Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Epilepsy and meta-analysis and SCN1A[original query] |
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| Physicochemical property changes of amino acid residues that accompany missense mutations in SCN1A affect epilepsy phenotype severity. Journal of medical genetics 2009 Jul . Kanai K, Yoshida S, Hirose S, Oguni H, Kuwabara S, Sawai S, Hiraga A, Fukuma G, Iwasa H, Kojima T, Kaneko S |
| SCN1A IVS5N+5 polymorphism and response to sodium valproate: a multicenter study. Pharmacogenomics 2012 Oct 13 (13): 1477-85. Haerian Batoul Sadat, Baum Larry, Tan Hui Jan, Kwan Patrick, Raymond Azman Ali, Saruwatari Junji, Nakagawa Kazuko, Mohamed Zahur |
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain : a journal of neurology 2013 Oct 136 (Pt 10): 3140-50. Kasperaviciute Dalia, Catarino Claudia B, Matarin Mar, Leu Costin, Novy Jan, Tostevin Anna, Leal Bárbara, Hessel Ellen V S, Hallmann Kerstin, Hildebrand Michael S, Dahl Hans-Henrik M, Ryten Mina, Trabzuni Daniah, Ramasamy Adaikalavan, Alhusaini Saud, Doherty Colin P, Dorn Thomas, Hansen Jörg, Krämer Günter, Steinhoff Bernhard J, Zumsteg Dominik, Duncan Susan, Kälviäinen Reetta K, Eriksson Kai J, Kantanen Anne-Mari, Pandolfo Massimo, Gruber-Sedlmayr Ursula, Schlachter Kurt, Reinthaler Eva M, Stogmann Elisabeth, Zimprich Fritz, Théâtre Emilie, Smith Colin, O'Brien Terence J, Meng Tan K, Petrovski Slave, Robbiano Angela, Paravidino Roberta, Zara Federico, Striano Pasquale, Sperling Michael R, Buono Russell J, Hakonarson Hakon, Chaves João, Costa Paulo P, Silva Berta M, da Silva António M, de Graan Pierre N E, Koeleman Bobby P C, Becker Albert, Schoch Susanne, von Lehe Marec, Reif Philipp S, Rosenow Felix, Becker Felicitas, Weber Yvonne, Lerche Holger, Rössler Karl, Buchfelder Michael, Hamer Hajo M, Kobow Katja, Coras Roland, Blumcke Ingmar, Scheffer Ingrid E, Berkovic Samuel F, Weale Michael E, , Delanty Norman, Depondt Chantal, Cavalleri Gianpiero L, Kunz Wolfram S, Sisodiya Sanjay |
| The SCN1A gene variants and epileptic encephalopathies. Journal of human genetics 2013 Sep 58 (9): 573-80. Parihar Rashmi, Ganesh Subramani |
| SCN1A, SCN2A and SCN3A gene polymorphisms and responsiveness to antiepileptic drugs: a multicenter cohort study and meta-analysis. Pharmacogenomics 2013 Jul 14 (10): 1153-66. Haerian Batoul Sadat, Baum Larry, Kwan Patrick, Tan Hui Jun, Raymond Azman Ali, Mohamed Zahur |
| Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy. Human genetics 2014 May 133 (5): 651-9. Baum Larry, Haerian Batoul Sadat, Ng Ho-Keung, Wong Virginia C N, Ng Ping Wing, Lui Colin H T, Sin Ngai Chuen, Zhang Chunbo, Tomlinson Brian, Wong Gary Wing-Kin, Tan Hui Jan, Raymond Azman Ali, Mohamed Zahurin, Kwan Patri |
| SCN1A rs3812718 polymorphism and susceptibility to epilepsy with febrile seizures: a meta-analysis. Gene 2014 Jan 533 (1): 26-31. Tang Linjun, Lu Xiaocheng, Tao Yi, Zheng Jinyu, Zhao Penglai, Li Kai, Li Lix |
| Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2014 Sep 13 (9): 893-903. Authors are not available |
| SCN1A rs3812718 polymorphism is associated with epilepsy: An updated meta-analysis. Epilepsy research 2018 Mar 142 81-87. Zhi Haiyang, Wu Changan, Yang Ziqi |
| Association between two SCN1A polymorphisms and resistance to sodium channel blocking AEDs: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2018 Mar . Bao Yi, Liu Xinzhu, Xiao Zhe |
| Association between SCN1A polymorphism rs3812718 and valproic acid resistance in epilepsy children: a case-control study and meta-analysis. Bioscience reports 2018 Nov . Wang Zhi Jian, Chen Jie, Chen Hai Liang, Zhang Lin Yan, Xu Duo, Jiang Wen Ti |
| Association between SCN1A polymorphism and carbamazepine responsiveness in epilepsy: A meta-analysis. Epilepsy research 2021 7 176 106627. Zhang Xuan, Liu Jia, Ye Ji |
| Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variants. Neurogenetics 2021 5 22 (2): 105-115. Rampazzo Ana Carla Mondek, Dos Santos Rafael Rodrigues Pinheiro, Maluf Fernando Arfux, Simm Renata Faria, Marson Fernando Augusto Lima, Ortega Manoela Marques, de Aguiar Paulo Henrique Pir |
| Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children: A protocol for systematic review and meta-analysis. Medicine 2021 5 100 (20): e25831. Wen Zhuangfei, Chen Jiang, Zhu Bin, Lu Yan, Chen Liji |
| Associations between CYP3A4, CYP3A5 and SCN1A polymorphisms and carbamazepine metabolism in epilepsy: A meta-analysis. Epilepsy research 2021 Mar 173 106615. Zhao Gui-Xin, Zhang Zheng, Cai Wen-Ke, Shen Ming-Li, Wang Ping, He Gong-H |
| SCN1A IVS5N+5 G>A Polymorphism and Risk of Febrile Seizure and Epilepsy: A Systematic Review and Meta-Analysis. Frontiers in neurology 2021 1 11 581539. Hao Jindou, Liu Haiying, Ma Jiying, Liu Guosheng, Dong Guoqing, Liu Peihui, Xiao F |
| Association between SCN1A polymorphism and risk of epilepsy in children: A systematic review and meta-analysis. Seizure 2023 9 112 40-47. Zhihong Zhou, Shuihua Wu, Xin Zou, Shuo |
- Page last reviewed:Feb 1, 2024
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