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Frayling, Timothy M., Timpson, Nicholas J., Weedon, Michael N., Zeggini, Eleftheria, Freathy, Rachel M., Lindgren, Cecilia M., Perry, John R. B., Elliott, Katherine S., Lango, Hana, Rayner, Nigel W., Shields, Beverley, Harries, Lorna W., Barrett, Jeffrey C., Ellard, Sian, Groves, Christopher J., Knight, Bridget, Patch, Ann-Marie, Ness, Andrew R., Ebrahim, Shah, Lawlor, Debbie A., Ring, Susan M., Ben-Shlomo, Yoav, Jarvelin, Marjo-Riitta, Sovio, Ulla, Bennett, Amanda J., Melzer, David, Ferrucci, Luigi, Loos, Ruth J. F., Barroso, Inês, Wareham, Nicholas J., Karpe, Fredrik, Owen, Katharine R., Cardon, Lon R., Walker, Mark, Hitman, Graham A., Palmer, Colin N. A., Doney, Alex S. F.Graham A., Morris, Andrew D., Smith, George Davey, Hattersley, Andrew T., McCarthy, Mark I. and Wellcome Trust Case Control (2007) A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science, 316 5826: 889-894. doi:10.1126/science.1141634 116   1675 Cited 1667 times in Scopus1667 99
Rafiq, Meena, Flanagan, Sarah E., Patch, Ann-Marie, Shields, Beverley M., Ellard, Sian, Hattersley, Andrew T. and Neonatal Diabetes International Collaborative Group (2008) Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations. Diabetes Care, 31 2: 204-209. doi:10.2337/dc07-1785 37   73 Cited 93 times in Scopus93 0
Edghill, Emma L., Flanagan, Sarah E., Patch, Ann-Marie, Boustred, Chris, Parrish, Andrew, Shields, Beverley, Shepherd, Maggie H., Hussain, Khalid, Kapoor, Ritika R., Malecki, Maciej, MacDonald, Michael J., Støy, Julie, Steiner, Donald F., Philipson, Louis H., Bell, Graeme I., The Neonatal Diabetes International Collaborative Group, Hattersley, Andrew T. and Ellard, Sian (2008) Insulin mutation screening in 1,044 patients with diabetes: Mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. Diabetes, 57 4: 1034-1042. doi:10.2337/db07-1405 49   125 Cited 144 times in Scopus144 0
Freathy, Rachel M., Mook-Kanamor, Dennis O., Sovio, Ulla, Prokopenko, Inga, Timpson, Nicholas J., Berry, Diane J., Warrington, Nicole M., Widen, Elisabeth, Hottenga, Jouke Jan, Kaakinen, Marika, Lange, Leslie A., Bradfield, Jonathan P., Kerkhof, Marjan, Marsh, Julie A., Magi, Reedik, Chen, Chih-Mei, Lyon, Helen N., Kirin, Mirna, Adair, Linda S., Aulchenko, Yurii S., Bennett, Amanda J., Borja, Judith B., Bouatia-Naji, Nabila, Charoen, Pimphen, Coin, Lachlan ..J. M., Cousminer, Diana L., De Geus, Eco J. C., Deloukas, Panos, Elliott, Paul, Evans, David M., Froguel, Philippe, Glaser, Beate, Groves, Christopher J., Hartikainen, Anna-Liisa, Hassanali, Neelam, Hirschhorn, Joel N., Hofman, Albert, Holly, Jeff M. P., Hypponen, Elina, Kanoni, Stavroula, Knight, Bridget A., Laitinen, Jaana, Lindgren, Cecilia M., McArdle, Wendy L., O'Reilly, Paul F., Pennell, Craig E., Postma, Dirkje. S., Pouta, Anneli, Ramasamy, Adaikalavan, Rayner, Nigel W., Ring, Susan M., Rivadeneira, Femando, Shields, Beverley M., Strachan, David P., Surakka, Ida, Taanila, Anja, Tiesler, Carta, Uitterlinden, Andre G., van Duijn, Cornelia M., Wijga, Alet H., Willemsen, Gonneke, Zhang, Haitao, Zhao, Jianhua, Wilson, James F., Steegers, Eric A. P., Hattersley, Andrew T., Eriksson, Johan G., Peltonen, Leena, Mohlke, Karen L., Grant, Struan F. A., Hakonarson, Hakon, Koppelman, George H., Dedoussis, George V., Heinrich, Joachim, Gillman, Matthew W., Palmer, Lyle J., Frayling, Timothy M., Boomsma, Dorret I., Smith, George Davey, Power, Chris, Jaddoe, Vincent W. V., Jarvelin, Marjo-Riitta and McCarthy, Mark I. (2010) Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, 42 5: 430-435. doi:10.1038/ng.567 20   81 Cited 87 times in Scopus87 1