Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 24, 2025. (Total: 235644Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 6 (of 6 Records)

Query Trace: Schizophrenia and SHANK3[original query]
A promoter variant of SHANK1 affects auditory working memory in schizophrenia patients and in subjects clinically at risk for psychosis.
European archives of psychiatry and clinical neuroscience 2012 Mar 262 (2): 117-24.
Lennertz Leonhard, Wagner Michael, Wölwer Wolfgang, Schuhmacher Anna, Frommann Ingo, Berning Julia, Schulze-Rauschenbach Svenja, Landsberg Martin W, Steinbrecher Anja, Alexander Michael, Franke Petra E, Pukrop Ralf, Ruhrmann Stephan, Bechdolf Andreas, Gaebel Wolfgang, Klosterkötter Joachim, Häfner Heinz, Maier Wolfgang, Mössner Raina
Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects.
Neuron 2015 Dec .
Zhou Yang, Kaiser Tobias, Monteiro Patrícia, Zhang Xiangyu, Van der Goes Marie S, Wang Dongqing, Barak Boaz, Zeng Menglong, Li Chenchen, Lu Congyi, Wells Michael, Amaya Aldo, Nguyen Shannon, Lewis Michael, Sanjana Neville, Zhou Yongdi, Zhang Mingjie, Zhang Feng, Fu Zhanyan, Feng Guopi
Investigation of SHANK3 in schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Mar .
de Sena Cortabitarte Ana, Degenhardt Franziska, Strohmaier Jana, Lang Maren, Weiss Birgit, Roeth Ralph, Giegling Ina, Heilmann-Heimbach Stefanie, Hofmann Andrea, Rujescu Dan, Fischer Christine, Rietschel Marcella, Nöthen Markus M, Rappold Gudrun A, Berkel Simo
Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.
American journal of medical genetics. Part A 2018 12 176 (12): 2668-2676.
Li Ying, Jia Xiangbin, Wu Huidan, Xun Guanglei, Ou Jianjun, Zhang Qiumeng, Li Honghui, Bai Ting, Hu Zhengmao, Zou Xiaobing, Xia Kun, Guo H
Rare variations in the SHANK3 gene confers susceptibility to schizophrenia in Uygur Chinese population.
Schizophrenia research 2020 11 228 597-599.
Zhang Han, Wang Dong, Chen Jianhua, Wang Yonggang, Yi Qizhong, Shi Yongyo
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.
Human molecular genetics 2021 9 31 (4): 625-637.
Levy Tess, Foss-Feig Jennifer H, Betancur Catalina, Siper Paige M, Trelles-Thorne Maria Del Pilar, Halpern Danielle, Frank Yitzchak, Lozano Reymundo, Layton Christina, Britvan Bari, Bernstein Jonathan A, Buxbaum Joseph D, Berry-Kravis Elizabeth, Powell Craig M, Srivastava Siddharth, Sahin Mustafa, Soorya Latha, Thurm Audrey, Kolevzon Alexander,
TOP