Showing 1 - 20 results of 24 for search '"Hreidarsson, Ástrádur B."', query time: 3.51s Refine Results  

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

by Flannick, Jason, Thorleifsson, Gudmar, Beer, Nicola L, Jacobs, Suzanne B R, Grarup, Niels, Burtt, Noël P, Mahajan, Anubha, Fuchsberger, Christian, Atzmon, Gil, Benediktsson, Rafn, Blangero, John, Bowden, Don W, Brandslund, Ivan, Brosnan, Julia, Burslem, Frank, Chambers, John, Cho, Yoon Shin, Christensen, Cramer, Douglas, Desirée A, Duggirala, Ravindranath, Dymek, Zachary, Farjoun, Yossi, Fennell, Timothy, Fontanillas, Pierre, Forsén, Tom, Gabriel, Stacey, Glaser, Benjamin, Gudbjartsson, Daniel F, Hanis, Craig, Hansen, Torben, Hreidarsson, Astradur B, Hveem, Kristian, Ingelsson, Erik, Isomaa, Bo, Johansson, Stefan, Jørgensen, Torben, Jørgensen, Marit Eika, Kathiresan, Sekar, Kong, Augustine, Kooner, Jaspal, Kravic, Jasmina, Laakso, Markku, Lee, Jong-Young, Lind, Lars, Lindgren, Cecilia M, Linneberg, Allan, Masson, Gisli, Meitinger, Thomas, Mohlke, Karen L, Molven, Anders, Morris, Andrew P, Potluri, Shobha, Rauramaa, Rainer, Ribel-Madsen, Rasmus, Richard, Ann-Marie, Rolph, Tim, Salomaa, Veikko, Segrè, Ayellet V, Skärstrand, Hanna, Steinthorsdottir, Valgerdur, Stringham, Heather M, Sulem, Patrick, Tai, E Shyong, Teo, Yik Ying, Teslovich, Tanya, Thorsteinsdottir, Unnur, Trimmer, Jeff K, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Vaziri-Sani, Fariba, Voight, Benjamin F, Wilson, James G, Boehnke, Michael, McCarthy, Mark I, Njølstad, Pål R, Pedersen, Oluf, Groop, Leif, Cox, David R, Stefansson, Kari, Altshuler, David
Published in Nature genetics (01.04.2014)

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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

by Scott, Laura J, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Johnson, Andrew D, Eicher, John D, Lee, Yeji, Ma, Clement, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Van Zuydam, Natalie R, Chen, Han, Voight, Ben F, Grallert, Harald, Müller-Nurasyid, Martina, Karssen, Lennart C, van Leeuwen, Elisabeth M, Willems, Sara M, Fuchsberger, Christian, Teslovich, Tanya M, Chanda, Pritam, Dina, Christian, Yengo, Loic, Jiang, Longda, Sparso, Thomas, Kestler, Hans A, Eisele, Lewin, Strawbridge, Rona J, Benediktsson, Rafn, Kong, Augustine, Sigurðsson, Gunnar, Kerrison, Nicola D, Luan, Jian'an, Roden, Michael, Thorand, Barbara, Fox, Caroline, Liu, Ching-Ti, Rybin, Denis, Tuomi, Tiinamaija, Couper, David J, Jørgensen, Torben, Linneberg, Allan, Cornelis, Marilyn C, Hunter, David J, Kraft, Peter, Sun, Qi, Perry, John R B, Wood, Andrew R, Zeggini, Eleftheria, Chines, Peter S, Stringham, Heather M, Mühleisen, Thomas W, Nöthen, Markus M, Pechlivanis, Sonali, Humphries, Steve E, Tremoli, Elena, Klopp, Norman, Mӓnnistö, Satu, Charpentier, Guillaume, Eury, Elodie, Gigante, Bruna, Leander, Karin, Bottinger, Erwin P, Blüher, Matthias, Kovacs, Peter, Scapoli, Chiara, Erbel, Raimund, Jöckel, Karl-Heinz, Moebus, Susanne, de Faire, Ulf, Hamsten, Anders, Stumvoll, Michael, Donnelly, Peter J, Frayling, Timothy M, Hattersley, Andrew T, Salomaa, Veikko, Pedersen, Nancy L, Mohlke, Karen L, Barroso, Inês, Lannfelt, Lars, Ingelsson, Erik, Lind, Lars, Lindgren, Cecilia M, Froguel, Philippe, Palli, Domenico, van der Schouw, Yvonne T, Altshuler, David, Groop, Leif C, van Duijn, Cornelia M, Florez, Jose C, Meigs, James B, Boerwinkle, Eric, Strauch, Konstantin, Metspalu, Andres, Morris, Andrew D, Hu, Frank B, Thorsteinsdottir, Unnur, Dupuis, Josée, Morris, Andrew P, Prokopenko, Inga
Published in Diabetes (New York, N.Y.) (01.11.2017)

