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Analysis of shared heritability in common disorders of the ..:
Anttila, V
;
Bulik-Sullivan, B
;
Finucane, H.K
...
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757. , 2018
Link:
https://serval.unil.ch/notice/serval:BIB_77315235F9BB
RT Journal T1
Analysis of shared heritability in common disorders of the brain
UL https://suche.suub.uni-bremen.de/peid=base-ftunivlausanne:oai:serval.unil.ch:BIB_77315235F9BB&Exemplar=1&LAN=DE A1 Anttila, V A1 Bulik-Sullivan, B A1 Finucane, H.K A1 Walters, R.K A1 Bras, J A1 Duncan, L A1 Escott-Price, V A1 Falcone, G.J A1 Gormley, P A1 Malik, R A1 Patsopoulos, N.A A1 Ripke, S A1 Wei, Z A1 Yu, D A1 Lee, P.H A1 Turley, P A1 Grenier-Boley, B A1 Chouraki, V A1 Kamatani, Y A1 Berr, C A1 Letenneur, L A1 Hannequin, D A1 Amouyel, P A1 Boland, A A1 Deleuze, J.F A1 Duron, E A1 Vardarajan, B.N A1 Reitz, C A1 Goate, A.M A1 Huentelman, M.J A1 Kamboh, M.I A1 Larson, E.B A1 Rogaeva, E A1 St George-Hyslop, P A1 Hakonarson, H A1 Kukull, W.A A1 Farrer, L.A A1 Barnes, L.L A1 Beach, T.G A1 Demirci, F.Y A1 Head, E A1 Hulette, C.M A1 Jicha, G.A A1 Kauwe, JSK A1 Kaye, J.A A1 Leverenz, J.B A1 Levey, A.I A1 Lieberman, A.P A1 Pankratz, V.S A1 Poon, W.W A1 Quinn, J.F A1 Saykin, A.J A1 Schneider, L.S A1 Smith, A.G A1 Sonnen, J.A A1 Stern, R.A A1 Van Deerlin, V.M A1 Van Eldik, L.J A1 Harold, D A1 Russo, G A1 Rubinsztein, D.C A1 Bayer, A A1 Tsolaki, M A1 Proitsi, P A1 Fox, N.C A1 Hampel, H A1 Owen, M.J A1 Mead, S A1 Passmore, P A1 Morgan, K A1 Nöthen, M.M A1 Rossor, M A1 Lupton, M.K A1 Hoffmann, P A1 Kornhuber, J A1 Lawlor, B A1 McQuillin, A A1 Al-Chalabi, A A1 Bis, J.C A1 Ruiz, A A1 Boada, M A1 Seshadri, S A1 Beiser, A A1 Rice, K A1 van der Lee, S.J A1 De Jager, P.L A1 Geschwind, D.H A1 Riemenschneider, M A1 Riedel-Heller, S A1 Rotter, J.I A1 Ransmayr, G A1 Hyman, B.T A1 Cruchaga, C A1 Alegret, M A1 Winsvold, B A1 Palta, P A1 Farh, K.H A1 Cuenca-Leon, E A1 Furlotte, N A1 Kurth, T A1 Ligthart, L A1 Terwindt, G.M A1 Freilinger, T A1 Ran, C A1 Gordon, S.D A1 Borck, G A1 Adams, HHH A1 Lehtimäki, T A1 Wedenoja, J A1 Buring, J.E A1 Schürks, M A1 Hrafnsdottir, M A1 Hottenga, J.J A1 Penninx, B A1 Artto, V A1 Kaunisto, M A1 Vepsäläinen, S A1 Martin, N.G A1 Montgomery, G.W A1 Kurki, M.I A1 Hämäläinen, E A1 Huang, H A1 Huang, J A1 Sandor, C A1 Webber, C A1 Muller-Myhsok, B A1 Schreiber, S A1 Salomaa, V A1 Loehrer, E A1 Göbel, H A1 Macaya, A A1 Pozo-Rosich, P A1 Hansen, T A1 Werge, T A1 Kaprio, J A1 Metspalu, A A1 Kubisch, C A1 Ferrari, M.D A1 Belin, A.C A1 van den Maagdenberg, AMJM A1 Zwart, J.A A1 Boomsma, D A1 Eriksson, N A1 Olesen, J A1 Chasman, D.I A1 Nyholt, D.R A1 Avbersek, A A1 Baum, L A1 Berkovic, S A1 Bradfield, J A1 Buono, R A1 Catarino, C.B A1 Cossette, P A1 De Jonghe, P A1 Depondt, C A1 Dlugos, D A1 Ferraro, T.N A1 French, J A1 Hjalgrim, H A1 Jamnadas-Khoda, J A1 Kälviäinen, R A1 Kunz, W.S A1 Lerche, H A1 Leu, C A1 Lindhout, D A1 Lo, W A1 Lowenstein, D A1 McCormack, M A1 Møller, R.S A1 Molloy, A A1 Ng, P.W A1 Oliver, K A1 Privitera, M A1 Radtke, R A1 Ruppert, A.K A1 Sander, T A1 Schachter, S A1 Schankin, C A1 Scheffer, I A1 Schoch, S A1 Sisodiya, S.M A1 Smith, P A1 Sperling, M A1 Striano, P A1 Surges, R A1 Thomas, G.N A1 Visscher, F A1 Whelan, C.D A1 Zara, F A1 Heinzen, E.L A1 Marson, A A1 Becker, F A1 Stroink, H A1 Zimprich, F A1 Gasser, T A1 Gibbs, R A1 Heutink, P A1 Martinez, M A1 Morris, H.R A1 Sharma, M YR 2018 K1 Brain Diseases/classification K1 Brain Diseases/diagnosis K1 Brain Diseases/genetics K1 Genetic Variation K1 Genome-Wide Association Study K1 Humans K1 Mental Disorders/classification K1 Mental Disorders/diagnosis K1 Mental Disorders/genetics K1 Phenotype K1 Quantitative Trait K1 Heritable K1 Risk Factors JF info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757 LK http://dx.doi.org/https://serval.unil.ch/notice/serval:BIB_77315235F9BB DO https://serval.unil.ch/notice/serval:BIB_77315235F9BB SF ELIB - SuUB Bremen
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