Browse by all authors Browse By Author Name - Hattersley,+Andrew+T.

Browse Results (17 results found)

Subscribe to the RSS feed for this result setSubscribe to the RSS feed for this result set

  Abstract Views File Downloads Thomson Reuters Web of Science Citation Count Scopus Citation Count Altmetric Score
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 129   1744 Cited 1753 times in Scopus1753 102
Maller, Julian B., McVean, Gilean, Byrnes, Jake, Vukcevic, Damjan, Palin, Kimmo, Su, Zhan, Howson, Joanna M. M., Auton, Adam, Myers, Simon, Morris, Andrew, Pirinen, Matti, Brown, Matthew A., Burton, Paul R., Caulfield, Mark J., Compston, Alastair, Farrall, Martin, Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V. S., Mathew, Christopher G., Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R., Worthington, Jane, Craddock, Nick, Hurles, Matthew, Ouwehand, Willem, Parkes, Miles, Rahman, Nazneen, Duncanson, Audrey, Todd, John A., Kwiatkowski, Dominic P., Samani, Nilesh J., Gough, Stephen C. L., McCarthy, Mark I., Deloukas, Panagiotis and Donnelly, Peter (2012) Bayesian refinement of association signals for 14 loci in 3 common diseases. Nature Genetics, 44 12: 1294-1301. doi:10.1038/ng.2435 60   27 Cited 38 times in Scopus38 10
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group, Wellcome Trust Case Control Consortium 2, Zhou, Kaixin, Tavendale, Roger, Donnelly, Louise A., Schofield, Chris, Burch, Lindsay, Carr, Fiona, Colhoun, Helen, Morris, Andrew D., Sutherland, Calum, Palmer, Colin N. A., Pearson, Ewan, Bellenguez Celine, Spencer, Chris C. A., Strange, Amy, Freeman, Colin, Rautanen, Anna, McCarthy, Mark I., Donnelly, Peter, Bennett, Amanda J., Coleman, Ruth L., Groves, Christopher J., McCarthy, Mark I., Holman, Rury R., Hawley, Simon A., Hardie, Grahame, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Langford, Cordelia, Peltonen, Leena, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G, Trembath, Richard, Plomin, Robert, Sawcer, Stephen J., Samani, Nilesh J., Viswanathan, Aananth C., Wood, Nicholas W., Harries, Lorna W., Hattersley, Andrew T., Doney, Alex S. F., McCarthy, Mark I. and Donnelly, Peter (2011) Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nature Genetics, 43 2: 117-120. doi:10.1038/ng.735 154   118 Cited 147 times in Scopus147 2
Wood, Andrew R., Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune H., Gustafsson, Stefan, Chu, Audrey Y., Estrada, Karol, Luan, Jian'an, Kutalik, Zoltan, Amin, Najaf, Buchkovich, Martin L., Croteau-Chonka, Damien C., Day, Felix R., Duan, Yanan, Fall, Tove, Fehrmann, Rudolf, Ferreira, Teresa, Jackson, Anne U., Karjalainen, Juha, Lo, Ken Sin, Locke, Adam E., Magi, Reedik, Mihailov, Evelin, Porcu, Evelin, Randall, Joshua C., Scherag, Andre, Vinkhuyzen, Anne A. E., Westra, Harm-Jan, Winkler, Thomas W., Workalemahu, Tsegaselassie, Zhao, Jing Hua, Absher, Devin, Albrecht, Eva, Anderson, Denise, Baron, Jeffrey, Beekman, Marian, Demirkan, Ayse, Ehret, Georg B., Feenstra, Bjarke, Feitosa, Mary F., Fischer, Krista, Fraser, Ross M., Goel, Anuj, Gong, Jian, Justice, Anne E., Kanoni, Stavroula, Kleber, Marcus E., Kristiansson, Kati, Lim, Unhee, Lotay, Vaneet, Lui, Julian C., Mangino, Massimo, Leach, Irene Mateo, Medina-Gomez, Carolina, Nalls, Michael A., Nyholt, Dale R., Palmer, Cameron D., Pasko, Dorota, Pechlivanis, Sonali, Prokopenko, Inga, Ried, Janina