Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: 22q11 Deletion Syndrome and GNB1L[original query] |
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Strong evidence that GNB1L is associated with schizophrenia. Human molecular genetics 2008 Feb 17 (4): 555-66. Williams Nigel M, Glaser Beate, Norton Nadine, Williams Hywel, Pierce Timothy, Moskvina Valentina, Monks Stephen, Del Favero Jurgen, Goossens Dirk, Rujescu Dan, Giegling Ina, Kirov George, Craddock Nicholas, Murphy Kieran C, O'Donovan Michael C, Owen Michael |
Supportive evidence for reduced expression of GNB1L in schizophrenia. Schizophrenia bulletin 2010 Jul 36 (4): 756-65. Ishiguro Hiroki, Koga Minori, Horiuchi Yasue, Noguchi Emiko, Morikawa Miyuki, Suzuki Yoshimi, Arai Makoto, Niizato Kazuhiro, Iritani Shyuji, Itokawa Masanari, Inada Toshiya, Iwata Nakao, Ozaki Norio, Ujike Hiroshi, Kunugi Hiroshi, Sasaki Tsukasa, Takahashi Makoto, Watanabe Yuichiro, Someya Toshiyuki, Kakita Akiyoshi, Takahashi Hitoshi, Nawa Hiroyuki, Arinami Tad |
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