Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: UFD1L[original query] |
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A family- and population-based study of the UFD1L gene for schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1076-9. Xie Lin, Ye Lin, Ju Guizhi, Xu Qi, Zhang Xuan, Liu Shuzheng, Shi Jieping, Yu Yaqin, Wang Zhenqi, Shen Yan, Wei J |
The UFD1L rs5992403 polymorphism is associated with age at onset of schizophrenia. Journal of psychiatric research 2010 Nov 44 (15): 1113-5. Ota Vanessa Kiyomi, Belangero Sintia Iole, Gadelha Ary, Bellucco Fernanda Teixeira, Christofolini Denise Maria, Mancini Tatiane Iris, Ribeiro-dos-Santos Andrea Kelly, Santos Sidney Emanuel, Mari Jair de Jesus, Bressan Rodrigo Affonseca, Melaragno Maria Isabel, Smith Marilia de Arruda Cardo |
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. European journal of human genetics : EJHG 2012 Oct 20 (10): 1051-7. Shashi Vandana, Francis Alan, Hooper Stephen R, Kranz Peter G, Zapadka Michael, Schoch Kelly, Ip Edward, Tandon Neeraj, Howard Timothy D, Keshavan Matcheri |
Polymorphisms in schizophrenia candidate gene UFD1L may contribute to cognitive deficits. Psychiatry research 2013 Aug 209 (1): 110-3. Ota Vanessa K, Berberian Arthur A, Gadelha Ary, Santoro Marcos L, Ottoni Gustavo L, Matsuzaka Camila T, Mari Jair J, Melaragno Maria I, Lara Diogo R, Smith Marília A C, Belangero Sintia I, Bressan Rodrigo |
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis. Frontiers in physiology 2017 8 612. Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi |
Accessing Gene Expression in Treatment-Resistant Schizophrenia. Molecular neurobiology 2018 1 55 (8): 7000-7008. Moretti Patricia N, Ota Vanessa K, Gouvea Eduardo S, Pedrini Mariana, Santoro Marcos L, Talarico Fernanda, Spindola Leticia M, Carvalho Carolina Muniz, Noto Cristiano, Xavier Gabriela, Brietzke Elisa, Gadelha Ary, Bressan Rodrigo, Mari Jair, Belangero Sint |
Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia. Schizophrenia research. Cognition 2019 Sep 17 100134. Akiyama Kazufumi, Saito Atsushi, Saito Satoshi, Ozeki Yuji, Watanabe Takashi, Fujii Kumiko, Shimoda Kazuta |
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development. PLoS genetics 2021 8 17 (8): e1009698. Kuil Laura E, MacKenzie Katherine C, Tang Clara S, Windster Jonathan D, Le Thuy Linh, Karim Anwarul, de Graaf Bianca M, van der Helm Robert, van Bever Yolande, Sloots Cornelius E J, Meeussen Conny, Tibboel Dick, de Klein Annelies, Wijnen René M H, Amiel Jeanne, Lyonnet Stanislas, Garcia-Barcelo Maria-Mercè, Tam Paul K H, Alves Maria M, Brooks Alice S, Hofstra Robert M W, Brosens Erw |
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- Page last updated:Apr 16, 2024
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