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

by Mahajan, Anubha, Go, Min Jin, Gaulton, Kyle J, Prokopenko, Inga, Wang, Xu, Abecasis, Goncalo R, Balkau, Beverley, Barnett, Anthony H, Beilby, John, Bell, Graeme I, Burtt, Noël, Chang, Li-Ching, Chen, Han, Chidambaram, Manickam, Chines, Peter S, Cho, Nam H, Cho, Young Min, van Dam, Rob M, Danesh, John, Dedoussis, George, Doney, Alex S, Donnelly, Peter J, Emilsson, Valur, Eriksson, Johan G, Florez, Jose C, Forsen, Tom, Fox, Caroline, Fraser, Ross M, Gigante, Bruna, Grant, George B, Grundberg, Elin, Hamsten, Anders, Hara, Kazuo, Hattersley, Andrew T, Herder, Christian, Hveem, Kristian, Hydrie, Zafar I, Ingelsson, Erik, Islam, Muhammed, Jackson, Anne U, Jafar, Tazeen, Kadowaki, Takashi, Kang, Hyun Min, Kao, Wen Hong L, Kato, Norihiro, Kelly, Ann M, Kim, Sangsoo, Kong, Augustine, Kraft, Peter, Kravic, Jasmina, Kumar, Ashish, Kuusisto, Johanna, Lagou, Vasiliki, Langenberg, Claudia, Lee, Jen-Mai, Li, Yun, Lindholm, Eero, Loos, Ruth J F, Maeda, Shiro, Mägi, Reedik, Männisto, Satu, Matthews, David R, Morris, Andrew D, Navarro, Pau, Pankow, James S, Park, Kyong Soo, Platou, Carl G, Qi, Lu, Rauramaa, Rainer, Raychaudhuri, Soumya, Rybin, Denis, Saaristo, Timo E, Saltevo, Juha, Segrè, Ayellet V, Sennblad, Bengt, Sigurđsson, Gunnar, Stefansson, Kari, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Stringham, Heather M, Suo, Chen, Thorleifsson, Gudmar, Tremoli, Elena, Tsai, Fuu Jen, Tuomilehto, Jaakko, Veglia, Fabrizio, Wareham, Nicholas J, Wilsgaard, Tom, Wilson, James F, Wong, Tien Yin, Wu, Ying, Yamamoto, Ken, Zhang, Fan, Zheng, Wei, Bowden, Donald W, Cox, Nancy J, Cruz, Miguel, Seielstad, Mark, Parra, Esteban J, Morris, Andrew P
Published in Nature genetics (01.03.2014)

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

by Mägi, Reedik, Robertson, Neil, Prokopenko, Inga, Green, Todd, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Kwan, Phoenix, Lu, Yingchang, van de Bunt, Martijn, Chalisey, Anil, Abecasis, Gonçalo R, Charpentier, Guillaume, Chines, Peter S, Doney, Alex S F, Edkins, Sarah, Esko, Tonu, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Gieger, Christian, Hassinen, Maija, Have, Christian T, Herder, Christian, Hreidarsson, Astradur B, Hunter, David J, Jørgensen, Marit E, Jørgensen, Torben, Kong, Augustine, Kraft, Peter, Kravic, Jasmina, Liang, Liming, Lindholm, Eero, Liu, Ching-Ti, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Müller-Nurasyid, Martina, Navarro, Carmen, Oskolkov, Nikolay N, Palli, Domenico, Perry, John R B, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Stančáková, Alena, Steinbach, Gerald, Strauch, Konstantin, Stringham, Heather M, Thorand, Barbara, Tonjes, Anke, Wiltshire, Steven, Zeggini, Eleftheria, Dunham, Ian, Pasquali, Lorenzo, Loos, Ruth J F, Boerwinkle, Eric, Thorsteinsdottir, Unnur, Stefansson, Kari, Rauramaa, Rainer, Stumvoll, Michael, Pedersen, Nancy L, Keinanen-Kiukaanniemi, Sirkka M, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Laakso, Markku, Jöcke, Karl-Heinz, Ripatti, Samuli, Boehm, Bernhard O, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Hveem, Kristian, Njølstad, Inger, Deloukas, Panagiotis, Frayling, Timothy M, Hattersley, Andrew T, de Faire, Ulf, Hamsten, Anders, Illig, Thomas, Cauchi, Stephane, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Pedersen, Oluf, Morris, Andrew D, Palmer, Collin N A, Kathiresan, Sekar, Melander, Olle, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, McCarthy, Mark I, Morris, Andrew P
Published in Nature genetics (01.12.2015)

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