Vomiting During Anaesthesia von Pembrey, R. E. J.

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National Health Service von Pembrey, R. E. J.

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National Health Service von Pembrey, R. E. J.

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Strong Position von Pembrey, R. E. J.

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Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms von Vella, Adrian, Cooper, Jason D., Lowe, Christopher E., Walker, Neil, Nutland, Sarah, Widmer, Barry, Jones, Richard, Ring, Susan M., McArdle, Wendy, Pembrey, Marcus E., Strachan, David P., Dunger, David B., Rebecca Twells, C.J., Clayton, David G., Todd, John A.

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Neural Basis of an Inherited Speech and Language Disorder von Vargha-Khadem, F., Watkins, K. E., Price, C. J., Ashburner, J., Alcock, K. J., Connelly, A., Frackowiak, R. S. J., Friston, K. J., Pembrey, M. E., Mishkin, M., Gadian, D. G., Passingham, R. E.

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Genome-wide association study identifies eight loci associated with blood pressure von Jackson, Anne U, Burton, Paul R, Di Gregorio, Alessandra, Mohlke, Karen L, Galan, Pilar, Syvänen, Ann-Christine, Marrugat, Jaume, Jarvelin, Marjo-Riitta, Newton-Cheh, Christopher, Meitinger, Thomas, Watkins, Hugh, Lucas, Gavin, Soranzo, Nicole, Tobin, Martin D, Wain, Louise V, Kooner, Jaspal S, Wallace, Chris, Altshuler, David, Najjar, Samer S, Zeggini, Eleftheria, Felix, Stephan B, Freimer, Nelson B, Laakso, Markku, Homuth, Georg, Ferrucci, Luigi, Brown, Morris, Snieder, Harold, Wichmann, H Erich, Orho-Melander, Marju, Chambers, John C, Valle, Timo T, van der Schouw, Yvonne T, Ernst, Florian, Strachan, David P, van der Harst, Pim, Kathiresan, Sekar, Romanazzi, Valeria, Dörr, Marcus, McArdle, Wendy L, Peden, John F, Beckmann, Jacques S, Song, Kijoung, Yuan, Xin, Melander, Olle, Coin, Lachlan, Lim, Noha, Barroso, Inês, Eyheramendy, Susana, O'Reilly, Paul F, Salomaa, Veikko, Gut, Ivo G, Tuomilehto, Jaakko, Peltonen, Leena, Morken, Mario A, Org, Elin, Luan, Jian'an, Panico, Salvatore, de Jong, Paul E, Schwartz, Stephen M, Matullo, Giuseppe, Wareham, Nicholas J, Seedorf, Udo, Laan, Maris, Uiterwaal, Cuno S, Boehnke, Michael, Farrall, Martin, Elosua, Roberto, Webster, John, Vollenweider, Peter, Reffelmann, Thorsten, Abecasis, Gonçalo R, Rettig, Rainer, Zhao, Jing Hua, Khaw, Kay-Tee, Elliott, Katherine S, Forouhi, Nita G, Voight, Benjamin F, Caulfield, Mark, Dominiczak, Anna, Munroe, Patricia B, Zhai, Guangju, Loos, Ruth JF, Sacerdote, Carlotta, Mooser, Vincent, Bergmann, Sven, Lakatta, Edward G, Bingham, Sheila A, Numans, Mattijs E, Völker, Uwe, Stringham, Heather M, Jousilahti, Pekka, Williams, Frances M, Clarke, Robert, Allione, Alessandra, Spector, Tim D, Elliott, Paul, Collins, Francis S, Lorbeer, Roberto, Sanna, Serena, Ricceri, Fulvio

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National Health Service von Pembrey, R. E. J.

