학술논문

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
Document Type
Article
Author
Gaulton, K.J.Ferreira, T.Mahajan, A.Rayner, N.W.Robertson, N.Beer, N.L.Van De Bunt, M.Lindgren, C.M.Trakalo, J.Wiltshire, S.Ingelsson, E.Donnelly, P.J.Gloyn, A.L.McCarthy, M.I.Morris, A.P.Lee, Y.Locke, A.Scott, L.J.Fuchsberger, C.Kwan, P.Ma, C.Kang, H.M.Abecasis, G.R.Jackson, A.U.Stringham, H.M.Boehnke, M.Teslovich, T.M.Raimondo, A.Thomsen, S.K.Rundle, J.K.Groves, C.J.Owen, K.R.Mägi, R.Esko, T.Mihailov, E.Metspalu, A.Reschen, M.E.Chalisey, A.O'Callaghan, C.A.Edkins, S.Langford, C.Peltonen, L.Zeggini, E.Ripatti, S.Deloukas, P.Barroso, I.Scott, R.A.Willems, S.M.Kerrison, N.D.Luan, J.Perry, J.R.B.Loos, R.J.F.Langenberg, C.Wareham, N.J.Prokopenko, I.Froguel, P.Green, T.Burtt, N.P.Carey, J.Crenshaw, A.T.Flannick, J.Fontanillas, P.Grant, G.B.Kathiresan, S.Altshuler, D.Sparso, T.Grarup, N.Have, C.T.Hansen, T.Pedersen, O.Thuillier, D.Yengo, L.Cauchi, S.Grallert, H.Wahl, S.Gieger, C.Klopp, N.Illig, T.Thorand, B.Peters, A.Frånberg, M.Strawbridge, R.J.Gertow, K.McLeod, O.Sennblad, B.Hamsten, A.Kestler, H.Chheda, H.Tikkanen, E.Tuomi, T.Groop, L.C.Eisele, L.Pechlivanis, S.Jöckel, K.-H.Moebus, S.Gustafsson, S.Steinthorsdottir, V.Thorleifsson, G.Kong, A.Thorsteinsdottir, U.Stefansson, K.Qi, L.Hunter, D.J.Kraft, P.Liang, L.Hu, F.B.Van Dam, R.M.Franks, P.W.Sun, Q.Karssen, L.C.Van Leeuwen, E.M.Van Duijn, C.Li, M.Kao, W.-H.L.Chen, H.Liu, C.-T.Dupuis, J.Linderman, M.Lu, Y.Voight, B.F.Almgren, P.Fadista, J.Jonsson, A.Kravic, J.Lindholm, E.Lyssenko, V.Oskolkov, N.N.Storm, P.Melander, O.Nilsson, P.M.Baldassarre, D.Tremoli, E.Balkau, B.Benediktsson, R.Hreidarsson, A.B.Sigurosson, G.Blüher, M.Kovacs, P.Tonjes, A.Stumvoll, M.Boeing, H.Bonnycastle, L.L.Chines, P.S.Collins, F.S.Bottinger, E.P.Gottesman, O.Charpentier, G.Cornelis, M.C.Couper, D.J.Doney, A.S.F.Palmer, C.N.A.Dorkhan, M.Eriksson, J.G.Kinnunen, L.Männistö, S.Salomaa, V.Koistinen, H.Tuomilehto, J.Florez, J.C.Eury, E.Lobbens, S.Fox, C.Gigante, B.Leander, K.De Faire, U.Hassinen, M.Lakka, T.A.Rauramaa, R.Herder, C.Roden, M.Holmen, O.L.Platou, C.G.P.Hveem, K.Humphries, S.E.Jørgensen, M.E.Jørgensen, T.Linneberg, A.Lichtner, P.Meyer, J.Müller-Nurasyid, M.Strauch, K.Mirza, G.Mühleisen, T.W.Nöthen, M.M.Navarro, C.Palli, D.Ruderfer, D.Rybin, D.Van Der Schouw, Y.T.Stančáková, A.Kuusisto, J.Laakso, M.Steinbach, G.Wennauer, R.Sijbrands, E.Wood, A.R.Frayling, T.M.Dunham, I.Birney, E.Pasquali, L.Ferrer, J.Meigs, J.B.Boerwinkle, E.Pankow, J.S.Pedersen, N.L.Lind, L.Keinanen-Kiukaanniemi, S.M.Korpi-Hyövälti, E.Saaristo, T.E.Saltevo, J.Erbel, R.Boehm, B.O.Bergman, R.N.Mohlke, K.L.Njølstad, I.Hattersley, A.T.Sladek, R.Morris, A.D.
Source
In: Nature Genetics. (Nature Genetics, 1 December 2015, 47(12):1415-1425)
Subject
Language
English
ISSN
15461718
10614036