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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 95   229 Cited 224 times in Scopus224 30
Claushuis, Dorith, Cortes, Adrian, Bradbury, Linda A., Martin, Tammy M., Rosenbaum, James T., Reveille, John D., Wordsworth, Paul, Pointon, Jennifer, Evans, David, Leo, Paul, Mukhopadhyay, Pamela and Brown, Matthew A. (2012). A genomewide association study of anterior uveiti. In: Abstracts of the American College of Rheumatology & Association of Rheumatology Health Professionals, Annual Scientific Meeting. Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, DC, United States, (S259-S259). 9-14 November 2012. doi:10.1002/art.37735 48   0 0
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 58   491 Cited 511 times in Scopus511 16
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 87   634 Cited 648 times in Scopus648 24
Codd, Veryan, Mangino, Massimo, van der Harst, Pim, Braund, Peter S., Kaiser, Michael, Beveridge, Alan J., Rafelt, Suzanne, Moore, Jasbir, Nelson, Chris, Soranzo, Nicole, Zhai, Guangju, Valdes, Ana M., Blackburn, Hannah, Mateo Leach, Irene, de Boer, Rudolf A., Kimura, Masayuki, Aviv, Abraham, Wellcome Trust Case Control Consortium, Goodall, Alison H., Ouwehand, Willem, van Veldhuisen, Dirk J., van Gilst, Wiek H., Navis, Gerjan, Burton, Paul R., Tobin, Martin D., Hall, Alistair S., Thompson, John R., Spector, Tim, Samani, Nilesh J., Brown, Matthew Arthur, Bradbury, Linda A. and Pointon, Jennifer J. (2010) Common variants near TERC are associated with mean telomere length. Nature Genetics, 42 3: 197-199. doi:10.1038/ng.532 223   105 Cited 111 times in Scopus111 15
Fischer, Roman, Trudgian, David C., Wright, Cynthia, Thomas, Gethin, Bradbury, Linda A., Brown, Matthew A., Bowness, Paul and Kessler, Benedikt M. (2012) Discovery of candidate serum proteomic and metabolomic biomarkers in ankylosing spondylitis. Molecular and Cellular Proteomics, 11 2: 013904.1-013904.11. doi:10.1074/mcp.M111.013904 62   1 Cited 23 times in Scopus23 2
Kenna, Tony J., Davidson, Stuart I., Duan, Ran, Bradbury, Linda A., McFarlane, Janelle, Smith, Malcolm, Weedon, Helen, Street, Shayna, Thomas, Ranjeny, Thomas, Gethin P. and Brown, Matthew A. (2012) Enrichment of circulating IL-17-secreting IL-23 receptor-positive gamma-delta T cells in patients with active ankylosing spondylitis. Arthritis and Rheumatism, 64 5: 1420-1429. doi:10.1002/art.33507 227 1 39 Cited 43 times in Scopus43 2
Karaderi, T., Pointon, J. J., Wordsworth, T. W. H., Harvey, D., Appleton, L. H., Cohen, C. J., Farrar, C., Harin, A., Brown, M. A., Wordsworth, B. P., The Australo-Anglo-American Spondyloarthritis Consortium, Kenna, Tony J., Gethin, Thomas P., Bradbury, Linda A. and Danoy, Patrick (2012) Evidence of genetic association between TNFRSF1A encoding the p55 tumour necrosis factor receptor, and ankylosing spondylitis in UK Caucasians. Clinical and Experimental Rheumatology, 30 1: 110-113. 107 15 4 Cited 4 times in Scopus4
Fisher, Sheila A., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Nature Genetics, 40 6: 710-712. doi:10.1038/ng.145 86   248 Cited 268 times in Scopus268 1