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls von Clayton, David G, Cardon, Lon R, Duncanson, Audrey, Ouwehand, Willem H, Todd, John A, Donnelly, Peter, Easton, Doug, Evans, David, Morris, Andrew P, Spencer, Chris C. A, Boorman, James P, Cant, Barbara, Everson, Ursula, Hussey, Judith M, Knight, Alexandra S, Nutland, Sarah, Stevens, Helen E, Watkins, Nicholas A, Jones, Richard W, Ring, Susan M, Breen, Gerome, Caesar, Sian, Green, Elaine K, Grozeva, Detelina, Jones, Ian R, Kirov, George, Moskvina, Valentina, Nikolov, Ivan, Collier, David A, Farmer, Anne, Williamson, Richard, Young, Allan H, Ball, Stephen G, Balmforth, Anthony J, Bishop, D. Timothy, Iles, Mark M, Dixon, Richard J, Stevens, Suzanne, Thompson, John R, Bredin, Francesca, Tremelling, Mark, Drummond, Hazel, Nimmo, Elaine R, Fisher, Sheila A, Forbes, Alastair, Lewis, Cathryn M, Prescott, Natalie J, Barbour, Jamie, Mohiuddin, M. Khalid, Mansfield, John C, Cummings, Fraser R, Connell, John, Dobson, Richard, Gungadoo, Johannie, Newhouse, Stephen J, Barton, Anne, Bruce, Ian N, John, Sally L, Potter, Catherine, Silman, Alan J, Symmons, Deborah P. M, Dunger, David B, Widmer, Barry, Frayling, Timothy M, Lango, Hana, Perry, John R. B, Groves, Christopher J, Rayner, Nigel W, Timpson, Nicholas J, Zeggini, Eleftheria, Newport, Melanie, Vannberg, Fredrik, Farrar, Claire, Wordsworth, Paul, Brown, Matthew A, Franklyn, Jayne A, Heward, Joanne M, Simmonds, Matthew J, Seal, Sheila, Stratton, Michael R, Ban, Maria, Conway, David, Chaney, Amy, Ghori, Mohammed J. R, Gwilliam, Rhian, Hunt, Sarah E, McGinnis, Ralph, Potter, Simon, Whittaker, Pamela, Widden, Claire, Withers, David, Hallgrimsdottir, Ingileif B, Vukcevic, Damjan, Bentley, David, Caulfield, Mark, Compston, Alistair, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Mathew, Christopher G

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Common variants near MC4R are associated with fat mass, weight and risk of obesity von Day, Ian, Dermitzakis, Emmanouil T, Randall, Joshua C, Weedon, Michael N, Hinney, Anke, Evans, David M, Qi, Lu, Bennett, Amanda J, Munroe, Patricia B, Herrera, Blanca, Johnson, Toby, Elliott, Katherine S, Song, Kijoung, Zeggini, Eleftheria, Cauchi, Stéphane, Teichmann, Sarah A, Lindgren, Cecilia M, Brown, Morris, Sims, Matthew A, Karpe, Fredrik, O'Rahilly, Stephen, Hattersley, Andrew T, Scherag, André, Samani, Nilesh J, Keniry, Andrew, Li, Shengxu, Beckmann, Jacques S, Cooper, Cyrus, Caulfield, Mark J, Owen, Katharine R, Luben, Robert N, McGinnis, Ralph, Ghori, Jilur, Ness, Andrew R, Bochud, Murielle, Jarvelin, Marjo-Riitta, Hebebrand, Johannes, Ong, Ken K, Freathy, Rachel M, McArdle, Wendy L, Potter, Simon, Wareham, Nicholas J, Ganz Vogel, Carla I, Mooser, Vincent, Barroso, Inês, Deloukas, Panos, Waterworth, Dawn M, Bergmann, Sven, Elliott, Paul, Gwilliam, Rhian, Tobias, Jonathan H, Jolley, Jennifer D M, Morris, Andrew D, Loos, Ruth J F, Yuan, Xin, Smith, George Davey, Palmer, Colin N A, Groves, Christopher J, Dina, Christian, Syddall, Holly E, Waeber, Gerard, Zhao, Jing Hua, Sandhu, Manjinder S, Doney, Alex S F, Hunt, Sarah E, Pouta, Anneli, Speliotes, Elizabeth K, Connell, John M, Timpson, Nicholas J, Wallace, Chris, Attwood, Antony P, Hall, Alistair S, Khaw, Kay-Tee, Meyre, David, Vollenweider, Peter, Bingham, Sheila A, Berndt, Sonja I, Hadley, David, Rayner, Nigel W, Frayling, Timothy M, Sadaf Farooqi, I, Hirschhorn, Joel N, Strachan, David P, Inouye, Michael, Papadakis, Konstantinos, Ring, Susan M, Wraight, Vicki L, Willer, Cristen J, Marchini, Jonathan, Uda, Manuela, Nica, Alexandra C, Mangino, Massimo, Soranzo, Nicole, McCarthy, Mark I, De, Subhajyoti, Neville, Matthew J, Prokopenko, Inga, Wheeler, Eleanor, Heid, Iris M, Froguel, Philippe

