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Visscher, Peter M., Wray, Naomi R., Zhang, Qian, Sklar, Pamela, McCarthy, Mark I., Brown, Matthew A. and Yang, Jian (2017) 10 years of GWAS discovery: biology, function, and translation. American Journal of Human Genetics, 101 1: 5-22. doi:10.1016/j.ajhg.2017.06.005     174 Cited 189 times in Scopus189 248
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: e63300. doi:10.1371/journal.pone.0063300     17 Cited 19 times in Scopus19 13
Aung, Tin, Ozaki, Mineo, Mizoguchi, Takanori, Allingham, R. Rand, Li, Zheng, Haripriya, Aravind, Nakano, Satoko, Uebe, Steffen, Harder, Jeffrey M., Chan, Anita S. Y., Lee, Mei Chin, Burdon, Kathryn P., Astakhov, Yury S., Abu-Amero, Khaled K., Zenteno, Juan C., Nilguen, Yildirim, Zarnowski, Tomasz, Pakravan, Mohammad, Abu Safieh, Leen, Jia, Liyun, Wang, Ya Xing, Williams, Susan, Paoli, Daniela, Schlottmann, Patricio G., Huang, Lulin, Sim, Kar Seng, Foo, Jia Nee, Nakano, Masakazu, Ikeda, Yoko, Kumar, Rajesh S., Ueno, Morio, Manabe, Shin-Ichi, Hayashi, Ken, Kazama, Shigeyasu, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Ishiko, Satoshi, Yoshida, Akitoshi, Yanagi, Masahide, Kiuchi, Yoshiaki, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Matsuda, Fumihiko, Yamashiro, Kenji, Gotoh, Norimoto, Miyake, Masahiro, Astakhov, Sergei Y., Osman, Essam A., Al-Obeidan, Saleh A., Owaidhah, Ohoud, Al-Jasim, Leyla, Al Shahwan, Sami, Fogarty, Rhys A., Leo, Paul, Yetkin, Yaz, Oguz, Cilingir, Kanavi, Mozhgan Rezaei, Beni, Afsaneh Nederi, Yazdani, Shahin, Akopov, Evgeny L., Toh, Kai-Yee, Howell, Gareth R., Orr, Andrew C., Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Kosior-Jarecka, Ewa, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N., Wong, Tien Yin, Liu, Yutao, Koch, Allison E. Ashley, Challa, Pratap, Rautenbach, Robyn M., Mackey, David A., Hewitt, Alex W., Mitchell, Paul, Wang, Jie Jin, Ziskind, Ari, Carmichael, Trevor, Ramakrishnan, Rangappa, Narendran, Kalpana, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Chen, Xueyi, Guadarrama-Vallejo, Dalia, Cheng, Ching Yu, Perera, Shamira A., Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Mardin, Christian, Schloetzer-Schrehardt, Ursula, Hillmer, Axel M., Herms, Stefan, Moebus, Susanne, Noethen, Markus M., Weisschuh, Nicole, Shetty, Rohit, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A., Lischinsky, Ignacio, Crowston, Jonathan G., Coote, Michael, Zhao, Bowen, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Vysochinskaya, Vera, Founti, Panayiota, Chatzikyriakidou, Anthoula, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Coleman, Anne L., Wilson, M. Roy, Rhee, Douglas J., Kang, Jae Hee, May-Bolchakova, Inna, Heegaard, Steffen, Mori, Kazuhiko, Alward, Wallace L. M., Jonas, Jost B., Xu, Liang, Liebmann, Jeffrey M., Chowbay, Balram, Schaeffeler, Elke, Schwab, Matthias, Lerner, Fabian, Wang, Ningli, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Fingert, John H., Inatani, Masaru, Tashiro, Kei, Reis, Andre, Edward, Deepak P., Pasquale, Louis R., Kubota, Toshiaki, Wiggs, Janey L., Pasutto, Francesca, Topouzis, Fotis, Dubina, Michael, Craig, Jamie E., Yoshimura, Nagahisa, Sundaresan, Periasamy, John, Simon W. M., Ritch, Robert, Hauser, Michael A. and Khor, Chiea-Chuen (2015) A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics, 47 4: 387-392. doi:10.1038/ng.3226     30 Cited 32 times in Scopus32 42
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     272 Cited 280 times in Scopus280 58
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     27 Cited 24 times in Scopus24 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     542 Cited 580 times in Scopus580 17
