Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: CACNA1I[original query] |
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CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population. Pediatric neurology 2006 Sep 35 (3): 187-90. Wang Juli, Zhang Yuehua, Liang Jianmin, Pan Hong, Wu Husheng, Xu Keming, Liu Xiaoyan, Jiang Yuwu, Shen Yan, Wu Xi |
Support for calcium channel gene defects in autism spectrum disorders. Molecular autism 2012 Dec 3 (1): 1. Lu AT, Dai X, Martinez-Agosto JA, Cantor RM |
A rare schizophrenia risk variant of CACNA1I disrupts Ca3.3 channel activity. Scientific reports 2016 10 6 34233. Andrade A, Hope J, Allen A, Yorgan V, Lipscombe D, Pan J |
Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy. Annals of neurology 2017 Mar 81 (3): 444-453. Glauser Tracy A, Holland Katherine, O'Brien Valerie P, Keddache Mehdi, Martin Lisa J, Clark Peggy O, Cnaan Avital, Dlugos Dennis, Hirtz Deborah G, Shinnar Shlomo, Grabowski Gregory, |
Further evidence for the genetic association between CACNA1I and schizophrenia. Hereditas 2018 155 16. Xie Yijun, Huang Di, Wei Li, Luo Xiong-Ji |
Genome-Wide Association Studies of Impulsive Personality Traits (BIS-11 and UPPS-P) and Drug Experimentation in up to 22,861 Adult Research Participants Identify Loci in the CACNA1I and CADM2 genes.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2019 Mar 39 (13): 2562-2572. Sanchez-Roige Sandra, Fontanillas Pierre, Elson Sarah L, Gray Joshua C, de Wit Harriet, MacKillop James, Palmer Abraham |
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels. Science translational medicine 2020 8 12 (556): . Heyne Henrike O, Baez-Nieto David, Iqbal Sumaiya, Palmer Duncan S, Brunklaus Andreas, May Patrick, , Johannesen Katrine M, Lauxmann Stephan, Lemke Johannes R, Møller Rikke S, Pérez-Palma Eduardo, Scholl Ute I, Syrbe Steffen, Lerche Holger, Lal Dennis, Campbell Arthur J, Wang Hao-Ran, Pan Jen, Daly Mark |
Functional multigenic variations associated with hodgkin lymphoma.
International journal of laboratory hematology 2021 Jul . Osman Yasser, Elsharkawy Tarek, Hashim Tariq Mohammad, Alratroot Jumana Abdulwahab, Alsuwat Hind Saleh, Otaibi Waad Mohammed Al, Hegazi Fatma Mohammed, AbdulAzeez Sayed, Borgio J Franc |
The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms. Neurobiology of disease 2021 May 155 105394. Hidalgo Sergio, Campusano Jorge M, Hodge James J |
Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort. Brain : a journal of neurology 2021 12 145 (5): 1839-1853. Baez-Nieto David, Allen Andrew, Akers-Campbell Seth, Yang Lingling, Budnik Nikita, Pupo Amaury, Shin Young-Cheul, Genovese Giulio, Liao Maofu, Pérez-Palma Eduardo, Heyne Henrike, Lal Dennis, Lipscombe Diane, Pan Jen |
Contribution of rare genetic variants to drug response in absence epilepsy. Epilepsy research 2021 Jan 170 106537. Myers Kenneth A, Bennett Mark F, Grinton Bronwyn E, Dabscheck Gabriel, Chan Eunice K, Bello-Espinosa Luis E, Sadleir Lynette G, D'Alfonso Sabrina, Schneider Amy L, Damiano John A, Hildebrand Michael S, Bahlo Melanie, Berkovic Samuel F, Buchhalter Jeffrey, Scheffer Ingrid |
[Whole exome sequencing analysis of a patient with 45,X/46,XY mosaicism and autism spectrum disorder]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 3 39 (3): 297-300. Yuan Danfeng, Jiao Jian, Zhang Manxue, Li Sixun, Wang Zhuo, Yang Yanping, Situ Mingjing, Wang Meiwen, Luo Tingting, Huang |
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder. Translational psychiatry 2022 2 12 (1): 84. Wang Chenyao, Horigane Shin-Ichiro, Wakamori Minoru, Ueda Shuhei, Kawabata Takeshi, Fujii Hajime, Kushima Itaru, Kimura Hiroki, Ishizuka Kanako, Nakamura Yukako, Iwayama Yoshimi, Ikeda Masashi, Iwata Nakao, Okada Takashi, Aleksic Branko, Mori Daisuke, Yoshida Takashi, Bito Haruhiko, Yoshikawa Takeo, Takemoto-Kimura Sayaka, Ozaki Nor |
Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes. Molecular neurobiology 2023 2 . Maksemous Neven, Harder Aster V E, Ibrahim Omar, Vijfhuizen Lisanne S, Sutherland Heidi, Pelzer Nadine, de Boer Irene, Terwindt Gisela M, Lea Rodney A, van den Maagdenberg Arn M J M, Griffiths Lyn |
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- Page last updated:Apr 22, 2024
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