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Mechelli, Rosella, Umeton, Renato, Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, Ricigliano, Vito A. G., Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium,2, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni and Brown, Matthew A. (2013) A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. PLoS One, 8 5: . doi:10.1371/journal.pone.0063300 62   3 Cited 6 times in Scopus6 10
Weedon, M. N., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2007) A common variant of HMGA2 is associated with adult and childhood height in the general population. Nature Genetics, 39 10: 1245-1250. doi:10.1038/ng2121 96   230 Cited 226 times in Scopus226 30
Psychosis Endophenotypes International Consortium, Wellcome Trust Case-Control Consortium and Brown, Matthew A. (2014) A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. Biological Psychiatry, 75 5: 386-397. doi:10.1016/j.biopsych.2013.03.033 41   3 Cited 1 times in Scopus1 1
Strange, Amy, Capon, Francesca, Spencer, Chris C. A., Knight, Jo, Weale, Michael E., Allen, Michael H., Barton, Anne, Band, Gavin, Bellenguez, Céline, Bergboer, Judith G. M., Blackwell, Jenefer M., Bramon, Elvira, Bumpstead, Suzannah J., Casas, Juan P., Cork, Michael J., Corvin, Aiden, Deloukas, Panos, Dilthey, Alexander, Duncanson, Audrey, Edkins, Sarah, Estivill, Xavier, Fitzgerald, Oliver, Freeman, Colin, Giardina, Emiliano, Gray, Emma, Hofer, Angelika, Hüffmeier, Ulrike, Hunt, Sarah E., Irvine, Alan D., Jankowski, Janusz, Kirby, Brian, Langford, Cordelia, Lascorz, Jesús, Leman, Joyce, Leslie, Stephen, Mallbris, Lotus, Markus, Hugh S., Mathew, Christopher G., McLean, W. H. Irwin, McManus, Ross, Mössner, Rotraut, Moutsianas, Loukas, Naluai, Åsa T., Nestle, Frank O., Novelli, Giuseppe, Onoufriadis, Alexandros, Palmer, Colin N. A., Perricone, Carlo, Pirinen, Matti, Plomin, Robert, Potter, Simon C., Pujol, Ramon M., Rautanen, Anna, Riveira-Munoz, Eva, Ryan, Anthony W., Salmhofer, Wolfgang, Samuelsson, Lena, Sawcer, Stephen J., Schalkwijk, Joost, Smith, Catherine H., Ståhle, Mona, Su, Zhan, Tazi-Ahnini, Rachid, Traupe, Heiko, Viswanathan, Ananth C., Warren, Richard B., Weger, Wolfgang, Wolk, Katarina, Wood, Nicholas, Worthington, Jane, Young, Helen S., Zeeuwen, Patrick L. J. M., Hayday, Adrian, Burden, A. David, Griffiths, Christopher E. M., Kere, Juha, Reis, André, McVean, Gilean, Evans, David M., Brown, Matthew A., Barker, Jonathan N., Peltonen, Leena, Donnelly, Peter and Trembath, Richard C. (2010) A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nature Genetics, 42 11: 985-990. doi:10.1038/ng.694 490   304 Cited 317 times in Scopus317 10
Claushuis, Dorith, Cortes, Adrian, Bradbury, Linda A., Martin, Tammy M., Rosenbaum, James T., Reveille, John D., Wordsworth, Paul, Pointon, Jennifer, Evans, David, Leo, Paul, Mukhopadhyay, Pamela and Brown, Matthew A. (2012). A genomewide association study of anterior uveiti. In: Abstracts of the American College of Rheumatology & Association of Rheumatology Health Professionals, Annual Scientific Meeting. Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, DC, United States, (S259-S259). 9-14 November 2012. doi:10.1002/art.37735 48   0 0