S., Ripke, Stephan, Shungin, Dmitry, Stancakova, Alena, Strawbridge, Rona J., Sung, Yun Ju, Tanaka, Toshiko, Teumer, Alexander, Trompet, Stella, van der Laan, Sander W., van Setten, Jessica, Van Vliet-Ostaptchouk, Jana V., Wang, Zhaoming, Yengo, Loic, Zhang, Weihua, Afzal, Uzma, Arnlov, Johan, Arscott, Gillian M., Bandinelli, Stefania, Barrett, Amy, Bellis, Claire, Bennett, Amanda J., Berne, Christian, Bluher, Matthias, Bolton, Jennifer L., Bottcher, Yvonne, Boyd, Heather A., Bruinenberg, Marcel, Buckley, Brendan M., Buyske, Steven, Caspersen, Ida H., Chines, Peter S., Clarke, Robert, Claudi-Boehm, Simone, Cooper, Matthew, Daw, E. Warwick, De Jong, Pim A., Deelen, Joris, Delgado, Graciela, Denny, Josh C., Dhonukshe-Rutten, Rosalie, Dimitriou, Maria, Doney, Alex S. F., Dorr, Marcus, Eklund, Niina, Eury, Elodie, Folkersen, Lasse, Garcia, Melissa E., Geller, Frank, Giedraitis, Vilmantas, Go, Alan S., Grallert, Harald, Grammer, Tanja B., Grassler, Jurgen, Gronberg, Henrik, de Groot, Lisette C. P. G. M., Groves, Christopher J., Haessler, Jeffrey, Hall, Per, Haller, Toomas, Hallmans, Goran, Hannemann, Anke, Hartman, Catharina A., Hassinen, Maija, Hayward, Caroline, Heard-Costa, Nancy L., Helmer, Quinta, Hemani, Gibran, Henders, Anjali K., Hillege, Hans L., Hlatky, Mark A., Hoffmannm Wolfgang, Hoffmann, Per, Holmen, Oddgeir, Houwing-Duistermaat, Jeanine J., Illig, Thomas, Isaacs, Aaron, James, Alan L., Jeff, Jarina, Johansen, Berit, Johansson, Asa, Jolley, Jennifer, Juliusdottir, Thorhildur, Junttila, Juhani, Kho, Abel N., Kinnunen, Leena, Klopp, Norman, Kocher, Thomas, Kratzer, Wolfgang, Lichtner, Peter, Lind, Lars, Lindstrom, Jaana, Lobbens, Stephane, Lorentzon, Matthias, Lu, Yingchang, Lyssenko, Valeriya, Magnusson, Patrik K. E., Mahajan, Anubha, Maillard, Marc, McArdle, Wendy L., McKenzie, Colin A., McLachlan, Stela, McLaren, Paul J., Menni, Cristina, Merger, Sigrun, Milani, Lili, Moayyeri, Alireza, Monda, Keri L., Morken, Mario A., Muller, Gabriele, Muller-Nurasyid, Martina, Musk, Arthur W., Narisu, Narisu, Nauck, Matthias, Nolte, Ilja M., Nothen, Markus M., Oozageer, Laticia, Pilz, Stefan, Rayner, Nigel W., Renstrom, Frida, Robertson, Neil R., Rose, Lynda M., Roussel, Ronan, Sanna, Serena, Scharnagl, Hubert, Scholtens, Salome, Schumacher, Fredrick R., Schunkert, Heribert, Scott, Robert A., Sehmi, Joban, Seufferlein, Thomas, Shi, Jianxin, Silventoinen, Karri, Smit, Johannes H., Smith, Albert Vernon, Smolonska, Joanna, Stanton, Alice V., Stirrups, Kathleen, Stott, David J., Stringham, Heather M., Sundstrom, Johan, Swertz, Morris A., Syvanen, Ann-Christine, Tayo, Bamidele O., Thorleifsson, Gudmar, Tyrer, Jonathan P., van Dijk, Suzanne, van Schoor, Natasja M., van der Velde, Nathalie, van Heemst, Diana, van Oort, Floor V. A., Vermeulen, Sita H., Verweij, Niek, Vonk, Judith M., Waite, Lindsay L., Waldenberger, Melanie, Wennauer, Roman, Wilkens, Lynne R., Willenborg, Christina, Wilsgaard, Tom, Wojczynski, Mary K., Wong, Andrew, Wright, Alan F., Zhang, Qunyuan, Arveiler, Dominique, Bakker, Stephan J. L., Beilby, John, Bergman, Richard N., Bergmann, Sven, Biffar, Reiner, Blangero, John, Boomsma, Dorret I., Bornstein, Stefan R., Bovet, Pascal, Brambilla, Paolo, Brown, Morris J., Campbell, Harry, Caulfield, Mark J., Chakravarti, Aravinda, Collins, Rory, Collins, Francis S., Crawford, Dana C., Cupples, L. Adrienne, Danesh, John, de