Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Bipolar Disorder and S100B[original query] |
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| Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. Journal of psychiatric research 2010 Oct 44 (14): 971-8. Saus Ester, Brunet Anna, Armengol Lluís, Alonso Pino, Crespo José M, Fernández-Aranda Fernando, Guitart Miriam, Martín-Santos Rocío, Menchón José Manuel, Navinés Ricard, Soria Virginia, Torrens Marta, Urretavizcaya Mikel, Vallès Vicenç, Gratacòs Mònica, Estivill Xavi |
| Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Sep 156B (6): 691-9. Dagdan Elif, Morris Derek W, Campbell Matthew, Hill Matthew, Rothermundt Matthias, Kästner Florian, Hohoff Christa, von Eiff Christof, Krakowitzky Petra, Gill Michael, McKeon Patrick, Roche Siobh |
| Cerebrospinal fluid neuroplasticity-associated protein levels in patients with psychiatric disorders: a multiplex immunoassay study. Translational psychiatry 2020 5 10 (1): 161. Hidese Shinsuke, Hattori Kotaro, Sasayama Daimei, Tsumagari Takuya, Miyakawa Tomoko, Matsumura Ryo, Yokota Yuuki, Ishida Ikki, Matsuo Junko, Yoshida Sumiko, Ota Miho, Kunugi Hiros |
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