Claushuis, T., Cortes, A., Bradbury, L. A., Martin, T. M., Rosenbaum, J. T., Reveille, J. D., Pointon, J. J., Wordsworth, B. P., Evans, D. M., Leo, P., Mukhopadhyay, P. and Brown, M. A. (2012). A genomewide association study of anterior uveitis. In: Eighth International Congress on Spondyloarthritis, Meeting abstracts. 8th International Congress on Spondyloarthritis, Granada, Spain, (625-625). 9-13 May 2012. 35   0
Brown, Matthew A., Pile, Kevin D., Kennedy, L. Gail, Campbell, Duncan, Andrew, Lee, March, Ruth, Shatford, Jane L., Weeks, Daniel E., Calin, Andrei and Wordsworth, B. Paul (1998) A genome-wide screen for susceptibility loci in ankylosing spondylitis. Arthritis and Rheumatism, 41 4: 588-595. doi:10.1002/1529-0131(199804)41:4<588::AID-ART5>3.0.CO;2-0 57   146 Cited 164 times in Scopus164 0
Hall, F. C., Brown, M. A., Weeks, D. E., Walsh, S., Nicod, A., Butcher, S., Andrews, L. J. and Wordsworth, B. P. (1997) A linkage study across the T cell receptor A and T cell receptor B loci in families with rheumatoid arthritis. Arthritis and Rheumatism, 40 10: 1798-1802. doi:10.1002/art.1780401011 46   9 Cited 9 times in Scopus9 0
Thomas, G, Duan, R, Pettit, A, Glant, T and Brown, M (2011). Altered Wnt-Signalling Links Inflammation and Bony Ankylosis in a Mouse Model of Ankylosing Spondylitis. In: Internal Medicine Journal. Unknown, unknown, (3-3). unknown. 75   0
Brown, M. A., George, C. R. P., Dunstan, C. R., Kalowski, S. and Corrigan, A. B. (1993) Aluminum-related bone disease presenting with calcaneal stress fractures. British Journal of Rheumatology, 32 3: 260-262. doi:10.1093/rheumatology/32.3.260 37   0 Cited 1 times in Scopus1 0
Esapa, Christopher T., Hough, Tertius A., Testori, Sarah, Head, Rosie A., Crane, Elizabeth A., Chan, Carol P. S., Evans, Holly, Bassett, J. H. Duncan, Tylzanowski, Przemko, McNally, Eugene G., Carr, Andrew J., Boyde, Alan, Howell, Peter G. T., Clark, Anne, Williams, Graham R., Brown, Matthew A., Croucher, Peter I., Nesbit, M. Andrew, Brown, Steve D. M., Cox, Roger D., Cheeseman, Michael T. and Thakker, Rajesh V. (2012) A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation. Journal of Bone and Mineral Research, 27 2: 413-428. doi:10.1002/jbmr.547 77   8 Cited 10 times in Scopus10 0
Piret, Sian E., Esapa, Christopher T., Gorvin, Caroline M., Head, Rosie, Loh, Nellie Y., Devuyst, Olivier, Thomas, Gethin, Brown, Steve D. M., Brown, Matthew, Croucher, Peter, Cox, Roger and Thakker, Rajesh V. (2012) A mouse model of early-onset renal failure due to a Xanthine Dehydrogenase nonsense mutation. Plos One, 7 9: 45217-1-45217-10. doi:10.1371/journal.pone.0045217 53   0 Cited 1 times in Scopus1 0
Esapa, Christopher T., Head, Rosie A., Jeyabalan, Jeshmi, Evans, Holly, Hough, Tertius A., Cheeseman, Michael T., McNally, Eugene G., Carr, Andrew J., Thomas, Gethin P., Brown, Matthew A., Croucher, Peter I., Brown, Steve D. M., Cox, Roger D. and Thakker, Rajesh V. (2012) A Mouse with an N-Ethyl-N-Nitrosourea (ENU) Induced Trp589Arg Galnt3 Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis. PLoS One, 7 8 Article. No.e43205: . doi:10.1371/journal.pone.0043205 50   4 Cited 4 times in Scopus4 1
He, Ji, Mangelsdorf, Marie, Fan, Dongsheng, Bartlett, Perry and Brown, Matthew A. (2014) Amyotrophic lateral sclerosis genetic studies: from genome-wide association mapping to genome sequencing. The Neuroscientist, 1-17. doi:10.1177/1073858414555404 27 3 13