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Genome-wide and fine-resolution association analysis of malaria in West Africa von Jallow, Muminatou, Molyneux, Malcolm E, Singhasivanon, Pratap, Clark, Taane G, Donnelly, Peter, Parker, Michael, Mueller, Ivo, Pinder, Margaret, Karunaweera, Nadira, Dolo, Amagana, Fry, Andrew E, Gwilliam, Rhian, Bojang, Kalifa A, Williams, Thomas N, Amodu, Olukemi, Horstmann, Rolf D, Kokwaro, Gilbert, Rowlands, Kate, Drakeley, Chris, Auburn, Sarah, Bumpstead, Suzannah J, Doumbo, Ogobara K, Achidi, Eric Akum, Agbenyega, Tsiri, Peshu, Norbert, Somaskantharajah, Elilan, Mendy, Alieu, Marchini, Jonathan, Dunstan, Sarah, Lemnge, Martha, Teo, Yik Ying, Tall, Adama, Ibrahim, Muntaser, Deloukas, Panos, Makani, Julie, Rockett, Kirk A, Green, Angela, Jeffreys, Anna E, Sirima, Sodiomon, Koram, Kwadwo A, Campino, Susana, Morris, Andrew, Corran, Patrick, Modiano, David, Sisay-Joof, Fatou, Troye-Blomberg, Marita, Potter, Simon, Fernando, Deepika, Riley, Eleanor M, Evans, Jennifer, Sakuntabhai, Anavaj, Conway, David J, Widden, Claire, Ragoussis, Jiannis, Allen, Angela, Inouye, Michael, Hien, Tran Tinh, Palotie, Aarno, Sirugo, Giorgio, Taylor, Terrie E, Howie, Bryan, Kwiatkowski, Dominic P, Thera, Mahamadou, Kivinen, Katja, Small, Kerrin S, Puijalon, Odile, Hunt, Sarah E, Djimde, Abdoulaye, Farrar, Jeremy, Marsh, Kevin, Michon, Pascal, Reyburn, Hugh, Usen, Stanley, Wilson, Michael, Coffey, Alison, SanJoaquin, Miguel, Plowe, Christopher V, Dunham, Andrew, Rogers, Jane, Reeder, John, Whittaker, Pamela

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation von Knight, S.J.L., Flannery, A.V., Hirst, M.C., Campbell, L., Christodoulou, Z., Phelps, S.R., Pointon, J., Middleton-Price, H.R., Barnicoat, A., Pembrey, M.E., Holland, J., Oostra, B.A., Bobrow, M., Davies, K.E.

