) neurotransmission influence function in humans? American Journal of Medical Genetics, 120A(4), 566-567. eScholarID:17d816

2002

• Alansari,A., Hajeer,A., Teh,L.S., Bayat, A, Hinks, AM, Mysercough,A., Gul,A., Inanc,M., Ordi-Ros,J., Ollier, WER. (2002). Transforming growth factor-12 polymorphism and systemic lupus erythematosus. Journal of Rheumatology, 29, 6, 1189-1191. eScholarID:1d5750
• Amoli MM, Donn RP, Thomson W, HajeerA.H, Garcia-PorruaC, LueiroM, Ollier WER, Gonzalez-GayM.A. (2002). Macrophage migration inhibitory factor gene polymorphism is associated with sarcoidosis in biopsy proven erythema nodosum. Journal of Rheumatology, 29, 8, 1671-1673. eScholarID:1d5834
• Amoli MM, HandS, HajeerA.H, JonesK.P, RolfS, StingC, DaviesB.H, Ollier WER. (2002). Polymorphism in the STAT6 gene encodes risk for nut allergy. Genes Immun, 3, 4, 220-224. eScholarID:1d5762
• Amoli MM, ShelleyE, MatteyD.L, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER, Gonzalez-GayM.A. (2002). Intercellular adhesion molecule-1 gene polymorphisms in isolated polymyalgia rheumatica. Journal of Rheumatology, 29, 3, 502-504. eScholarID:1d5754
• Amoli MM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2002). Henoch-Schonlein purpura and cutaneous leukocytoclastic angiitis exhibit different HLA-DRB1 associations. Journal of Rheumatology, 29, 5, 945-947. eScholarID:1d5822
• Amoli MM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2002). HLA-B35 association with nephritis in Henoch-Schonlein purpura. Journal of Rheumatology, 29, 5, 948-949. eScholarID:1d5824
• Amoli MM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2002). Interleukin 1 receptor antagonist gene polymorphism is associated with severe renal involvement and renal sequelae in Henoch-Schonlein purpura. Journal of Rheumatology, 29, 7, 1404-1407. eScholarID:1d5756
• Amoli MM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2002). Interleukin 8 gene polymorphism is associated with increased risk of nephritis in cutaneous vasculitis. Journal of Rheumatology, 29, 11, 2367-2370. eScholarID:1d5830
• Barton A, Ollier WER. (2002). Genetic approaches to the investigation of rheumatoid arthritis. Current Opinion in Rheumatology, 14, 3, eScholarID:1d5738
• Bayat A, Alansari A, Hajeer AH, Shah M, Watson JS, Stanley JK, Ferguson MW.J, Ollier WER. (2002). Genetic susceptibility in Dupuytren's disease: lack of association of a novel transforming growth factor beta(2) polymorphism in Dupuytren's disease. J Hand Surg [Br], 27(1), 47-9. eScholarID:1d3240
• Bayat A, Bock O, Mrowietz U, Ollier WER, Ferguson M. W. (2002). Genetic susceptibility to keloid disease and transforming growth factor beta 2 polymorphisms. Br J Plast Surg, 55, 4, 283-6. eScholarID:1d3544
• Bayat A, Watson JS, Stanley JK, Alansari A, Shah M, Ferguson MW.J, Ollier WER. (2002). Genetic susceptibility in Dupuytren's disease: TGF-β1 Polymorphisms and Dupuytren's disease. J Bone Joint Surg Br, 84(2), 211-5. eScholarID:1d3238
• Bayat A, WatsonJ.S, StanleyJ.K, FergusonM.W, Ollier WER. (2002). Novel single nucleotide polymorphisms in the 3'-UTR of the TGFbetaRI and TGFbetaRIII genes. European Journal of Immunogenetics, 29, 5, 445-446. eScholarID:1d5768
• BazrafshaniM.R, HajeerA.H, Ollier WER, ThornhillM.H. (2002). IL-1B and IL-6 gene polymorphisms encode significant risk for the development of recurrent aphthous stomatitis (RAS). Genes Immun, 3, 5, 302-305. eScholarID:1d5769
• BazrafshaniM.R, HajeerA.H, Ollier WER, ThornhillM.H. (2002). Recurrent aphthous stomatitis and gene polymorphisms for the inflammatory markers TNF-alpha, TNF-beta and the vitamin D receptor: no association detected. Oral Diseases, 8, 6, 303-307. eScholarID:1d5771
• Donaldson,I.J., Shefta,J., Lawson,C.A., Bushnell,J.R., Morgan,A.W., Isaacs,J.D., Carpenter,D., Shaw,M.A., Rooth,I., Quinnell,R.J., Zumla,A.M., Ollier, WER, Chintu,C.Z., Muyinda,G.P., Hill,A.S., Boylston,A.W. (2002). Unique TCR beta-subunit variable gene haplotypes in Africans. Immunogenetics, 53, 10-11, 884-893. eScholarID:1d5772
• Donn RP, Alourfi Z, De Benedetti F, Meazza C, Zeggini E, Lunt M, Stevens A, Shelley E, Lamb E, Ollier WER, Thomson W, Ray DW. (2002). Mutation screening of the macrophage migration inhibitory factor (MIF) gene: positive association of a functional polymorphism of MIF with juvenile idiopathic arthritis. Arthritis and Rheumatism, 46, 2402-2409. eScholarID:1d2604 | DOI:10.1002/art.10492
• Donn RP, FarhanA, StevansA, RamananA, Ollier WER, Thomson W. (2002). Neuroendocrine gene polymorphisms and susceptibility to juvenile idiopathic arthritis. Rheumatology (Oxford), 41, 8, 930 - 936. eScholarID:1d3743
• Donn RP, ShelleyE, Ollier WER, Thomson W. (2002). Lack of association between juvenile idiopathic arthritis and fas gene polymorphism. Journal of Rheumatology, 29, 1, 166 - 168. eScholarID:1d3649
• Fife,M., Steer,S., Fisher,S., Newton,J., McKay,K., Worthington, J, Shah,C., Polley,A., Rosenthal,A., Ollier, WER, Lewis,C., Wordsworth,P., Lanchbury,J. (2002). Association of familial and sporadic rheumatoid arthritis with a single corticotropin-releasing hormone genomic region (8q12.3) haplotype. Arthritis and Rheumatism, 46, 1, 75-82. eScholarID:1d5643
• Gonzalez-GayM.A, HajeerA.H, DababnehA, Garcia-PorruaC, Amoli MM, Thomson W, Ollier WER. (2002). Corticotropin releasing hormone promoter polymorphisms in giant cell arteritis and polymyalgia rheumatica. Clinical and Experimental Rheumatology, 20, 2, 133-138. eScholarID:1d5774
• Gonzalez-GayM.A, HajeerA.H, DababnehA, Garcia-PorruaC, MatteyD.L, Amoli MM, Thomson W, Ollier WER. (2002). IL-6 promoter polymorphism at position -174 modulates the phenotypic expression of polymyalgia rheumatica in biopsy-proven giant cell arteritis. Clinical and Experimental Rheumatology, 20, 2, 179-184. eScholarID:1d5776
• Gonzalez-GayM.A, HajeerA.H, Garcia-PorruaC, DababnehA, Thomson W, Ollier WER, MatteyD.L. (2002). Patients chosen for treatment with cyclosporine because of severe rheumatoid arthritis are more likely to carry HLA-DRB1 shared epitope alleles, and have earlier disease onset. Journal of Rheumatology, 29, 2, 271-275. eScholarID:1d5777
• Hajeer AH, Fakhoury H, Ollier WER. (2002). Diagnostic molecular techniques in clinical medicine. Middle East Laboratory, 5(3), 6-13. eScholarID:1d9729
• Holmes,J., Payton, A, Barrett,J., Harrington,R., McGuffin,P., Owen,M., Ollier, WER, Worthington, J, Gill,M., Kirley,A., Hawi,Z., Fitzgerald,M., Asherson,P., Curran,S., Mill,J., Gould,A., Taylor,E., Kent,L., Craddock,N., Thapar,A. (2002). Association of DRD4 in children with ADHD and comorbid conduct problems. American Journal of Medical Genetics, 114, 2, 150-153. eScholarID:1d5780
• Kennedy LJ, Barnes A, Happ G, Quinnell R, Courtenay O, Carter S, Ollier WER, Thomson W. (2002). Evidence for extensive DLA polymorphism in different dog populations. Tissue Antigens, 60( 1), 43-52. eScholarID:1d15749
• Kennedy LJ, Ryvar R, Gaskell R. M, Addie D. D, Willoughby K, Carter S. D, Thomson W, Ollier WER, Radford A. D. (2002). Sequence analysis of MHC DRB alleles in domestic cats from the United Kingdom. Immunogenetics, 54, 5, 348-52. eScholarID:1d3536
• Kennedy, LJ, Barnes, A, Happ, G. M., Quinnell, R. J., Bennett, D., Angles, J. M., Day, M. J., Carmichael, N., Innes, J. F., Isherwood, D., Carter, S. D., Thomson, W, Ollier, WER. (2002). Extensive interbreed, but minimal intrabreed, variation of DLA class II alleles and haplotypes in dogs. Tissue Antigens, 59, 3, 194-204. eScholarID:1d3537
• KerrJ.R, MatteyD.L, Thomson W, Poulton K, Ollier WER. (2002). Association of symptomatic acute human parvovirus B19 infection with human leukocyte antigen class I and II alleles. Journal of Infectious Diseases, 186, 4, 447-452. eScholarID:1d5782
• Low,A.S., Gonzalez-Gay,M.A., Akil,M., Amos,R.S., Bax,D.E., Cannings,C., Hajeer,A., Till,S.H., Winfield,J., Ollier, WER, Wilson,A.G. (2002). TNF +489 polymorphism does not contribute to susceptibility to rheumatoid arthritis. Clinical and Experimental Rheumatology, 20, 6, 829-832. eScholarID:1d5784
• MacKay,K., Eyre, SS, Myerscough,A., Milicic,A., Barton, A, Laval,S., Barrett,J., Lee,D., White,S., John, S, Brown,M.A., Bell,J., Silman, AJ, Ollier, WER, Wordsworth,P., Worthington, J. (2002). Whole-genome linkage analysis of rheumatoid arthritis susceptibility loci in 252 affected sibling pairs in the United Kingdom. Arthritis and Rheumatism, 46, 3, 632 - 639. eScholarID:1d3669 | DOI:10.1002/art.10147
• Massa,M., Mazzoli,F., Pignatti,P., De Benedetti,F., Passalia,M., Viola,S., Samodal,R., La Cava,A., Giannoni,F., Ollier, WER, Martini,A., Albani,S. (2002). Proinflammatory responses to self HLA epitopes are triggered by molecular mimicry to Epstein-Barr virus proteins in oligoarticular juvenile idiopathic arthritis. Arthritis and Rheumatism, 46, 10, 2721-2729. eScholarID:1d5785
• MatteyD.L, DawesP.T, ClarkeS, FisherJ, BrownfieldA, Thomson W, HaajeerA.H, Ollier WER. (2002). Relationship among the HLA-DRB1 shared epitope, smoking, and rheumatoid factor production in rheumatoid arthritis. Arthritis and Rheumatism, 47, 4, 403-407. eScholarID:1d5789
• MatteyD.L, DawesP.T, FisherJ, BrownfieldA, ThomsonW, HajeerA.H, Ollier WER. (2002). Nodular disease in rheumatoid arthritis: association with cigarette smoking and HLA-DRB1/TNF gene interaction. Journal of Rheumatology, 29, 11, 2313-2318. eScholarID:1d5788
• McGinnis,R., Child,F., Clayton,S., Davies,S., Lenney,W., Illig,T., Wjst,M., Spurr,N., Debouck,C., Hajeer,A.H., Ollier, WER, Strange,R., Fryer,A.A. (2002). Further support for the association of CCR5 allelic variants with asthma susceptibility. European Journal of Immunogenetics, 29, 6, 525-528. eScholarID:1d5791
• Pendleton N, Payton A, van den Boogerd EH, Holland F, Diggle P, Rabbitt PM, Horan M A, Worthington J, Ollier WER. (2002). Apolipoprotein E genotype does not predict decline in intelligence in healthy older adults. Neuroscience Letters, 324(1), 74-6. eScholarID:1d2377
• Thomson W, BarrettJ.H, Donn RP, PepperL, Kennedy LJ, Ollier WER, Silman AJ, WooP, SouthwoodT. (2002). Juvenile idiopathic arthritis classified by the ILAR criteria: HLA associations in UK patients. Rheumatology (Oxford), 41, 10, 1183-1189. eScholarID:1d5948
• VencovskyJ, Zd'arskyE, MoyesS.P, HajeerA, RuzickovaS, CimburekZ, Ollier WER, MainiR.N, MageedR.A. (2002). Polymorphism in the immunoglobulin VH gene V1-69 affects susceptibility to rheumatoid arthritis in subjects lacking the HLA-DRB1 shared epitope. Rheumatology (Oxford), 41, 4, 401-410. eScholarID:1d5802
• Zeggini E, Donn RP, Ollier WER, Thomson W. (2002). Evidence for linkage of HLA loci in juvenile idiopathic oligoarthritis: independent effects of HLA-A and HLA-DRB1. Arthritis and Rheumatism, 46, 10, 2716-2720. eScholarID:1d5842
• Zeggini E, Thomson W, AlansariA, Ollier WER, Donn RP, British Paediatric Rheumatology Study Group. (2002). Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritis. Rheumatology (Oxford), 41, 4, 462 - 465. eScholarID:1d3698
• Zeggini E, Thomson W, KwiatkowskiD, RichardsonA, Ollier WER, Donn RP. (2002). Linkage and association studies of single-nucleotide polymorphism-tagged tumor necrosis factor haplotypes in juvenile oligoarthritis. Arthritis and Rheumatism, 46, 12, 3304-3311. eScholarID:1d5844
• Amoli MM, AlansariA, El MagadmiM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2002). Lack of association between A561C E-selectin polymorphism and large and small-sized blood vessel vasculitides. Clinical and Experimental Rheumatology, 20, 4, 575-576. eScholarID:17d146
• Gonzalez-GayM.A, Di GiovineF.S, SilvestriT, Amoli MM, Garcia-PorruaC, Thomson W, Ollier WER, HajeerA.H. (2002). Lack of association between IL-1 cluster and TNF-alpha gene polymorphisms and giant cell arteritis. Clinical and Experimental Rheumatology, 20, 3, 431. eScholarID:17d900