Weedon, Michael N., Evans, David M., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008) Genome-wide association analysis identifies 20 loci that influence adult height. Nature Genetics, 40 5: 575-583. doi:10.1038/ng.121 69   426 Cited 417 times in Scopus417 27
Samani, Nilesh J., Erdmann, Jeanette, Hall, Alistair S., Hengstenberg, Christian, Mangino, Mangino, Mayer, Bjoern, Dixon, Richard J., Meitinger, Thomas, Braund, Peter, Wichmann, H. Erich, Barrett, Jennifer H., Konig, Inke R., Stevens, Suzanne E., Szymczak, Silke, Tregouet, David-Alexandre, Iles, Mark M., Pahlke, Friedrich, Pollard, Helen, Lieb, Wolfgang, Cambien, Francois, Fischer, Marcus, Ouwehand, Willem, Blankenberg, Stefan, Balmforth, Anthony J., Baessler, Andrea, Ball, Steven G., Strom, Tim M., Braenne, Ingrid, Gieger, Christian, Deloukas, Panos, Tobin, Martin D., Ziegler, Andreas, Thompson, John R., Schunkert, Heribert, for the WTCCC and the Cardiogenics Consortium, Bradbury, Linda A. and Brown, Matthew A. (2007) Genomewide association analysis of coronary artery disease. The New England Journal of Medicine, 357 5: 443-453. doi:10.1056/NEJMoa072366 155   975 Cited 1013 times in Scopus1013 3
Barrett, Jeffrey C., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics, 40 8: 955-962. doi:10.1038/ng.175 59   1261 Cited 1325 times in Scopus1325 25
Reveille, John D., Sims, Anne-Marie, Danoy, Patrick, Evans, David M., Leo, Paul, Pointon, Jennifer J., Jin, Rui, Zhou, Xiaodong, Bradbury, Linda A., Appleton, Louise H., Davis, John C., Diekman, Laura, Doan, Tracey, Dowling, Alison, Duan, Ran, Duncan, Emma L., Farrar, Claire, Hadler, Johanna, Harvey, David, Karaderi, Tugce, Mogg, Rebecca, Pomeroy, Emma, Pryce, Karena, Taylor, Jacqueline, Savage, Laurie, Deloukas, Panos, Kumanduri, Vasudev, Peltonen, Leena, Ring, Sue M., Whittaker, Pamela, Glazov, Evgeny, Thomas, Gethin P., Maksymowych, Walter P., Inman, Robert D., Ward, Michael M., Stone, Millicent A., Weisman, Michael H., Wordsworth, B. Paul and Brown, Mathew A. (2010) Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nature Genetics, 42 2: 123-127. doi:10.1038/ng.513 198   189 Cited 195 times in Scopus195 9
Duncan, Emma L., Danoy, Patrick, Kemp, John P., Leo, Paul J., McCloskey, Eugene, Nicholson, Geoffrey C., Eastell, Richard, Prince, Richard L., Eisman, John A., Jones, Graeme, Sambrook, Philip N., Reid, Ian R., Dennison, Elaine M., Wark, John, Richards, J. Brent, Uitterlinden, Andre G., Spector, Tim D., Esapa, Chris, Cox, Roger D., Brown, Steve D. M., Thakker, Rajesh V., Addison, Kathryn A., Bradbury, Linda A., Center, Jacqueline R., Cooper, Cyrus, Cremin, Catherine, Estrada, Karol, Felsenberg, Dieter, Glueer, Claus-C., Hadler, Johanna, Henry, Margaret J., Hofman, Albert, Kotowicz, Mark A., Makovey, Joanna, Nguyen, Sing C., Nguyen, Tuan V., Pasco, Julie A., Pryce, Karena, Reid, David M., Rivadeneira, Fernando, Roux, Christian, Stefansson, Kari, Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Tichawangana, Rumbidzai, Evans, David M. and Brown, Matthew A. (2011) Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. PLoS Genetics, 7 4: e1001372.1-e1001372.10. doi:10.1371/journal.pgen.1001372 142 34 62 Cited 65 times in Scopus65 0
