Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Schizophrenia and FOXP2[original query] |
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FOXP2 polymorphisms in patients with schizophrenia. Schizophrenia research 2005 Mar 73 (2-3): 253-6. Sanjuan Julio, Tolosa Amparo, González Jose Carlos, Aguilar Eduardo Jesus, Moltó Maria Dolores, Nájera Carmen, de Frutos Ro |
Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. Psychiatric genetics 2006 Apr 16 (2): 67-72. Sanjuán Julio, Tolosa Amparo, González José C, Aguilar Eduardo J, Pérez-Tur Jordi, Nájera Carmen, Moltó María Dolores, de Frutos Ro |
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatric genetics 2008 Dec 18 (6): 295-301. Laroche Fabrice, Ramoz Nicolas, Leroy Sophie, Fortin Célia, Rousselot-Paillet Bérangère, Philippe Anne, Colleaux Laurence, Bresson Jean-Louis, Mogenet Agnès, Golse Bernard, Mouren-Simeoni Marie-Christine, Gorwood Philip, Galli Thierry, Simonneau Michel, Krebs Marie-Odile, Robel Lauren |
FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies. BMC medical genetics 2010 11 (1): 114. Tolosa Amparo, Sanjuán Julio, Dagnall Adam M, Moltó María D, Herrero Neus, de Frutos Ro |
Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia. Schizophrenia research 2011 Jul 129 (2-3): 141-8. Jamadar S, Powers N R, Meda S A, Gelernter J, Gruen J R, Pearlson G |
Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients. Neuroscience letters 2011 Apr 493 (3): 131-5. Španiel Filip, Horá?ek Ji?í, Tint?ra Jaroslav, Ibrahim Ibrahim, Novák Tomáš, ?ermák Jan, Klírová Monika, Höschl Cyr |
FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2013 Mar 14 (2): 146-50. Li Tao, Zeng Zhen, Zhao Qian, Wang Ti, Huang Ke, Li Junyan, Li You, Liu Jie, Wei Zhiyun, Wang Yang, Feng Guoyin, He Lin, Shi Yongyo |
Preliminary evidence of an interaction between the FOXP2 gene and childhood emotional abuse predicting likelihood of auditory verbal hallucinations in schizophrenia. Journal of psychiatric research 2014 Mar 50 66-72. McCarthy-Jones Simon, Green Melissa J, Scott Rodney J, Tooney Paul A, Cairns Murray J, Wu Jing Qin, Oldmeadow Christopher, Carr Vaughan, |
Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population. Journal of child neurology 2014 Dec 29 (12): NP207-11. Park YoungJoon, Won SeongSik, Nam Min, Chung Joo-Ho, Kwack KyuB |
Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population. Journal of neural transmission (Vienna, Austria : 1996) 2017 Apr . Rao Wenwang, Du Xiangdong, Zhang Yingyang, Yu Qiong, Hui Li, Yu Yaqin, Kou Changgui, Yin Guangzhong, Zhu Xiaomin, Man Lijuan, Soares Jair C, Zhang Xiang Ya |
Meta-analysis of FOXP2 rs10447760 polymorphism with schizophrenia. Asian journal of psychiatry 2018 5 35 50-51. Chen Yan, Fang Xinyu, Wang Yewei, Zhang Ch |
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
No association between common genetic variation in FOXP2 and language impairment in schizophrenia. Psychiatry research 2019 01 271 590-597. McCarthy Nina S, Clark Melanie L, Jablensky Assen, Badcock Johanna |
No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population. Psychiatric genetics 2018 Jan . Yin Jiajun, Jia Ningren, Liu Yansong, Jin Chunhui, Zhang Fuquan, Yu Shui, Wang Jun, Yuan Jianm |
FOXP2 contributes to the cognitive impairment in chronic patients with schizophrenia. Aging 2019 8 11 (16): 6440-6448. Lang Xiaoe, Zhang Wenzhong, Song Xinxin, Zhang Guangya, Du Xiangdong, Zhou Yongjie, Li Zezhi, Zhang Xiang Ya |
Deciphering the Biological Mechanisms Underlying the Genome-Wide Associations between Computerized Device Use and Psychiatric Disorders. Journal of clinical medicine 2019 11 8 (12): . Wendt Frank R, Muniz Carvalho Carolina, Pathak Gita A, Gelernter Joel, Polimanti Rena |
FOXP2 expression and gray matter density in the male brains of patients with schizophrenia. Brain imaging and behavior 2020 Jul . Sanjuán Julio, Castro-Martínez Xochitl Helga, García-Martí Gracián, González-Fernández Javier, Sanz-Requena Roberto, Haro Josep María, Meana J Javier, Martí-Bonmatí Luis, Nacher Juan, Sebastiá-Ortega Noelia, Gilabert-Juan Javier, Moltó María Dolor |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression. Brain : a journal of neurology 2021 9 145 (2): 770-786. Li Shiwu, Li Jiao, Liu Jiewei, Wang Junyang, Li Xiaoyan, Huo Yongxia, Li Yifan, Liu Yixing, Li Ming, Xiao Xiao, Luo Xiong-Ji |
The genetic determinants of language network dysconnectivity in drug-naïve early stage schizophrenia. NPJ schizophrenia 2021 Mar 7 (1): 18. Du Jingnan, Palaniyappan Lena, Liu Zhaowen, Cheng Wei, Gong Weikang, Zhu Mengmeng, Wang Jijun, Zhang Jie, Feng Jianfe |
Sexual dimorphism in the relationship between Forkhead-Box P2 and BMI with cognitive deficits in schizophrenia. Frontiers in aging neuroscience 2022 8 14 920352. Yang Mi, Cui Ying, Xue Mei, Forster Mattew T, Lang Xiaoe, Xiu Meihong, Li Zezhi, Zhang Xiangya |
Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder. Psychiatric genetics 2023 1 33 (1): 8-19. Yaz?c? Merve, Yekta? Çi?dem, Eröz Recep, Kaplan Karakaya Elif Sümeyra, Sar?gedik En |
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- Page last updated:Apr 16, 2024
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