Browse by all authors Browse By Author Name - Brown,+Matthew+A.

Browse Results (221 results found)

Subscribe to the RSS feed for this result setSubscribe to the RSS feed for this result set

Page 1 of 5

Result Pages:    1 2 3 4 5  next › last »

  Abstract Views File Downloads Thomson Reuters Web of Science Citation Count Scopus Citation Count Altmetric Score
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 66   6 Cited 6 times in Scopus6 10
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-U145. doi:10.1038/ng.3226 9   1 37
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 97   231 Cited 230 times in Scopus230 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 49   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.694 496   310 Cited 326 times in Scopus326 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 50   0 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 59   147 Cited 164 times in Scopus164 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 80   8 Cited 10 times in Scopus10 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 52   5 Cited 5 times in Scopus5 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 37 6 13
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 66 4 5 Cited 6 times in Scopus6 6
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 86   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 74   3 Cited 3 times in Scopus3 1
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 63   0 0
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 39   2 Cited 2 times in Scopus2 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 81   15 Cited 16 times in Scopus16 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 108   16 Cited 17 times in Scopus17 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 42   13 Cited 10 times in Scopus10 42
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 118 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 172   331 Cited 341 times in Scopus341 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 48   6 Cited 3 times in Scopus3 0
Pointon, Jennifer J., Harvey, David, Karaderi, Tugce, Appleton, Louise H., Farrar, Claire, Brown, Matthew A. and Wordsworth, Bryan P. (2009). A Region On Chromosome 16 Associated with Ankylosing Spondylitis. In: Rheumatology. Annual Meeting of the British-Society-of-Rheumatology, Glasgow Scotland, (I53-I53). Apr 28-May 01, 2009. 4   0
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 43   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. 29  
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 98 1 32 Cited 33 times in Scopus33 0
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 84 3 9 Cited 7 times in Scopus7 0
Pimentel-Santos, F. M., Costantino, Felicie, Cortes, Adrian, Garchon, Henri-Jean, Hadler, Johanna, Breban, Maxime, Brown, Matthew A. and Branco, Jaime C. (2014). Association study in portuguese patients with ankylosing spondylitis using the immunochip. In: European Workshop for Rheumatology Research, Lisbon, Portugal, (A39-A40). 20-22 February 2014. doi:10.1136/annrheumdis-2013-205124.90 9   0 0
Sparrow, Duncan B., McInerney-Leo, Aideen, Gucev, Zoran S., Gardiner, Brooke, Marshall, Mhairi, Leo, Paul J., Chapman, Deborah L., Tasic, Velibor, Shishko, Abduhadi, Brown, Matthew A., Duncan, Emma L. and Dunwoodie, Sally L. (2013) Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics, 22 8: 1625-1631. doi:10.1093/hmg/ddt012 65   11 Cited 10 times in Scopus10 0