Harvey, D, Pointon, JJ, Sleator, C, Meenagh, A, Farrar, C, Sun, JY, Senitzer, D, Middleton, D, Brown, MA and Wordsworth, BP (2009) Analysis of killer immunoglobulin-like receptor genes in ankylosing spondylitis. Annals of the Rheumatic Diseases, 68 4: 595-598. doi:10.1136/ard.2008.095927 75   13 Cited 17 times in Scopus17 0
Pointon, JJ, Timms, AE, Bradbury, L and Brown, MA (2006) Analysis of positional candidate genes in ankylosing spondylitis: A possible role for ENPP1. Rheumatology, 45 I60-I60. 67   0
Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013) A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 7: 441-446. doi:10.1038/gene.2013.38 63 4 4 Cited 6 times in Scopus6 6
Charlesworth, J., Stankovich, J., Lewis, P., Byron, J., Stevens, W., Sahhar, J., Roddy, J., Nash, P., Tymms, K., Rischmueller, M., Lester, S., Brown, M., Proudman, S. and Zochling, J. (2012). An immunochip based interrogation of scleroderma susceptibility variants. In: Internal Medicine Journal. unknown, unknown, (2-2). unknown. 42   0
Charlesworth, J., Stankovich, J., Lewis, P., Byron, J., Stevens, W., Sahhar, J., Proudman, S., Roddy, J., Nash, P., Tymms, K., Brown, M. and Zochling, J. (2012). An immunochip-based interrogation of scleroderma susceptibility variants. In: Rheumatology. 2nd Systemic Sclerosis World Congress, Madrid, Spain, (15-16). Feb 02-04, 2012. 41   0
Zochling, Jane, Newell, Felicity, Charlesworth, Jac C., Leo, Paul, Stankovich, Jim, Cortes, Adrian, Zhou, Yuan, Stevens, Wendy, Sahhar, Joanne, Roddy, Janet, Nash, Peter, Tymms, Kathleen, Rischmueller, Maureen, Lester, Sue, Proudman, Susanna and Brown, Matthew A. (2014) An immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Arthritis Research & Therapy, 16 5: 1-7. doi:10.1186/s13075-014-0438-8 71   0 0
Pimentel-Santos, Fernando Manuel, Ligeiro, Dario, Matos, Mafalda, Mourao, Ana Filipa, de Sousa, Elsa Vieira, Pinto, Patricia, Ribeiro, Ana, Santos, Helena, Barcelos, Anabela, Godinho, Fatima, Cruz, Margarida, Fonseca, Joao Eurico, Guedes-Pinto, Henrique, Trindade, Helder, Brown, Matthew A., Branco, Jaime C. and CORPOREA Study Group (2012) ANKH and susceptibility to and severity of ankylosing spondylitis. Journal of Rheumatology, 39 1: 131-134. doi:10.3899/jrheum.110681 72   3 Cited 3 times in Scopus3 1
Zhang, Y, Johnson, K, Wordsworth, P, Russell, G, Carr, A, Terkeltaub, RA and Brown, MA (2004) ANKH mutations cause both familial and sporadic calcium pyrophosphate dihydrate chondrocalcinosis and increase ANKH transcription/2 translation.. Arthritis And Rheumatism, 50 9: S240-S240. 119   0
Brown, M. (2009) Anktylosing spondylitls and the spondyloar thropathies. Australian Doctor, 27/Feb: 25-32. 18   Cited 0 times in Scopus0
Brown, M. A., Jepson, A., Young, A., Whittle, H. C., Greenwood, B. M. and Wordsworth, B. P. (1997) Ankylosing spondylitis in west Africans - Evidence for a non-HLA-B27 protective effect. Annals of the Rheumatic Diseases, 56 1: 68-70. doi:10.1136/ard.56.1.68 72   74 Cited 80 times in Scopus80 0