2001

• Alansari A, Hajeer A. H, Bayat A, Eyre SS, Carthy D, Ollier WER. (2001). Two novel polymorphisms in the human transforming growth factor beta 2 gene. Genes Immun, 2, 5, 295-6. eScholarID:1d3543
• Amoli MM, MatteyD.L, CalvinoM.C, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER, Gonzalez-GayM.A. (2001). Polymorphism at codon 469 of the intercellular adhesion molecule-1 locus is associated with protection against severe gastrointestinal complications in Henoch-Schonlein purpura. Journal of Rheumatology, 28, 5, 1014-1018. eScholarID:1d5760
• Amoli MM, ShelleyE, MatteyD.L, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER, Gonzalez-GayM.A. (2001). Lack of association between intercellular adhesion molecule-1 gene polymorphisms and giant cell arteritis. Journal of Rheumatology, 28, 7, 1600-1604. eScholarID:1d5832
• Amoli MM, Thomson W, HajeerA.H, CalvinoM.C, Garcia-PorruaC, Ollier WER, Gonzalez-GayM.A. (2001). HLA-DRB1*01 association with Henoch-Schonlein purpura in patients from northwest Spain. Journal of Rheumatology, 28, 6, 1266-1270. eScholarID:1d5828
• Amoli MM, Thomson W, HajeerA.H, Garcia-PorruaC, LueiroM, Ollier WER, Gonzalez-GayM.A. (2001). HLA-DRB1 associations in biopsy proven erythema nodosum. Journal of Rheumatology, 28, 12, 2660-2662. eScholarID:1d5826
• Barton A, John S, Ollier WER, Silman AJ, Worthington J. (2001). Association between rheumatoid arthritis and polymorphism of tumor necrosis factor receptor II, but not tumor necrosis factor receptor I, in Caucasians. Arthritis and Rheumatism, 44, 1, 61 - 65. eScholarID:1d3737
• Barton, A, Eyre, SS, Myerscough,A., Brintnell,B., Ward,D., Ollier, WER, Lorentzen,J.C., Klareskog,L., Silman, AJ, John, S, Worthington, J, The Arthritis Rheumatism Campaign National Repository. (2001). High resolution linkage and association mapping identifies a novel rheumatoid arthritis susceptibility locus homologous to one linked to two rat models of inflammatory arthritis. Human Molecular Genetics, 10 (18), 1901 - 1906. eScholarID:1d3624 | DOI:10.1093/hmg/10.18.1901
• Crosdale D, Poulton K, Ollier WER, Thomson W, Denning DW. (2001). Mannose binding lectin gene polymorphisms as a susceptibility factor for chronic necrotisng pulmonary aspergillosis. J Infect Dis, 184, 5, 653-656. eScholarID:1d4449
• Donn RP, ShelleyE, Ollier WER, Thomson W, British Paediatric Rheumatology Study Group. (2001). A novel 5'-flanking region polymorphism of macrophage migration inhibitory factor is associated with systemic-onset juvenile idiopathic arthritis. Arthritis and Rheumatism, 44, 8, 1782 - 1785. eScholarID:1d3651 | DOI:10.1002/1529-0131(200108)44:8<1782::AID-ART314>3.0.CO;2-#
• Donn, RP, Barrett,J.H., Farhan,A., Stopford,A., Pepper,L., Shelley,E., Davies,N., Ollier, WER, Thomson, W, British Paediatric Rheumatology Study Group. (2001). Cytokine gene polymorphisms and susceptibility to juvenile idiopathic arthritis. Arthritis and Rheumatism, 44, 4, 802 - 810. eScholarID:1d3650 | DOI:10.1002/1529-0131(200104)44:4<802::AID-ANR136>3.0.CO;2-G
• Gonzalez-GayM.A, HajeerA.H, DababnehA, MakkiR, Garcia-PorruaC, Thomson W, Ollier WER. (2001). Seronegative rheumatoid arthritis in elderly and polymyalgia rheumatica have similar patterns of HLA association. Journal of Rheumatology, 28, 1, 122-125. eScholarID:1d5778
• GulA, HajeerA.H, Worthington J, BarrettJ.H, Ollier WER, Silman AJ. (2001). Evidence for linkage of the HLA-B locus in Behcet's disease, obtained using the transmission disequilibrium test. Arthritis and Rheumatism, 44, 1, 239-240. eScholarID:1d5645
• GulA, HajeerA.H, Worthington J, Ollier WER, Silman AJ, Silman AJ. (2001). Linkage mapping of a novel susceptibility locus for Behcet's disease to chromosome 6p22-23. Arthritis and Rheumatism, 44, 11, 2693-2696. eScholarID:1d5647
• John S, Eyre SS, MyerscoughA, BarrettJ, Silman AJ, Ollier WER, Worthington J. (2001). Linkage and association analysis of candidate genes in rheumatoid arthritis. Journal of Rheumatology, 28, 8, 1752-1755. eScholarID:1d3555
• Kennedy, LJ, Angles, J, Barnes, A, Carter, S, Francino, O, Gerlach, J, Happ, G, Ollier, WER, Thomson, W, Wagner, J. (2001). Nomenclature for factors of the dog major histocompatibility system (DLA), 2000: second report of the ISAG DLA Nomenclature Committee. Anim Genet, 32(4), eScholarID:1d15802
• MatteyD.L, DawesP.T, Gonzalez-GayM.A, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER. (2001). HLA-DRB1 alleles encoding an aspartic acid at position 70 protect against development of rheumatoid arthritis. Journal of Rheumatology, 28, 2, 232-239. eScholarID:1d5786
• MatteyD.L, Gonzalez-GayM.A, Garcia-PorruaC, Thomson W, HajeerA.H, Ollier WER. (2001). Influence of HLA-DRB1 and TNF microsatellite polymorphisms on the expression of extraarticular manifestations in rheumatoid arthritis patients from northwest Spain. Clinical and Experimental Rheumatology, 19, 6, 703-708. eScholarID:1d5787
• MatteyD.L, HassellA.B, DawesP.T, CheungN.T, Poulton K, Thomson W, HajeerA.H, Ollier WER. (2001). Independent association of rheumatoid factor and the HLA-DRB1 shared epitope with radiographic outcome in rheumatoid arthritis. Arthritis and Rheumatism, 44, 7, 1529-1533. eScholarID:1d5838
• MatthiasC, JahnkeV, HajeerA, Ollier WER, FryerA.A, StrangeR.C. (2001). Influence of genetic variation in the major histocompatibility complex on head and neck cancer susceptibility. Laryngorhinootologie, 80, 10, 595-600. eScholarID:1d5790
• MuldoonJ, UrielA, KhooS, Ollier WER, HajeerA.H. (2001). Novel IFN-alpha receptor promoter polymorphisms. Genes Immun, 2, 3, 159-160. eScholarID:1d5793
• Ollier WER, HarrisonB, SymmonsD. (2001). What is the natural history of rheumatoid arthritis? Best Pract Res Clin Rheumatol, 15, 1, 27-48. eScholarID:1d5794
• Ollier WER, Kennedy LJ, Thomson W, Barnes A, BellS.C, BennettD, AnglesJ.M, InnesJ.F, CarterS.D. (2001). Dog MHC alleles containing the human RA shared epitope confer susceptibility to canine rheumatoid arthritis. Immunogenetics, 53, 8, 669-673. eScholarID:1d5840
• Payton, A, Holmes,J., Barrett,J.H., Hever,T., Fitzpatrick,H., Trumper,A.L., Harrington,R., McGuffin,P., O'Donovan,M., Owen,M., Ollier, WER, Worthington, J, Thapar,A. (2001). Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. American Journal of Medical Genetics, 105, 5, 464-470. eScholarID:1d5797
• Payton, A, Holmes,J., Barrett,J.H., Sham,P., Harrington, R, McGuffin,P., Owen,M., Ollier, WER, Worthington, J, Thapar,A. (2001). Susceptibility genes for a trait measure of attention deficit hyperactivity disorder: a pilot study in a non-clinical sample of twins. Psychiatry Research, 105, 3, 273-278. eScholarID:1d5799
• Stevens F, Ray DW, Alansari A, Hajeer A, Thomson W, Donn RP, Ollier WER, Worthington J, Davis JRE. (2001). Characterization of a prolactin gene polymorphism and its associations with systemic lupus erythematosus. Arthritis Rheum, 44( 10), 2358-66. eScholarID:1d15733
• Vencovsky,J., Jarosova,K., Ruzickova,S., Nemcova,D., Niederlova,J., Ozen,S., Alikasifoglu,M., Bakkaloglu,A., Ollier, WER, Mageed,R.A. (2001). Higher frequency of allele 2 of the interleukin-1 receptor antagonist gene in patients with juvenile idiopathic arthritis. Arthritis and Rheumatism, 44, 10, 2387-2391. eScholarID:1d5801
• Villarreal, J., Crosdale, D., Ollier, WER, Hajeer, A., Thomson, W, Ordi, J., Balada, E., Villardell, M., Teh, L. S., Poulton, K. (2001). Mannose binding lectin and FcgammaRIIa (CD32) polymorphism in Spanish systemic lupus erythematosus patients. Rheumatology (Oxford), 40, 9, 1009-12. eScholarID:1d3535
• Weatherby,S.J., Thomson, W, Pepper,L., Donn, RP, Worthington, J, Mann,C.L., Davies,M.B., Fryer,A.A., Boggild,M.D., Young,C.A., Jones,P.W., Strange,R.C., Ollier, WER, Hawkins,C.P. (2001). HLA-DRB1 and disease outcome in multiple sclerosis. Journal of Neurology, 248, 4, 304-310. eScholarID:1d5652
• AlansariA.S, HajeerA.H, Garcia-PorruaC, Thomson W, Ollier WER, Gonzalez-GayM.A. (2001). HLA-DRB1 associations in systemic lupus erythematosus patients from northwest Spain. Clinical and Experimental Rheumatology, 19, 3, 352. eScholarID:17d815