Robinson, Philip Cameron, Wordsworth, Bryan Paul, Reveille, John D. and Brown, Matthew A. (2013) Axial spondyloarthritis: a new disease entity, not necessarily early ankylosing spondylitis. Annals of the Rheumatic Diseases, 72 2: 162-164. doi:10.1136/annrheumdis-2012-202073 58   18 Cited 20 times in Scopus20 3
Maller, Julian B., McVean, Gilean, Byrnes, Jake, Vukcevic, Damjan, Palin, Kimmo, Su, Zhan, Howson, Joanna M. M., Auton, Adam, Myers, Simon, Morris, Andrew, Pirinen, Matti, Brown, Matthew A., Burton, Paul R., Caulfield, Mark J., Compston, Alastair, Farrall, Martin, Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Mathew, Christopher G., Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R., Worthington, Jane, Craddock, Nick, Hurles, Matthew, Ouwehand, Willem, Parkes, Miles, Rahman, Nazneen, Duncanson, Audrey, Todd, John A., Kwiatkowski, Dominic P., Samani, Nilesh J., Gough, Stephen C. L., McCarthy, Mark I., Deloukas, Panagiotis and Donnelly, Peter (2012) Bayesian refinement of association signals for 14 loci in 3 common diseases. Nature Genetics, 44 12: 1294-1301. doi:10.1038/ng.2435 60   25 Cited 36 times in Scopus36 10
Patterson, Sarah L., Reveille, John D., Lee, MinJae, Ward, Michael M., Rahbar, Mohammad H., Brown, Matthew A., Weisman, Michael H. and Gensler, Lianne S. (2014). Better Outcomes in Ankylosing Spondylitis: The Synergistic Association Between Exercise and Tumor Necrosis Factor Inhibitors.. In: Arthritis & Rheumatology. , , (S250-S251). . 17   0
Okada, Yukinori, Wu, Di, Terao, Chikashi, Ikari, Katsunori, Kochi, Yuta, Ohmura, Koichiro, Suzuki, Akari, Yamanaka, Hisashi, Denny, Joshua C., Greenberg, Jeffrey D., Graham, Robert R., Brown, Matthew A., Bae, Sang-Cheol, Worthington, Jane, Padyukov, Leonid, Klareskog, Lars, Gregersen, Peter K., Visscher, Peter M., Siminovitch, Katherine A. and Plenge, Robert M. (2013). Biological Insights From Genetics Of Rheumatoid Arthritis Contribute To Drug Discovery. In: 77th Annual Meeting of the American-College-of-Rheumatology / 48th Annual Meeting of the Association-of-Rheumatology-Health-Professionals, San Diego Ca, (S723-S724). Oct 25-30, 2013. doi:10.1002/art.38216 73   0 0
Pointon, Jennifer J., Karaderi, Tugce, Appleton, Louise H., Harvey, David, Farrar, Claire, Brown, Matthew A. and Wordsworth, Bryan P. (2009). Candidate Genes for Ankylosing Spondylitis. In: Rheumatology. Annual Meeting of the British-Society-of-Rheumatology, Glasgow Scotland, (I53-I53). Apr 28-May 01, 2009. 48   0
Gensler, Lianne S., Ward, Michael M., Lee, MinJae, Rahbar, Mohammad, Brown, Matthew A., Reveille, John D. and Weisman, Michael H. (2013). Cardiovascular Disease Is Associated With Worse Functional Outcomes In Ankylosing Spondylitis. In: 77th Annual Meeting of the American-College-of-Rheumatology / 48th Annual Meeting of the Association-of-Rheumatology-Health-Professionals, San Diego Ca, (S1047-S1047). Oct 25-30, 2013. doi:10.1002/art.38216 24   0 0
Pahau, Helen, Brown, Matthew A., Paul, Sanjoy, Thomas, Ranjeny and Videm, Vibeke (2014) Cardiovascular disease is increased prior to onset of rheumatoid arthritis but not osteoarthritis: the population-based Nord-Trøndelag health study (HUNT). Arthritis Research and Therapy, 16 2: 1-9. doi:10.1186/ar4527 27   0 Cited 0 times in Scopus0 0
