Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: GPHN[original query] |
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Pathway-based association analysis of genome-wide screening data suggest that genes associated with the gamma-aminobutyric acid receptor signaling pathway are involved in neuroleptic-induced, treatment-resistant tardive dyskinesia. Pharmacogenetics and genomics 2008 Apr 18 (4): 317-23. Inada Toshiya, Koga Minori, Ishiguro Hiroki, Horiuchi Yasue, Syu Aoi, Yoshio Takashi, Takahashi Nagahide, Ozaki Norio, Arinami Tad |
A discovery resource of rare copy number variations in individuals with autism spectrum disorder. G3 (Bethesda, Md.) 2012 Dec 2 (12): 12. Prasad A, Merico D, Thiruvahindrapuram B, Wei J, Lionel AC, Sato D, Rickaby J, Lu C, Szatmari P, Roberts W, Fernandez BA, Marshall CR, Hatchwell E, Eis PS, Scherer SW |
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics 2014 May 15 (2): 117-27. Egger Gerald, Roetzer Katharina M, Noor Abdul, Lionel Anath C, Mahmood Huda, Schwarzbraun Thomas, Boright Oliver, Mikhailov Anna, Marshall Christian R, Windpassinger Christian, Petek Erwin, Scherer Stephen W, Kaschnitz Wolfgang, Vincent John |
Genetic effects influencing risk for major depressive disorder in China and Europe. Translational psychiatry 2017 03 7 (3): e1074. Bigdeli T B, Ripke S, Peterson R E, Trzaskowski M, Bacanu S-A, Abdellaoui A, Andlauer T F M, Beekman A T F, Berger K, Blackwood D H R, Boomsma D I, Breen G, Buttenschøn H N, Byrne E M, Cichon S, Clarke T-K, Couvy-Duchesne B, Craddock N, de Geus E J C, Degenhardt F, Dunn E C, Edwards A C, Fanous A H, Forstner A J, Frank J, Gill M, Gordon S D, Grabe H J, Hamilton S P, Hardiman O, Hayward C, Heath A C, Henders A K, Herms S, Hickie I B, Hoffmann P, Homuth G, Hottenga J-J, Ising M, Jansen R, Kloiber S, Knowles J A, Lang M, Li Q S, Lucae S, MacIntyre D J, Madden P A F, Martin N G, McGrath P J, McGuffin P, McIntosh A M, Medland S E, Mehta D, Middeldorp C M, Milaneschi Y, Montgomery G W, Mors O, Müller-Myhsok B, Nauck M, Nyholt D R, Nöthen M M, Owen M J, Penninx B W J H, Pergadia M L, Perlis R H, Peyrot W J, Porteous D J, Potash J B, Rice J P, Rietschel M, Riley B P, Rivera M, Schoevers R, Schulze T G, Shi J, Shyn S I, Smit J H, Smoller J W, Streit F, Strohmaier J, Teumer A, Treutlein J, Van der Auwera S, van Grootheest G, van Hemert A M, Völzke H, Webb B T, Weissman M M, Wellmann J, Willemsen G, Witt S H, Levinson D F, Lewis C M, Wray N R, Flint J, Sullivan P F, Kendler K |
Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia. Schizophrenia research 2017 Jan . Balan Shabeesh, Yamada Kazuo, Iwayama Yoshimi, Hashimoto Takanori, Toyota Tomoko, Shimamoto Chie, Maekawa Motoko, Takagai Shu, Wakuda Tomoyasu, Kameno Yosuke, Kurita Daisuke, Yamada Kohei, Kikuchi Mitsuru, Hashimoto Tasuku, Kanahara Nobuhisa, Yoshikawa Tak |
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific reports 2020 Feb 10 (1): 3198. Bacchelli Elena, Cameli Cinzia, Viggiano Marta, Igliozzi Roberta, Mancini Alice, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
Gephyrin and CYP2C9 Genetic Polymorphisms in Patients with Pharmacoresistant Epilepsy. Pharmacogenomics and personalized medicine 2021 9 14 1133-1140. El-Tallawy Hamdy N, Abuhamdah Sawsan, Nassar Ahmed Y, Farghaly Wafaa M A, Saleem Tahia H, Atta Sara A, Sayed Ayat A, Tohamy Amal M, Hassan Mohammed |
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