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     1 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.     0
Merriman, T. R., Cadzow, M., Merriman, M., Phipps-Green, A., Topless, R., Abhishek, A., Andres, M., Bradbury, L., Buchanan, R., Cremin, K., de Guzman, E., de Zoysa, J., Doherty, M., Hill, C., Huizinga, T., Jansen, T., Janssen, M., Joosten, L., Kurreeman, F., Lester, S., Liote, F., Macartney-Coxson, D., Matsuo, H., McCarthy, G., McCormick, S., Murphy, R., Pavelka, K., Perez-Ruiz, F., Puig, J., Radstake, T., Riches, P., Rischmueller, M., Roddy, E., Smith, M., Stahl, E., Stiburkova, B., Stubbs, R., Tausche, A-K., Torres, R., Walker, R., Yamamoto, K., Brown, M., Choi, H., Dalbeth, N., So, A., Stamp, L. and Flynn, T. (2017). A GENOME-WIDE ASSOCIATION STUDY OF GOUT IN PEOPLE OF EUROPEAN ANCESTRY. In: Annual European Congress of Rheumatology, Madrid Spain, (383-383). Jun 14-17, 2017. doi:10.1136/annrheumdis-2017-eular.5634     0 0
Meng, Weihua, Deshmukh, Harshal A., Donnelly, Louise A., Torrance, Nicola, Colhoun, Helen M., Palmer, Colin N. A., Smith, Blair H., Wellcome Trust Case Control Consortium 2 and Brown, Matthew (2015) A genome-wide association study provides evidence of sex-specific involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) with diabetic neuropathic pain. EBioMedicine, 2 10: 1386-1393. doi:10.1016/j.ebiom.2015.08.001     17 Cited 15 times in Scopus15 3
Merriman, Tony R., Cadzow, Murray, Tanner, Callum, Brown, Matthew A., Cremin, Katie, Janssen, Matthijs, Jansen, Tim, Joosten, Leo A., Radstake, Timothy, Riches, Philip L., Tausche, Anne-Kathrin, Liote, Frederic, So, Alex, van Rij, Andre M., Jones, Gregory T., Stamp, Lisa K., Dalbeth, Nicola and McKinney, Cushla (2015). A genome-wide association study reveals association of the transferrin receptor locus with gout. In: American College Of Rheumatology (ACR/ARHP) Annual Meeting, San Francisco, United States, (). 6 - 11 November, 2015. doi:10.1002/art.39448     0 1
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     156 Cited 176 times in Scopus176 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     9 Cited 9 times in Scopus9 3
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.     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     0 Cited 1 times in Scopus1 0
Karaderi, T., Pointon, J. J., Harrison, P., Harvey, D., Farrar, C., Brown, M. A. and Wordsworth, B. P. (2008). A meta-analysis of IL23R associations with ankylosing spondylitis. In: Clinical and Experimental Rheumatology. , , (723-723). .     0
Bodea, Corneliu A., Neale, Benjamin M., Ripke, Stephan, Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, The International IBD Genetics Consortium and Brown, Matthew A. (2016) A method to exploit the structure of genetic ancestry space to enhance case-control studies. American Journal of Human Genetics, 98 5: 857-868. doi:10.1016/j.ajhg.2016.02.025     4 Cited 4 times in Scopus4 8
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     12 Cited 17 times in Scopus17 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     4 Cited 5 times in Scopus5 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: e0122650-e0122650. doi:10.1371/journal.pone.0043205     9 Cited 10 times in Scopus10 1
Lee, MinJae, Rahbar, Mohammad H., Brown, Matthew, Gensler, Lianne, Weisman, Michael, Diekman, Laura and Reveille, John D. (2018) A multiple imputation method based on weighted quantile regression models for longitudinal censored biomarker data with missing values at early visits. BMC Medical Research Methodology, 18 1: . doi:10.1186/s12874-017-0463-9     2 Cited 2 times in Scopus2 2
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, 21 6: 1-17. doi:10.1177/1073858414555404   10 14 Cited 14 times in Scopus14 20