Lill, Christina M., Liu, Tian, Schjeide, Brit-Marem, Roehr, Johannes T., Akkad, Denis A., Damotte, Vincent, Alcina, Antonio, Ortiz, Migual A., Arroyo, Rafa, Lopez de Lapuente, Aitzkoa, Blaschke, Paul, Winkelmann, Alexander, Gerdes, Lisa-Ann, Luessi, Felix, Fernadez, Oscar, Izquierdo, Guillermo, Antiguedad, Alfredo, Hoffjan, Sabine, Cournu-Reibeix, Isabelle, Gromoller, Silvana, Faber, Hans, Liebsch, Maria, Meissner, Esther, Chanvillard, Coralie, Touze, Emmanuel, Pico, Fernando, Corcia, Philippe, 19ANZgene Consortium, Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Browning, Brian L., Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Cox, Mathew B., Chapman, Caron, Clarke, Glynnis, Danoy, Patrick, Drysdale, Karen, Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R., Hadler, Johanna, Jensen, Cathy J., Johnson, Laura J., Kermode, Allan G., Heard, Rober N., Kilpatrick, Trevor J., Lechner-Scott, Jeanette, Marriott, Mark, Mason, Deborah, Moscato, Pablo, Pender, Michael P., Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Slee, Mark, Stankovich, Jim, Stewart, Graeme J., Tajouri, Lotfi, Taylor, Bruce V., Wiley, James, Wilkins, Ella J., Dorner, Thomas, Steinhagen-Thiessen, Elisabeth, Baeckman, Lars, Heekeren, Hauke R., Li, Shu-Chen, Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Kumpfel, Tania, Kubisch, Christian, Epplen, Joerg T., Zettl, Uwe K., Fontaine, Bertrand, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena, Bertram, Lars and Zipp, Frauke (2012) Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Journal of Medical Genetics, 49 9: 558-562. doi:10.1136/jmedgenet-2012-101175 131   8 Cited 7 times in Scopus7 1
Ferreira, Manuel A. R., Welcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nature genetics, 40 9: 1056-1058. doi:10.1038/ng.209 59   508 Cited 533 times in Scopus533 16
Orozco, G., Hinks, A., Eyre, S., Ke, X. Y., Gibbons, L. J., Bowes, J., Flynn, E., Martin, P., Wellcome Trust Case Control Consortium, Brown, Matthew A., Linda Bradbury and et al (2009) Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.. Human Molecular Genetics, 18 14: 2693-2699. doi:10.1093/hmg/ddp193 59   54 Cited 55 times in Scopus55 7
van Koolwijk, Leonieke M. E., Ramdas, Wishal D., Ikram, M. Kamran, Jansonius, Nomdo M., Pasutto, Francesca, Hysi, Pirro G., Macgregor, Stuart, Janssen, Sarah F., Hewitt, Alex W., Viswanathan, Ananth C., ten Brink, Jacoline B., Hosseini, S. Mohsen, Amin, Najaf, Despriet, Dominiek D. G., Willemse-Assink, Jacqueline J. M., Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S., Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y., Gramer, Eugen, Welge-Luessen, Ulrich, Montgomery, Grant W., Carbonaro, Francis, Young, Terri L., The DCCT/EDIC Research Group, Bellenguez, Celine, McGuffin, Peter, Foster, Paul J., Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y., Czudowska, Monika A., Hofman, Albert, Uitterlinden, Andre G., Wolfs, Roger C. W., de Jong, Paulus T. V. M., Oostra, Ben A., Paterson, Andrew D., Wellcome Trust Case Control Consortium 2, Mackey, David A., Bergen, Arthur A. B., Reis, Andre, Hammond, Christopher J., Vingerling, Johannes R., Lemij, Hans G., Klaver, Caroline C. W., van Duijn, Cornelia M. and Brown, Matthew A. (2012) Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genetics, 8 5: e1002611.1-e1002611.13. doi:10.1371/journal.pgen.1002611 60   38 Cited 38 times in Scopus38 2