Faire, Ulf, den Ruijter Hester M., Erbel, Raimund, Erdmann, Jeanette, Eriksson, Johan G., Farrall, Martin, Ferrannini, Ele, Ferrieres, Jean, Ford, Ian, Forouhi, Nita G., Forrester, Terrence, Gansevoort, Ron T., Gejman, Pablo V., Gieger, Christian, Golay, Alain, Gottesman, Omri, Gudnason, Vilmundur, Gyllensten, Ulf, Haas, David W., Hall, Alistair S., Harris, Tamara B., Hattersley, Andrew T., Heath, Andrew C., Hengstenberg, Christian, Hicks, Andrew A., Hindorff, Lucia A., Hingorani, Aroon D., Hofman, Albert, Hovingh, G. Kees, Humphries, Steve E., Hunt, Steven C., Hypponen, Elina, Jacobs, Kevin B., Jarvelin, Marjo-Riitta, Jousilahti, Pekka, Jula, Antti M., Kaprio, Jaakko, Kastelein, John J. P., Kayser, Manfred, Kee, Frank, Keinanen-Kiukaanniemi, Sirkka M., Kiemeney, Lambertus A., Kooner, Jaspal S., Kooperberg, Charles, Koskinen, Seppo, Kovacs, Peter, Kraja, Aldi T., Kumari, Meena, Kuusisto, Johanna, Lakka, Timo A., Langenberg, Claudia, Le Marchandm Loic, Lehtimaki, Terho, Lupoli, Sara, Madden, Pamela A. F., Mannisto, Satu, Manunta, Paolo, Marette, Andre, Matise, Tara C., McKnight, Barbara, Meitinger, Thomas, Moll, Frans L., Montgomery, Grant W., Morris, Andrew D., Morris, Andrew P., Murray, Jeffrey C., Nelis, Mari, Ohlsson, Claes, Oldehinkel, Albertine J., Ong, Ken K., Ouwehand, Willem H., Pasterkamp, Gerard, Peters, Annette, Pramstaller, Peter P., Price, Jackie F., Qi, Lu, Raitakari, Olli T., Rankinen, Tuomo, Rao, D. C., Rice, Treva K., Ritchie, Marylyn, Rudan, Igor, Salomaa, Veikko, Samani, Nilesh J., Saramies, Jouko, Sarzynski, Mark A., Schwarz, Peter E. H., Sebert, Sylvain, Sever, Peter, Shuldiner, Alan R., Sinisalo, Juha, Steinthorsdottir, Valgerdur, Stolk, Ronald P., Tardif, Jean-Claude, Tonjes, Anke, Tremblay, Angelo, Tremoli, Elena, Virtamo, Jarmo, Vohl, Marie-Claude, Amouyel, Philippe, Asselbergs, Folkert W., Assimes, Themistocles L., Bochud, Murille, Boehm, Bernhard O., Boerwinkle, Eric, Bottinger, Erwin P., Bouchard, Claude, Cauchi, Stephane, Chambers, John C., Chanock, Stephen J., Cooper, Richard S., de Bakker Paul I. W., Dedoussis, George, Ferrucci, Luigi, Franks, Paul W., Froguel, Philippe, Groop, Leif C., Haiman, Christopher A., Hamsten, Anders, Hayes, M. Geoffrey, Hui, Jennie, Hunter, David J., Hveem, Kristian, Jukema, J. Wouter, Kaplan, Robert C., Kivimaki, Mika, Kuh, Diana, Laakso, Markku, Liu, Yongmei, Martin, Nicholas G., Marz, Winfried, Melbye, Mads, Moebus, Susanne, Munroe, Patricia B., Njolstad, Inger, Oostra, Ben A., Palmer, Colin N. A., Pedersen, Nancy L., Perola, Markus, Perusse, Louis, Peters, Ulrike, Powell, Joseph E., Power, Chris, Quertermous, Thomas, Rauramaa, Rainer, Reinmaa, Eva, Ridker, Paul M., Rivadeneira, Fernando, Rotter, Jerome I., Saaristo, Timo E., Saleheen, Danish, Schlessinger, David, Slagboom, P. Eline, Snieder, Harold, Spector, Tim D., Strauch, Konstantin, Stumvoll, Michael, Tuomilehto, Jaakko, Uusitupa, Matti, van der Harst, Pim, Volzke, Henry, Walker, Mark, Wareham, Nicholas J., Watkins, Hugh, Wichmann, H.-Erich, Wilson, James F., Zanen, Pieter, Deloukas, Panos, Heid, Iris M., Lindgren, Cecilia M., Mohlke, Karen L., Speliotes, Elizabeth K., Thorsteinsdottir, Unnur, Barroso, Ines, Fox, Caroline S., North, Kari E., Strachan, David P., Beckmann, Jacques S., Berndt, Sonja I., Boehnke, Michael, Borecki, Ingrid B., McCarthy, Mark I., Metspalu, Andres, Stefansson, Kari, Uitterlinden, Andre G., van Duijn Cornelia M., Franke, Lude, Willer, Cristen J., Price, Alkes L., Lettre, Guillaume, Loos, Ruth J. F., Weedon, Michael N., Ingelsson, Erik, O'Connell, Jeffrey R., Abecasis, Goncalo R., Chasman, Daniel I., Goddard, Michael E., Visscher, Peter M., Hirschhorn, Joel N. and Frayling, Timothy M. (2014) Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46 11: 1173-1186. doi:10.1038/ng.3097 50   16 Cited 18 times in Scopus18 414
