Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: GRIN1[original query] |
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Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Dec 156B (8): 913-22. Demontis Ditte, Nyegaard Mette, Buttenschøn Henriette N, Hedemand Anne, Pedersen Carsten B, Grove Jakob, Flint Tracey J, Nordentoft Merete, Werge Thomas, Hougaard David M, Sørensen Karina M, Yolken Robert H, Mors Ole, Børglum Anders D, Mortensen Preben |
Genetic variants of the NMDA receptor influence cortical excitability and plasticity in humans. Journal of neurophysiology 2011 Oct 106 (4): 1637-43. Mori Francesco, Ribolsi Michele, Kusayanagi Hajime, Siracusano Alberto, Mantovani Vilma, Marasco Elena, Bernardi Giorgio, Centonze Die |
Gene-gene interaction analyses between NMDA receptor subunit and dopamine receptor gene variants and clozapine response. Pharmacogenomics 2011 Feb 12 (2): 277-91. Hwang Rudi, Souza Renan P, Tiwari Arun K, Zai Clement C, Müller Daniel J, Potkin Steven G, Lieberman Jeffrey A, Meltze Herbert Y, Kennedy James |
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia. Translational psychiatry 2012 7 1 (11): e55. Tarabeux J, Kebir O, Gauthier J, Hamdan F F, Xiong L, Piton A, Spiegelman D, Henrion É, Millet B, , Fathalli F, Joober R, Rapoport J L, DeLisi L E, Fombonne É, Mottron L, Forget-Dubois N, Boivin M, Michaud J L, Drapeau P, Lafrenière R G, Rouleau G A, Krebs M |
[Correlation between genetic polymorphisms of -855 G/C and -1140 G/A in GRIN1 gene and paranoid schizophrenia]. Fa yi xue za zhi 2013 Apr 29 (2): 107-9. Li Zhong-Jie, Ding Mei, Pang Hao, Sun Xue-Fei, Xing Jia-Xin, Xuan Jin-Feng, Wang Bao-J |
Genetic variation of GRIN1 confers vulnerability to methamphetamine-dependent psychosis in a Thai population. Neuroscience letters 2013 Sep 551 58-61. Chanasong Rachanee, Thanoi Samur, Watiktinkorn Paritat, Reynolds Gavin P, Nudmamud-Thanoi Suti |
Association of genetic variation in pharmacodynamic factors with methadone dose required for effective treatment of opioid addiction. Pharmacogenomics 2013 May 14 (7): 755-68. Levran Orna, Peles Einat, Randesi Matthew, Shu Xu, Ott Jurg, Shen Pei-Hong, Adelson Miriam, Kreek Mary Jean |
A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity. Psychiatry research 2014 Aug 218 (3): 356-8. Lin Yi-Ting, Hsieh Ming H, Liu Chen-Chung, Hwang Tzung-Jeng, Chien Yi-Ling, Hwu Hai-Gwo, Liu Chih-M |
The effects of single nucleotide polymorphisms in glutamatergic neurotransmission genes on neural response to alcohol cues and craving. Addiction biology 2015 Aug . Bach Patrick, Kirsch Martina, Hoffmann Sabine, Jorde Anne, Mann Karl, Frank Josef, Charlet Katrin, Beck Anne, Heinz Andreas, Walter Henrik, Rietschel Marcella, Kiefer Falk, Vollstädt-Klein Sabi |
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis. Neurology® neuroimmunology & neuroinflammation 2015 Oct 2 (5): e153. Day Gregory S, Prüss Harald, Benseler Susanne M, Paton Tara A, Paterson Andrew D, Andrade Danielle |
Additive effect of MTHFR and GRIN1 genetic polymorphisms on the risk of schizophrenia. Molecular biology research communications 2016 11 4 (1): 33-42. Foroughmand Ali Mohammad, Galehdari Hamid, Pooryasin Atefeh, Ajam Tahereh, Kazemi-Nezhad Seyed Re |
Influence of Genetic Variants of the N-Methyl-D-Aspartate Receptor on Emotion and Social Behavior in Adolescents. Neural plasticity 2016 2016 6851592. Lee Li-Ching, Cho Ying-Chun, Lin Pei-Jung, Yeh Ting-Chi, Chang Chun-Yen, Yeh Ting-Kua |
N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) G1001C polymorphism and susceptibility to schizophrenia: A meta-analysis. EXCLI journal 2017 12 9 11-16. Saadat Mosta |
Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology. Behavior genetics 2018 3 48 (3): 198-208. Curtis David, Coelewij Leda, Liu Shou-Hwa, Humphrey Jack, Mott Richa |
Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.
