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pro vyhledávání: '"Frayling T.M."'
Autor:
Wood, A.R., Tyrrell, J., Beaumont, R., Jones, S.E., Tuke, M.A., Ruth, K.S., Yaghootkar, H., Freathy, R.M., Murray, A., Frayling, T.M., Weedon, M.N., GIANT Consortium (Chen, C.M., Gieger, C., Grallert, H., Heid, I.M., Heinrich, J., Illig, T., Lamina, C., Meitinger, T., Peters, A., Rzehak, P., Thiering, E., Wichmann, H.-E.)
Publikováno v:
Diabetologia 59, 1214-1221 (2016)
Diabetologia
Diabetologia
Aims/hypothesis Genome-wide association (GWA) studies have identified hundreds of common genetic variants associated with obesity and type 2 diabetes. These studies have usually focused on additive association tests. Identifying deviations from addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b78acf411eb5db3041fcb95daf212dc6
https://doi.org/10.1101/027490
https://doi.org/10.1101/027490
Autor:
Voight, B.F., Raychaudhuri, S., Purcell, S., McCarroll, S.A., Segrè, A.V., Ardlie, K., Burtt, N.P., Crawford, G., Elliott, A.L., Green, T., Guiducci, C., Saxena, R., Daly, M.J., Florez, J.C., Altshuler, D., Meigs, J.B., Scott, L.J., Welch, R.P., Willer, C.J., Ganser, M., Jackson, A.U., Stringham, H.M., Abecasis, G.R., Boehnke, M., Steinthorsdottir, V., Thorleifsson, G., Kong, A., Walters, G.B., Thorsteinsdottir, U., Stefansson, K., Dina, C., Proença, C., Cauchi, S., Froguel, P., Zeggini, E., Bumpstead, S., Payne, F., Smith, N., Barroso, I., Ferreira, T., Elliott, K.S., Lindgren, C.M., Prokopenko, I., Rayner, N.W., Robertson, N.R., Morris, A.P., McCarthy, M.I., Huth, C., Grallert, H., Gieger, C., Klopp, N., Meitinger, T., Petersen, A.-K., Thorand, B., Wichmann, H.-E., Illig, T., Aulchenko, Y.S., Amin, N., Witteman, J., Hofman, A., Van Duijn, C.M., McCulloch, L.J., Bennett, A.J., Groves, C.J., Hassanali, N., Owen, K.R., Gloyn, A.L., Wu, G., Stein, L.D., Langenberg, C., Griffin, S., Wareham, N.J., Hoffmann, O.M., Hide, W.A., Dupuis, J., Qi, L., Kraft, P., Sun, Q., Hunter, D., Hu, F.B., Cornelis, M., VanDam, R., Van Hoek, M., Van Herpt, T., Sijbrands, E., Uitterlinden, A., Navarro, P., Balkau, B., Benediktsson, R., Sigurdsson, G., Blagieva, R., Boehm, B.O., Boerwinkle, E., Bonnycastle, L.L., Chines, P.S., Erdos, M.R., Morken, M.A., Narisu, N., Swift, A.J., Boström, K.B., Bravenboer, B., Charpentier, G., Couper, D.J., Doney, A.S.F., Morris, A.D., Palmer, C.N.A., Fox, C.S., Franklin, C.S., Rudan, I., Grarup, N., Hadjadj, S., Thomas Sparsø, [No Value], Campbell, H., Wilson, J.F., Hansen, T., Pedersen, O., Herder, C., Roden, M., Isomaa, B., Tuomi, T., Johnson, P.R.V., Jørgensen, T., Kao, W.H.L., Kuusisto, J., Laakso, M., Lauritzen, T., Li, M., Lieverse, A., Lyssenko, V., Nilsson, P., Groop, L., Marre, M., Midthjell, K., Platou, C., Hveem, K., Perry, J.R.B., Shields, B.M., Weedon, M.N., Frayling, T.M., Hattersley, A.T., Rathmann, W., Strassburger, K., Rocheleau, G., Sladek, R., Sampson, M.J., Shrader, P., Tichet, J., Bergman, R.N., Collins, F.S., Gyllensten, U., Hitman, G.A., Mohlke, K.L., Pramstaller, P.P., Tuomilehto, J., Walker, M., Watanabe, R.M., Pankow, J.S.