2000

• al AnsariA.S, Ollier WER, VillarrealJ, OrdiJ, TehL.S, HajeerA.H. (2000). Tumor necrosis factor receptor II (TNFRII) exon 6 polymorphism in systemic lupus erythematosus. Tissue Antigens, 55, 1, eScholarID:1d22728
• AmoliM, Ollier WER, HajeerA.H. (2000). A novel PCR-RFLP assay for the detection of a polymorphism in the 3' of STAT6 gene. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 1, 5, eScholarID:1d22729
• BaerwaldC.G, MokC.C, TicklyM, LauC.S, WordsworthB.P, Ollier WER, PanayiG.S, LanchburyJ.S. (2000). Corticotropin releasing hormone (CRH) promoter polymorphisms in various ethnic groups of patients with rheumatoid arthritis. Zeitschrift fur Rheumatologie, 59, 1, eScholarID:1d21932
• BarrettJ.H, ThomsonW, Ollier WER, Bidwell JL, NavarreteC. (2000). HLA and disease association studies - statistical considerations. Histocompatibility testing, eScholarID:1d22730
• Barton A, MyerscoughA, John S, Gonzalez-GayM, Ollier WER, Worthington J. (2000). A single nucleotide polymorphism in exon 1 of cytotoxic T-lymphocyte-associated-4 (CTLA-4) is not associated with rheumatoid arthritis. Rheumatology, 39, 1, 63 - 66. eScholarID:1d3622
• BartonA, WorthingtonJ, Ollier WER. (2000). Syntenic mapping of human disease genes using animal models of autoimmunity. GeneScreen, 1, 1, eScholarID:1d22731
• BazrafshaniM.R, Ollier WER, HajeerA.H. (2000). A novel PCR-RFLP assay for the detection of the single nucleotide polymorphism at position -1082 in the human IL-10 gene promoter. European Journal of Immunogenetics, 27, 3, eScholarID:1d22732
• CheungN.T, DawesP.T, PoultonK.V, Ollier WER, TaylorD.J, MatteyD.L. (2000). High serum levels of pro-matrix metalloproteinase-3 are associated with greater radiographic damage and the presence of the shared epitope in patients with rheumatoid arthritis. Journal of Rheumatology, 27, 4, eScholarID:1d22733
• CraddockT.P, ZumlaA.M, Ollier WER, ChintuC.Z, MuyindaG.P, LancasterF.C, BoylstonA.W. (2000). Predominance of one T-cell antigen receptor BV haplotype in African populations. Immunogenetics, 51, 3, eScholarID:1d21933
• Crosdale D. J, Ollier WER, Thomson W, Philip Dyer, Jensenious J, Johnson R. W, Poulton K. (2000). Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids. Eur J Immunogenet, 27, 3, 111-7. eScholarID:1d21928
• FifeM.S, FisherS.A, John S, Worthington J, ShahC.J, Ollier WER, PanayiG.S, LewisC.M, LanchburyJ.S. (2000). Multipoint linkage analysis of a candidate gene locus in rheumatoid arthritis demonstrates significant evidence of linkage and association with the corticotropin-releasing hormone genomic region. Arthritis and Rheumatism, 43, 8, 1673 - 1678. eScholarID:1d3549
• Fryer,A.A., Spiteri,M.A., Bianco,A., Hepple,M., Jones,P.W., Strange,R.C., Makki,R., Tavernier,G., Smilie,F.I., Custovic, A, Woodcock,A.A., Ollier, WER, Hajeer,A.H. (2000). The -403 G-->A promoter polymorphism in the RANTES gene is associated with atopy and asthma. Genes Immun, 1, 8, eScholarID:1d21935
• Gonzalez-Gay,M.A., Garcia-Porrua,C., Llorca,J., Hajeer,A.H., Branas,F., Dababneh,A., Gonzalez-Louzao,C., Rodriguez-Gil,E., Rodriguez-Ledo,P., Ollier, WER. (2000). Visual manifestations of giant cell arteritis. Trends and clinical spectrum in 161 patients. Histocompatibility testing, 79, 5, eScholarID:1d22734
• Gonzalez-GayM.A, Garcia-PorruaC, HajeerA.H, DababnehA, Ollier WER. (2000). HLA-DRB1*04 may be a marker of severity in giant cell arteritis. Annals of the Rheumatic Diseases, 59, 7, eScholarID:1d22735
• Hajeer A. H, Dababneh A, Makki R. F, Thomson W, Poulton K, Gonzalez-Gay M. A, Garcia-Porrua C, Mattey D. L, Ollier WER. (2000). Different gene loci within the HLA-DR and TNF regions are independently associated with susceptibility and severity in Spanish rheumatoid arthritis patients. Tissue Antigens, 55, 4, 319-25. eScholarID:1d21929
• Hajeer,A.H., Lear,J.T., Ollier, WER, Naves,M., Worthington,J., Bell,D.A., Smith,A.G., Bowers,W.P., Jones,P.W., Strange,R.C., Fryer,A.A. (2000). Preliminary evidence of an association of tumour necrosis factor microsatellites with increased risk of multiple basal cell carcinomas. British Journal of Dermatology, 142, 3, eScholarID:1d22736
• Hall,M.A., McGlinn,E., Coakley,G., Fisher,S.A., Boki,K., Middleton,D., Kaklamani,E., Moutsopoulos,H., Loughran,T.P.,Jr., Ollier, WER, Panayi,G.S., Lanchbury,J.S. (2000). Genetic polymorphism of IL-12 p40 gene in immune-mediated disease. Histocompatibility testing, 1, 3, eScholarID:1d22737
• Holmes J, Payton, A, Barrett J H, Hever T, Fitzpatrick H, Trumper A L, Harrington, R, McGuffin P, Owen M, Ollier, WER, Worthington J, Thapar A. (2000). A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder. Molecular Psychiatry, 5, 523-530. eScholarID:1d23950
• Kennedy LJ, Carter S, Barnes A, Bell S, Bennett D, Ollier WER, Thomson W. (2000). DLA-DQA1 polymorphisms in dogs defined by sequence-specific oligonucleotide probes (SSOP). Tissue Antigens, 55( 3), eScholarID:1d21693
• Kennedy LJ, Hall L, Carter S, Barnes A, Bell S, Bennett D, Ollier WER, Thomson W. (2000). Identification of further DLA-DRB1 and DQA1 alleles in the dog. Eur J Immunogenet, 27( 1), eScholarID:1d21692
• Kennedy, LJ, Altet, L, Angles, J, Barnes, A, Carter, S, Francino, O, Gerlach, J, Happ, G, Ollier, WER, Polvi, A, Thomson, W, Wagner, J. (2000). Nomenclature for factors of the dog major histocompatibility system (DLA), 1998: first report of the ISAG DLA Nomenclature Committee. Anim Genet, 31( 1), eScholarID:1d21694
• Kennedy,L.J., Altet,L., Angles,J.M., Barnes,A., Carter,S.D., Francino,O., Gerlach,J.A., Happ,G.M., Ollier, WER, Polvi,A., Thomson,W., Wagner,J.L. (2000). Nomenclature for factors of the dog major histocompatibility system (DLA), 1998: first report of the ISAG DLA Nomenclature Committee. Histocompatibility testing, 31, 1, eScholarID:1d22739
• KennedyL.J, CarterS.D, BarnesA, BellS, BennettD, Ollier WER, ThomsonW. (2000). DLA-DQA1 polymorphisms in dogs defined by sequence-specific oligonucleotide probes (SSOP). Tissue Antigens, 55, 3, eScholarID:1d22738
• MakkiR.F, al SharifF, Gonzalez-GayM.A, Garcia-PorruaC, Ollier WER, HajeerA.H. (2000). RANTES gene polymorphism in polymyalgia rheumatica, giant cell arteritis and rheumatoid arthritis. Clinical and Experimental Rheumatology, 18, 3, eScholarID:1d22740
• MatteyD.L, Gonzalez-GayM.A, HajeerA.H, DababnehA, ThomsonW, Garcia-PorruaC, Ollier WER. (2000). Association between HLA-DRB1*15 and secondary Sjogren's syndrome in patients with rheumatoid arthritis. Journal of Rheumatology, 27, 11, eScholarID:1d22741
• MatteyD.L, HajeerA.H, DababnehA, ThomsonW, Gonzalez-GayM.A, Garcia-PorruaC, Ollier WER. (2000). Association of giant cell arteritis and polymyalgia rheumatica with different tumor necrosis factor microsatellite polymorphisms. Arthritis and Rheumatism, 43, 8, eScholarID:1d22742
• McDermott,D.H., Beecroft,M.J., Kleeberger,C.A., Al Sharif,F.M., Ollier, WER, Zimmerman,P.A., Boatin,B.A., Leitman,S.F., Detels,R., Hajeer,A.H., Murphy,P.M. (2000). Chemokine RANTES promoter polymorphism affects risk of both HIV infection and disease progression in the Multicenter AIDS Cohort Study. AIDS, 14, 17, eScholarID:1d22743
• MyerscoughA, John S, BarrettJ.H, Ollier WER, Worthington J. (2000). Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci. Arthritis and Rheumatism, 43, 12, 2771 - 2775. eScholarID:1d3679
• Ollier WER. (2000). Rheumatoid arthritis and Epstein-Barr Virus: a case of living with the enemy? Annals of the Rheumatic Diseases, 59, 7, eScholarID:1d22744
• Ollier WER. (2000). Role of interferon-gamma gene in rheumatoid arthritis? Lancet, 356, 9232, eScholarID:1d22745
• SusolE, MacGregorA.J, BarrettJ.H, WilsonH, BlackC, WelshK, Silman AJ, Ollier WER, Worthington J. (2000). A two-stage, genome-wide screen for susceptibility loci in primary Raynaud's phenomenon. Arthritis and Rheumatism, 43, 7, 1641 - 1646. eScholarID:1d3685
• SusolE, RandsA.L, HerrickA, McHughN, BarrettJ.H, Ollier WER, Worthington J. (2000). Association of markers for TGFbeta3, TGFbeta2 and TIMP1 with systemic sclerosis. Rheumatology, 39, 12, 1332 - 1336. eScholarID:1d3739
• Weatherby,S.J., Mann,C.L., Davies,M.B., Carthy,D., Fryer,A.A., Boggild,M.D., Young,C., Strange,R.C., Ollier, WER, Hawkins,C.P. (2000). Polymorphisms of apolipoprotein E; outcome and susceptibility in multiple sclerosis. Multiple Sclerosis, 6, 1, eScholarID:1d22746