Nolte, Ilja M., Wallace, Chris, Newhouse, Stephen J., Waggott, Daryl, Fu, Jingyuan, Soranzo, Nicole, Gwilliam, Rhian, Deloukas, Panos, Savelieva, Irina, Zheng, Dongling, Dalageorgou, Chrysoula, Farrall, Martin, Samani, Nilesh J., Connell, John, Brown, Morris, Dominiczak, Anna, Lathrop, Mark, Zeggini, Eleftheria, Wain, Louise V., The DCCT/EDIC Research Group, Newton-Cheh, Christopher, Eijgelsheim, Mark, Rice, Kenneth, de Bakke, Paul I. W., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Asselbergs, Folkert W., Spector, Tim D., Carter, Nicholas D., Jeffery, Steve, Tobin, Martin, Caulfield, Mark, Snieder, Harold, Paterson, Andrew D., Munroe, Patricia B., Jamshidi, Yalda, The Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda (2009) Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies. PLoS One, 4 7: e6138-1-e6138-10. doi:10.1371/journal.pone.0006138 110   30 Cited 33 times in Scopus33 0
Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F. J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debta, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark, de Bruijn, Renée F.A.G., Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J., Chibnik, Lori B., Gislason, Gauti K., Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B., Phan, Thanh G., Oostra, Ben A., Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Wright, Margaret J., Franke, Barbara, Martin, Nicholas G., Thompson, Paul M., Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Nalls, Michael A., Uitterlinden, Andre G., Au, Rhoda, Elbaz, Alexis, Beare, Richard J., van Swieten, John C., Lopez, Oscar L., Harris, Tamara B., Chouraki, Vincent, Breteler, Monique M.B., De Jager, Philip L., Becker, James T., Vernooij, Meike W., Knopman, David, Fazekas, Franz, Wolf, Philip A., van der Lugt, Aad, Gudnason, Vilmundur, Longstreth Jr, W.T., Brown, Matthew A., Bennett, David A., van Duijn, Cornelia M., Mosley, Thomas H., Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J., Ikram, M. Arfan, Seshadri, Sudha and Cohorts Heart Aging Res Genomic Ep (2012) Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics, 44 5: 545-551. doi:10.1038/ng.2237 100   53 Cited 58 times in Scopus58 43
Holliday, Elizabeth G., Maguire, Jane M., Evans, Tiffany-Jane, Koblar, Simon A., Jannes, Jim, Sturm, Jonathan W., Hankey, Graeme J., Baker, Ross, Golledge, Jonathan, Parsons, Mark W., Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D., Lincz, Lisa F., Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Bevan, Steve, Bis, Joshua C., Boerwinkle, Eric, Boncoraglio, Giorgio B., Brott, Thomas G., Brown, Robert D., Jr., Cheng, Yu-Ching, Cole, John W., Cotlarciuc, Ioana, Devan, William J., Fornage, Myriam, Furie, Karen L., Gretarsdottir, Solveig, Gschwendtner, Andreas, Ikram, M. Arfan, Longstreth, W. T., Jr., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., Parati, Eugenio A., Psaty, Bruce M., Sharma, Pankaj, Stefansson, Kari, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Traylor, Matthew, Verhaaren, Benjamin F. J., Wiggins, Kerri L., Worrall, Bradford B., The Australian Stroke Genetics Collaborative, The International Stroke Genetics Consortium, The Wellcome Trust Case Control Consortium 2, Brown, Matthew A., Sudlow, Cathie, Rothwell, Peter M., Farrall, Martin, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S., Scott, Rodney J., Levi, Christopher and Attia, John (2012) Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nature Genetics, 44 10: 1147-1151. doi:10.1038/ng.2397 78   42 Cited 41 times in Scopus41 2