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 95 times in Scopus95 0
Lindgren, Cecilia M., Heid, Iris M., Randall, Joshua C., Lamina, Claudia, Steinthorsdottir, Valgerdur, Qi, Lu, Speliotes, Elizabeth K, Thorleifsson,Gudmar, Willer, Cristen J., Herrera, Blanca M., Jackson, Anne U., Lim, Noha, Scheet, Paul, Soranzo, Nicole, Amin, Najaf, Aulchenko, Yurii S., Chambers, John C., Drong, Alexander, Luan, Jian'an, Lyon, Helen N., Rivadeneira, Fernando, Sanna, Serena, Timpson, Nicholas J., Zillikens, M. Carola, Zhao, Jing Hua, Almgren, Peter, Bandinelli, Stefania, Bennett, Amanda J., Bergman, Richard N., Bonnycastle, Lori L., Bumpstead, Suzannah J., Chanock, Stephen J., Cherkas, Lynn, Chines, Peter, Coin, Lachlan, Cooper, Cyrus, Crawford, Gabriel, Doering, Angela, Dominiczak, Anna, Doney, Alex S. F., Ebrahim, Shah, Elliott, Paul, Erdos, Michael R., Estrada, Karol, Ferrucci, Luigi, Fischer, Guido, Forouhi, Nita G., Gieger, Christian, Grallert, Harald, Groves, Christopher J., Grundy, Scott, Guiducci, Candace, Hadley, David, Hamsten, Anders, Havulinna, Aki S., Hofman, Albert, Holle, Rolf, Holloway, John W., Illig, Thomas, Isomaa, Bo, Jacobs,Leonie C., Jameson, Karen, Jousilahti, Pekka, Karpe, Fredrik, Kuusisto, Johanna, Laitinen, Jaana, Lathrop, G. Mark, Lawlor, Debbie A. L., Mangino, Massimo, McArdle, Wendy L., Meitinger, Thomas, Morken, Mario A., Morris, Andrew P., Munroe, Patricia, Narisu, Narisu, Nordstrom, Anna, Nordstrom , Peter, Oostra, Ben A., Palmer, Colin N. A., Payne, Felicity, Peden, John F., Prokopenko, Inga, Renstrom, Frida, Ruokonen, Aimo, Salomaa, Veikko, Sandhu, Manjinder S., Scott, Laura J., Scuteri, Angelo, Silander, Kaisa, Song, Kijoung, Yuan, Xin, Stringham, Heather M., Swift, Amy J., Tuomi, Tiinamaija, Uda, Manuela, Vollenweider, Peter, Waeber, Gerard, Wallace, Chris, Walters, G. Bragi, Weedon, Michael N., The Wellcome Trust Case Control Consortium, Witteman, Jacqueline C. M., Zhang, Cuilin, Zhang, Weihua, Caulfield, Mark J., Collins, Francis S., Davey Smith, George, Day, Ian N. M., Franks, Paul W., Hattersley, Andrew T., Hu, Frank B., Jarvelin, Marjo-Riitta, Kong, Augustine, Kooner, Jaspal S., Laakso, Markku, Lakatta, Edward, Mooser, Vincent, Morris, Andrew D., Peltonen, Leena, Samani, Nilesh J., Spector, Timothy D., Strachan, David P., Tanaka, Toshiko, Tuomilehto, Jaakko, Uitterlinden, Andre G., van Duijn, Cornelia M., Wareham, Nicholas J., Watkins, Hugh, Waterworth, Dawn M., Boehnke, Michael, Deloukas, Panos, Groop, Leif, Hunter. David J., Thorsteinsdottir, Unnur, Schlessinger, David, Wichmann, H.-Erich, Frayling, Timothy M., Abecasis, Goncalo R., Hirschhorn, Joel N., Loos, Ruth J. F., Stefansson, Kari, Mohlke, Karen L., Barroso, Ines, McCarthy, Mark I., Brown, Matthew A. and Bradbury, Linda (2009) Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genetics, 5 6: e1000508-1-e1000508-13. doi:10.1371/journal.pgen.1000508 255   237 Cited 255 times in Scopus255 3
