Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and GRIN2B[original query] |
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Association analysis for NMDA receptor subunit 2B (GRIN2B) genetic variants and psychopathology and clozapine response in schizophrenia. Psychiatric genetics 2001 Dec 11 (4): 219-22. Hong C J, Yu Y W, Lin C H, Cheng C Y, Tsai S |
Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol. Pharmacogenetics and genomics 2011 Apr 21 (4): 206-16. Giegling Ina, Drago Antonio, Dolžan Vita, Plesni?ar Blanka Kores, Schäfer Martin, Hartmann Annette M, Sander Thomas, Toliat Mohammad Reza, Möller Hans-Jürgen, Stassen Hans H, Rujescu Dan, Serretti Alessand |
The role of GRIN2B in Tourette syndrome: Results from a transmission disequilibrium study. Journal of affective disorders 2015 Aug 187 62-65. Che Fengyuan, Zhang Ying, Wang Guiju, Heng Xueyuan, Liu Shiguo, Du Yife |
GRIN2B Gene Polymorphism in Chronic Ketamine Users. The American journal on addictions 2020 Jan . Fan Ni, An Lina, Zhang Minling, He Hongbo, Zhou Yanling, Ou Yuf |
A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European journal of human genetics : EJHG 2022 11 . Garret Philippine, Chevarin Martin, Vitobello Antonio, Verdez Simon, Fournier Cyril, Verloes Alain, Tisserant Emilie, Vabres Pierre, Prevel Orlane, Philippe Christophe, Denommé-Pichon Anne-Sophie, Bruel Ange-Line, Mau-Them Frédéric Tran, Safraou Hana, Boughalem Aïcha, Costa Jean-Marc, Trost Detlef, Thauvin-Robinet Christel, Faivre Laurence, Duffourd Yann |
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