Imielinski, M., Baldassano, R. N., Griffiths, A., Russell, R. K., Annese, V., Dubinsky, M., Kugathasan, S., Bradfield, J. P., Walters, T. D., et al, International IBD Genetics Consortium, Brown, Matthew A. and Bradbury, Linda (2009) Common variants at five new loci associated with early-onset inflammatory bowel disease.. Nature Genetics, 41 12: 1335-1340. doi:10.1038/ng.489 86   203 Cited 222 times in Scopus222 5
Su, Zhan, Gay, Laura J., Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David C., Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Edkins, Sarah, van der Winkel, Anouk, Levine, David, Sasieni, Peter, Bellenguez, Celine, Howarth, Kimberley, Freeman, Colin, Trudgill, Nigel, Tucker, Art T., Pirinen, Matti, Peppelenbosch, Maikel P., van der Laan, Luc J. W., Kuipers, Ernst J., Drenth, Joost P. H., Peters, Wilbert H., Reynolds, John V., Kelleher, Dermot P., McManus, Ross, Grabsch, Heike, Prenen, Hans, Bisschops, Raf, Krishnadath, Kausila, Siersema, Peter D., van Baal, Jantine W. P. M., Middleton, Mark, Petty, Russell, Gillies, Richard, Burch, Nicola, Bhandari, Pradeep, Paterson, Stuart, Edwards, Cathryn, Penman, Ian, Vaidya, Kishor, Ang, Yeng, Murray, Iain, Patel, Praful, Ye, Weimin, Mullins, Paul, Wu, Anna H., Bird, Nigel C., Dallal, Helen, Shaheen, Nicholas J., Murray, Liam J., Koss, Konrad, Bernstein, Leslie, Romero, Yvonne, Hardie, Laura J., Zhang, Rui, Winter, Helen, Corley, Douglas A., Panter, Simon, Risch, Harvey A., Reid, Brian J., Sargeant, Ian, Gammon, Marilie D., Smart, Howard, Dhar, Anjan, McMurtry, Hugh, Ali, Haythem, Liu, Geoffrey, Casson, Alan G., Chow, Wong-Ho, Rutter, Matt, Tawil, Ashref, Morris, Danielle, Nwokolo, Chuka, Isaacs, Peter, Rodgers, Colin, Ragunath, Krish, MacDonald, Chris, Haigh, Chris, Monk, David, Davies, Gareth, Wajed, Saj, Johnston, David, Gibbons, Michael, Cullen, Sue, Church, Nicholas, Langley, Ruth, Griffin, Michael, Alderson, Derek, Deloukas, Panos, Hunt, Sarah E., Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Anderson, Mark, Brooks, Claire, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas, Trynka, Gosia, Wijmenga, Cisca, Cazier, Jean-Baptiste, Atherfold, Paul, Nicholson, Anna M., Gellatly, Nichola L., Glancy, Deborah, Cooper, Sheldon C., Cunningham, David, Lind, Tore, Hapeshi, Julie, Ferry, David, Rathbone, Barrie, Brown, Julia, Love, Sharon, Attwood, Stephen, MacGregor, Stuart, Watson, Peter, Sanders, Scott, Ek, Weronica, Harrison, Rebecca F., Moayyedi, Paul, de Caestecker, John, Barr, Hugh, Stupka, Elia, Vaughan, Thomas L., Peltonen, Leena, Spencer, Chris C. A., Tomlinson, Ian, Donnelly, Peter and Jankowski, Janusz A. Z. (2012) Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nature Genetics, 44 10: 1131-1136. doi:10.1038/ng.2408 410   39 Cited 41 times in Scopus41 17
Fakiola, Michaela, Strange, Amy, Cordell, Heather J., Miller, E. Nancy, Pirinen, Matti, Su, Zhan, Mishra, Anshuman, Mehrotra, Sanjana, Monteiro, Gloria R., Band, Gavin, Bellenguez, Celine, Dronov, Serge, Edkins, Sarah, Freeman, Colin, Giannoulatou, Eleni, Gray, Emma, Hunt, Sarah E., Lacerda, Henio G., Langford, Cordelia, Pearson, Richard, Pontes, Nubia N., Rai, Madhukar, Singh, Shri P., Smith, Linda, Sousa, Olivia, Vukcevic, Damjan, Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Wilson, Mary E., Deloukas, Panos, Peltonen, Leena, Christiansen, Frank, Witt, Campbell, Jeronimo, Selma M. B., Sundar, Shyam, Spencer, Chris C. A., Blackwell, Jenefer M., Donnelly, Peter, LeishGEN Consortium and Wellcome Trust Case Control Consortium 2 (2013) Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. Nature Genetics, 45 2: 208-213. doi:10.1038/ng.2518 76   20 Cited 20 times in Scopus20 12