1999

• al SharifF, Ollier WER, HajeerA.H. (1999). A rare polymorphism at position -28 in the human RANTES promoter. European Journal of Immunogenetics, 26, 5, eScholarID:1d22716
• Al SharifF.M, MakkiR.F, Ollier WER, HajeerA.H. (1999). A new microsatellite marker within the promoter region of the MIP-1A gene. Immunogenetics, 49, 7-8, eScholarID:1d22717
• Cox,A., Camp,N.J., Cannings,C., di Giovine,F.S., Dale,M., Worthington, J, John, S, Ollier, WER, Silman, AJ, Duff,G.W. (1999). The Combined sib-TDT and TDT provide evidence for linkage of the interleukin-1 gene cluster to erosive rheumatoid arthritis. Human Molecular Genetics, 8, 9, eScholarID:1d3547
• DonnR.P, FarhanA.J, BarrettJ.H, ThomsonW, WorthingtonJ, Ollier WER. (1999). Absence of association between interleukin 1 alpha and oligoarticular juvenile chronic arthritis in UK patients. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 38, 2, eScholarID:1d22718
• FRA Stevens, A Hajeer, John S, W Thompson, J Worthington, Davis JRE, Ollier WER. (1999). The Bgll polymorphism of the human prolactin gene lies within intron C and can be detected by PCR/RFLP. European Journal of Immunogenetics, 26, 261-263. eScholarID:1d25192
• Gonzalez-GayM.A, Garcia-PorruaC, HajeerA, Ollier WER. (1999). Can HLA-DR explain the varying frequency of synovitis in polymyalgia rheumatica? Comment on the article by Salvarani et al. Arthritis and Rheumatism, 42, 7, eScholarID:1d22719
• Gonzalez-GayM.A, Garcia-PorruaC, Vazquez-CarunchoM, DababnehA, HajeerA, Ollier WER. (1999). The spectrum of polymyalgia rheumatica in northwestern Spain: incidence and analysis of variables associated with relapse in a 10 year study. Journal of Rheumatology, 26, 6, eScholarID:1d21936
• HajeerA.H, al SharifF, Ollier WER. (1999). A polymorphism at position -403 in the human RANTES promoter. European Journal of Immunogenetics, 26, 5, eScholarID:1d22720
• John S, MyerscoughA, Eyre SS, RobyP, HajeerA, Silman AJ, Ollier WER, Worthington J. (1999). Linkage of a marker in intron D of the estrogen synthase locus to rheumatoid arthritis. Arthritis and Rheumatism, 42, 8, eScholarID:1d3553
• JonesF.I, RamachandranS, LearJ, SmithA, BowersB, Ollier WER, JonesP, FryerA.A, StrangeR.C. (1999). The melanocyte stimulating hormone receptor polymorphism: association of the V92M and A294H alleles with basal cell carcinoma. Clinica Chimica Acta, 282, 1-2, eScholarID:1d22721
• Kennedy LJ, Carter S. D, Barnes A, Bell S, Bennett D, Ollier WER, Thomson W. (1999). Interbreed variation of DLA-DRB1, DQA1 alleles and haplotypes in the dog. Vet Immunol Immunopathol, 69, 2-4, 101-11. eScholarID:1d3539
• Kennedy,L.J., Altet,L., Angles,J.M., Barnes,A., Carter,S.D., Francino,O., Gerlach,J.A., Happ,G.M., Ollier, WER, Polvi,A., Thomson,W., Wagner,J.L. (1999). Nomenclature for factors of the dog major histocompatibility system (DLA), 1998. First report of the ISAG DLA Nomenclature Committee. International Society for Animals Genetics. Tissue Antigens, 54, 3, eScholarID:1d22722
• Mattey,D.L., Hassell,A.B., Plant,M.J., Cheung,N.T., Dawes,P.T., Jones,P.W., Thomson,W., Poulton,K.V., Hajeer,A.H., Ollier, WER. (1999). The influence of HLA-DRB1 alleles encoding the DERAA amino acid motif on radiological outcome in rheumatoid arthritis. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 38, 12, eScholarID:1d22725
• MatteyD.L, HassellA.B, DawesP.T, Ollier WER, HajeerA. (1999). Interaction between tumor necrosis factor microsatellite polymorphisms and the HLA-DRB1 shared epitope in rheumatoid arthritis: influence on disease outcome. Arthritis and Rheumatism, 42, 12, eScholarID:1d22724
• MatteyD.L, HassellA.B, PlantM, DawesP.T, Ollier WER, JonesP.W, FryerA.A, AllderseaJ.E, StrangeR.C. (1999). Association of polymorphism in glutathione S-transferase loci with susceptibility and outcome in rheumatoid arthritis: comparison with the shared epitope. Annals of the Rheumatic Diseases, 58, 3, eScholarID:1d22723
• Ollier WER, WinchesterR. (1999). The germline and somatic genetic basis for rheumatoid arthritis. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 1, eScholarID:1d22726
• PickardC, MannC, SinnottP, BoggildM, HawkinsC, StrangeR.C, HutchinsonI.V, Ollier WER, DonnR.P. (1999). Interleukin-10 (IL10) promoter polymorphisms and multiple sclerosis. Journal of Neuroimmunology, 101, 2, eScholarID:1d22727