Biological psychiatry 2018 Jan . Cheng Zhongshan, Zhou Hang, Sherva Richard, Farrer Lindsay A, Kranzler Henry R, Gelernter Jo |
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a journal of neurology 2018 1 141 (3): 698-712. Fry Andrew E, Fawcett Katherine A, Zelnik Nathanel, Yuan Hongjie, Thompson Belinda A N, Shemer-Meiri Lilach, Cushion Thomas D, Mugalaasi Hood, Sims David, Stoodley Neil, Chung Seo-Kyung, Rees Mark I, Patel Chirag V, Brueton Louise A, Layet Valérie, Giuliano Fabienne, Kerr Michael P, Banne Ehud, Meiner Vardiella, Lerman-Sagie Tally, Helbig Katherine L, Kofman Laura H, Knight Kristin M, Chen Wenjuan, Kannan Varun, Hu Chun, Kusumoto Hirofumi, Zhang Jin, Swanger Sharon A, Shaulsky Gil H, Mirzaa Ghayda M, Muir Alison M, Mefford Heather C, Dobyns William B, Mackenzie Amanda B, Mullins Jonathan G L, Lemke Johannes R, Bahi-Buisson Nadia, Traynelis Stephen F, Iago Heledd F, Pilz Daniela |
Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility. Translational psychiatry 2018 01 8 (1): 12. Yu Yanjie, Lin Yingni, Takasaki Yuto, Wang Chenyao, Kimura Hiroki, Xing Jingrui, Ishizuka Kanako, Toyama Miho, Kushima Itaru, Mori Daisuke, Arioka Yuko, Uno Yota, Shiino Tomoko, Nakamura Yukako, Okada Takashi, Morikawa Mako, Ikeda Masashi, Iwata Nakao, Okahisa Yuko, Takaki Manabu, Sakamoto Shinji, Someya Toshiyuki, Egawa Jun, Usami Masahide, Kodaira Masaki, Yoshimi Akira, Oya-Ito Tomoko, Aleksic Branko, Ohno Kinji, Ozaki Nor |
Association between polymorphisms in the GRIN1 gene 5' regulatory region and schizophrenia in a northern Han Chinese population and haplotype effects on protein expression in vitro. BMC medical genetics 2019 2 20 (1): 26. Liu Yong-Ping, Ding Mei, Zhang Xi-Cen, Liu Yi, Xuan Jin-Feng, Xing Jia-Xin, Xia Xi, Yao Jun, Wang Bao-J |
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia. Psychiatric genetics 2019 1 29 (2): 44-50. Tsavou Antonia, Curtis Dav |
Modulation on Glutamic Pathway of Frontal-Striatum-Thalamus by rs11146020 and rs3813296 Gene Polymorphism in First-Episode Negative Schizophrenia. Frontiers in neuroscience 2020 14 351. Cai Suping, Lv Yahui, Huang Kexin, Zhang Wei, Wang Qiang, Huang Liyu, Wang Jij |
The association between eating behavior and polymorphisms in GRIN2B, GRIK3, GRIA1 and GRIN1 genes in people with type 2 diabetes mellitus. Molecular biology reports 2020 Feb . Kochetova Olga V, Avzaletdinova Diana S, Korytina Gulnaz F, Morugova Tatyana V, Mustafina Olga |
A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study. Journal of personalized medicine 2020 12 10 (4): . Hong Syuan-Yu, Yang Jiann-Jou, Li Shuan-Yow, Lee Inn-C |
Exploratory study of selected nucleotide variants in GRIN1, GRIN2A and GRIN2B encoding subunits of the NMDA receptor in a targeted group of schizophrenia patients with chronic cognitive impairment. Pharmacological reports : PR 2020 11 73 (1): 269-277. Krzystanek Marek, Asman Marek, Witecka Joanna, Pa?asz Artur, Wiaderkiewicz Rysza |
Selected single-nucleotide variants in GRIN1, GRIN2A, and GRIN2B encoding subunits of the NMDA receptor are not biomarkers of schizophrenia resistant to clozapine: exploratory study. Pharmacological reports : PR 2020 10 73 (1): 309-315. Krzystanek Marek, Asman Marek, Witecka Joanna, Pa?asz Artur, Wiaderkiewicz Rysza |
Association between well-characterized gene polymorphisms and the hypnosis response caused by sevoflurane-induced anaesthesia. Journal of clinical pharmacy and therapeutics 2020 10 45 (6): 1442-1451. Chen Ming-Hua, Ouyang Wen, Xia Yu-Hao, Zeng You-Jie, Wang Sai-Ying, Duan Kai-Ming, Fang Ch |
Genetic variation of rs12918566 affects GRIN2A expression and is associated with spontaneous movement response during sevoflurane anesthesia induction. Brain and behavior 2021 Jul e02165. Chen Ming-Hua, Fang Chao, Wu Na-Yiyuan, Xia Yu-Hao, Zeng You-Jie, Ouyang W |
Association of CaMK2A and MeCP2 signaling pathways with cognitive ability in adolescents. Molecular brain 2021 Oct 14 (1): 152. Lee Li-Ching, Su Ming-Tsan, Huang Hsing-Ying, Cho Ying-Chun, Yeh Ting-Kuang, Chang Chun-Y |
Association between NMDA gene polymorphism (rs4880213) and GRIN2B blood serum levels in thyroid pathology patients. Journal of medicine and life 2022 Jan 15 (1): 109-116. Kamyshna Iryna Ivanivna, Pavlovych Larysa Borysivna, Kamyshnyi Aleksandr Mychailovi |
Lifetime cannabis use and childhood trauma associated with CNR1 genetic variants increase the risk of psychosis: findings from the STREAM study. Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999) 2023 3 . Loureiro Camila Marcelino, Corsi-Zuelli Fabiana, Fachim Helene Aparecida, Shuhama Rosana, de Oliveira Adrielle Martins, Menezes Paulo Rossi, Dalton Caroline F, Louzada-Junior Paulo, Belangero Sintia Iole, Coeli-Lacchini Fernanda, Reynolds Gavin P, Lacchini Riccardo, Del-Ben Cristina Mar |
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- Page last updated:Apr 16, 2024
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