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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 52   3 Cited 4 times in Scopus4 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 91   225 Cited 224 times in Scopus224 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 35   2 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.694 483   278 Cited 299 times in Scopus299 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 46   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 56   146 Cited 163 times in Scopus163 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 75   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 47   4 Cited 4 times in Scopus4 1
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 58   4 Cited 5 times in Scopus5 5
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 71   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 59   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 29   0 Cited 0 times in Scopus0 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 78   14 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 101   15 Cited 15 times in Scopus15 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 31   11 Cited 8 times in Scopus8 41
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 115 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 167   312 Cited 326 times in Scopus326 7
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 43   6 Cited 3 times in Scopus3 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 39   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. 25  
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 94 1 30 Cited 29 times in Scopus29 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 79 3 8 Cited 6 times in Scopus6 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: Annals of the Rheumatic Diseases. European Workshop for Rheumatology Research, Lisbon Portugal, (A39-A40). Feb 20-22, 2014. doi:10.1136/annrheumdis-2013-205124.90 5   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 54   6 Cited 7 times in Scopus7 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 54   13 Cited 16 times in Scopus16 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 55   18 Cited 25 times in Scopus25 2
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 66   0 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 18   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 1-9. doi:10.1186/ar4527 18   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 120   6 Cited 4 times in Scopus4 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 56   477 Cited 502 times in Scopus502 13
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 55   51 Cited 53 times in Scopus53 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 55   33 Cited 33 times in Scopus33 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 107   29 Cited 31 times in Scopus31 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 89   44 Cited 50 times in Scopus50 44
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 74   35 Cited 31 times in Scopus31 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 83   192 Cited 208 times in Scopus208 2
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 403   28 Cited 32 times in Scopus32 16
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 64   16 Cited 16 times in Scopus16 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 106   54 Cited 58 times in Scopus58 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 17 1 0 42
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.735 144   106 Cited 134 times in Scopus134 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 85   626 Cited 638 times in Scopus638 26
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 73 9 11 Cited 13 times in Scopus13 1
Jiang, Lei, Willner, Dana, Danoy, Patrick, Xu, Huji and Brown, Matthew A. (2013) Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. G3-Genes Genomes Genetics, 3 1: 23-29. doi:10.1534/g3.112.004069 43   5 Cited 2 times in Scopus2 0
Knight, Jo, Spain, Sarah L., Capon, Francesca, Hayday, Adrian, Nestle, Frank O., Clop, Alex, Wellcome Trust Case Control Consortium, Brown, Matthew A., Genetic Analysis of Psoriasis Consortium, Barker, Jonathan N., Weale, Michael E. and Trembath, Richard C. (2012) Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis. Human Molecular Genetics, 21 23: 5185-5192. doi:10.1093/hmg/dds344 41   11 Cited 12 times in Scopus12 1
Kochan, Grazyna, Krojer, Tobias, Harvey, David, Fischer, Roman, Chen, Liye, Vollmar, Melanie, von Delft, Frank, Kavanagh, Kathryn L., Brown, Matthew A., Bowness, Paul, Wordsworth, Paul, Kessler, Benedikt M. and Oppermann, Udo (2011) Crystal structures of the endoplasmic reticulum aminopeptidase-1 (ERAP1) reveal the molecular basis for N-terminal peptide trimming. Proceedings of the National Academy of Sciences of the United States of America, 108 19: 7745-7750. doi:10.1073/pnas.1101262108 59   49 Cited 54 times in Scopus54 1
Peach, Chris A., Zhang, Yun, Dunford, James E., Brown, Matthew A. and Carr, Andrew J. (2007) Cuff tear arthropathy - Evidence of functional variation in pyrophosphate metabolism genes. Clinical Orthopaedics and Related Research, 462: 67-72. doi:10.1097/BLO.0b013e31811f39de 33   7 Cited 10 times in Scopus10 0
Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschke, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stephane, Szabo, Attila J., Tory, Kalman, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hulya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie and Hildebrandt, Friedhelm (2013) Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. American Journal of Human Genetics, 93 5: 915-925. doi:10.1016/j.ajhg.2013.09.012 34   9 Cited 9 times in Scopus9 3
Cortes, Adrian, Robinson, Philip and Brown, Matthew A. (2012). Dense genotyping of candidate genes identifies 16 new susceptibility loci in ankylosing spondylitis. 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, (S1053-S1054). 9-14 November 2012. doi:10.1002/art.37735 32   1 0

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