Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 42 Records) |
| Query Trace: Disease and GRIN2B[original query] |
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| Psychosis and relapse in bipolar disorder are related to GRM3, DAOA, and GRIN2B genotype. African journal of psychiatry 2010 Sep 13 (4): 297-301. Dalvie S, Horn N, Nossek C, van der Merwe L, Stein D J, Ramesar |
| NMDA receptor gene variations as modifiers in Huntington disease: a replication study. PLoS currents 2011 3 RRN1247. Saft Carsten, Epplen Jörg T, Wieczorek Stefan, Landwehrmeyer G Bernhard, Roos Raymund A C, de Yebenes Justo Garcia, Dose Matthias, Tabrizi Sarah J, Craufurd David, , Arning Laris |
| 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 |
| Increasing power for voxel-wise genome-wide association studies: the random field theory, least square kernel machines and fast permutation procedures. NeuroImage 2012 Nov 63 (2): 858-73. Ge Tian, Feng Jianfeng, Hibar Derrek P, Thompson Paul M, Nichols Thomas |
| Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS computational biology 2012 8 (7): e1002587. Jia Peilin, Wang Lily, Fanous Ayman H, Pato Carlos N, Edwards Todd L, , Zhao Zhongmi |
TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample.
Journal of molecular neuroscience : MN 2012 Dec . Aragam N, Wang KS, Anderson JL, Liu X |
| [Association polymorphic variants of GRIN2B gene with paranoid schizophrenia and response to common neuroleptics in Russians and Tatars from Bashkortostan Republic]. Genetika 2013 Sep 49 (9): 1106-13. Gareeva A E, Zakirov D F, Khusnutdinova E |
| Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics 2013 Nov 14 (3-4): 173-9. Ramos Eliana Marisa, Latourelle Jeanne C, Gillis Tammy, Mysore Jayalakshmi S, Squitieri Ferdinando, Di Pardo Alba, Di Donato Stefano, Gellera Cinzia, Hayden Michael R, Morrison Patrick J, Nance Martha, Ross Christopher A, Margolis Russell L, Gomez-Tortosa Estrella, Ayuso Carmen, Suchowersky Oksana, Trent Ronald J, McCusker Elizabeth, Novelletto Andrea, Frontali Marina, Jones Randi, Ashizawa Tetsuo, Frank Samuel, Saint-Hilaire Marie-Helene, Hersch Steven M, Rosas Herminia D, Lucente Diane, Harrison Madaline B, Zanko Andrea, Abramson Ruth K, Marder Karen, Gusella James F, Lee Jong-Min, Alonso Isabel, Sequeiros Jorge, Myers Richard H, Macdonald Marcy |
| Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease. Journal of neural transmission (Vienna, Austria : 1996) 2014 May 121 (5): 533-42. Andreoli Virginia, De Marco Elvira Valeria, Trecroci Francesca, Cittadella Rita, Di Palma Gemma, Gambardella Anton |
| Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain imaging and behavior 2014 Jun 8 (2): 183-207. Shen Li, Thompson Paul M, Potkin Steven G, Bertram Lars, Farrer Lindsay A, Foroud Tatiana M, Green Robert C, Hu Xiaolan, Huentelman Matthew J, Kim Sungeun, Kauwe John S K, Li Qingqin, Liu Enchi, Macciardi Fabio, Moore Jason H, Munsie Leanne, Nho Kwangsik, Ramanan Vijay K, Risacher Shannon L, Stone David J, Swaminathan Shanker, Toga Arthur W, Weiner Michael W, Saykin Andrew J, |
| Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
| DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson's disease patients. BMC neurology 2015 15 59. Zainal Abidin Shahidee, Tan Eng Liang, Chan Soon-Choy, Jaafar Ameerah, Lee Alex Xuen, Abd Hamid Mohd Hamdi Noor, Abdul Murad Nor Azian, Pakarul Razy Nur Fadlina, Azmin Shahrul, Ahmad Annuar Azlina, Lim Shen Yang, Cheah Pike-See, Ling King-Hwa, Mohamed Ibrahim Norlin |
| Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphisms. Parkinsonism & related disorders 2015 Nov . Hassan Anhar, Heckman Michael G, Ahlskog J E, Wszolek Zbigniew K, Serie Daniel J, Uitti Ryan J, van Gerpen Jay A, Okun Michael S, Rayaprolu Sruti, Ross Owen |
| Dopamine D3 receptor Ser9Gly variant is associated with impulse control disorders in Parkinson's disease patients. Parkinsonism & related disorders 2016 Jun . Krishnamoorthy Soumya, Rajan Roopa, Banerjee Moinak, Kumar Hardeep, Sarma Gangadhara, Krishnan Syam, Sarma Sankara, Kishore As |
| Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease. Journal of neurology, neurosurgery, and psychiatry 2016 Apr . Kraemmer Julia, Smith Kara, Weintraub Daniel, Guillemot Vincent, Nalls Mike A, Cormier-Dequaire Florence, Moszer Ivan, Brice Alexis, Singleton Andrew B, Corvol Jean-Christop |
| Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiology of aging 2016 Feb 38 141-50. Hohman Timothy J, Bush William S, Jiang Lan, Brown-Gentry Kristin D, Torstenson Eric S, Dudek Scott M, Mukherjee Shubhabrata, Naj Adam, Kunkle Brian W, Ritchie Marylyn D, Martin Eden R, Schellenberg Gerard D, Mayeux Richard, Farrer Lindsay A, Pericak-Vance Margaret A, Haines Jonathan L, Thornton-Wells Tricia A, |
| [Polymorphic Variants of Glutamate Receptor (GRIK5, GRIN2B) and Serotonin Receptor (HTR2A) Genes Are Associated with Chronic Obstructive Pulmonary Disease]. Molekuliarnaia biologiia 0 51 (4): 603-614. Korytina G F, Akhmadishina L Z, Kochetova O V, Aznabaeva Y G, Zagidullin Sh Z, Victorova T |
| Using an Event-History with Risk-Free Model to Study the Genetics of Alcoholism. Scientific reports 2017 May 7 (1): 1975. Yang Hsin-Chou, Chen I-Chen, Tsay Yuh-Chyuan, Li Zheng-Rong, Chen Chun-Houh, Hwu Hai-Gwo, Chen Chen-Hs |
| Convergent functional genomics of cocaine misuse in humans and animal models. The American journal of drug and alcohol abuse 2019 8 46 (1): 22-30. Forero Diego A, González-Giraldo Yei |
| 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 |
| 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 |
| Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes. Noro psikiyatri arsivi 2021 9 58 (3): 171-175. Yalçintepe Sinem, Görker I??k, Demir Selma, Atli Emine ?kbal, Atli Engin, Tozkir Hilmi, Süt Necdet, Özen Yasemin, Eker Damla, Mail Çisem, Güler Hazal Sezginer, Zhuri Drenushe, Gurkan Hak |
| Biallelic ADGRV1 variants are associated with Rolandic epilepsy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 6 43 (2): 1365-1374. Liu Zhigang, Ye Xingguang, Zhang Jieyan, Wu Benze, Dong Shiwei, Gao Pingmi |
| Polymorphism of neurodegeneration-related genes associated with Parkinson's disease risk. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 6 43 (9): 5301-5312. Li Jiaxin, Yi Minhan, Li Binbin, Yin Shujuan, Zhang Ying, Huang Zini, Shu Li, Zhang Yu |
| 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 |
| Analysis of the Pathogenic Variants of Genes Using a Gene Panel in Turkish Epilepsy Patients. Clinical laboratory 2022 Jun 68 (6): . Gun-Bilgic Dilek, Polat Muzaff |
| Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population. American journal of medical genetics. Part A 2024 10 e63914. Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, Selinda Mascarenhas, Lakshmi Priya Rao, Karthik Vijay Nair, Bhagesh Hunakunti, Adarsh Pooradan Prasannakumar, Rohit Naik, Dhanya Lakshmi Narayanan, Shalini S Nayak, Vivekananda Bhat, Suvasini Sharma, Y Ramesh Bhat, B L Yatheesha, Rajesh Kulkarni, Siddaramappa J Patil, Sheela Nampoothiri, Shahyan Siddiqui, Katta Mohan Girisha, Stephanie Bielas, Anju Shuk |
| Changes in Expression of Key Genes in Alzheimer's Disease: A Specific Brain Tissue Change. The journals of gerontology. Series A, Biological sciences and medical sciences 2024 1 . Lucas Trevizani Rasmussen, Roger Willian de Labio, Mônica Pezenatto Dos Santos, Bruno Mari Fredi, Eduardo Federighi Baisi Chagas, Elizabeth Suchi Chen, Gustavo Turecki, Marília de Arruda Cardoso Smith, Spencer Luiz Marques Pay |
| Association between GRIN2B polymorphism and Parkinson's disease risk, age at onset, and progression in Southern China. Frontiers in neurology 2025 1 15 1459576. Can Cui, Hongxia Li, Yiwen Bao, Yingying Han, Hongxiang Yu, Huan Song, Bei Zha |
- Page last reviewed:Feb 1, 2024
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