1998

• CoakleyG, MokC.C, HajeerA.H, Ollier WER, TurnerD, SinnottP.J, HutchinsonI.V, PanayiG.S, LanchburyJ.S. (1998). Interleukin-10 promoter polymorphisms in rheumatoid arthritis and Felty's syndrome. British Journal of Rheumatology, 37, 9, eScholarID:1d22699
• DababnehA, Gonzalez-GayM.A, Garcia-PorruaC, HajeerA, ThomsonW, Ollier WER. (1998). Giant cell arteritis and polymyalgia rheumatica can be differentiated by distinct patterns of HLA class II association. Journal of Rheumatology, 25, 11, eScholarID:1d22700
• DaviesE.J, TiklyM, WordsworthB.P, Ollier WER. (1998). Mannose-binding protein gene polymorphism in South African systemic lupus erythematosus. British Journal of Rheumatology, 37, 4, eScholarID:1d22701
• GhodsiK, TaylorG.M, GokhaleD.A, DeardenS, StevensR.F, BirchJ.M, FergussonW.D, EdenO.B, Ollier WER. (1998). Lack of association between childhood common acute lymphoblastic leukaemia and an HLA-C locus dimorphism influencing the specificity of natural killer cells. British Journal of Haematology, 102, 5, eScholarID:1d22702
• HajeerA.H, LazarusM, TurnerD, MageedR.A, VencovskyJ, SinnottP, HutchinsonI.V, Ollier WER. (1998). IL-10 gene promoter polymorphisms in rheumatoid arthritis. Scandinavian Journal of Rheumatology, 27, 2, eScholarID:1d22703
• Ichii-Jones,F., Lear,J.T., Heagerty,A.H., Smith,A.G., Hutchinson,P.E., Osborne,J., Bowers,B., Jones,P.W., Davies,E., Ollier, WER, Thomson,W., Yengi,L., Bath,J., Fryer,A.A., Strange,R.C. (1998). Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 111, 2, eScholarID:1d22704
• JohnS, KormanY, Ollier WER, WorthingtonJ. (1998). Integrated microsatellite markers suitable for genetic studies of cytokine genes. Cytokine, 10, 6, eScholarID:1d22705
• JohnS, MyerscoughA, MarlowA, HajeerA, SilmanA, Ollier WER, WorthingtonJ. (1998). Linkage of cytokine genes to rheumatoid arthritis. Evidence of genetic heterogeneity. Annals of the Rheumatic Diseases, 57, 6, eScholarID:1d22706
• JohnS, TurnerD, DonnR, SinnottP, WorthingtonJ, Ollier WER, HutchinsonI.V, HajeerA.H. (1998). Two novel biallelic polymorphisms in the IL-2 gene. European Journal of Immunogenetics, 25, 6, eScholarID:1d22707
• KennedyL.J, CarterS.D, BarnesA, BellS, BennettD, Ollier WER, ThomsonW. (1998). Nine new dog DLA-DRB1 alleles identified by sequence-based typing. Immunogenetics, 48, 4, eScholarID:1d22708
• KollintzaA, WorthingtonJ, JohnS, Ollier WER, HajeerA.H. (1998). A new polymorphism in the promoter of the interleukin 5 receptor alpha subunit (IL-5RA) gene. Immunogenetics, 48, 1, eScholarID:1d22709
• MatthiasC, JahnkeV, FryerA, StrangeR, Ollier WER, HajeerA. (1998). Influence of tumour necrosis factor microsatellite polymorphisms on susceptibility to head and neck cancer. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 118, 2, eScholarID:1d22710
• Naves,M., Hajeer,A.H., Teh,L.S., Davies,E.J., Ordi-Ros,J., Perez-Pemen,P., Vilardel-Tarres,M., Thomson,W., Worthington,J., Ollier, WER. (1998). Complement C4B null allele status confers risk for systemic lupus erythematosus in a Spanish population. European Journal of Immunogenetics, 25, 4, eScholarID:1d22711
• PlantM.J, JonesP.W, SaklatvalaJ, Ollier WER, DawesP.T. (1998). Patterns of radiological progression in early rheumatoid arthritis: results of an 8 year prospective study. Journal of Rheumatology, 25, 3, eScholarID:1d22712
• PoultonK.V, KennedyL.J, RossJ, ThomsonW, MbanyaJ.C, Ollier WER. (1998). A study of HLA-DPB1 phenotypes reveals DPB1*6301 in a rural population from Cameroon. European Journal of Immunogenetics, 25, 5, eScholarID:1d22713
• StanworthS.J, DonnR.P, HassallA, DawesP, Ollier WER, SnowdenN. (1998). Absence of an association between mannose-binding lectin polymorphism and rheumatoid arthritis. British Journal of Rheumatology, 37, 2, eScholarID:1d22714
• TarassiK, CarthyD, PapasteriadesC, BokiK, NikolopoulouN, CarcassiC, Ollier WER, HajeerA.H. (1998). HLA-TNF haplotype heterogeneity in Greek SLE patients. Clinical and Experimental Rheumatology, 16, 1, eScholarID:1d22715

1997

• AH Hajeer, J Worthington, EJ Davies, Hillarby M, Poulton K, Ollier WER. (1997). TNF microsatellite A2, B3 and D2 alleles are associated with systemic lupus erythematosus. Tissue Antigens, 49, 222-227. eScholarID:1d25563
• CarterS.D, Ollier WER, BennettD. (1997). Canine immunogenetics and autoimmune diseases. Veterinary Record, 141, eScholarID:1d22674
• EJ Davies, LS Teh, J Ordiros, N Snowden, Hillarby, M, A Hajeer, Donn, RP, P Perez-Pemen, M Vilardell-Tarres, Ollier, WER. (1997). A dysfunctional allele of the mannose binding protein gene associates with systemic lupus erythematosus in a Spanish population. Journal of Rheumatology, 24, 485-488. eScholarID:1d25565
• Hajeer,A., John,S., Ollier, WER, Silman,A.J., Dawes,P., Hassell,A., Mattey,D., Fryer,A., Strange,R., Worthington,J. (1997). Tumor necrosis factor microsatellite haplotypes are different in male and female patients with RA. Journal of Rheumatology, 24, 1, eScholarID:1d22675
• HajeerA.H, WorthingtonJ, SilmanA.J, Ollier WER. (1997). Tumor necrosis factor a microsatellite polymorphism in rheumatoid arthritis:reply to the letter by Perdriger et al. Arthritis and Rheumatism, 40, eScholarID:1d22676
• HarrisonB.J, ThomsonW, PepperL, Ollier WER, ChakravartyK, BarrettE.M, SilmanA.J, SymmonsD.P. (1997). Patients who develop inflammatory polyarthritis (IP) after immunization are clinically indistinguishable from other patients with IP. British Journal of Rheumatology, 36, 3, eScholarID:1d22677
• Hay,C.R., Ollier, WER, Pepper,L., Cumming,A., Keeney,S., Goodeve,A.C., Colvin,B.T., Hill,F.G., Preston,F.E., Peake,I.R. (1997). HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party. Thrombosis and Haemostasis, 77, 2, eScholarID:1d22678
• JohnS, HajeerA, MarlowA, MyerscoughA, SilmanA.J, Ollier WER, WorthingtonJ. (1997). Investigation of candidate disease susceptibility genes in rheumatoid arthritis: principles and strategies. Journal of Rheumatology, 24, 1, eScholarID:1d22680
• JohnS, MarlowA, HajeerA, Ollier WER, SilmanA, WorthingtonJ. (1997). Linkage and association studies of the natural resistance associated macrophage protein 1 (NRAMP1) locus in rheumatoid arthritis. Journal of Rheumatology, 24, 3, eScholarID:1d22679
• Kennedy,L.J., Poulton,K.V., Thomson,W., Williams,F., Middleton,D., Howell,W.M., Tarassi,K., Papasteriades,C., Albert,E., Fleischhauer,K., Chandanayingyong,D., Tiercy,J.M., Juji,T., Tokunaga,K., Ollier, WER, Charron,D. (1997). HLA Class I DNA typing using sequence specific oligonucleotide probes (SSOP). HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 1, eScholarID:1d22681
• KhooS.H, PepperL, SnowdenN, HajeerA.H, VallelyP, WilkinsE.G, MandalB.K, Ollier WER. (1997). Tumour necrosis factor c2 microsatellite allele is associated with the rate of HIV disease progression. AIDS, 11, 4, eScholarID:1d22682
• La Cava,A., Nelson,J.L., Ollier, WER, MacGregor,A., Keystone,E.C., Thorne,J.C., Scavulli,J.F., Berry,C.C., Carson,D.A., Albani,S. (1997). Genetic bias in immune responses to a cassette shared by different microorganisms in patients with rheumatoid arthritis. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 100, 3, eScholarID:1d22683
• LazarusM, HajeerA.H, TurnerD, SinnottP, WorthingtonJ, Ollier WER, HutchinsonI.V. (1997). Genetic variation in the interleukin 10 gene promoter and systemic lupus erythematosus. Journal of Rheumatology, 24, 12, eScholarID:1d22684
• Lopez-Larrea,C., Alvarez,V., du Tait,E., Fan,L., Grosse-Wilde,H., Grunnet,N., Hashemi,S., Holdsworth,R., Jersild,C., Mehra,N.K., Mercier,P., Ohya,K., Ollier, WER, Charron,D. (1997). AHS#5: HLA-B7, B27, B22, B42, B47, B73, B81, B703. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 1, eScholarID:1d22685
• MarlowA, JohnS, HajeerA, Ollier WER, SilmanA.J, WorthingtonJ. (1997). The sensitivity of different analytical methods to detect disease susceptibility genes in rheumatoid arthritis sibling pair families. Journal of Rheumatology, 24, 1, eScholarID:1d22686
• McDonaghJ.E, DunnA, Ollier WER, WalkerD.J. (1997). Compound heterozygosity for the shared epitope and the risk and severity of rheumatoid arthritis in extended pedigrees. British Journal of Rheumatology, 36, 3, eScholarID:1d22687
• MizushimaN, KohsakaH, NankiT, Ollier WER, CarsonD.A, MiyasakaN. (1997). HLA-dependent peripheral T cell receptor (TCR) repertoire formation and its modification by rheumatoid arthritis (RA). Clinical and Experimental Immunology, 110, 3, eScholarID:1d22688
• MurdochM.E, PaytonA, AbioseA, ThomsonW, PanickerV.K, DyerP.A, JonesB.R, MaizelsR.M, Ollier WER. (1997). HLA-DQ alleles associate with cutaneous features of onchocerciasis. The Kaduna-London-Manchester Collaboration for Research on Onchocerciasis. Human Immunology, 55, 1, eScholarID:1d22689
• Ollier WER, DayI.N.M. (1997). HLA genes and rheumatoid arthritis susceptibility. Genetics of common diseases. Future therapeutic and diagnostic possibilities, eScholarID:1d22692
• Ollier WER, HajeerA, IsenbergD.A. (1997). Does the HLA-DRB1 shared epitope really contribute that much to the development or severity of rheumatoid arthritis? Controversies in Rheumatology, eScholarID:1d22693
• Ollier WER, WorthingtonJ. (1997). New horizons in rheumatoid arthritis genetics. Journal of Rheumatology, 24, eScholarID:1d22691
• Ollier WER, WorthingtonJ. (1997). Small fish in a big pond. British Journal of Rheumatology, 36, 9, eScholarID:1d22690
• RiderJ.R, Ollier WER, LockR.J, BrookesS.T, PamphilonD.H. (1997). Human cytomegalovirus infection and systemic lupus erythematosus. Clinical and Experimental Rheumatology, 15, 4, eScholarID:1d22694
• SmythL.J, SnowdenN, CarthyD, PapasteriadesC, HajeerA, Ollier WER. (1997). Fc gamma RIIa polymorphism in systemic lupus erythematosus. Annals of the Rheumatic Diseases, 56, 12, eScholarID:1d22695
• SnowdenN, PepperL, KhooS, HajeerA, MandalB.K, WilkinsE.G.L, Ollier WER, CharronD. (1997). MHC polymorphisms are associated with the rate of disease progression in HIV infection. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 2, eScholarID:1d22696
• Stasny,P., Carcassi,C., Mehra,N.K., Alcalay,D., Chan,S., Gonzalez-Escribano,M., Guo,S., Hammond,M., Hashemi,S., Hsu,S., Inoko,H., Ivaskova,E., Layrisse,Z., Konenkov,V., Berg-Loonen,E., Loeliger,C., Manzo,C., Morellini,M., Nose,Y., Ollier, WER, Papasteriades,C., Sachs,J., Scorza,C., Tait,B., Testi,M., Tilanus,M., Xiao,L., Zmijewski,C., Charron,D. (1997). AHS#13: HLA-DR4, DR53. HLA Genetic diversity of HLA. Functional and medical implication. Proceedings of the Twelfth International Histocompatibility Workshop and Conference, 1, eScholarID:1d22697
• VencovskyJ, MainiR.N, Ollier WER, MageedR.A. (1997). Immunoglobulin variable region (IgV) gene expression in rheumatoid factors from monozygotic twins with rheumatoid arthritis. Annals of the New York Academy of Sciences, 815, eScholarID:1d22698