Ellinghaus, David, Jostins, Luke, Spain, Sarah L., Cortes, Adrian, Bethune, Joern, Han, Buhm, Park, Yu Rang, Raychaudhuri, Soumya, Pouget, Jennie G., Hubenthal, Matthias, Folseraas, Trine, Wang, Yupeng, Esko, Tonu, Metspalu, Andres, Westra, Harm-Jan, Franke, Lude, Pers, Tune H., Weersma, Rinse K., Collij, Valerie, D'Amato, Mauro, Halfvarson, Jonas, Jensen, Anders Boeck, Lieb, Wolfgang, Degenhardt, Franziska, Forstner, Andreas J., Hofmann, Andrea, Schreiber, Stefan, Mrowietz, Ulrich, Juran, Brian D., Lazaridis, Kostantinos N., Brunak, Soren, Dale, Anders M., Trembath, Richard C., Weidinger, Stephan, Weichenthal, Michael, Ellinghaus, Eva, Elder, James T., Barker, Jonathan N. W. N., Andreassen, Ole A., McGovern, Dermot P., Karlsen, Tom H., Barrett, Jeffrey C., Parkes, Miles, Brown, Matthew A. and Franke, Andre (2016) Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. Nature Genetics, 48 5: 510-518. doi:10.1038/ng.3528     114 Cited 123 times in Scopus123 137
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     27 Cited 30 times in Scopus30 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.     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     14 Cited 14 times in Scopus14 5
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). 2-4 February 2012.     0
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: Australian Rheumatology Association in conjunction with Rheumatology Health Professionals 53rd Annual Scientific Meeting Conference Abstracts. Australian Rheumatology Association in conjunction with Rheumatology Health Professionals 53rd Annual Scientific Meeting, Canberra, Australia, (2-2). 12‐15 May 2012.     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     17 Cited 19 times in Scopus19 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     6 Cited 6 times in Scopus6 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.     0
Brown, M. (2009) Anktylosing spondylitls and the spondyloar thropathies. Australian Doctor, 27/Feb: 25-32.     0
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     83 Cited 90 times in Scopus90 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     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.     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     14 Cited 16 times in Scopus16 2
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     11 Cited 9 times in Scopus9 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     31 Cited 34 times in Scopus34 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     6 Cited 7 times in Scopus7 3
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     21 Cited 25 times in Scopus25 0
Haynes, Katelin, Kenna, Tony, Glazov, Evgeny, Brown, Matthew A. and Thomas, Gethin (2014). A Novel Monocyte-Specific Transcript Underlies the Chromosome 21q22 Intergenic Genetic Association in Ankylosing Spondylitis. In: , , (S830-S830). .     1
Haynes, K., Kenna, T., Glazov, E., Brown, M. A. and Thomas, G. P. (2014). A Novel Monocyte-Specific Transcript Underlies the Chromosome 21Q22 Intergenic Genetic Association in Ankylosing Spondylitis. In: 9th International Cogress on Spondyloarthritis: Abstracts. 9th International Cogress on Spondyloarthritis, Gent, Belgium, (775-775). 23-25 October 2014.     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     45 Cited 52 times in Scopus52 48
Brown, MA (2005) Antibody treatments of inflammatory arthritis. Current Medicinal Chemistry, 12 25: 2943-2946. doi:10.2174/092986705774462842     13 Cited 16 times in Scopus16 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.    
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.    
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   2 27 Cited 34 times in Scopus34 0
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