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Analysis of shared heritability in common disorders of the ..:
Anttila, Verneri
;
Sullivan, Brenda
;
Finucane, Hilary
...
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757. , 2018
Link:
https://cea.hal.science/cea-01870483
RT Journal T1
Analysis of shared heritability in common disorders of the brain
UL https://suche.suub.uni-bremen.de/peid=base-ftunivlille:oai:HAL:cea-01870483v1&Exemplar=1&LAN=DE A1 Anttila, Verneri A1 Sullivan, Brenda A1 Finucane, Hilary A1 Walters, Walter A1 Bras, Jose A1 Duncan, Laramie A1 Price, Valentina A1 Falcone, Guido A1 Gormley, Padhraig A1 Malik, Rainer A1 Patsopoulos, Pat A1 Ripke, Stephan A1 Wei, Wei A1 Yu, Dongmei A1 Lee, Phil, L A1 Turley, Patrick A1 Grenier-Boley, Benjamin A1 Chouraki, Vincent A1 Kamatani, Yoichiro A1 Berr, Claudine A1 Letenneur, Luc A1 Hannequin, Didier A1 Amouyel, Philip A1 Boland, Anne A1 Deleuze, Jean-François A1 Duron, Emmanuelle A1 Vardarajan, N A1 Reitz, Chris A1 Goate, Alison A1 Huentelman, Matthew A1 Kamboh, M. Ilyas A1 Larson, Lars A1 Rogaeva, Ekaterina A1 St George-Hyslop, Peter A1 Hakonarson, Hakon A1 Kukull, Walter A1 Li, Lindsay A1 Li, Lisa A1 Thomas, Thomas A1 Demirci, F. Yesim A1 Head, Eli A1 Hulette, Chris A1 Jicha, Gregory A1 Kauwe, John A1 Kaye, Jeffrey A1 Leverenz, James A1 Levey, Allan A1 Li, Andrew A1 Pankratz, Vernon A1 Poon, Wayne A1 Quinn, Joseph A1 Saykin, Andrew A1 Lo, Lon A1 Smit, Amanda A1 So, Joshua A1 Stern, Robert A1 van Deerlin, Vivianna A1 Li, Linda A1 Harold, Denise A1 Russo, Giancarlo A1 Rubinsztein, David, C A1 Bayer, Anthony A1 Tsolaki, Magda A1 Proitsi, Petra A1 Fox, Nick A1 Hampel, Harald A1 Owen, Michael A1 Sim, Simon A1 Passmore, Peter A1 Morgan, Kevin A1 Markus, Mark A1 Schott, Jonathan A1 Kauffmann, Martin A1 Lupton, Michel A1 Hoffmann, Per A1 Kornhuber, Johannes A1 Lawlor, Brian A1 Mcquillin, Andrew A1 Al-Chalabi, Ammar A1 Bis, Joshua A1 Ruiz, Agustin A1 Boada, Mercè A1 Seshadri, Sudha A1 Beiser, Alexa A1 Rice, Kenneth A1 van Der Lee, Sven A1 de Jager, Philip A1 Geschwind, Dan A1 Riemenschneider, Matthias A1 Riedel-Heller, Helle A1 Rotter, Jerome A1 Ran, Gerhard A1 Hyman, Bradley, T A1 Cruchaga, Carlos A1 Alegret, Montserrat A1 Winsvold, Bendik A1 Palta, Priit A1 Farh, Kai-How A1 Cuenca-Leon, Ester A1 Furlotte, Nicholas A1 Kurth, Tobias A1 Li, Lannie A1 Terwindt, Gisela A1 Freilinger, Tobias A1 Ran, Carol A1 Scott, Scott A1 Borck, Guntram A1 Adams, Hieab H.H A1 Lehtimaki, Terho A1 Wedenoja, Juho A1 Buring, Julie A1 Hrafnsdottir, Maria A1 Hottenga, Jan A1 Penninx, Brenda A1 Artto, Ville A1 Kaunisto, Mari A1 Vepsäläinen, Salli A1 Martin, Nicholas, M A1 Montgomery, Grant, W A1 Kurki, Mitja A1 Hämäläinen, Eija A1 Huang, Hailiang A1 Huang, Jie A1 Sandor, Cynthia A1 Webb, Caleb A1 Müller-Myhsok, Bertram A1 Schreiber, Stefan A1 Salomaa, Veikko A1 Lo, Eli A1 Göbel, Hartmut A1 Macaya, Alfons A1 Pozo-Rosich, Pat A1 Kaprio, Jaakko A1 Metspalu, Andres A1 Kubisch, Chris A1 Ferrari, Michel A1 Belin, Andrea A1 van den Maagdenberg, Arn M.J.M A1 Zwart, John A1 Boomsma, Dorret, I A1 Eriksson, Nicholas A1 Olesen, Ole A1 Chasman, Dan A1 Nyholt, Dale A1 Anney, Richard A1 Avbersek, Andreja A1 Bau, Larry A1 Berkovic, Samuel, F A1 Bradfield, Jonathan A1 Buono, Russell A1 Catarino, Claudia A1 Cossette, Patrick A1 de Jonghe, Peter A1 Depondt, Chantal A1 Dlugos, Dennis A1 French, Jacqueline A1 Hjalgrim, Helle A1 Jamnadas-Khoda, Jennifer A1 Kälviäinen, Reetta A1 Kunz, Wolfram A1 Lerche, Holger A1 Leu, Costin A1 Li, Dick A1 Lo, Warren A1 Lowenstein, Dan A1 Mccormack, Mark A1 Møller, Rikke A1 Molloy, Anne A1 Ng, Ping-Wing A1 Oliver, Oliver A1 Privitera, Michael A1 Radtke, Rodney A1 Ruppert, Ann-Kathrin A1 Schachter, Steve A1 Schankin, Chris A1 Scheffer, Ingrid, E A1 Schoch, Susan A1 Sisodiya, Sanjay A1 Smit, Philip A1 Sperling, Michael A1 Striano, Pasquale A1 Surges, Rainer A1 Visscher, Frank A1 Whelan, Chris A1 Zara, Federico A1 Heinzen, Erin A1 Marson, Anthony A1 Becker, Felicitas A1 Stroink, Hans A1 Zimprich, Fritz A1 Gasser, Thomas A1 Gibbs, Raphael A1 Heutink, Peter A1 Martinez, Matias A1 Morris, Huw A1 Sharma, Manu A1 Ryten, Mina A1 Mok, Kin A1 Pulit, Sara A1 Bevan, Steve PB HAL CCSD; American Association for the Advancement of Science (AAAS) YR 2018 K1 MESH: Brain Diseases K1 MESH: Genetic Variation K1 MESH: Genome-Wide Association Study K1 MESH: Humans K1 MESH: Mental Disorders K1 MESH: Phenotype K1 MESH: Quantitative Trait K1 Heritable K1 MESH: Risk Factors K1 [SDV]Life Sciences [q-bio] K1 [SDV.GEN]Life Sciences [q-bio]/Genetics K1 [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology K1 [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC] JF info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757 LK http://dx.doi.org/https://cea.hal.science/cea-01870483 DO https://cea.hal.science/cea-01870483 SF ELIB - SuUB Bremen
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