1996

• Dearden,S.P., Taylor,G.M., Gokhale,D.A., Robinson,M.D., Thompson,W., Ollier, WER, Binchy,A., Birch,J.M., Stevens,R.F., Carr,T., Bardsley,W.G. (1996). Molecular analysis of HLA-DQB1 alleles in childhood common acute lymphoblastic leukaemia. British Journal of Cancer, 73, 5, eScholarID:1d22660
• DonnR.P, Ollier WER. (1996). Juvenile chronic arthritis--a time for change? European Journal of Immunogenetics, 23, 3, eScholarID:1d22661
• GrennanD.M, Ollier WER. (1996). Associations of HLA-DRB and HLA-DRQ genes with two and five year outcomes in rheumatoid arthritis. Annals of the Rheumatic Diseases, 55, 7, eScholarID:1d22662
• HajeerA.H, WorthingtonJ, SilmanA.J, Ollier WER. (1996). Association of tumor necrosis factor microsatellite polymorphisms with HLA-DRB1*04-bearing haplotypes in rheumatoid arthritis patients. Arthritis and Rheumatism, 39, 7, eScholarID:1d22663
• HaworthS, RidgewayJ, StewartI, DyerP.A, PepperL, Ollier WER. (1996). Polymyalgia rheumatica is associated with both HLA-DRB1*0401 and DRB1*0404. British Journal of Rheumatology, 35, 7, eScholarID:1d22664
• Hillarby M, EJ Davies, Donn RP, DM Grennan, Ollier WER. (1996). TAP2D is associated with HLA-B44 and DR4 and may contribute to rheumatoid arthritis and Felty's syndrome susceptibility. Clin Exp Rheumatol, 14, 67-70. eScholarID:1d6936
• JawaheerD, MacGregorA.J, GregersenP.K, SilmanA.J, Ollier WER. (1996). Unexpected HLA haplotype sharing in dizygotic twin pairs discordant for rheumatoid arthritis. Journal of Medical Genetics, 33, 12, eScholarID:1d22665
• KohsakaH, CarsonD.A, RassentiL.Z, Ollier WER, ChenP.P, KippsT.J, MiyasakaN. (1996). The human immunoglobulin V(H) gene repertoire is genetically controlled and unaltered by chronic autoimmune stimulation. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 98, 12, eScholarID:1d22667
• KohsakaH, NankiT, Ollier WER, MiyasakaN, CarsonD.A. (1996). Influence of the rheumatoid arthritis-associated shared epitope on T- cell receptor repertoire formation. Proceedings of the Association of American Physicians, 108, 4, eScholarID:1d22666
• NankiT, KohsakaH, MizushimaN, Ollier WER, CarsonD.A, MiyasakaN. (1996). Genetic control of T cell receptor BJ gene expression in peripheral lymphocytes of normal and rheumatoid arthritis monozygotic twins. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 98, 7, eScholarID:1d22668
• Ollier WER, DaviesE, SnowdenN, AllderseaJ, FryerA, JonesP, StrangeR. (1996). Association of homozygosity for glutathione-S-transferase GSTM1 null alleles with the Ro+/La- autoantibody profile in patients with systemic lupus erythematosus. Arthritis and Rheumatism, 39, 10, eScholarID:1d22669
• PoultonK.V, SinnottP.J, KennedyL.J, Ollier WER, BurkeJ.F. (1996). Protocol 28a. Sequence-specific oligonucleotide typing (SSOP). PCR Essential Techniques, eScholarID:1d22672
• PoultonK.V, SinnottP.J, KennedyL.J, Ollier WER, BurkeJ.F. (1996). Sequence specific primer typing (SSP). PCR Essential Techniques, eScholarID:1d22670
• PoultonK.V, SinnottP.J, KennedyL.J, Ollier WER, BurkeJulian. (1996). Sequence-specific oligonucleotide typing (SSOP). PCR : essential techniques, eScholarID:1d22671
• SymmonsD.P, Ollier WER, BrennanP, SilmanA.J. (1996). Should patients with recent onset rheumatoid arthritis be offered genetic screening? Annals of the Rheumatic Diseases, 55, 7, eScholarID:1d22673

