EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA

Autor:	Di Florio A, Peter P. Zandi, St. Clair D, Annabel Vreeker, Mikael Landén, Daniel P. Howrigan, Laura J. Scott, Michael Conlon O'Donovan, Benjamin M. Neale, I. Jones, Weiqing Wang, N. Craddock, Fernando S. Goes, Faith Dickerson, Robert H. Yolken, Eli A. Stahl, Nicholas A. Watts, Nancy L. Pedersen, Duncan Palmer, James T.R. Walters, Neil Risch, Aiden Corvin, Lina Jonsson, Chia-Yen Chen, Adam E. Locke, D. H. R. Blackwood, Marco P. Boks, Catherine Schaefer, Tarjinder Singh, Matthew Solomonson, Derrek Morris, L. A. Jones, Andrew McQuillin, Roel A. Ophoff, Rolf Adolfsson, Danielle Posthuma, Andrew M. McIntosh, R.S. Kahn, Sinéad B. Chapman, M J Owen, Claire Churchhouse, N Bass, Xiaoming Jia, Andreas Reif, Jordan W. Smoller
Rok vydání:	2021
Předmět:	Pharmacology business.industry Schizophrenia (object-oriented programming) Risk gene Computational biology medicine.disease Psychiatry and Mental health Text mining Neurology medicine Pharmacology (medical) Neurology (clinical) Bipolar disorder business Biological Psychiatry Exome sequencing
Zdroj:	European Neuropsychopharmacology. 51:e24
ISSN:	0924-977X
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::1403a2a06ec30b2f4552fe0594216beb https://doi.org/10.1016/j.euroneuro.2021.07.057 Zobrazit plný text záznamu Full Text from ScienceDirect