Publikováno v:
Voight, B F, Raychaudhuri, S, Purcell, S, McCarroll, S A, Segrè, A V, Ardlie, K, Burtt, N P, Crawford, G, Elliott, A L, Green, T, Guiducci, C, Saxena, R, Daly, M J, Florez, J C, Altshuler, D, Meigs, J B, Scott, L J, Welch, R P, Willer, C J, Ganser, M, Jackson, A U, Stringham, H M, Abecasis, G R, Boehnke, M, Steinthorsdottir, V, Thorleifsson, G, Kong, A, Walters, G B, Thorsteinsdottir, U, Stefansson, K, Dina, C, Proença, C, Cauchi, S, Froguel, P, Zeggini, E, Bumpstead, S, Payne, F, Smith, N, Barroso, I, Ferreira, T, Elliott, K S, Lindgren, C M, Prokopenko, I, Rayner, N W, Robertson, N R, Morris, A P, McCarthy, M I, Huth, C, Grallert, H, Gieger, C, Klopp, N, Meitinger, T, Petersen, A-K, Thorand, B, Wichmann, H-E, Illig, T, Aulchenko, Y S, Amin, N, Witteman, J, Hofman, A, Van Duijn, C M, McCulloch, L J, Bennett, A J, Groves, C J, Hassanali, N, Owen, K R, Gloyn, A L, Wu, G, Stein, L D, Langenberg, C, Griffin, S, Wareham, N J, Hoffmann, O M, Hide, W A, Dupuis, J, Qi, L, Kraft, P, Sun, Q, Hunter, D, Hu, F B, Cornelis, M, VanDam, R, Van Hoek, M, Van Herpt, T, Sijbrands, E, Uitterlinden, A, Navarro, P, Balkau, B, Benediktsson, R, Sigurdsson, G, Blagieva, R, Boehm, B O, Boerwinkle, E, Bonnycastle, L L, Chines, P S, Erdos, M R, Morken, M A, Narisu, N, Swift, A J, Boström, K B, Bravenboer, B, Charpentier, G, Couper, D J, Doney, A S F, Morris, A D, Palmer, C N A, Fox, C S, Franklin, C S, Rudan, I, Grarup, N, Hadjadj, S, Thomas Sparsø, N V, Campbell, H, Wilson, J F, Hansen, T, Pedersen, O, Herder, C, Roden, M, Isomaa, B, Tuomi, T, Johnson, P R V, Jørgensen, T, Kao, W H L, Kuusisto, J, Laakso, M, Lauritzen, T, Li, M, Lieverse, A, Lyssenko, V, Nilsson, P, Groop, L, Marre, M, Midthjell, K, Platou, C, Hveem, K, Perry, J R B, Shields, B M, Weedon, M N, Frayling, T M, Hattersley, A T, Rathmann, W, Strassburger, K, Rocheleau, G, Sladek, R, Sampson, M J, Shrader, P, Tichet, J, Bergman, R N, Collins, F S, Gyllensten, U, Hitman, G A, Mohlke, K L, Pramstaller, P P, Tuomilehto, J, Walker, M, Watanabe, R M & Pankow, J S 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-874 . https://doi.org/10.1038/nature08625
Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K T, Jonasdottir, A, Frigge, M L, Gylfason, A, Olason, P I, Gudjonsson, S A, Sverrisson, S, Stacey, S N, Sigurgeirsson, B, Benediktsdottir, K R, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J H, Johannsson, O T, Hreidarsson, A B, Sigurdsson, G, Ferguson-Smith, A C, Gudbjartsson, D F, Thorsteinsdottir, U, Stefansson, K, DIAGRAM Consortium & Lauritzen, T 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-74 . https://doi.org/10.1038/nature08625
Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K T, Jonasdottir, A, Frigge, M L, Gylfason, A, Olason, P I, Gudjonsson, S A, Sverrisson, S, Stacey, S N, Sigurgeirsson, B, Benediktsdottir, K R, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J H, Johannsson, O T, Hreidarsson, A B, Sigurdsson, G, Ferguson-Smith, A C, Gudbjartsson, D F, Thorsteinsdottir, U, Stefansson, K, DIAGRAM Consortium & Lauritzen, T 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-74 . https://doi.org/10.1038/nature08625
To access publisher full text version of this article. Please click on the hyperlink in Additional Links field Effects of susceptibility variants may depend on from which parent they are inherited. Although many associations between sequence variants
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