Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: SLC1A2[original query] |
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Synergistic association of PI4KA and GRM3 genetic polymorphisms with poor antipsychotic response in south Indian schizophrenia patients with low severity of illness. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 635-46. Kaur Harpreet, Jajodia Ajay, Grover Sandeep, Baghel Ruchi, Jain Sanjeev, Kukreti Ritushr |
Combined effect of common gene variants on response to drug withdrawal therapy in medication overuse headache. European journal of clinical pharmacology 2014 Oct 70 (10): 1195-202. Cargnin Sarah, Viana Michele, Sances Grazia, Bianchi Marika, Ghiotto Natascia, Tassorelli Cristina, Nappi Giuseppe, Canonico Pier Luigi, Genazzani Armando A, Terrazzino Salvato |
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS.
Molecular psychiatry 2015 Mar 20 (3): 337-44. Mattheisen M, Samuels J F, Wang Y, Greenberg B D, Fyer A J, McCracken J T, Geller D A, Murphy D L, Knowles J A, Grados M A, Riddle M A, Rasmussen S A, McLaughlin N C, Nurmi E L, Askland K D, Qin H-D, Cullen B A, Piacentini J, Pauls D L, Bienvenu O J, Stewart S E, Liang K-Y, Goes F S, Maher B, Pulver A E, Shugart Y Y, Valle D, Lange C, Nestadt |
Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. European journal of human genetics : EJHG 2015 Sep 23 (9): 1200-6. Fiorentino Alessia, Sharp Sally I, McQuillin Andr |
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, |
SLC1A2 rs3794087 variant and risk for essential tremor: a systematic review and meta-analysis. Pharmacogenetics and genomics 2015 Aug . Jiménez-Jiménez Félix J, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
Common variants in SLC1A2 and schizophrenia: Association and cognitive function in patients with schizophrenia and healthy individuals. Schizophrenia research 2015 Oct . Zhang Bao, Guan Fanglin, Chen Gang, Lin Huali, Zhang Tianxiao, Feng Jiali, Li Lu, Fu Dong |
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 |
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy. American journal of human genetics 2017 8 101 (2): 300-310. Guella Ilaria, McKenzie Marna B, Evans Daniel M, Buerki Sarah E, Toyota Eric B, Van Allen Margot I, , Suri Mohnish, Elmslie Frances, , Simon Marleen E H, van Gassen Koen L I, Héron Delphine, Keren Boris, Nava Caroline, Connolly Mary B, Demos Michelle, Farrer Matthew |
Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.
Schizophrenia bulletin 2017 May . Ortega-Alonso Alfredo, Ekelund Jesper, Sarin Antti-Pekka, Miettunen Jouko, Veijola Juha, Järvelin Marjo-Riitta, Hennah Willi |
Pharmacogenetic Analysis of Functional Glutamate System Gene Variants and Clinical Response to Clozapine. Molecular neuropsychiatry 2017 Feb 2 (4): 185-197. Taylor Danielle L, Tiwari Arun K, Lieberman Jeffrey A, Potkin Steven G, Meltzer Herbert Y, Knight Joanne, Remington Gary, Müller Daniel J, Kennedy James |
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 |
Variability with Astroglial Glutamate Transport Genetics Is Associated with Increased Risk for Post-Traumatic Seizures. Journal of neurotrauma 2018 Jul . Kumar Raj G, Breslin Kristen B, Ritter Anne C, Conley Yvette P, Wagner Amy |
Clozapine pharmacogenomics: a review of efficacy, pharmacokinetics, and agranulocytosis. Current opinion in psychiatry 2018 Jul . Li Kevin J, Solomon Haley V, DeLisi Lynn |
Psychological and genetic risk factors associated with suicidal behavior in Korean patients with mood disorders. Journal of affective disorders 2018 Apr 235 489-498. Choi Hee-Yeon, Kim Ga Eun, Kong Kyoung Ae, Lee Yu Jin, Lim Weon-Jeong, Park So-Hyun, Ha Su Hee, Kim Soo |
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 testing in fetuses with isolated agenesis of the corpus callosum. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 8 34 (14): 2227-2234. She Qin, Fu Fang, Guo Xiaoyan, Tan Weihe, Liao C |
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 |
Association study of the excitatory amino acid transporter 2 (EAAT2) and glycine transporter 1 (GlyT1) gene polymorphism with schizophrenia in a Polish population. Neuropsychiatric disease and treatment 2019 15 989-1000. Merk Wojciech, Kucia Krzysztof, M?drala Tomasz, Kowalczyk Ma?gorzata, Owczarek Aleksander, Kowalski J |
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 |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
Genomic Markers for Essential Tremor. Pharmaceuticals (Basel, Switzerland) 2021 6 14 (6): . Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, García-Martín Elena, Álvarez Ignacio, Pastor Pau, Agúndez José A |
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 |
The Associations between Metalloestrogens, GSTP1, and SLC11A2 Polymorphism and the Risk of Endometrial Cancer. Nutrients 2022 Jul 14 (15): . Michalczyk Kaja, Kapczuk Patrycja, Witczak Grzegorz, Bosiacki Mateusz, Kurzawski Mateusz, Chlubek Dariusz, Cymbaluk-P?oska Ane |
Association Study of the SLC1A2 (rs4354668), SLC6A9 (rs2486001), and SLC6A5 (rs2000959) Polymorphisms in Major Depressive Disorder. Journal of clinical medicine 2022 10 11 (19): . Rodek Patryk, Kowalczyk Ma?gorzata, Kowalski Jan, Owczarek Aleksander, Chor?za Piotr, Kucia Krzyszt |
Astrocytes Differentiated from LRRK2-I1371V Parkinson's-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery. Cells 2023 6 12 (12): . Roon Banerjee, Aishwarya Raj, Chandrakanta Potdar, Pramod Kumar Pal, Ravi Yadav, Nitish Kamble, Vikram Holla, Indrani Dat |
SLC1A2 Gene Polymorphism Influences Methamphetamine-Induced Psychosis. Journal of personalized medicine 2023 2 13 (2): . Yahya Dayang Nooreffazleen, Guad Rhanye Mac, Wu Yuan-Seng, Gan Siew Hua, Gopinath Subash C B, Zakariah Hasif Adli, Rashid Rusdi Abdul, Sim Maw Sh |
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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- Page last updated:Apr 22, 2024
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