1995

• Albani,S., Keystone,E.C., Nelson,J.L., Ollier, WER, La Cava,A., Montemayor,A.C., Weber,D.A., Montecucco,C., Martini,A., Carson,D.A. (1995). Positive selection in autoimmunity: abnormal immune responses to a bacterial dnaJ antigenic determinant in patients with early rheumatoid arthritis. Nature Medicine, 1, 5, eScholarID:1d22645
• AwomoyiA.A, DonnR.P, DaviesE.J, CarthyD, ThomsonW, Ollier WER. (1995). Absence of TAP 2D in Yoruba Nigerians. European Journal of Immunogenetics, 22, 2, eScholarID:1d22646
• CarthyD, MacGregorA, AwomoiA, RigbyA.S, ThomsonW, DonnR, SilmanA, Ollier WER. (1995). HLA-DPB1*0201 is associated with particular clinical features of rheumatoid arthritis. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 62, 3, eScholarID:1d22647
• DaviesE.J, SnowdenN, HillarbyM.C, CarthyD, GrennanD.M, ThomsonW, Ollier WER. (1995). Mannose-binding protein gene polymorphism in systemic lupus erythematosus. Arthritis and Rheumatism, 38, 1, eScholarID:1d22648
• DaviesE.J, SteersG, Ollier WER, GrennanD.M, CooperR.G, HayE.M, HillarbyM.C. (1995). Relative contributions of HLA-DQA and complement C4A loci in determining susceptibility to systemic lupus erythematosus. British Journal of Rheumatology, 34, 3, eScholarID:1d22649
• DonnR.P, ThomsonW, PepperL, CarthyD, FarhanA, RyderC, SouthwoodT, HoltL, Ollier WER. (1995). Antinuclear antibodies in early onset pauciarticular juvenile chronic arthritis (JCA) are associated with HLA-DQB1*0603: a possible JCA- associated human leucocyte antigen haplotype. British Journal of Rheumatology, 34, 5, eScholarID:1d22650
• EJ Davies, G Steers, Ollier WER, Hillarby M. (1995). A possible interaction of the HLA-DQA and complement C4A loci in determining susceptibility to SLE. British Journal of Rheumatology, 34, eScholarID:1d25560
• EJ Davies, NS Snowden, Hillarby M, Carthy D, Thomson Wendy, Ollier WER. (1995). A dysfunctional allele of the mannose binding protein gene in SLE: relationship to C4 null alleles. Arthritis Rheum, 34, 110-114. eScholarID:1d25559
• KayR.A, HutchingsC.J, Ollier WER. (1995). A subset of Sj"gren's syndrome associates with the TCRBV13S2 locus but not the TCRBV2S1 locus. Human Immunology, 42, 4, eScholarID:1d22651
• KennedyL.J, PoultonK.V, DyerP.A, Ollier WER, ThomsonW. (1995). Definition of HLA-C alleles using sequence-specific oligonucleotide probes (PCR-SSOP). Tissue Antigens, 46, 3 ( Pt 1), eScholarID:1d22652
• MacGregorA, Ollier WER, ThomsonW, JawaheerD, SilmanA. (1995). HLA-DRB1*0401/0404 genotype and rheumatoid arthritis: increased association in men, young age at onset, and disease severity. Journal of Rheumatology, 22, 6, eScholarID:1d22653
• MacGregorA.J, BamberS, CarthyD, VencovskyJ, MageedR.A, Ollier WER, SilmanA.J. (1995). Heterogeneity of disease phenotype in monozygotic twins concordant for rheumatoid arthritis. British Journal of Rheumatology, 34, 3, eScholarID:1d22654
• MacGregorA.J, Ollier WER, VenkovskyJ, MageedR.A, CarthyD, SilmanA.J. (1995). Rheumatoid factor isotypes in monozygotic and dizygotic twins discordant for rheumatoid arthritis. Journal of Rheumatology, 22, 12, eScholarID:1d22655
• Ollier WER, MacGregorA. (1995). Genetic epidemiology of rheumatoid disease. British Medical Bulletin, 51, 2, eScholarID:1d22657
• Ollier WER. (1995). Genes and rheumatic diseases. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 14, eScholarID:1d22656
• SilmanA.J, HayE.M, WorthingtonJ, ThomsonW, PepperL, DavidsonJ, DyerP, Ollier WER. (1995). Lack of influence of non-inherited maternal HLA-DR alleles on susceptibility to rheumatoid arthritis. Annals of the Rheumatic Diseases, 54, eScholarID:1d22658
• VencovskyJ, MageedR.A, Ollier WER, MainiR.N. (1995). Monozygotic rheumatoid arthritis twin pairs express similar levels of conserved immunoglobulin V gene in polyclonal rheumatoid factors irrespective of disease status. Scandinavian Journal of Immunology, 42, 1, eScholarID:1d22659

1994

• BansalA.S, MacGregorA.J, PumphreyR.S, SilmanA.J, Ollier WER, WilsonP.B. (1994). Increased levels of sCD23 in rheumatoid arthritis are related to disease status. Clinical and Experimental Rheumatology, 12, 3, eScholarID:1d22633
• Davies,E.J., Hutchings,C.J., Hillarby,M.C., Donn,R.P., Cooper,R.G., Hay,E.M., Bernstein,R.M., Holt,P.J., Grennan,D.M., Ollier, WER. (1994). HLA-DP does not contribute towards susceptibility to systemic lupus erythematosus. Annals of the Rheumatic Diseases, 53, 3, eScholarID:1d22634
• Donn RP, EJ Davies, W Thomson, Hillarby M, Ollier WER. (1994). TAP gene associations in UK Caucasoids. European Journal of Immunogenetics, 21, 159-167. eScholarID:1d25557
• DonnR.P, DaviesE.J, ThomsonW, Ollier WER, HoltP.L. (1994). Increased frequency of TAP2B in early in early onset pauciarticular juvenile chronic arthritis. Annals of the Rheumatic Diseases, 53, eScholarID:1d22635
• EJ Davies, Donn RP, Hillarby M, DM Grennan, Ollier WER. (1994). Polymorphisms of the TAP2 transporter gene in systemic lupus erythematosus. Annals Of Rheumatic Diseases, 53, 61-63. eScholarID:1d25553
• GarleppM.J, LaingB, ZilkoP.J, Ollier WER, MastagliaF.L. (1994). HLA associations with inclusion body myositis. Clinical and Experimental Immunology, 98, 1, eScholarID:1d22636
• HajeerA.H, MacGregorA.J, RigbyA.S, Ollier WER, CarthyD, SilmanA.J. (1994). Influence of previous exposure to human parvovirus B19 infection in explaining susceptibility to rheumatoid arthritis: an analysis of disease discordant twin pairs. Annals of the Rheumatic Diseases, 53, 2, eScholarID:1d22637
• JawaheerD, ThomsonW, MacGregorA.J, CarthyD, DavidsonJ, DyerP.A, SilmanA.J, Ollier WER. (1994). "Homozygosity" for the HLA-DR shared epitope contributes the highest risk for rheumatoid arthritis concordance in identical twins. Arthritis and Rheumatism, 37, 5, eScholarID:1d22638
• KayR.A, HayE.M, HoltP.J, BernsteinR.M, Ollier WER. (1994). Serological and immunogenetic markers of extraglandular primary Sj"gren's syndrome. British Journal of Rheumatology, 33, 2, eScholarID:1d22642
• KayR.A, Ollier WER. (1994). Idiotypic T-lymphocyte receptor in animal and human autoimmune diseases. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 61, 7-8, eScholarID:1d22639
• KayR.A, Ollier WER. (1994). T-lymphocyte receptor genes: genome organization and genetic mechanisms of repertoire diversity. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 61, 7-8, eScholarID:1d22640
• KayR.A, SnowdenN, HajeerA.H, BoylstonA.W, Ollier WER. (1994). Genetic control of the human V beta 13.2 T cell repertoire: importance of allelic variation outside the coding regions of the TCRBV13S2 gene. European Journal of Immunology, 24, 11, eScholarID:1d22641
• TrejoV, DeromC, VlietinckR, Ollier WER, SilmanA, EbersG, DeromR, GregersenP.K. (1994). X chromosome inactivation patterns correlate with fetal-placental anatomy in monozygotic twin pairs: implications for immune relatedness and concordance for autoimmunity. Molecular Medicine, 1, 1, eScholarID:1d22643
• Worthington,J., Ollier, WER, Leach,M.K., Smith,I., Hay,E.M., Thomson,W., Pepper,L., Carthy,D., Farhan,A., Martin,S.. (1994). The Arthritis and Rheumatism Council's National Repository of Family Material: pedigrees from the first 100 rheumatoid arthritis families containing affected sibling pairs. British Journal of Rheumatology, 33, 10, eScholarID:1d22644

1993

• BansalA.S, Ollier WER, MarshM.N, PumphreyR.S, WilsonP.B. (1993). Variations in serum sCD23 in conditions with either enhanced humoral or cell-mediated immunity. Immunology, 79, 2, eScholarID:1d22618
• CarthyD, Ollier WER, PapasteriadesC, PappasH, ThomsonW. (1993). A shared HLA-DRB1 sequence confers RA susceptibility in Greeks. European Journal of Immunogenetics, 20, 5, eScholarID:1d22619
• CJ Hutchings, Hillarby M, MJ McMahon, Ollier WER. (1993). HLA-DPAI and HLA-DPBI in rheumatoid arthritis and its subsets. Disease Markers, 11, 37-44. eScholarID:1d25548
• HajeerA.H, SnowdenN, WilsonP, DroverS, Ollier WER. (1993). Antibodies to major histocompatibility complex class II inhibit proliferation, but increase production of soluble CD23 in lymphoblastoid B-cell lines. Immunology, 80, 4, eScholarID:1d22620
• HayE.M, Ollier WER, SilmanA.J. (1993). The Arthritis and Rheumatism Council's national family material repository. British Journal of Rheumatology, 32, 6, eScholarID:1d22621
• Hillarby M, Ollier WER, M Davis, J Davidson, PA Sanders, DM Grennan. (1993). Unusual DQA-DR haplotypes in rheumatoid vasculitis. British Journal of Rheumatology, 32, 93-96. eScholarID:1d25546
• JawaheerD, Ollier WER, ThomsonW. (1993). Multiplex ARMS-RFLP: a simple and rapid method for HLA-DR4 subtyping. European Journal of Immunogenetics, 20, 3, eScholarID:1d22622
• KohsakaH, ChenP.P, TaniguchiA, Ollier WER, CarsonD.A. (1993). Divergent T cell receptor gamma repertoires in rheumatoid arthritis monozygotic twins. Arthritis and Rheumatism, 36, 2, eScholarID:1d22625
• KohsakaH, ChenP.P, TaniguchiA, Ollier WER, CarsonD.A. (1993). Regulation of the mature human T cell receptor gamma repertoire by biased V-J gene rearrangement. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 91, 1, eScholarID:1d22623
• KohsakaH, TaniguchiA, ChenP.P, Ollier WER, CarsonD.A. (1993). The expressed T cell receptor V gene repertoire of rheumatoid arthritis monozygotic twins: rapid analysis by anchored polymerase chain reaction and enzyme-linked immunosorbent assay. European Journal of Immunology, 23, 8, eScholarID:1d22624
• MacGregorA.J, FoxH, Ollier WER, SnaithM.L, SilmanA.J. (1993). An identical twin pair discordant for rheumatoid arthritis and ankylosing spondylitis. Clinical and Experimental Rheumatology, 11, 4, eScholarID:1d22626
• Obata,F., Tsunoda,M., Kaneko,T., Ito,K., Ito,I., Masewicz,S., Mickelson,E.M., Ollier, WER, Pawelec,G., Cella,M.. (1993). Human T-cell receptor TCRAV, TCRBV, and TCRAJ sequences newly found in T-cell clones reactive with allogeneic HLA class II antigens. Immunogenetics, 38, 1, eScholarID:1d22627
• SilmanA.J, MacGregorA.J, ThomsonW, HolliganS, CarthyD, FarhanA, Ollier WER. (1993). Twin concordance rates for rheumatoid arthritis: results from a nationwide study. British Journal of Rheumatology, 32, 10, eScholarID:1d22629
• SilmanA.J, Ollier WER, HolliganS, BirrellF, AdebajoA, AsuzuM.C, ThomsonW, PepperL. (1993). Absence of rheumatoid arthritis in a rural Nigerian population. Journal of Rheumatology, 20, 4, eScholarID:1d22628
• ThomsonW, PepperL, PaytonA, CarthyD, ScottD, Ollier WER, SilmanA, SymmonsD. (1993). Absence of an association between HLA-DRB1*04 and rheumatoid arthritis in newly diagnosed cases from the community. Annals of the Rheumatic Diseases, 52, 7, eScholarID:1d22630
• TurnerS, Ollier WER, MorganK, WorthingtonJ. (1993). Frequency of alleles of type II collagen in collagen antibody-positive rheumatoid arthritis patients. British Journal of Rheumatology, 32, 12, eScholarID:1d22631
• WorthingtonJ, RigbyA.S, MacGregorA.J, SilmanA.J, CarthyD, Ollier WER. (1993). Lack of association of increased antibody levels to mycobacterial hsp65 with rheumatoid arthritis: results from a study of disease discordant twin pairs. Annals of the Rheumatic Diseases, 52, 7, eScholarID:1d22632

