Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and GRIN2A[original query] |
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| A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia. Pharmacogenetics 2003 May 13 (5): 271-8. Itokawa Masanari, Yamada Kazuo, Yoshitsugu Kiyoshi, Toyota Tomoko, Suga Toshiro, Ohba Hisako, Watanabe Akiko, Hattori Eiji, Shimizu Hiromitsu, Kumakura Tetsuo, Ebihara Mitsuru, Meerabux Joanne M, Toru Michio, Yoshikawa Tak |
| NR2A and NR2B receptor gene variations modify age at onset in Huntington disease. Neurogenetics 2005 Feb 6 (1): 25-8. Arning Larissa, Kraus Peter H, Valentin Sandra, Saft Carsten, Andrich Jürgen, Epplen Jörg |
| Extended analyses support the association of a functional (GT)n polymorphism in the GRIN2A promoter with Japanese schizophrenia. Neuroscience letters 2005 Apr 378 (2): 102-5. Iwayama-Shigeno Yoshimi, Yamada Kazuo, Itokawa Masanari, Toyota Tomoko, Meerabux Joanne M A, Minabe Yoshio, Mori Norio, Inada Toshio, Yoshikawa Tak |
| Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes. Neuroscience letters 2006 Feb 394 (2): 101-4. Iwayama Yoshimi, Hashimoto Kenji, Nakajima Mizuho, Toyota Tomoko, Yamada Kazuo, Shimizu Eiji, Itokawa Masanari, Hoshika Akinori, Iyo Masaomi, Yoshikawa Tak |
| NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner. Human genetics 2007 Sep 122 (2): 175-82. Arning Larissa, Saft Carsten, Wieczorek Stefan, Andrich Jürgen, Kraus Peter H, Epplen Jörg |
| 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 |
| Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. PLoS genetics 2011 Aug 7 (8): e1002237. Hamza Taye H, Chen Honglei, Hill-Burns Erin M, Rhodes Shannon L, Montimurro Jennifer, Kay Denise M, Tenesa Albert, Kusel Victoria I, Sheehan Patricia, Eaaswarkhanth Muthukrishnan, Yearout Dora, Samii Ali, Roberts John W, Agarwal Pinky, Bordelon Yvette, Park Yikyung, Wang Liyong, Gao Jianjun, Vance Jeffery M, Kendler Kenneth S, Bacanu Silviu-Alin, Scott William K, Ritz Beate, Nutt John, Factor Stewart A, Zabetian Cyrus P, Payami Hayd |
A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection.
Viral immunology 2011 Oct 24 (5): 397-402. Liu Lifeng, Li Jin, Yao Jinjian, Yu Jinling, Zhang Jinliang, Ning Qin, Wen Zirong, Yang Daguo, He Yongwen, Kong Xinjuan, Song Qilong, Chen Man, Yang Hong, Liu Qing, Li Senlin, Lin Jushe |
| 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 |
| 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 |
| Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population. PloS one 2014 9 (6): e99294. Yamada-Fowler Naomi, Fredrikson Mats, Söderkvist Pet |
| Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
| Glutamatergic and GABAergic susceptibility loci for heroin and cocaine addiction in subjects of African and European ancestry. Progress in neuro-psychopharmacology & biological psychiatry 2016 Jan 64 118-23. Levran Orna, Peles Einat, Randesi Matthew, Correa da Rosa Joel, Ott Jurg, Rotrosen John, Adelson Miriam, Kreek Mary Jean |
| Caffeine, creatine, GRIN2A and Parkinson's disease progression. Journal of the neurological sciences 2017 Apr 375 355-359. Simon David K, Wu Cai, Tilley Barbara C, Lohmann Katja, Klein Christine, Payami Haydeh, Wills Anne-Marie, Aminoff Michael J, Bainbridge Jacquelyn, Dewey Richard, Hauser Robert A, Schaake Susen, Schneider Jay S, Sharma Saloni, Singer Carlos, Tanner Caroline M, Truong Daniel, Wei Peng, Wong Pei Shieen, Yang Tianzho |
| Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individuals. Neuropsychologia 2018 7 117 347-351. Jha Siddharth, Read Silven, Hurd Peter, Crespi Berna |
| Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. European journal of human genetics : EJHG 2018 1 26 (2): 258-264. Bobbili Dheeraj R, Lal Dennis, May Patrick, Reinthaler Eva M, Jabbari Kamel, Thiele Holger, Nothnagel Michael, Jurkowski Wiktor, Feucht Martha, Nürnberg Peter, Lerche Holger, Zimprich Fritz, Krause Roland, Neubauer Bernd A, Reinthaler Eva M, Zimprich Fritz, Feucht Martha, Steinböck Hannelore, Neophytou Birgit, Geldner Julia, Gruber-Sedlmayr Ursula, Haberlandt Edda, Ronen Gabriel M, Altmüller Janine, Lal Dennis, Nürnberg Peter, Sander Thomas, Thiele Holger, Krause Roland, May Patrick, Balling Rudi, Lerche Holger, Neubauer Bernd A, |
| Interaction between caffeine and polymorphisms of glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) and cytochrome P450 1A2 (CYP1A2) on Parkinson's disease risk. Movement disorders : official journal of the Movement Disorder Society 2018 Jan . Kim Iris Y, O'Reilly Éilis J, Hughes Katherine C, Gao Xiang, Schwarzschild Michael A, McCullough Marjorie L, Hannan Marian T, Betensky Rebecca A, Ascherio Alber |
| 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 |
| 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 |
| Glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) gene polymorphism (rs4998386) and Parkinson's disease susceptibility: A meta-analysis. Aging medicine (Milton (N.S.W)) 2019 Sep 2 (3): 174-183. Nepal Gaurav, Rehrig Jessica Holly, Ojha Raje |
| Genome-wide conditional association study reveals the influences of lifestyle cofactors on genetic regulation of body surface area in MESA population. PloS one 2021 6 16 (6): e0253167. Khatun Mita, Monir Md Mamun, Xu Ting, Xu Haiming, Zhu J |
| Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 2022 4 604 (7906): 509-516. Singh Tarjinder, Poterba Timothy, Curtis David, Akil Huda, Al Eissa Mariam, Barchas Jack D, Bass Nicholas, Bigdeli Tim B, Breen Gerome, Bromet Evelyn J, Buckley Peter F, Bunney William E, Bybjerg-Grauholm Jonas, Byerley William F, Chapman Sinéad B, Chen Wei J, Churchhouse Claire, Craddock Nicholas, Cusick Caroline M, DeLisi Lynn, Dodge Sheila, Escamilla Michael A, Eskelinen Saana, Fanous Ayman H, Faraone Stephen V, Fiorentino Alessia, Francioli Laurent, Gabriel Stacey B, Gage Diane, Gagliano Taliun Sarah A, Ganna Andrea, Genovese Giulio, Glahn David C, Grove Jakob, Hall Mei-Hua, Hämäläinen Eija, Heyne Henrike O, Holi Matti, Hougaard David M, Howrigan Daniel P, Huang Hailiang, Hwu Hai-Gwo, Kahn René S, Kang Hyun Min, Karczewski Konrad J, Kirov George, Knowles James A, Lee Francis S, Lehrer Douglas S, Lescai Francesco, Malaspina Dolores, Marder Stephen R, McCarroll Steven A, McIntosh Andrew M, Medeiros Helena, Milani Lili, Morley Christopher P, Morris Derek W, Mortensen Preben Bo, Myers Richard M, Nordentoft Merete, O'Brien Niamh L, Olivares Ana Maria, Ongur Dost, Ouwehand Willem H, Palmer Duncan S, Paunio Tiina, Quested Digby, Rapaport Mark H, Rees Elliott, Rollins Brandi, Satterstrom F Kyle, Schatzberg Alan, Scolnick Edward, Scott Laura J, Sharp Sally I, Sklar Pamela, Smoller Jordan W, Sobell Janet L, Solomonson Matthew, Stahl Eli A, Stevens Christine R, Suvisaari Jaana, Tiao Grace, Watson Stanley J, Watts Nicholas A, Blackwood Douglas H, Børglum Anders D, Cohen Bruce M, Corvin Aiden P, Esko Tõnu, Freimer Nelson B, Glatt Stephen J, Hultman Christina M, McQuillin Andrew, Palotie Aarno, Pato Carlos N, Pato Michele T, Pulver Ann E, St Clair David, Tsuang Ming T, Vawter Marquis P, Walters James T, Werge Thomas M, Ophoff Roel A, Sullivan Patrick F, Owen Michael J, Boehnke Michael, O'Donovan Michael C, Neale Benjamin M, Daly Mark |
| Interaction between Caffeine Consumption & Genetic susceptibility in Parkinson's disease: a systematic review. Ageing research reviews 2024 6 102381. Yujuan Yang, Zhi-Dong Zhou, Ling Xiao Yi, Brendan Jen-Wei Tan, Eng-King T |
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