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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 128   1741 Cited 1746 times in Scopus1746 102
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 38   74 Cited 94 times in Scopus94 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 52   130 Cited 150 times in Scopus150 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 24   89 Cited 99 times in Scopus99 1