Boraska, Vesna, Jeroncic, Ana, Colonna, Vincenza, Southam, Lorraine, Nyholt, Dale R., Rayner, Nigel William, Perry, John R. B., Toniolo, Daniela, Albrecht, Eva, Ang, Wei, Bandinelli, Stefania, Barbalic, Maja, Barroso, Ines, Beckmann, Jacques S., Biffar, Reiner, Boomsma, Dorret, Campbell, Harry, Corre, Tanguy, Erdmann, Jeanette, Esko, Tonu, Fischer, Krista, Franceschini, Nora, Frayling, Timothy M., Girotto, Giorgia, Gonzalez, Juan R., Harris, Tamara B., Heath, Andrew C., Heid, Iris M., Hoffmann, Wolfgang, Hofman, Albert, Horikoshi, Momoko, Zhao, Jing Hua, Jackson, Anne U., Hottenga, Jouke-Jan, Jula, Antti, Kahonen, Mika, Khaw, Kay-Tee, Kiemeney, Lambertus A., Klopp, Norman, Kutalik, Zoltan, Lagou, Vasiliki, Launer, Lenore J., Lehtimaki, Terho, Lemire, Mathieu, Lokki, Marja-Liisa, Loley, Christina, Luan, Jian'an, Mangino, Massimo, Leach, Irene Mateo, Medland, Sarah E., Mihailov, Evelin, Montgomery, Grant W., Navis, Gerjan, Newnham, John, Nieminen, Markku S., Palotie, Aarno, Panoutsopoulou, Kalliope, Peters, Annette, Pirastu, Nicola, Polasek, Ozren, Rehnstrom, Karola, Ripatti, Samuli, Ritchie, Graham R. S., Rivadeneira, Fernando, Robino, Antonietta, Samani, Nilesh J., Shin, So-Youn, Sinisalo, Juha, Smit, Johannes H., Soranzo, Nicole, Stolk, Lisette, Swinkels, Dorine W., Tanaka, Toshiko, Teumer, Alexander, Tonejes, Anke, Traglia, Michela, Tuomilehto, Jaakko, Valsesia, Armand, van Gilst, Wiek H., van Meurs, Joyce B. J., Smith, Albert Vernon, Viikari, Jorma, Vink, Jacqueline M., Waeber, Gerard, Warrington, Nicole M., Widen, Elisabeth, Willemsen, Gonneke, Wright, Alan F., Zanke, Brent W., Zgaga, Lina, Wellcome Trust Case Control Consortium, Bradbury, Linda A., Pointon, Jennifer J., Brown, Matthew A., Boehnke, Michael, d'Adamo, Adamo Pio, de Geus, Eco, Demerath, Ellen W., den Heijer, Martin, Eriksson, Johan G., Ferrucci, Luigi, Gieger, Christian, Gudnason, Vilmundur, Hayward, Caroline, Hengstenberg, Christian, Hudson, Thomas J., Jarvelin, Marjo-Riitta, Kogevinas, Manolis, Loos, Ruth J. F., Martin, Nicholas G., Metspalu, Andres, Pennell, Craig E., Penninx, Brenda W., Perola, Markus, Raitakari, Olli, Salomaa, Veikko, Schreiber, Stefan, Schunkert, Heribert, Spector, Tim D., Stumvoll, Michael, Uitterlinden, Andre G., Ulivi, Sheila, van der Harst, Pim, Vollenweider, Peter, Volzke, Henry, Wareham, Nicholas J., Wichmann, H-Erich, Wilson, James F., Rudan, Igor, Xue, Yali and Zeggini, Eleftheria (2012) Genome-wide meta-analysis of common variant differences between men and women. Human Molecular Genetics, 21 21: 4805-4815. doi:10.1093/hmg/dds304 71   4 Cited 3 times in Scopus3 2
Eyre, Steve, Bowes, John, Diogo, Dorothee, Lee, Annette, Barton, Anne, Martin, Paul, Zhernakova, Alexandra, Stahl, Eli, Viatte, Sebastien, McAllister, Kate, Amos, Christopher I., Padyukov, Leonid, Toes, Rene E. M., Huizinga, Tom W. J., Wijmenga, Cisca, Trynka, Gosia, Franke, Lude, Westra, Harm-Jan, Alfredsson, Lars, Hu, Xinli, Sandor, Cynthia, de Bakker, Paul I. W., Davila, Sonia, Khor, Chiea Chuen, Heng, Khai Koon, Andrews, Robert, Edkins, Sarah, Hunt, Sarah E., Langford, Cordelia, Symmons, Deborah, Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate, Wellcome Trust Case Control Consortium, Concannon, Pat, Onengut-Gumuscu, Suna, Rich, Stephen S., Deloukas, Panos, Gonzalez-Gay, Miguel A., Rodriguez-Rodriguez, Luis, Arlsetig, Lisbeth, Martin, Javier, Rantapaa-Dahlqvist, Solbritt, Plenge, Robert M., Raychaudhuri, Soumya, Klareskog, Lars, Gregersen, Peter K., Worthington, Jane, Bradbury, Linda A., Pointon, Jennifer J. and Brown, Matthew A. (2012) High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics, 44 12: 1336-1340. doi:10.1038/ng.2462 45 2 102 Cited 98 times in Scopus98 29