1992

• CarthyD, FarhanA, GreenL.M, Ollier WER, TsujiK. (1992). Characterization of anti DRB1*0402 - specific T-cell clones. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 1, eScholarID:1d22609
• HammondA, Ollier WER, WalportM.J. (1992). Effects of C4 null alleles and homoduplications on quantitative expression of C4A and C4B. Clinical and Experimental Immunology, 88, 1, eScholarID:1d22610
• Kay,R.A., Thomson,W., Hay,E.M., Dyer,P.A., Green,L.M., Forster,H., Holt,P.J.L., Bernstein,R.M., Griffiths,I., Pumphrey,R., Boylston,A.W., Ollier, WER, Tsuji,K. (1992). The influence of HLA and primary Sj"gren's syndrome on VB6.7 T cell receptor gene expression. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 2, eScholarID:1d22611
• Nelson,J.L., Hansen,J.A., Singal,D., Buchanan,W., Marshall,W., Larsen,B., Feng,L., Feng,C.H., Thomson,W., Ollier, WER, Howell,W., Smith,J., Eliaou,J.F., Clot,J., Taneja,V., Mehra,N., Naik,S., Agarwal,S., Angelini,G., Ferrara,G., Delfino,L., Morozzi,G., Marcolongo,R., Tsuchiya,K., Sasazuki,T., Chandanayingyong,D., Charoenwongse,P., Deesomchok,U., Templin,D., Sartakova,M., Konenkov,V., Tsuji,K. (1992). Rheumatoid arthritis-joint report. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 1, eScholarID:1d22612
• Ollier WER, SymmonsD.P.M, ReadA.P. (1992). Autoimmunity. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, eScholarID:1d22614
• Ollier WER, ThomsonW. (1992). Population genetics of rheumatoid arthritis. Rheumatic Diseases Clinics of North America, 18, 4, eScholarID:1d22613
• RileyG.S, WorthingtonJ, DyerP.A, Ollier WER, TsujiK. (1992). Epitope scanning of the HLA-DRB1 allele sequences with monoclonal antibodies. HLA 1991. Proceedings of the Eleventh International Histocompatibility Workshop and Conference, 2, eScholarID:1d22615
• ThomsonW, Ollier WER. (1992). Non-radioactive ASO typing for class II--the way forward. European Journal of Immunogenetics, 19, 3, eScholarID:1d22616
• WalportM.J, Ollier WER, SilmanA.J. (1992). Immunogenetics of rheumatoid arthritis and the Arthritis and Rheumatism Council's National Repository. British Journal of Rheumatology, 31, 10, eScholarID:1d22617

1991

• DizierM.H, SilmanA.J, Ollier WER, GrennanD.M, Clerget-DarpouxF. (1991). Interactive effect of HLA and Gm and genetic heterogeneity tested in 79 rheumatoid arthritis families. Disease Markers, 9, 1, eScholarID:1d22603
• Hillarby, M, R Clarkson, DM Grennan, AS Bate, Ollier, WER, Sanders, PP, D Chattophadhyay, M Davis, MM O'Sullivan, B Williams. (1991). Immunogenetic heterogeneity in rheumatoid disease as illustrated by different MHC associations (DQ, Dw, C4) in articular and extra-articular subsets. British Journal of Rheumatology, 30, 5-9. eScholarID:1d25542
• Kay,R.A., Hay,E.M., Dyer,P.A., Dennett,C., Green,L.M., Bernstein,R.M., Holt,P.J., Pumphrey,R.S., Boylston,A.W., Ollier, WER. (1991). An abnormal T cell repertoire in hypergammaglobulinaemic primary Sj"gren's syndrome. Clinical and Experimental Immunology, 85, 2, eScholarID:1d22604
• KayR.A, HayE.M, DavidsonJ.A, DennettC, GreenL, BoylstonA.W, DyerP.A, Ollier WER. (1991). A specific T cell gene product is present in abnormal amounts in hypergammaglobulinaemic primary Sj"gren's syndrome. European Journal of Immunogenetics, 18, eScholarID:1d22605
• Ollier WER, StephensC, AwadJ, CarthyD, GuptaA, PerryD, JawadA, FestensteinH. (1991). Is rheumatoid arthritis in Indians associated with HLA antigens sharing a DR beta 1 epitope? Annals of the Rheumatic Diseases, 50, 5, eScholarID:1d22606
• RigbyA.S, SilmanA.J, VoelmL, GregoryJ.C, Ollier WER, KhanM.A, NepomG.T, ThomsonG. (1991). Investigating the HLA component in rheumatoid arthritis: an additive (dominant) mode of inheritance is rejected, a recessive mode is preferred. Genetic Epidemiology, 8, 3, eScholarID:1d22607
• SidebottomD, GrennanD.M, GreenJ.R, SandersP.A, Ollier WER, De LangeG. (1991). Ig CH and D14S1 variants in rheumatoid arthritis--linkage and association studies. British Journal of Rheumatology, 30, 3, eScholarID:1d22608

1990

• Awad,J., Ollier, WER, Cutbush,S., Papasteriadis,C., Gupta,A., Carthy,D., McCloskey,D., Brown,C.J., Boki,K., Fostizopoulos,G.. (1990). Heterogeneity of HLA-DR4 in Greeks including a unique DR4-DQw2 association. Tissue Antigens, 35, 1, eScholarID:1d22598
• BateA.S, Ollier WER, GrennanD.M. (1990). Lack of association between DQ A and DX A polymorphisms with rheumatoid arthritis and Felty's syndrome. Disease Markers, 8, 2, eScholarID:1d22599
• CutbushS, Ollier WER, PapasteriadesC, AwadJ, BokiK, MoutsopoulosH, BiroA, SachsJ. (1990). Association of DR4 related RFLP bands and RA in Greeks. Autoimmunity, 8, 2, eScholarID:1d22600
• PapasteriadesC, al MahmoudI, PapageorgakisN, RomaniaS, KatsasA, Ollier WER, EconomidouI. (1990). HLA antigens in Greek patients with cholelithiasis. Disease Markers, 8, 1, eScholarID:1d22601
• SilmanA.J, Ollier WER. (1990). Age and calendar year of onset in sibling pairs with rheumatoid arthritis. British Journal of Rheumatology, 29, 5, eScholarID:1d22602

1989

• FestensteinH, CutbushS.D, Ollier WER, AwadJ, Pachoula-PapasteriadisC, GarleppM.J. (1989). New HLA DNA polymorphisms associated with rheumatoid arthritis. Immunology of HLA, eScholarID:1d22588
• FielderA.H, Ollier WER, LordD.K, BurleyM.W, SilmanA, AwadJ, FestensteinH, BatchelorJ.R. (1989). HLA class III haplotypes in multicase rheumatoid arthritis families. Human Immunology, 25, 2, eScholarID:1d22589
• JassimA, Ollier WER, PayneA, BiroA, OliverR.T, FestensteinH. (1989). Analysis of HLA antigens on germ cells in human semen. European Journal of Immunology, 19, 7, eScholarID:1d22590
• OkoyeR.C, Ollier WER, JaraquemadaD, AwadJ, NavarreteC, CutbushS, CarthyD, Dos-SantosA, FestensteinH. (1989). HLA-D region heterogeneity in a Nigerian population. Tissue Antigens, 33, 4, eScholarID:1d22591
• Ollier WER, CarthyD, CutbushS, OkoyeR, AwadJ, FielderA, SilmanA, FestensteinH. (1989). HLA-DR4 associated Dw types in rheumatoid arthritis. Tissue Antigens, 33, 1, eScholarID:1d22592
• Ollier WER, SpectorT, SilmanA, PerryL, OrdJ, ThomsonW, FestensteinH. (1989). Are certain HLA haplotypes responsible for low testosterone levels in males? Disease Markers, 7, 3, eScholarID:1d22593
• Pachoula-PapasteriadisC, Ollier WER, CutbushS, EconomidouJ, FestensteinH. (1989). HLA antigen and haplotype frequencies in Greeks. Tissue Antigens, 33, 4, eScholarID:1d22594
• SilmanA, HennessyE, DitriM, Ollier WER. (1989). Co-segregation of HLA and rheumatoid arthritis in multicase families. Tissue Antigens, 33, 1, eScholarID:1d22595
• SilmanA.J, Ollier WER, BubelM.A. (1989). Autoimmune thyroid disease and thyroid autoantibodies in rheumatoid arthritis patients and their families. British Journal of Rheumatology, 28, 1, eScholarID:1d22596
• SpectorT.D, Ollier WER, PerryL.A, SilmanA.J, ThompsonP.W, EdwardsA. (1989). Free and serum testosterone levels in 276 males: a comparative study of rheumatoid arthritis, ankylosing spondylitis and healthy controls. Clinical Rheumatology, 8, 1, eScholarID:1d22597