Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Schizophrenia and NT5C2[original query] |
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A comprehensive family-based replication study of schizophrenia genes.
![]() JAMA psychiatry 2013 Jun 70 (6): 573-81. Aberg Karolina A, Liu Youfang, Bukszár Jozsef, McClay Joseph L, Khachane Amit N, Andreassen Ole A, Blackwood Douglas, Corvin Aiden, Djurovic Srdjan, Gurling Hugh, Ophoff Roel, Pato Carlos N, Pato Michele T, Riley Brien, Webb Todd, Kendler Kenneth, O'Donovan Mick, Craddock Nick, Kirov George, Owen Mike, Rujescu Dan, St Clair David, Werge Thomas, Hultman Christina M, Delisi Lynn E, Sullivan Patrick, van den Oord Edwin |
The impact of the genome-wide supported variant in the cyclin M2 gene on gray matter morphology in schizophrenia. Behavioral and brain functions : BBF 2013 9 (1): 40. Ohi Kazutaka, Hashimoto Ryota, Yamamori Hidenaga, Yasuda Yuka, Fujimoto Michiko, Umeda-Yano Satomi, Fukunaga Masaki, Watanabe Yoshiyuki, Iwase Masao, Kazui Hiroaki, Takeda Masatos |
Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2016 Jul . Hauberg Mads Engel, Holm-Nielsen Marie Hebsgaard, Mattheisen Manuel, Askou Anne Louise, Grove Jakob, Børglum Anders Dupont, Corydon Thomas Ju |
Two-stage replication of previous genome-wide association studies of AS3MT-CNNM2-NT5C2 gene cluster region in a large schizophrenia case-control sample from Han Chinese population. Schizophrenia research 2016 Jul . Guan Fanglin, Zhang Tianxiao, Li Lu, Fu Dongke, Lin Huali, Chen Gang, Chen Te |
The rs11191580 variant of the NT5C2 gene is associated with schizophrenia and symptom severity in a South Chinese Han population: evidence from GWAS. Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999) 2016 Nov 0. Li Zhen, Jiang Juan, Long Jianxiong, Ling Weijun, Huang Guifeng, Guo Xiaojing, Su |
Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort. Bipolar disorders 2016 Sep 18 (6): 520-527. Gonzalez Suzanne, Gupta Jayanta, Villa Erika, Mallawaarachchi Indika, Rodriguez Marco, Ramirez Mercedes, Zavala Juan, Armas Regina, Dassori Albana, Contreras Javier, Flores Deborah, Jerez Alvaro, Ontiveros Alfonso, Nicolini Humberto, Escamilla Micha |
Association of MAD1L1 polymorphism (rs871925) with prenatal famine exposure and schizophrenia in a Chinese population: A case-control study. IUBMB life 2019 Sep . Sun Yaoyao, Kang Guojun, Zhu Xiaojing, Li Rixin, Kang Qi, Zhang Mingyuan, Wang Yueying, Chen Xin, Yu Yaqin, Yu Qio |
AS3MT Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China. Frontiers in neuroscience 2021 12 15 705297. Fan Xiaomei, Chen Yuna, Lu Jieluan, Li Wenzhou, Li Xi, Guo Huijuan, Chen Qing, Yang Yanxia, Xia Hanbi |
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