De Wet, Heidi, Rees, Mathew G., Shimomura, Kenju, Aittoniemi, Jussi, Patch, Ann-Marie, Flanagan, Sarah E., Ellard, Sian, Hattersley, Andrew T., Sansom, Mark S. P. and Ashcroft, Frances M. (2007) Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes. Proceedings of the National Academy of Sciences of the United States of America, 104 48: 18988-18992. doi:10.1073/pnas.0707428104 38   26 Cited 29 times in Scopus29 0
Støy, Julie, Edghill, Emma L., Flanagan, Sarah E., Ye, Honggang, Paz, Veronica P., Pluzhnikov, Anna, Below, Jennifer E., Hayes, M. Geoffrey, Cox, Nancy J., Lipkind, Gregory M., Lipton, Rebecca B., Greeley, Siri Atma W., Patch, Ann-Marie, Ellard, Sian, Steiner, Donald F., Hattersley, Andrew T., Philipson, Louis H. and Bell, Graeme I. (2007) Insulin gene mutations as a cause of permanent neonatal diabetes. Proceedings of the National Academy of Sciences of USA, 104 38: 15040-15044. doi:10.1073/pnas.0707291104 38   201 Cited 227 times in Scopus227 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   132 Cited 150 times in Scopus150 0
Morris, Andrew P., Voight, Benjamin F., Teslovich, Tanya M., Ferreira, Teresa, Segre, Ayellet V., Steinthorsdottir, Valgerdur, Strawbridge, Rona J., Khan, Hassan, Grallert, Harald, Mahajan, Anubha, Prokopenko, Inga, Kang, Hyun Min, Dina, Christian, Esko, Tonu, Fraser, Ross M., Kanoni, Stavroula, Kumar, Ashish, Lagou, Vasiliki, Langenberg, Claudia, Luan, Jian'an, Lindgren, Cecilia M., Mueller-Nurasyid, Martina, Pechlivanis, Sonali, Rayner, N. William, Scott, Laura J., Wiltshire, Steven, Yengo, Loic, Kinnunen, Leena, Rossin, Elizabeth J., Raychaudhuri, Soumya, Johnson, Andrew D., Dimas, Antigone S., Loos, Ruth J. F., Vedantam, Sailaja, Chen, Han, Florez, Jose C., Fox, Caroline, Liu, Ching-Ti, Rybin, Denis, Couper, David J., Kao, Wen Hong L., Li, Man, Cornelis, Marilyn C., Kraft, Peter, Sun, Qi, van Dam, Rob M., Stringham, Heather M., Chines, Peter S., Fischer, Krista, Fontanillas, Pierre, Holmen, Oddgeir L., Hunt, Sarah E., Jackson, Anne U., Kong, Augustine, Lawrence, Robert, Meyer, Julia, Perry, John R. B., Platou, Carl G. P., Potter, Simon, Rehnberg, Emil, Robertson, Neil, Sivapalaratnam, Suthesh, Stancakova, Alena, Stirrups, Kathleen, Thorleifsson, Gudmar, Tikkanen, Emmi, Wood, Andrew R., Almgren, Peter, Atalay, Mustafa, Benediktsson, Rafn, Bonnycastle, Lori L., Burtt, Noel, Carey, Jason, Charpentier, Guillaume, Crenshaw, Andrew T., Doney, Alex S. F., Dorkhan, Mozhgan, Edkins, Sarah, Emilsson, Valur, Eury, Elodie, Forsen, Tom, Gertow, Karl, Gigante, Bruna, Grant, George B., Groves, Christopher J., Guiducci, Candace, Herder, Christian, Hreidarsson, Astradur B., Hui, Jennie, James, Alan, Jonsson, Anna, Rathmann, Wolfgang, Klopp, Norman, Kravic, Jasmina, Krjutskov, Kaarel, Langford, Cordelia, Leander, Karin, Lindholm, Eero, Lobbens, Stephane, Mannisto, Satu, Mirza, Ghazala, Muehleisen, Thomas W., Musk, Bill, Parkin, Melissa, Rallidis, Loukianos, Saramies, Jouko, Sennblad, Bengt, Shah, Sonia, Sigurdsson, Gunnar, Silveira, Angela, Steinbach, Gerald, Thorand, Barbara, Trakalo, Joseph, Veglia, Fabrizio, Wennauer, Roman, Winckler, Wendy, Zabaneh, Delilah, Campbell, Harry, van Duijn, Cornelia, Uitterlinden, Andre G., Hofman, Albert, Sijbrands, Eric, Abecasis, Goncalo R., Owen, Katharine R., Zeggini, Eleftheria, Trip, Mieke D., Forouhi, Nita G., Syvanen, Ann-Christine, Eriksson, Johan G., Peltonen, Leena, Noethen, Markus