Cortes, Adrian, Hadler, Johanna, Pointon, Jenny P., Robinson, Philip C., Karaderi, Tugce, Leo, Paul, Cremin, Katie, Pryce, Karena, Harris, Jessica, Lee, Seunghun, Joo, Kyung Bin, Shim, Seung-Cheol, Weisman, Michael, Ward, Michael, Zhou, Xiaodong, Garchon, Henri-Jean, Chiocchia, Gilles, Nossent, Johannes, Lie, Benedicte A., Førre, Øystein, Tuomilehto, Jaakko, Laiho, Kari, Jiang, Lei, Liu, Yu, Wu, Xin, Bradbury, Linda A., Elewaut, Dirk, Burgos-Vargas, Ruben, Stebbings, Simon, Appleton, Louise, Farrah, Claire, Lau, Jonathan, Kenna, Tony J., Haroon, Nigil, Ferreira, Manuel A., Yang, Jian, Mulero, Juan, Fernandez-Sueiro, Jose Luis, Gonzalez-Gay, Miguel A., Lopez-Larrea, Carlos, Deloukas, Panos, Donnelly, Peter, Bowness, Paul, Gafney, Karl, Gaston, Hill, Gladman, Dafna D., Rahman, Proton, Maksymowych, Walter P., Xu, Huji, Crusius, J. Bart A., van der Horst-Bruinsma, Irene E., Chou, Chung-Tei, Valle-Oñate, Raphael, Romero-Sánchez, Consuelo, Hansen, Inger Myrnes, Pimentel-Santos, Fernando M., Inman, Robert D., Videm, Vibeke, Martin, Javier, Breban, Maxime, Reveille, John D., Evans, David M., Kim, Tae-Hwan, Wordsworth, Bryan Paul, Brown, Matthew A., Australo-Anglo-American Spondyloarthritis Consortium (TASC), Groupe Française d?Etude Génétique des Spondylarthrites (GFEGS), Nord-Trøndelag Health Study (HUNT), Spondyloarthritis Research Consortium of Canada (SPARCC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) (2013) Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nature Genetics, 45 7: 730-740. doi:10.1038/ng.2667 140   52 Cited 57 times in Scopus57 17
The Australo-Anglo-American Spondyloarthritis Consortium (TASC), Wellcome Trust Case Control Consortium 2 (WTCCC2), Evans, David M., Spencer, Chris C. A., Pointon, Jennifer J., Su, Zhan, Harvey, David, Kochan, Grazyna, Opperman, Udo, Dilthey, Alexander, Pirinen, Matti, Stone, Millicent A., Appleton, Louise, Moutsianis, Loukas, Leslie, Stephen, Wordsworth, Tom, Kenna, Tony J., Karaderi, Tugce, Thomas, Gethin P., Ward, Michael M., Weisman, Michael H., Farrar, Claire, Bradbury, Linda A., Danoy, Patrick, Inman, Robert D., Maksymowych, Walter, Gladman, Dafna, Rahman, Proton, Spondyloarthritis Research Consortium of Canada (SPARCC), Morgan, Ann, Marzo-Ortega, Helena, Bowness, Paul, Gaffney, Karl, Gaston, J. S. Hill, Smith, Malcolm, Bruges-Armas, Jacome, Couto, Ana-Rita, Sorrentino, Rosa, Paladini, Fabiana, Ferreira, Manuel A., Xu, Huji, Liu, Yu, Jiang, Lei, Lopez-Larrea, Carlos, Díaz-Pena, Roberto, López-Vázquez, Antonio, Zayats, Tetyana, Band, Gavin, Bellenguez, Céline, Blackburn, Hannah, Blackwell, Jenefer M., Bramon, Elvira, Bumpstead, Suzannah J., Casas, Juan P., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Duncanson, Audrey, Edkins, Sarah, Freeman, Colin, Gillman, Matthew, Gray, Emma, Gwilliam, Rhian, Hammond, Naomi, Hunt, Sarah E., Jankowski, Janusz, Jayakumar, Alagurevathi, Langford, Cordelia, Liddle, Jennifer, Markus, Hugh S., Mathew, Christopher G., McCann, Owen T., McCarthy, Mark I., Palmer, Colin