Robinson, Philip, Cortes, Adrian, Leo, Paul, Evans, David and Brown, Matthew A. (2012). Ankylosing spondylitis is associated with single nucleotide polymorphisms in loci implicating four aminopeptidases. In: Abstracts of the American College of Rheumatology & Association of Rheumatology Health Professionals, Annual Scientific Meeting. Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, DC, United States, (S688-S689). 9-14 November 2012. doi:10.1002/art.37735 61   0 0
Robinson, P. C., Cortes, A., Leo, P., Evans, D. M. and Brown, M. A. (2012). Ankylosing spondylitis is associated with snps in loci implicating four aminopeptidases. In: Eighth International Congress on Spondyloarthritis, Meeting abstracts. 8th International Congress on Spondyloarthritis, Granada, Spain, (602-603). 9-13 May 2012. 38   0
Karaderi, T., Keidel, S. M., Pointon, J. J., Appleton, L. H., Brown, M. A., Evans, D. M. and Wordsworth, B. P. (2014) Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). Annals of the Rheumatic Diseases, 73 11: 2054-2058. doi:10.1136/annrheumdis-2014-205643 27   1 Cited 0 times in Scopus0 3
Bentley, Liz, Esapa, Christopher T., Nesbit, M. Andrew, Head, Rosie A., Evans, Holly, Lath, Darren, Scudamore, Cheryl L., Hough, Tertius A., Podrini, Christine, Hannan, Fadil M., Fraser, William D., Croucher, Peter I., Brown, Matthew A., Brown, Steve D. M., Cox, Roger D. and Thakker, Rajesh V. (2014) An N-ethyl-n-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess. Endocrinology, 155 3: 908-922. doi:10.1210/en.2013-1247 35   1 Cited 1 times in Scopus1 0
Gregson, Celia L., Hollingworth, Peter, Williams, Martin, Petrie, Kirsten A., Bullock, Alex N., Brown, Matthew A., Tobias, Jon H. and Triffitt, James T. (2011) A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date. Bone, 48 3: 654-658. doi:10.1016/j.bone.2010.10.164 80   14 Cited 16 times in Scopus16 0
Jaakkola, E, Herzberg, I, Crane, AM, Pointon, JJ, Laiho, K, Kauppi, M, Kaarela, K, Wordsworth, BP, Tuomilehto, J and Brown, MA (2004) A novel human leucocyte antigen-DRB1 genotyping method based on multiplex primer extension reactions. Tissue Antigens, 64 1: 88-95. doi:10.1111/j.1399-0039.2004.00241.x 95   5 Cited 7 times in Scopus7 0
Couto, Ana. R., Bruges-Armas, Jacome, Peach, Chris A., Chapmsn, Kay, Brown, Matthew A., Wordsworth, B. Paul and Zhang, Yun (2007) A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81 2: 81-84. doi:10.1007/s00223-007-9043-z 106   16 Cited 16 times in Scopus16 0
Anderson, Robert P., Henry, Margaret J., Taylor, Roberta, Duncan, Emma L., Danoy, Patrick, Costa, Marylia J., Addison, Kathryn, Tye-Din, Jason A., Kotowicz, Mark A., Knight, Ross E., Pollock, Wendy, Nicholson, Geoffrey C., Toh, Ban-Hock, Brown, Matthew A. and Pasco, Julie A. (2013) A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways. BMC Medicine, 11 1: 188.1-188.13. doi:10.1186/1741-7015-11-188 37   11 Cited 10 times in Scopus10 42
Brown, MA (2005) Antibody treatments of inflammatory arthritis. Current Medicinal Chemistry, 12 25: 2943-2946. doi:10.2174/092986705774462842 176   12 Cited 14 times in Scopus14 0
Sims, A. M., Duncan, E. L., Dowling, A., Doan, T., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Wass, J. and Brown, M. A. (2007). A Phase 1 Genomewide Association Study in Osteoporosis. In: GeneMappers 2007 Conference, Brisbane, Queensland, Australia, (). 29-31 August 2007. 53  