M., Balkau, Beverley, Palmer, Colin N. A., Lyssenko, Valeriya, Tuomi, Tiinamaija, Isomaa, Bo, Hunter, David J., Qi, Lu, Wellcome Trust Case Control Consortium, Brown, Matthew A., Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators, Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Asian Genetic Epidemiology Network–Type 2 Diabetes (AGEN-T2D) Consortium, South Asian Type 2 Diabetes (SAT2D) Consortium, Shuldiner, Alan R., Roden, Michael, Barroso, Ines, Wilsgaard, Tom, Beilby, John, Hovingh, Kees, Price, Jackie F., Wilson, James F., Rauramaa, Rainer, Lakka, Timo A., Lind, Lars, Njolstad, Inger, Pedersen, Nancy L., Dedoussis, George, Khaw, Kay-Tee, Wareham, Nicholas J., Keinanen-Kiukaanniemi, Sirkka M., Saaristo, Timo E., Korpi-Hyovalti, Eeva, Saltevo, Juha, Laakso, Markku, Kuusisto, Johanna, Metspalu, Andres, Collins, Francis S., Mohlke, Karen L., Bergman, Richard N., Tuomilehto, Jaakko, Boehm, Bernhard O., Gieger, Christian, Hveem, Kristian, Cauchi, Stephane, Froguel, Philippe, Baldassarre, Damiano, Tremoli, Elena, Humphries, Steve E., Saleheen, Danish, Danesh, John, Ingelsson, Erik, Ripatti, Samuli, Salomaa, Veikko, Erbel, Raimund, Joeckel, Karl-Heinz, Moebus, Susanne, Peters, Annette, Hamsten, Anders, Illig, Thomas, de Faire, Ulf, Morris, Andrew D., Donnelly, Peter J., Frayling, Timothy M., Hattersley, Andrew T., Boerwinkle, Eric, Melander, Olle, Kathiresan, Sekar, Nilsson, Peter M., Deloukas, Panos, Thorsteinsdottir, Unnur, Groop, Leif C., Stefansson, Kari, Hu, Frank, Pankow, James S., Dupuis, Josee, Meigs, James B., Altshuler, David, Boehnke, Michael, McCarthy, Mark I. and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nature Genetics, 44 9: 981-990. doi:10.1038/ng.2383 143   299 Cited 307 times in Scopus307 11
Heid, Iris M., Jackson, Anne U., Randall, Joshua C., Winkler, Thomas W., Qi, Lu, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Zillikens, M. Carola, Speliotes, Elizabeth K., Maegi, Reedik, Workalemahu, Tsegaselassie, White, Charles C., Bouatia-Naji, Nabila, Harris, Tamara B., Berndt, Sonja I., Ingelsson, Erik, Willer, Cristen J., Weedon, Michael N., Luan, Jianan, Vedantam, Sailaja, Esko, Tonu, Kilpelaeinen, Tuomas O., Kutalik, Zoltan, Li, Shengxu, Monda, Keri L., Dixon, Anna L., Holmes, Christopher C., Kaplan, Lee M., Liang, Liming, Min, Josine L., Moffatt, Miriam F., Molony, Cliona, Nicholson, George, Schadt, Eric E., Zondervan, Krina T., Feitosa, Mary F., Ferreira, Teresa, Allen, Hana Lango, Weyant, Robert J., Wheeler, Eleanor, Wood, Andrew R., Estrada, Karol, Goddard, Michael E., Lettre, Guillaume, Mangino, Massimo, Nyholt, Dale R., Purcell, Shaun, Smith, Albert Vernon, Visscher, Peter M., Yang, Jian, McCarroll, Steven A., Nemesh, James, Voight, Benjamin F., Absher, Devin, Amin, Najaf, Aspelund, Thor, Coin, Lachlan, Glazer, Nicole L., Hayward, Caroline, Heard-Costa, Nancy L., Hottenga, Jouke-Jan, Johansson, Asa, Johnson, Toby, Kaakinen, Marika, Kapur, Karen, Ketkar, Shamika, Knowles, Joshua W., Kraft, Peter, Kraja, Aldi T., Lamina, Claudia, Leitzmann, Michael F., McKnight, Barbara, Morris, Andrew P., Ong, Ken K., Perry, John R. B., Peters, Marjolein J., Polasek, Ozren, Prokopenko, Inga, Rayner, Nigel W., Ripatti, Samuli, Rivadeneira, Fernando, Robertson, Neil R., Sanna, Serena, Sovio, Ulla, Surakka, Ida, Teumer, Alexander, van Wingerden, Sophie, Vitart, Veronique, Zhao, Jing