Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways von Soranzo, N, Sanna, S, Langenberg, C, Prokopenko, I, Stolerman, E, Sandhu, MS, Devaney, JM, Reilly, MP, Ricketts, SL, Stewart, AF, Arking, D, Balkau, B, Böhm, B, Bonnefond, A, Bonnycastle, LL, Bornstein, SR, Burnett-Miller, MS, Campbell, H, Cao, A, Chambers, J, Clark, R, Collins, FS, Deloukas, P, Egan, JM, Ferrucci, L, Forouhi, N, Fox, CS, Franzosi, MG, Goel, A, Grallert, H, Hadley, D, Hamsten, A, Hayward, C, Heath, S, Herder, C, Homuth, G, Hottenga, JJ, Hunter-Merrill, R, Illig, T, Jackson, AU, Kleber, M, Knouff, CW, Kooner, J, Köttgen, A, Kovacs, P, Kühnel, B, Lathrop, M, Loos, RJ, Mägi, R, Magnusson, PK, Mangino, M, McArdle, WL, McPherson, R, Meitinger, T, Melander, O, Mohlke, KL, Morken, MA, Nathan, DM, Oexle, K, Olla, N, Pankow, JS, Pedersen, NL, Peltonen, L, Perola, M, Polasek, O, Porcu, E, Rathmann, W, Rocheleau, G, Roden, M, Rudan, I, Salomaa, V, Schlessinger, D, Seedorf, U, Selvin, E, Serrano-Ríos, M, Shrader, P, Siscovick, D, Song, K, Spector, TD, Stefansson, K, Strawbridge, R, Stumvoll, M, Tanaka, T, Teumer, A, Thorsteinsdottir, U, Tönjes, A, Wallaschofski, H, Watkins, H, Wild, SH, Willemsen, G, Williams, GH, Wright, AF, Epstein, SE, Hakonarson, HH, Roberts, R, Fleming, MD, Sladek, R, Froguel, P, McCarthy, MI, Uda, M

Volltext

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits — The Hispanic/Latino Anthropometry Consortium von Fernández-Rhodes, L, Graff, M, Buchanan, VL, Justice, AE, Highland, HM, Guo, X, Zhu, W, Chen, HH, Young, KL, Adhikari, K, Palmer, ND, Below, JE, Bradfield, J, Pereira, AC, Glover, LS, Kim, D, Lilly, AG, Shrestha, P, Thomas, AG, Zhang, X, Chen, M, Chiang, CWK, Pulit, S, Horimoto, A, Krieger, JE, Guindo-Martínez, M, Preuss, M, Schumann, C, Smit, RAJ, Torres-Mejía, G, Acuña-Alonzo, V, Bedoya, G, Bortolini, MC, Canizales-Quinteros, S, Gallo, C, González-José, R, Poletti, G, Rothhammer, F, Hakonarson, H, Igo, R, Adler, SG, Iyengar, SK, Nicholas, SB, Gogarten, SM, Isasi, CR, Papnicolaou, G, Stilp, AM, Qi, Q, Kho, M, Smith, JA, Langefeld, CD, Wagenknecht, L, Mckean-Cowdin, R, Gao, XR, Nousome, D, Conti, DV, Feng, Y, Allison, MA, Arzumanyan, Z, Buchanan, TA, Ida Chen, YD, Genter, PM, Goodarzi, MO, Hai, Y, Hsueh, W, Ipp, E, Kandeel, FR, Lam, K, Li, X, Nadler, JL, Raffel, LJ, Roll, K, Sandow, K, Tan, J, Taylor, KD, Xiang, AH, Yao, J, Audirac-Chalifour, A, de Jesus Peralta Romero, J, Hartwig, F, Horta, B, Blangero, J, Curran, JE, Duggirala, R, Lehman, DE, Puppala, S, Fejerman, L, John, EM, Aguilar-Salinas, C, Burtt, NP, Florez, JC, García-Ortíz, H, González-Villalpando, C, Mercader, J, Orozco, L, Tusié-Luna, T, Blanco, E, Gahagan, S, Cox, NJ, Hanis, C

Volltext bestellen

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A von Kasperaviciute, D, Catarino, CB, Matarin, M, Leu, C, Novy, J, Tostevin, A, Leal, B, Hessel, EV, Hallmann, K, Hildebrand, MS, Dahl, HH, Ryten, M, Trabzuni, D, Ramasamy, A, Alhusaini, S, Doherty, CP, Dorn, T, Hansen, J, Krämer, G, Steinhoff, BJ, Zumsteg, D, Duncan, S, Kälviäinen, RK, Eriksson, KJ, Kantanen, AM, Pandolfo, M, Gruber-Sedlmayr, U, Schlachter, K, Reinthaler, EM, Stogmann, E, Zimprich, F, Théâtre, E, Smith, C, O'Brien, TJ, Meng Tan, K, Petrovski, S, Robbiano, A, Paravidino, R, Zara, F, Striano, P, Sperling, MR, Buono, RJ, Hakonarson, H, Chaves, J, Costa, PP, Silva, BM, da Silva, AM, de Graan, PN, Koeleman, BP, Becker, A, Schoch, S, von Lehe, M, Reif, PS, Rosenow, F, Becker, F, Weber, Y, Lerche, H, Rössler, K, Buchfelder, M, Hamer, HM, Kobow, K, Coras, R, Blumcke, I, Scheffer, IE, Berkovic, SF, Weale, ME, UK Brain Expression Consortium, The, Delanty, N, Depondt, C, Cavalleri, GL, Kunz, WS, Sisodiya, SM

Volltext bestellen