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Neuromolecular Medicine|September 18, 2009
Translin-associated factor X gene (TSNAX) may be associated with female major depressive disorder in the Japanese populationAkiko Okuda, Taro Kishi, Tomo Okochi, et al.
Human Molecular Genetics|July 29, 2008
Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophreniaMasashi Ikeda, Takao Hikita, Shinichiro Taya, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2016
Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophreniaRyoko Higashiyama, Tohru Ohnuma, Yuto Takebayashi, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|February 25, 2014
The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and orbitofrontal sulcogyral pattern in patients with schizophrenia and healthy subjectsTsutomu Takahashi, Yumiko Nakamura, Yukako Nakamura, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 26, 2011
Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trialGlyn Lewis, Jean Mulligan, Nicola Wiles, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 3, 2008
No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese populationKunihiro Kawashima, Taro Kishi, Masashi Ikeda, et al.
Nature Human Behaviour|January 22, 2020
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habitsNana Matoba, Masato Akiyama, Kazuyoshi Ishigaki, et al.
Schizophrenia Research|March 27, 2007
Association analysis of AKT1 and schizophrenia in a UK case control sampleNadine Norton, Hywel J Williams, Sarah Dwyer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 19, 2016
Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control studyJun Egawa, Satoshi Hoya, Yuichiro Watanabe, et al.
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