Hua, Cavalcanti-Proenca, Christine, Chines, Peter S., Fisher, Eva, Kulzer, Jennifer R., Lecoeur, Cecile, Narisu, Narisu, Sandholt, Camilla, Scott, Laura J., Silander, Kaisa, Stark, Klaus, Tammesoo, Mari-Liis, Teslovich, Tanya M., Timpson, Nicholas John, Watanabe, Richard M., Welch, Ryan, Chasman, Daniel I., Cooper, Matthew N., Jansson, John-Olov, Kettunen, Johannes, Lawrence, Robert W., Pellikka, Niina, Perola, Markus, Vandenput, Liesbeth, Alavere, Helene, Almgren, Peter, Atwood, Larry D., Bennett, Amanda J., Biffar, Reiner, Bonnycastle, Lori L., Bornstein, Stefan R., Buchanan, Thomas A., Campbell, Harry, Day, Ian N. M., Dei, Mariano, Doerr, Marcus, Elliott, Paul, Erdos, Michael R., Eriksson, Johan G., Freimer, Nelson B., Fu, Mao, Gaget, Stefan, Geus, Eco J. C., Gjesing, Anette P., Grallert, Harald, Graessler, Juergen, Groves, Christopher J., Guiducci, Candace, Hartikainen, Anna-Liisa, Hassanali, Neelam, Havulinna, Aki S., Herzig, Karl-Heinz, Hicks, Andrew A., Hui, Jennie, Igl, Wilmar, Jousilahti, Pekka, Jula, Antti, Kajantie, Eero, Kinnunen, Leena, Kolcic, Ivana, Koskinen, Seppo, Kovacs, Peter, Kroemer, Heyo K., Krzelj, Vjekoslav, Kuusisto, Johanna, Kvaloy, Kirsti, Laitinen, Jaana, Lantieri, Olivier, Lathrop, G. Mark, Lokki, Marja-Liisa, Luben, Robert N., Ludwig, Barbara, McArdle, Wendy L., McCarthy, Anne, Morken, Mario A., Nelis, Mari, Neville, Matt J., Pare, Guillaume, Parker, Alex N., Peden, John F., Pichler, Irene, Pietilainen, Kirsi H., Platou, Carl G. P., Pouta, Anneli, Ridderstrale, Martin, Samani, Nilesh J., Saramies, Jouko, Sinisalo, Juha, Smit, Jan H., Strawbridge, Rona J., Stringham, Heather M., Swift, Amy J., Teder-Laving, Maris, Thomson, Brian, Usala, Gianluca, van Meurs, Joyce B. J., van Ommen, Gert-Jan, Vatin, Vincent, Volpato, Claudia B., Wallaschofski, Henri, Walters, G. Bragi, Widen, Elisabeth, Wild, Sarah H., Willemsen, Gonneke, Witte, Daniel R., Zgaga, Lina, Zitting, Paavo, Beilby, John P., James, Alan L., Kahonen, Mika, Lehtimaki, Terho, Nieminen, Markku S., Ohlsson, Claes, Palmer, Lyle J., Raitakari, Olli, Ridker, Paul M., Stumvoll, Michael, Toenjes, Anke, Viikari, Jorma, Balkau, Beverley, Ben-Shlomo, Yoav, Bergman, Richard N., Boeing, Heiner, Smith, George Davey, Ebrahim, Shah, Froguel, Philippe, Hansen, Torben, Hengstenberg, Christian, Hveem, Kristian, Isomaa, Bo, Jorgensen, Torben, Karpe, Fredrik, Khaw, Kay-Tee, Laakso, Markku, Lawlor, Debbie A., Marre, Michel, Meitinger, Thomas, Metspalu, Andres, Midthjell, Kristian, Pedersen, Oluf, Salomaa, Veikko, Schwarz, Peter E. H., Tuomi, Tiinamaija, Tuomilehto, Jaakko, Valle, Timo T., Wareham, Nicholas J., Arnold, Alice M., Beckmann, Jacques S., Bergmann, Sven, Boerwinkle, Eric, Boomsma, Dorret I., Caulfield, Mark J., Collins, Francis S., Eiriksdottir, Gudny, Gudnason, Vilmundur, Gyllensten, Ulf, Hamsten, Anders, Hattersley, Andrew T., Hofman, Albert, Hu, Frank B., Illig, Thomas, Iribarren, Carlos, Jarvelin, Marjo-Riitta, Kao, W. H. Linda, Kaprio, Jaakko, Launer, Lenore J., Munroe, Patricia B., Oostra, Ben, Penninx, Brenda W., Pramstaller, Peter P., Psaty, Bruce M., Quertermous, Thomas, Rissanen, Aila, Rudan, Igor, Shuldiner, Alan R., Soranzo, Nicole, Spector, Timothy D., Syvanen, Ann-Christine, Uda, Manuela, Uitterlinden, Andre, Voelzke, Henry, Vollenweider, Peter, Wilson, James F., Witteman, Jacqueline C., Wright, Alan F., Abecasis, Goncalo