N. A., Peltonen, Leena, Plomin, Robert, Potter, Simon C., Rautanen, Anna, Ravindrarajah, Radhi, Ricketts, Michelle, Samani, Nilesh, Sawcer, Stephen J., Strange, Amy, Trembath, Richard C., Viswanathan, Ananth C., Waller, Matthew, Weston, Paul, Whittaker, Pamela, Widaa, Sara, Wood, Nicholas W., McVean, Gilean, Reveille, John D., Wordsworth, B. Paul, Brown, Matthew A. and Donnelly, Peter (2011) Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nature Genetics, 43 8: 761-767. doi:10.1038/ng.873 148   181 Cited 187 times in Scopus187 6
Sandhu, M. S., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008) LDL-cholesterol concentrations: a genome-wide association study. The Lancet, 371 9611: 483-491. doi:10.1016/S0140-6736(08)60208-1 64   198 Cited 202 times in Scopus202 0
Linsel-Nitschke, Patrick, Gotz, Anika, Braenne, Ingrid, Erdmann, Jeanette, Braund, Peter, Hengstenberg, Christian, Stark, Klaus, Fischer, Marcus, Chreiber, Stefan, El Mokhtari, Nour Eddine, Schaefer, Arne, Schrezenmeier, Jurgen, Rubin, Diana, Hinney, Anke, Reinehr, Thomas, Roth, Christian, Ortlepp, Jan, Hanrath, Peter, Hall, Alistair, S., Mangino, Massimo, Lieb, Wolfgang, Lamina, Claudia, Heid, Iris M., Doering, Angela, Gieger, Christian, Peters, Annette, Meitinger, Thomas, Wichmann, H.-Erich, Konig, Inke R., Ziegler, Andreas, Kronenberg, Florian, Samani, Nilesh J., Schunkert, Heribert, for the Wellcome Trust Case Control Consortium (WTCCC), Bradbury, Linda A., Brown, Matthew A. and Cardiogenics Consortium (2008) Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease: A Mendelian Randomisation study. PLoS One, 3 8: e2986-1-e2986-9. doi:10.1371/journal.pone.0002986 146 3 46 Cited 54 times in Scopus54 9
Nejentsev, S., Howson, J. M. M., Walker, N. M., Szeszko, J., Field, S. F., Stevens, H. E., Reynolds, P., Hardy, M., King, E., Masters, J., Hulme, J., Maier, L. M., Smyth, D., Bailey, R., Cooper, J. D., Ribas, G., Campbell, R. D., The Wellcome Trust Case Control Consortium, Bradbury, Linda A. and Brown, Matthew A. (2007) Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature, 450 7171: 887-892. doi:10.1038/nature06406 89   267 Cited 269 times in Scopus269 1
Grozeva, Detelina, Kirov, George, Ivanov, Dobril, Jones, Ian R., Jones, Lisa, Green, Elaine K., St Clair, David M., Young, Allan H., Ferrier, Nicol, Farmer, Anne E., McGuffin, Peter, Holmans, Peter A., Owen, Michael J., O'Donovan, Michael C., Craddock, Nick, Wellcome Trust Case Control Consortuim, Bradbury, Linda A., Pointon, Jennifer J. and Brown, Matthew A. (2010) Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and schizophrenia. Archives of General Psychiatry, 67 4: 318-327. doi:10.1001/archgenpsychiatry.2010.25 83   93 Cited 94 times in Scopus94 0
Barton, Anne, Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility. Human Molecular Genetics, 17 15: 2274-2279. doi:10.1093/hmg/ddn128 30   94 Cited 105 times in Scopus105 0
Thompson, Wendy, Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2007) Rheumatoid arthritis association at 6q23. Nature Genetics, 39 12: 1431-1433. doi:10.1038/ng.2007.32 58   245 Cited 253 times in Scopus253 0
Barton, Anne, Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. Nature Genetics, 40 10: 1156-1159. doi:10.1038/ng.218 45   92 Cited 95 times in Scopus95 0