Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: ALDH5A1[original query] |
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An association study between polymorphisms in five genes in glutamate and GABA pathway and paranoid schizophrenia. European psychiatry : the journal of the Association of European Psychiatrists 2005 Jan 20 (1): 45-9. Zhang Boyu, Yuan Yanbo, Jia Yanbin, Yu Xin, Xu Qi, Shen Yucun, Shen Y |
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. Neuroscience letters 2006 Apr 397 (3): 234-9. Lorenz Susanne, Heils Armin, Taylor Kirsten P, Gehrmann Anne, Muhle Hiltrud, Gresch Meike, Becker Tim, Tauer Ulrike, Stephani Ulrich, Sander Thom |
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. The Lancet. Neurology 2007 Nov 6 (11): 970-80. Cavalleri Gianpiero L, Weale Michael E, Shianna Kevin V, Singh Rinki, Lynch John M, Grinton Bronwyn, Szoeke Cassandra, Murphy Kevin, Kinirons Peter, O'Rourke Deirdre, Ge Dongliang, Depondt Chantal, Claeys Kristl G, Pandolfo Massimo, Gumbs Curtis, Walley Nicole, McNamara James, Mulley John C, Linney Kristen N, Sheffield Leslie J, Radtke Rodney A, Tate Sarah K, Chissoe Stephanie L, Gibson Rachel A, Hosford David, Stanton Alice, Graves Tracey D, Hanna Michael G, Eriksson Kai, Kantanen Anne-Mari, Kalviainen Reetta, O'Brien Terence J, Sander Josemir W, Duncan John S, Scheffer Ingrid E, Berkovic Samuel F, Wood Nicholas W, Doherty Colin P, Delanty Norman, Sisodiya Sanjay M, Goldstein David |
Cognitive functioning and survival in the elderly: the SSADH C538T polymorphism. Annals of human genetics 2008 Sep 72 (Pt 5): 630-5. De Rango F, Leone O, Dato S, Novelletto A, Bruni A C, Berardelli M, Mari V, Feraco E, Passarino G, De Benedictis |
Suggestive association with ocular phoria at chromosome 6p22. Investigative ophthalmology & visual science 2014 Jan 55 (1): 345-52. Bosten Jenny M, Hogg Ruth E, Bargary Gary, Goodbourn Patrick T, Lawrance-Owen Adam J, Mollon John |
ALDH5A1 variability in opioid dependent patients could influence response to methadone treatment. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2014 Mar 24 (3): 420-4. Fonseca Francina, Gratacòs Mònica, Escaramís Geòrgia, De Cid Rafael, Martín-Santos Rocío, Farré Magi, Estivill Xavier, Torrens Mar |
Polymorphisms of ABAT, SCN2A and ALDH5A1 may affect valproic acid responses in the treatment of epilepsy in Chinese. Pharmacogenomics 2016 Dec 17 (18): 2007-2014. Li Xi, Zhang Jun, Wu Xi, Yan Han, Zhang Yin, He Ruo-Hui, Tang Yong-Jun, He Yi-Jing, Tan Dan, Mao Xiao-Yuan, Yin Ji-Ye, Liu Zhao-Qian, Zhou Hong-Hao, Liu J |
Novel ALDH5A1 variants and genotype: Phenotype correlation in SSADH deficiency. Neurology 2020 Sep . DiBacco Melissa L, Pop Ana, Salomons Gajja S, Hanson Ellen, Roullet Jean-Baptiste, Gibson K Michael, Pearl Phillip |
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population. Human genomics 2020 Sep 14 (1): 28. Tsang Mandy H Y, Kwong Anna K Y, Chan Kate L S, Fung Jasmine L F, Yu Mullin H C, Mak Christopher C Y, Yeung Kit-San, Rodenburg Richard J T, Smeitink Jan A M, Chan Rachel, Tsoi Thomas, Hui Joannie, Wong Shelia S N, Tai Shuk-Mui, Chan Victor C M, Ma Che-Kwan, Fung Sharon T H, Wu Shun-Ping, Chak W K, Chung Brian H Y, Fung Cheuk-Wi |
Polymorphic Genetic Markers of the GABA Catabolism Pathway in Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2020 Aug . Ciminelli Bianca Maria, Menduti Giovanna, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Squitti Rosanna, Rongioletti Mauro, Nica Sabrina, Novelletto Andrea, Rossi Luisa, Malaspina Patriz |
Clinical and molecular characterization of pediatric mitochondrial disorders in south of China. European journal of medical genetics 2020 4 63 (8): 103898. Hu Chaoping, Li Xihua, Zhao Lei, Shi Yiyun, Zhou Shuizhen, Wu Bingbing, Wang |
Genetic 3'UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients. Scientific reports 2020 Mar 10 (1): 5736. Pamu?a-Pi?at Jolanta, T?cza Karolina, Kalinowska-Herok Magdalena, Grzybowska E |
Assessing Prevalence and Carrier Frequency of Succinic Semialdehyde Dehydrogenase Deficiency. Journal of child neurology 2021 12 36 (13-14): 1218-1222. Martin Kirt, McConnell Alice, Elsea Sarah |
Phenotypic Correlates of Structural and Functional Protein Impairments Resultant from ALDH5A1 Variants. Research square 2023 7 . Itay Tokatly Latzer, Jean-Baptiste Roullet, Samuele Cesaro, Melissa L DiBacco, Erland Arning, Alexander Rotenberg, Henry H C Lee, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mariarita Bertoldi, Phillip L Pea |
Coexistence of temporal lobe epilepsy and idiopathic generalized epilepsy. Epilepsy & behavior : E&B 2023 12 151 109602. Ali A Asadi-Pooya, Mahdi Malekpour, Ehsan Taherifard, Arashk Mallahzadeh, Mohsen Farjoud Kouhanja |
Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants. Human genetics 2023 11 . Itay Tokatly Latzer, Jean-Baptiste Roullet, Samuele Cesaro, Melissa L DiBacco, Erland Arning, Alexander Rotenberg, Henry H C Lee, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mariarita Bertoldi, Phillip L Pea |
Proteome-wide Mendelian randomization identifies therapeutic targets for ankylosing spondylitis. Frontiers in immunology 2024 4 15 1366736. Wenlong Zhao, Peng Fang, Chengteng Lai, Xiaoyu Xu, Yang Wang, Hao Liu, Hui Jiang, Xiaozhou Liu, Jun L |
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- Page last updated:Apr 29, 2024
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