Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: DOCK4[original query] |
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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular psychiatry 2010 Sep 15 (9): 954-68. Maestrini E, Pagnamenta A T, Lamb J A, Bacchelli E, Sykes N H, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri T S, Minopoli F, Reichert J, Cai G, Buxbaum J D, Korvatska O, Schellenberg G D, Dawson G, de Bildt A, Minderaa R B, Mulder E J, Morris A P, Bailey A J, Monaco A P, |
Analysis of DNA copy number alterations in ovarian serous tumors identifies new molecular genetic changes in low-grade and high-grade carcinomas. Cancer research 2009 May 69 (9): 4036-42. Kuo Kuan-Ting, Guan Bin, Feng Yuanjian, Mao Tsui-Lien, Chen Xu, Jinawath Natini, Wang Yue, Kurman Robert J, Shih Ie-Ming, Wang Tian- |
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological psychiatry 2010 Aug 68 (4): 320-8. Pagnamenta Alistair T, Bacchelli Elena, de Jonge Maretha V, Mirza Ghazala, Scerri Thomas S, Minopoli Fiorella, Chiocchetti Andreas, Ludwig Kerstin U, Hoffmann Per, Paracchini Silvia, Lowy Ernesto, Harold Denise H, Chapman Jade A, Klauck Sabine M, Poustka Fritz, Houben Renske H, Staal Wouter G, Ophoff Roel A, O'Donovan Michael C, Williams Julie, Nöthen Markus M, Schulte-Körne Gerd, Deloukas Panos, Ragoussis Jiannis, Bailey Anthony J, Maestrini Elena, Monaco Anthony P, |
DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2012 May 15 (4): 459-69. Alkelai Anna, Lupoli Sara, Greenbaum Lior, Kohn Yoav, Kanyas-Sarner Kyra, Ben-Asher Edna, Lancet Doron, Macciardi Fabio, Lerer Berna |
Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population. Journal of Zhejiang University. Science. B 2014 Mar 15 (3): 264-71. Liang Shuang, Wang Xue-lai, Zou Ming-yang, Wang Han, Zhou Xue, Sun Cai-hong, Xia Wei, Wu Li-jie, Fujisawa Takashi X, Tomoda Ake |
The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants. Molecular neurobiology 2015 Jul . Shao Shanshan, Kong Rui, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Guo Shengnan, Wang Jia, Zhang Xiaohui, Zhang Jiajia, Song Ranr |
Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.
Alzheimer's research & therapy 2021 02 13 (1): 34. Bone William P, Siewert Katherine M, Jha Anupama, Klarin Derek, Damrauer Scott M, , Chang Kyong-Mi, Tsao Philip S, Assimes Themistocles L, Ritchie Marylyn D, Voight Benjamin |
Genetic variations in DOCK4 contribute to schizophrenia susceptibility in a Chinese cohort: A genetic neuroimaging study. Behavioural brain research 2023 2 443 114353. Xu Xusan, He Bin, Zeng Jieqing, Yin Jingwen, Wang Xiaoxia, Luo Xudong, Liang Chunmei, Luo Shucun, Yan Haifeng, Xiong Susu, Tan Zhi, Lv Dong, Dai Zhun, Lin Zhixiong, Lin Juda, Ye Xiaoqing, Chen Riling, Li You, Wang Yajun, Chen Wubiao, Luo Zebin, Li Keshen, Ma Guo |
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