Timpson, Nicholas J., Tobias, Jon H., Richards, J. Brent, Soranzo, Nicole, Duncan, Emma L., Sims, Anne-Maree, Whittaker, Pamela, Kumanduri, Vasudev, Zhai, Guangju, Glaser, Beate, Eisman, John, Jones, Graeme, Nicholson, Geoff, Prince, Richard, Seeman, Ego, Spector, Tim D., Brown, Matthew A., Peltonen, Leena, Smith, George Davey, Deloukas, Panos and Evans, David M. (2009) Common variants in the region around Osterix are associated with bone mineral density and growth in childhood. Human Molecular Genetics, 18 8: 1510-1517. doi:10.1093/hmg/ddp052 110   55 Cited 59 times in Scopus59 0
Gharahkhani, Puya, Burdon, Kathryn P., Fogarty, Rhys, Sharma, Shiwani, Hewitt, Alex W., Martin, Sarah, Law, Matthew H., Cremin, Katie, Bailey, Jessica N. Cooke, Loomis, Stephanie J., Pasquale, Louis R., Haines, Jonathan L., Hauser, Michael A., Viswanathan, Ananth C., McGuffin, Peter, Topouzis, Fotis, Foster, Paul J., Graham, Stuart L., Casson, Robert J., Chehade, Mark, White, Andrew J., Zhou, Tiger, Souzeau, Emmanuelle, Landers, John, Fitzgerald, Jude T., Klebe, Sonja, Ruddle, Jonathan B., Goldberg, Ivan, Healey, Paul R., Wellcome Trust Case Control Consortium 2, NEIGHBORHOOD Consortium, Mills, Richard A., Wang, Jie Jin, Montgomery, Grant W., Martin, Nicholas G., Radford-Smith, Graham, Whiteman, David C., Brown, Matthew A., Wiggs, Janey L., Mackey, David A., Mitchell, Paul, MacGregor, Stuart and Craig, Jamie E. (2014) Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma. Nature Genetics, 46 10: 1120-1125. doi:10.1038/ng.3079 36 2 1 Cited 2 times in Scopus2 56
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group, Wellcome Trust Case Control Consortium 2, Zhou, Kaixin, Tavendale, Roger, Donnelly, Louise A., Schofield, Chris, Burch, Lindsay, Carr, Fiona, Colhoun, Helen, Morris, Andrew D., Sutherland, Calum, Palmer, Colin N. A., Pearson, Ewan, Bellenguez Celine, Spencer, Chris C. A., Strange, Amy, Freeman, Colin, Rautanen, Anna, McCarthy, Mark I., Donnelly, Peter, Bennett, Amanda J., Coleman, Ruth L., Groves, Christopher J., McCarthy, Mark I., Holman, Rury R., Hawley, Simon A., Hardie, Grahame, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Langford, Cordelia, Peltonen, Leena, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G, Trembath, Richard, Plomin, Robert, Sawcer, Stephen J., Samani, Nilesh J., Viswanathan, Aananth C., Wood, Nicholas W., Harries, Lorna W., Hattersley, Andrew T., Doney, Alex S. F., McCarthy, Mark I. and Donnelly, Peter (2011) Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nature Genetics, 43 2: 117-120. doi:10.1038/ng.735 154   118 Cited 146 times in Scopus146 2
Loos, Ruth J. F., Evans, David M., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008) Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nature Genetics, 40 6: 768-775. doi:10.1038/ng.140 89   650 Cited 665 times in Scopus665 27
Ritchie, Matthew E., Liu, Ruijie, Carvalho, Benilton S., The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene), Irizarry, Rafael A., Brown, Matthew A., Csurhes, Peter A., Danoy, Patrick, Greer, Judith M., Hadler, Johanna, Pryce, Karena and Pender, Michael P. (2011) Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips. BMC Bioinformatics, 12 68.1-68.12. doi:10.1186/1471-2105-12-68 79 12 11 Cited 13 times in Scopus13 1

Page 1 of 5

Result Pages:    1 2 3 4 5  next › last »