R., Boehnke, Michael, Borecki, Ingrid B., Deloukas, Panos, Frayling, Timothy M., Groop, Leif C., Haritunians, Talin, Hunter, David J., Kaplan, Robert C., North, Kari E., O'Connell, Jeffrey R., Peltonen, Leena, Schlessinger, David, Strachan, David P., Hirschhorn, Joel N., Assimes, Themistocles L., Wichmann, H-Erich, Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Stefansson, Kari, Cupples, L. Adrienne, Loos, Ruth J. F., Barroso, Ines, McCarthy, Mark I., Fox, Caroline S., Mohlke, Karen L. and Lindgren, Cecilia M. (2010) Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics, 42 11: 949-U160. doi:10.1038/ng.685 37   264 Cited 302 times in Scopus302 33
Flanagan, Sarah E., Patch, Ann-Marie, Mackay, Deborah J. G., Edghill, Emma L., Gloyn, Anna L., Robinson, David, Shield, Julian P. H., Temple, Karen, Ellard, Sian and Hattersley, Andrew T. (2007) Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood. Diabetes, 56 7: 1930-1937. doi:10.2337/db07-0043 36   134 Cited 153 times in Scopus153 0
Ellard, Sian, Flanagan, Sarah E., Girard, Christophe A., Patch, Ann-Marie, Harries, Lorna W., Parrish, Andrew, Edghill, Emma L., Mackay, Deborah J. G., Proks, Peter, Shimomura, Kenju, Haberland, Holger, Carson, Dennis J., Sheild, Julian P. H., Hattersley, Andrew T. and Ashcroft, Frances M. (2007) Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects. American Journal of Human Genetics, 81 2: 375-382. doi:10.1086/519174 53   76 Cited 90 times in Scopus90 0
Garin, Intza, Edghill, Emma L., Akerman, Ildem, Rubio-Cabezas, Oscar, Rica, Itxaso, Locke, Jonathan M., Maestro, Miguel Angel, Alshaikh, Adnan, Bundak, Ruveyde, del Castillo, Gabriel, Deeb, Asma, Deiss, Dorothee, Fernandez, Juan M., Godbole, Koumudi, Hussain, Khalid, O'Connell, Michele, Klupa, Thomasz, Kolouskova, Stanislava, Mohsin, Fauzia, Perlman, Kusiel, Sumnik, Zdenek, Rial, Jose M., Ugarte, Estibaliz, Vasanthi, Thiruvengadam, Neonatal Diabetes International Group, Johnstone, Karen, Flanagan, Sarah E., Martinez, Rosa, Castano, Carlos, Patch, Ann-Marie, Fernandez-Rebollo, Eduardo, Raile, Klemens, Morgan, Noel, Harries, Lorna W., Castano, Luis, Ellard, Sian, Ferrer, Jorge, de Nanclares, Guiomar Perez and Hattersley, Andrew T. (2010) Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis. Proceedings of the National Academy of Sciences of the USA, 107 7: 3105-3110. doi:10.1073/pnas.0910533107 92   51 Cited 57 times in Scopus57 1
Shaw-Smith, Charles, Flanagan, Sarah E., Patch, Ann-Marie, Grulich-Henn, Juergen, Habeb, Abdelhadi M., Hussain, Khalid, Pomahacova, Renata, Matyka, Krystyna, Abdullah, Mohamed, Hattersley, Andrew T. and Ellard, Sian (2012) Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. Pediatric Diabetes, 13 4: 307-314. doi:10.1111/j.1399-5448.2012.00855.x 32   0 Cited 5 times in Scopus5 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   90 Cited 99 times in Scopus99 1
Rubio-Cabezas, Oscar, Patch, Ann-Marie, Minton, Jayne A. L., Flanagan, Sarah E., Edghill, Emma L., Hussain, Khalid, Balafrej, Amina, Deeb, Asma, Buchanan, Charles R., Jefferson, Ian G., Mutair, Angham, The Neonatal Diabetes International Collaborative Group, Hattersley, Andrew T. and Ellard, Sian (2009) Wolcott-Rallison Syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families. The Journal of Clinical Endocrinology and Metabolism, 94 11: 4162-4170. doi:10.1210/jc.2009-1137 64   38 Cited 39 times in Scopus39 0