Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and SLC1A2[original query] |
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| Association study of polymorphisms in the excitatory amino acid transporter 2 gene (SLC1A2) with schizophrenia. BMC psychiatry 2004 4 (): 21. Deng Xiangdong, Shibata Hiroki, Ninomiya Hideaki, Tashiro Nobutada, Iwata Nakao, Ozaki Norio, Fukumaki Yasuyu |
| SLC1A2 rs3794087 does not associate with essential tremor. Neurobiology of aging 2014 Apr 35 (4): 935.e9-10. Ross Jay P, Rayaprolu Sruti, Bernales Cecily Q, Soto-Ortolaza Alexandra I, van Gerpen Jay, Uitti Ryan J, Wszolek Zbigniew K, Rajput Alex, Rajput Ali H, Rajput Michele L, Ross Owen A, Vilariño-Güell Carl |
| No evidence for genetic association between glutamate transporter EAAT2 and Devic's neuromyelitis optica in caucasians and afro-caribbeans. Multiple sclerosis and related disorders 2014 Jan 3 (1): 89-93. Hanoux Vincent, Coulbault Laurent, Derache Nathalie, Cabre Philippe, De Seze Jérôme, Marignier Romain, Rudolf Gabrielle, Emmanuelle Dugué Audrey, Allouche Stéphane, Defer Gilles, |
| A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor. Neurological research 2016 Oct 38 (10): 880-7. Jiménez-Jiménez Félix Javier, García-Martín Elena, Alonso-Navarro Hortensia, Lorenzo-Betancor Oswaldo, Ortega-Cubero Sara, Pastor Pau, Calleja Marisol, Agúndez José A |
| SLC1A2 rs3794087 are associated with susceptibility to Parkinson's disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population. Journal of the neurological sciences 2016 Jun 365 96-100. Xu Yaqian, Cao Bei, Chen YongPing, Ou RuWei, Wei QianQian, Yang Jing, Zhao Bi, Song Wei, Shang Hui-Fa |
Genome-wide association study in essential tremor identifies three new loci.
Brain : a journal of neurology 2016 Dec 139 (Pt 12): 3163-3169. Müller Stefanie H, Girard Simon L, Hopfner Franziska, Merner Nancy D, Bourassa Cynthia V, Lorenz Delia, Clark Lorraine N, Tittmann Lukas, Soto-Ortolaza Alexandra I, Klebe Stephan, Hallett Mark, Schneider Susanne A, Hodgkinson Colin A, Lieb Wolfgang, Wszolek Zbigniew K, Pendziwiat Manuela, Lorenzo-Betancor Oswaldo, Poewe Werner, Ortega-Cubero Sara, Seppi Klaus, Rajput Alex, Hussl Anna, Rajput Ali H, Berg Daniela, Dion Patrick A, Wurster Isabel, Shulman Joshua M, Srulijes Karin, Haubenberger Dietrich, Pastor Pau, Vilariño-Güell Carles, Postuma Ronald B, Bernard Geneviève, Ladwig Karl-Heinz, Dupré Nicolas, Jankovic Joseph, Strauch Konstantin, Panisset Michel, Winkelmann Juliane, Testa Claudia M, Reischl Eva, Zeuner Kirsten E, Ross Owen A, Arzberger Thomas, Chouinard Sylvain, Deuschl Günther, Louis Elan D, Kuhlenbäumer Gregor, Rouleau Guy |
| Analysis of variant rs3794087 in SLC1A2 and Parkinson's disease in a Chinese Han population: A case-control study and meta-analysis. Neuroscience letters 2017 Dec . Cheng Yuan, Mao Cheng-Yuan, Liu Yu-Tao, Li Fang, Yang Jing, Liu Han, Zhang Chan, Wang Yan-Lin, Wu Jun, Shi Chang-He, Xu Yu-Mi |
| A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
| Genetic variant in SLC1A2 is associated with elevated anterior cingulate cortex glutamate and lifetime history of rapid cycling. Translational psychiatry 2019 May 9 (1): 149. Veldic Marin, Millischer Vincent, Port John D, Ho Ada Man-Choi, Jia Yun-Fang, Geske Jennifer R, Biernacka Joanna M, Backlund Lena, McElroy Susan L, Bond David J, Villaescusa J Carlos, Skime Michelle, Choi Doo-Sup, Lavebratt Catharina, Schalling Martin, Frye Mark |
| Assessment of three essential tremor genetic loci in sporadic Parkinson's disease in Eastern China. CNS neuroscience & therapeutics 2019 Nov . Gao Ting, Wu Jiong, Zheng Ran, Fang Yi, Jin Chong-Yao, Ruan Yang, Cao Jin, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
| SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
| Atopic polygenic risk score is associated with paradoxical eczema developing in psoriasis patients treated with biologics.
The Journal of investigative dermatology 2023 2 . Al-Janabi Ali, Eyre Steve, Foulkes Amy C, Khan Adnan R, Dand Nick, Burova Ekaterina, DeSilva Bernadette, Makrygeorgou Areti, Davies Emily, Smith Catherine H, Griffiths Christopher Em, Morris Andrew P, Warren Richard B, |
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