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Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease von Ouwehand, Willem, Keniry, Andrew, Fisher, Sheila A, Jewell, Derek P, Anderson, Carl A, Prescott, Natalie J, Deloukas, Panos, Blaszczyk, Katarzyna, Mansfield, John C, Mathew, Christopher G, Watkins, Nick, Drummond, Hazel, Cummings, Fraser R, Forbes, Alastair, Barrett, Jeffrey C, Ravindrarajah, Radhi, Sanderson, Jeremy, Inouye, Mike, Hunt, Sarah, Nimmo, Elaine R, Johnson, Christopher, Bumpstead, Suzannah, Hanson, Catherine E, Lobo, Alan, Massey, Dunecan, Cardon, Lon, Ewels, Philip, Satsangi, Jack, Tremelling, Mark, Gwilliam, Rhian, Carter, Martyn, Berzuini, Carlo, Lees, Charlie W, Onnie, Clive M, Parkes, Miles, Lewis, Cathryn M

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Rheumatoid arthritis association at 6q23 von Worthington, Jane, Thomson, Wendy, Barton, Anne, Ke, Xiayi, Eyre, Steve, Hinks, Anne, Bowes, John, Donn, Rachelle, Symmons, Deborah, Hider, Samantha, Bruce, Ian N, Wilson, Anthony G, Marinou, Ioanna, Morgan, Ann, Emery, Paul, Carter, Angela, Steer, Sophia, Hocking, Lynne, Reid, David M, Wordsworth, Paul, Harrison, Pille, Strachan, David

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Availability and use of rapid diagnostic tests for the management of acute childhood infections in Europe: A cross-sectional survey of paediatricians von Dewez, JE, Pembrey, L, Nijman, RG, Del Torso, S, Grossman, Z, Hadjipanayis, A, Van Esso, D, Lim, E, Emonts, M, Burns, J, Gras-LeGuen, C, Kohlfuerst, D, Dornbusch, HJ, Brengel-Pesce, K, Mallet, F, Von Both, U, Tsolia, M, Eleftheriou, I, Zavadska, D, De Groot, R, Van der Flier, M, Moll, H, Hagedoorn, N, Borensztajn, D, Oostenbrink, R, Kuijpers, T, Pokorn, M, Vincek, K, Martinón-Torres, F, Rivero, I, Agyeman, P, Carrol, ED, Paulus, S, Cunnington, A, Herberg, J, Levin, M, Mujkić, A, Geitmann, K, Da Dalt, L, Valiulis, A, Lapatto, R, Syridou, G, Altorjai, P, Torpiano, P, Størdal, K, Illy, K, Mazur, A, Spreitzer, MV, Rios, J, Wyder, C, Romankevych, I, Basmaci, R, Ibanez-Mico, S, Yeung, S

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Radiological malformations of the ear in pendred syndrome von Phelps, P.D., Coffey, R.A., Trembath, R.C., Luxon, L.M., Grossman, A.B., Britton, K.E., Kendall-Taylor, P., Graham, J.M., Cadge, B.C., Stephens, S.G.D., Pembrey, M.E., Reardon, W.

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Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA von Reardon, W., Pembrey, M.E., Trembath, R.C., Ross, R.J.M., Sweeney, M.G., Harding, A.E., Luxon, L.M.

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Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study von Burn, J, Brennan, P, Little, J, Holloway, S, Coffey, R, Somerville, J, Dennis, NR, Allan, L, Arnold, R, Deanfield, JE, Godman, M, Houston, A, Keeton, B, Oakley, C, Scott, O, Silove, E, Wilkinson, J, Pembrey, M, Hunter, AS

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Factor V Leiden is associated with pre‐eclampsia but not with fetal growth restriction: a genetic association study and meta‐analysis von DUDDING, T., HERON, J., THAKKINSTIAN, A., NURK, E., GOLDING, J., PEMBREY, M., RING, S. M., ATTIA, J., SCOTT, R. J.

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Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13 von Barton, Anne, Thomson, Wendy, Ke, Xiayi, Eyre, Steve, Hinks, Anne, Bowes, John, Plant, Darren, Gibbons, Laura J, Wilson, Anthony G, Bax, Deborah E, Morgan, Ann W, Emery, Paul, Steer, Sophia, Hocking, Lynne, Reid, David M, Wordsworth, Paul, Harrison, Pille, Worthington, Jane

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