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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 91   225 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 46   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 56   477 Cited 502 times in Scopus502 13
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
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.532 217   103 Cited 107 times in Scopus107 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 56   0 Cited 21 times in Scopus21 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 219 1 33 Cited 39 times in Scopus39 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. 105 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 85   247 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 63   417 Cited 411 times in Scopus411 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 153   951 Cited 986 times in Scopus986 0
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 57   1242 Cited 1316 times in Scopus1316 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.513 195   182 Cited 189 times in Scopus189 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 137 24 58 Cited 63 times in Scopus63 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 69   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 84 Cited 88 times in Scopus88 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 134   43 Cited 50 times in Scopus50 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.873 142   167 Cited 179 times in Scopus179 3
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 62   195 Cited 199 times in Scopus199 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 144 3 44 Cited 53 times in Scopus53 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 86   261 Cited 267 times in Scopus267 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 82   88 Cited 90 times in Scopus90 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 29   93 Cited 104 times in Scopus104 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 56   243 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 44   91 Cited 95 times in Scopus95 0