Sims, A. M., Duncan, E. L., Dowling, A., Doan, T., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Wass, J. and Brown, M. A. (2007). A phase 1 Genome-wide association study in Ostoeporosis. In: 17th Annual Meeting of the Australian & New Zealand Bone & Mineral Society, Queenstown, New Zealand,, (). 9-12 September, 2007. 80  
Field, Judith, Browning, Sharon R., Johnson, Laura J., Danoy, Patrick, Varney, Michael D., Tait, Brian D., Gandhi, Kaushal S., Charlesworth Jac C., Heard, Robert N., Stewart, Graeme J., Kilpatrick, Trevor J., Foote, Simon J., Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R., Taylor, Bruce V., Brown, Matthew A., Rubio, Justin P. and Stankovich, Jim (2010) A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis. PLoS One, 5 10: e13454.1-e13454.7. doi:10.1371/journal.pone.0013454 117 2 15 Cited 18 times in Scopus18 0
Shore, Eileen M., Xu, Meiqi, Feldman, George J., Fenstermacher, David A., Brown, Matthew A., Kaplan, Frederick S., Cho, Tae-Joon, Choi, In Ho, Connor, J. Michael, Delai, Patricia, Zasloff, Michael, Glaser, David L., LeMerrer, Martine, Smith, Roger, Morhart, Rolf, Rogers, John G., Triffitt, James T. and Urtizberea, J. Andoni (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics, 38 5: 525-527. doi:10.1038/ng1783 169   323 Cited 339 times in Scopus339 10
Shore, Eileen M., Xu, Meiqi, Feldman, George J., Fenstermacher, David A., Brown, Matthew A., Kaplan, Frederick S. and FOP Int Res Consortium (2007) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527)). Nature Genetics, 39 2: 276-276. doi:10.1038/ng0207-276b 45   6 Cited 3 times in Scopus3 0
Newton, J. L., Harney, S. M. J., Wordsworth, B. P. and Brown, M. A. (2004) A review of the MHC genetics of rheumatoid arthritis. Genes and Immunity, 5 3: 151-157. doi:10.1038/sj.gene.6364045 100   130 Cited 142 times in Scopus142 12
Bellenguez, Celine, Strange, Amy, Freeman, Colin, Donnelly, Peter, Spencer, Chris C. A., Wellcome Trust Case Control Consortium and Brown, Matthew A. (2012) A robust clustering algorithm for identifying problematic samples in genome-wide association studies. Bioinformatics, 28 1: 134-135. doi:10.1093/bioinformatics/btr599 41   9 Cited 8 times in Scopus8 3
Pimental da Couto, A. and Brown, Matthew A. (2013). Articular chondrocalcinosis. In Michael F. Murray, Mark W. Babyatsky, Monica A. Giovanni, Fowzan S. Alkuraya and Douglas R. Stewart (Ed.), Clinical Genomics: Practical Applications in Adult Patient Care (pp. 704-708) United States: McGraw-Hill Professional Pub. 27  
Estrada, K, Evangelou, E, Hsu, YH, Styrkarsdottir, U, Liu, CT, Moayyeri, A, Kaptoge, S, Duncan, E, Amin, N, Kiel, D, Karasik, D, Albagha, OM, Brown, M, Spector, TD, Zillikens, MC, Ohlsson, C, Thorleifsson, G, Reeve, J, Vandenput, L, Pettersson, U, O'Neill, T, Riancho, JA, Ijunggren, O, Rousseau, F, Leslie, WD, Obermayer-Pietsch, B, Alonso, N, Langdahl, B, Nogues, X, Prince, R, Lips, P, Cheng, S, Marc, J, Kollia, P, Brandi, ML, Hocking, L, Khusnutdina, E, Cooper, C, Lehtimaki, T, Jackson, R, Koh, JM, Minster, RL, Yerges-Armstrong, L, Richards, B, Glazer, N, Kung, A, Koller, D, Evans, D, Ioannidis, J, Ralston, SH, Uitterlinden, AG, Rivadeneira, F, Aogc, Gefos and GENOMOS Consortia (2011). Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity. In: Bone. 3rd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society, Athens Greece, (S69-S69). May 07-11, 2011. doi:10.1016/j.bone.2011.03.070 66   2 0
