Tight junction dynamics: the role of junctional adhesion molecules (JAMs) von Garrido-Urbani, S, Bradfield, P. F, Imhof, B. A

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Detection of differentially expressed genes in synovial fibroblasts by restriction fragment differential display von Scaife, S., Brown, R., Kellie, S., Filer, A., Martin, S., Thomas, A. M. C., Bradfield, P. F., Amft, N., Salmon, M., Buckley, C. D.

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Persistent induction of the chemokine receptor CXCR4 by TGF-beta 1 on synovial T cells contributes to their accumulation within the rheumatoid synovium von Buckley, C D, Amft, N, Bradfield, P F, Pilling, D, Ross, E, Arenzana-Seisdedos, F, Amara, A, Curnow, S J, Lord, J M, Scheel-Toellner, D, Salmon, M

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Functional role of a polymorphism in the Pannexin1 gene in collagen-induced platelet aggregation von Molica, F, Morel, S, Meens, M J, Denis, J-F, Bradfield, P F, Penuela, S, Zufferey, A, Monyer, H, Imhof, B A, Chanson, M, Laird, D W, Fontana, P, Kwak, B R

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Persistent Induction of the Chemokine Receptor CXCR4 by TGF-β1 on Synovial T Cells Contributes to Their Accumulation Within the Rheumatoid Synovium von Buckley, Christopher D., Amft, Nicole, Bradfield, Paul F., Pilling, Darrell, Ross, Ewan, Arenzana-Seisdedos, Fernando, Amara, Ali, Curnow, S. John, Lord, Janet M., Scheel-Toellner, Dagmar, Salmon, Mike

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Cell adhesion: More than just glue (Review) von Buckley, Christopher D., Rainger, G. Ed, Bradfield, Paul F., Nash, Gerard B., Simmons, David L.

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LPS differentially regulates adhesion and transendothelial migration of human monocytes under static and flow conditions von Bradfield, Paul F., Johnson-Léger, Caroline A., Zimmerli, Claudia, Imhof, Beat A.

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Rheumatoid fibroblast‐like synoviocytes overexpress the chemokine stromal cell–derived factor 1 (CXCL12), which supports distinct patterns and rates of CD4+ and CD8+ T cell migrati... von Bradfield, Paul F., Amft, Nicole, Vernon‐Wilson, Elizabeth, Exley, Andrew E., Parsonage, Greg, Rainger, G. Ed, Nash, Gerard B., Thomas, Andrew M. C., Simmons, David L., Salmon, Mike, Buckley, Christopher D.

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Differential association of cytoplasmic signalling molecules SHP-1, SHP-2, SHIP and phospholipase C-gamma1 with PECAM-1/CD31 von Pumphrey, N J, Taylor, V, Freeman, S, Douglas, M R, Bradfield, P F, Young, S P, Lord, J M, Wakelam, M J, Bird, I N, Salmon, M, Buckley, C D

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A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci von Bradfield, Jonathan P, Qu, Hui-Qi, Wang, Kai, Zhang, Haitao, Sleiman, Patrick M, Kim, Cecilia E, Mentch, Frank D, Qiu, Haijun, Glessner, Joseph T, Thomas, Kelly A, Frackelton, Edward C, Chiavacci, Rosetta M, Imielinski, Marcin, Monos, Dimitri S, Pandey, Rahul, Bakay, Marina, Grant, Struan F A, Polychronakos, Constantin, Hakonarson, Hakon

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Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC von Mishra, Rajashree, Åkerlund, Mikael, Cousminer, Diana L, Ahlqvist, Emma, Bradfield, Jonathan P, Chesi, Alessandra, Hodge, Kenyaita M, Guy, Vanessa C, Brillon, David J, Pratley, Richard E, Rickels, Michael R, Vella, Adrian, Ovalle, Fernando, Harris, Ronald I, Melander, Olle, Varvel, Stephen, Hakonarson, Hakon, Froguel, Phillippe, Lonsdale, John T, Mauricio, Didac, Schloot, Nanette C, Khunti, Kamlesh, Greenbaum, Carla J, Yderstræde, Knud B, Tuomi, Tiinamaija, Voight, Benjamin F, Schwartz, Stanley, Boehm, Bernhard O, Groop, Leif, Leslie, Richard David, Grant, Struan F A

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genome-wide association study identifies KIAA0350 as a type 1 diabetes gene von HAKONARSON, Hakon, GRANT, Struan F. A, LAWSON, Margaret L, ROBINSON, Luke J, SKRABAN, Robert, YANG LU, CHIAVACCI, Rosetta M, STANLEY, Charles A, KIRSCH, Susan E, RAPPAPORT, Eric F, ORANGE, Jordan S, MONOS, Dimitri S, BRADFIELD, Jonathan P, DEVOTO, Marcella, QU, Hui-Qi, POLYCHRONAKOS, Constantin, MARCHAND, Luc, KIM, Cecilia E, GLESSNER, Joseph T, GRABS, Rosemarie, CASALUNOVO, Tracy, TABACK, Shayne P, FRACKELTON, Edward C

