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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
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.532 222   103 Cited 108 times in Scopus108 15
Jaakkola, Elisa, Herzberg, Ibi, Laiho, Kari, Barnardo, Martin C.N.M., Pointon, Jennifer J., Kauppi, Markku, Kaarela, Kalevi, Tuomilehto-Wolf, Eva, Tuomilehto, Jaakko, Wordsworth, B. Paul and Brown, Matthew A. (2006) Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitis. Annals of The Rheumatic Diseases, 65 6: 775-780. doi:10.1136/ard.2005.041103 174   33 Cited 50 times in Scopus50 0
Newby, Paul R., Pickles, Oliver J., Mazumdar, Samaresh, Brand, Oliver J., Carr-Smith, Jaqueline D., Pearce, Simon H. S., Franklyn, Jayne A., Wellcome Trust Case Control Consortium, Evans, David M., Simmonds, Matthew J., Gough, Stephen C. L., Brown, Matthew A., Bradbury, Linda and Pointon, Jennifer (2010) Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. European Journal of Human Genetics, 18 9: 1021-1026. doi:10.1038/ejhg.2010.55 95 5 8 Cited 9 times in Scopus9 3
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.513 197   187 Cited 193 times in Scopus193 9
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 92 Cited 93 times in Scopus93 29
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.873 147   176 Cited 181 times in Scopus181 6
Harvey, David, Pointon, Jennifer J., Evans, David M., Karaderi, Tugce, Farrar, Claire, Appleton, Louise H., Sturrock, Roger D., Stone, Millicent A., Oppermann, Udo, Brown, Matthew A. and Wordsworth, B. Paul (2009) Investigating the genetic association between ERAP1 and ankylosing spondylitis. Human Molecular Genetics, 18 21: 4204-4212. doi:10.1093/hmg/ddp371 83   54 Cited 50 times in Scopus50 0
Anderson, Carl, Massey, Dunecan, Barrett, Jeffrey, Prescott, Natalie, Tremelling, Mark, Fisher, Sheila, Gwilliam, Rhian, Jacob, Jemima, Nimmo, Elaine, Drummond, Hazel, Lees, Charlie, Onnie, Clive, Hanson, Catherine, Blaszczyk, Katarzyna, Ravindrarajah, Radhi, Hunt, Sarah, Varma, Dhiraj, Hammond, Naomi, Lewis, Gregory, Attlesey, Heather, Watkins, Nick, Ouwehand, Willem, Strachan, David, McArdle, Wendy, Lewis, Cathryn, Lobo, Alan, Sanderson, Jeremy, Jewell, Derek, Deloukas, Panos, Mansfield, John, Mathew, Christopher, Satsangi, Jack, Parkes, Miles, Bradbury, Linda, Brown, Matthew and Pointon, Jennifer (2009) Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. Gastroenterology, 136 2: 523-529.e3. doi:10.1053/j.gastro.2008.10.032 195   94 Cited 100 times in Scopus100 0
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   92 Cited 94 times in Scopus94 0
Pointon, Jennifer J., Harvey, David, Karaderi, Tugce, Appleton, Louise H., Farrar, Claire, Stone, Millicent A., Sturrock, Roger D., Reveille, John D., Weisman, Michael H., Ward, Michael M., Brown, Matthew A. and Wordsworth, B. Paul (2010) The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD). Annals of the Rheumatic Diseases, 69 6: 1243-1246. doi:10.1136/ard.2009.115147 85   15 Cited 17 times in Scopus17 0