Karaderi, T., Harvey, D., Farrar, C., Appleton, L. H., Stone, M. A., Sturrock, R. D., Brown, M. A., Wordsworth, P. and Pointon, J. J. (2009) Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case control study and meta-analysis of published series. Rheumatology, 48 4: 386-389. doi:10.1093/rheumatology/ken501 56   51 Cited 56 times in Scopus56 0
Davidson, Stuart, Wu, Xin, Liu, Yu, Wei, Meng, Danoy, Patrick, Thomas, Gethin, Cai, Qing, Sun, Linyun, Duncan, Emma, Wang, Niansong, Yu, Qinghong, Xu, Anlong, Fu, Yonggui, Brown, Matthew and Xu, Huji (2009) Association of ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population. Arthritis & Rheumatism, 60 11: 3263-3268. doi:10.1002/art.24933 72   62 Cited 56 times in Scopus56 0
Pimentel-Santos, F. M., Ligeiro, D., Matos, M., Mourao, A. F., Sousa, E., Pinto, P., Ribeiro, A., Sousa, M., Barcelos, A., Godinho, F., Cruz, M., Fonseca, J. E., Guedes-Pinto, H., Trindade, H., Evans, D. M., Brown, M. A. and Branco, J. C. (2009) Association of IL23R and ERAP1 genes with ankylosing spondylitis in a Portuguese population. Clinical And Experimental Rheumatology, 27 5: 800-806. 157 45 41 Cited 40 times in Scopus40
Dehghan, Abbas, Yang, Qiong, Peters, Annette, Basu, Saonli, Bis, Joshua, Rudnicka, Alicja, Kavousi, Maryam, Chen, Ming-Huei, Baumert, Jens, Lowe, Gordon, et al, Wellcome Trust Case Control Consortium, Brown, Matthew and Bradbury, Linda (2009) Association of novel genetic loci with circulating fibrinogen levels: A genome-wide association study in 6 population-based cohorts. Circulation: Cardiovascular Genetics, 2 2: 125-133. doi:10.1161/CIRCGENETICS.108.825224 81   45 Cited 49 times in Scopus49 0
Zhang, Y, Johnson, K, Russell, RGG, Wordsworth, BP, Carr, AJ, Terkeltaub, RA and Brown, MA (2005) Association of sporadic chondrocalcinosis with a-4-basepair g-to-a transition in the 5 '-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate. Arthritis And Rheumatism, 52 4: 1110-1117. doi:10.1002/art.20978 115   38 Cited 45 times in Scopus45 0
Davidson, Stuart I., Liu, Yu, Danoy, Patrick A., Wu, Xin, Thomas, Gethin P., Jiang, Lei, Sun, Linyun, Wang, Niansong, Han, Jun, Han, Huanxing, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011) Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese. Annals of the Rheumatic Diseases, 70 2: 289-292. doi:10.1136/ard.2010.133322 97 1 32 Cited 32 times in Scopus32 0
Danoy, P, Pryce, K, Hadler, J, Bradbury, LA, Farrar, C, Pointon, J, Ward, M, Weisman, M, Reveille, JD, Wordsworth, BP, Stone, MA, Maksymowych, WP, Rahman, P, Gladman, D, Inman, RD, Brown, MA, Australo-Anglo-Amer and Spondyloarthrit Res Consortium (2010) Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease. PLoS Genetics, 6 12: e1001195-1-e1001195-5. doi:10.1371/journal.pgen.1001195 89   69 Cited 80 times in Scopus80 1
Danoy, Patrick, Wei, Meng, Hadler, Johanna, Jiang, Lei, He, Dongyi, Sun, Linyun, Zeng, Xiaofeng, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011) Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese population. Annals of the Rheumatic Diseases, 70 10: 1793-1797. doi:10.1136/ard.2010.144576 83 3 9 Cited 7 times in Scopus7 0

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