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Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes von Forgetta, Vincenzo, Manousaki, Despoina, Istomine, Roman, Ross, Stephanie, Tessier, Marie-Catherine, Marchand, Luc, Li, Min, Qu, Hui-Qi, Bradfield, Jonathan P, Grant, Struan F A, Hakonarson, Hakon, Paterson, Andrew D, Piccirillo, Ciriaco, Polychronakos, Constantin, Richards, J Brent

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Common variations in BARD1 influence susceptibility to high-risk neuroblastoma von Devoto, Marcella, Hakonarson, Hakon, Maris, John M, Capasso, Mario, Hou, Cuiping, Asgharzadeh, Shahab, Glessner, Joseph T, Attiyeh, Edward F, Mosse, Yael P, Kim, Cecilia, Diskin, Sharon J, Cole, Kristina A, Bosse, Kristopher, Diamond, Maura, Laudenslager, Marci, Winter, Cynthia, Bradfield, Jonathan P, Scott, Richard H, Jagannathan, Jayanti, Garris, Maria, McConville, Carmel, London, Wendy B, Seeger, Robert C, Grant, Struan F A, Li, Hongzhe, Rahman, Nazneen, Rappaport, Eric

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A framework for conducting GWAS using repeated measures data with an application to childhood BMI von Burrows, Kimberley, Heiskala, Anni, Bradfield, Jonathan P., Balkhiyarova, Zhanna, Ning, Lijiao, Boissel, Mathilde, Chan, Yee-Ming, Froguel, Philippe, Bonnefond, Amelie, Hakonarson, Hakon, Alves, Alexessander Couto, Lawlor, Deborah A., Kaakinen, Marika, Järvelin, Marjo-Riitta, Grant, Struan F. A., Tilling, Kate, Prokopenko, Inga, Sebert, Sylvain, Canouil, Mickaël, Warrington, Nicole M.

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High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications von Shaikh, Tamim H, Gai, Xiaowu, Perin, Juan C, Glessner, Joseph T, Xie, Hongbo, Murphy, Kevin, O'Hara, Ryan, Casalunovo, Tracy, Conlin, Laura K, D'Arcy, Monica, Frackelton, Edward C, Geiger, Elizabeth A, Haldeman-Englert, Chad, Imielinski, Marcin, Kim, Cecilia E, Medne, Livija, Annaiah, Kiran, Bradfield, Jonathan P, Dabaghyan, Elvira, Eckert, Andrew, Onyiah, Chioma C, Ostapenko, Svetlana, Otieno, F George, Santa, Erin, Shaner, Julie L, Skraban, Robert, Smith, Ryan M, Elia, Josephine, Goldmuntz, Elizabeth, Spinner, Nancy B, Zackai, Elaine H, Chiavacci, Rosetta M, Grundmeier, Robert, Rappaport, Eric F, Grant, Struan F A, White, Peter S, Hakonarson, Hakon

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Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes von Mishra, Rajashree, Chesi, Alessandra, Cousminer, Diana L, Hawa, Mohammad I, Bradfield, Jonathan P, Hodge, Kenyaita M, Guy, Vanessa C, Hakonarson, Hakon, Mauricio, Didac, Schloot, Nanette C, Yderstræde, Knud B, Voight, Benjamin F, Schwartz, Stanley, Boehm, Bernhard O, Leslie, Richard David, Grant, Struan F A

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Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP von Grant, Struan F A, Li, Mingyao, Bradfield, Jonathan P, Kim, Cecilia E, Annaiah, Kiran, Santa, Erin, Glessner, Joseph T, Casalunovo, Tracy, Frackelton, Edward C, Otieno, F George, Shaner, Julie L, Smith, Ryan M, Imielinski, Marcin, Eckert, Andrew W, Chiavacci, Rosetta M, Berkowitz, Robert I, Hakonarson, Hakon

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Loss of BMAL1 in ovarian steroidogenic cells results in implantation failure in female mice von Liu, Yan, Johnson, Brian P., Shen, Anna L., Wallisser, Jacqueline A., Krentz, Kathy J., Moran, Susan M., Sullivan, Ruth, Glover, Edward, Parlow, Albert F., Drinkwater, Norman R., Schuler, Linda A., Bradfield, Christopher A.

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Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism von Solé-Navais, Pol, Juodakis, Julius, Ytterberg, Karin, Wu, Xiaoping, Bradfield, Jonathan P., Vaudel, Marc, LaBella, Abigail L., Helgeland, Øyvind, Flatley, Christopher, Geller, Frank, Finel, Moshe, Zhao, Mengqi, Lazarus, Philip, Hakonarson, Hakon, Magnus, Per, Andreassen, Ole A., Njølstad, Pål R., Grant, Struan F. A., Feenstra, Bjarke, Muglia, Louis J., Johansson, Stefan, Zhang, Ge, Jacobsson, Bo

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