Showing results (151-160 of 208) with videos related to
Sort By:
Pageof 21
Scientific Reports|October 24, 2015
Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese populationHiroki Kimura, Satoshi Tanaka, Itaru Kushima, et al.Neuroscience Letters|September 18, 2012
An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disordersShinji Matsunaga, Masashi Ikeda, Taro Kishi, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 31, 2012
Functional genetic variation at the NRGN gene and schizophrenia: evidence from a gene-based case-control study and gene expression analysisKazutaka Ohi, Ryota Hashimoto, Yuka Yasuda, et al.Neuropsychopharmacology Reports|February 28, 2026
Persistent Interleukin-1β Elevation in Post-COVID-19 Patients: Findings From a Nationwide Registry Study in JapanNaoki Takamatsu, Hiroki Kimura, Mari S Oba, et al.Psychiatric Genetics|June 8, 2015
A genome-wide association study of late-onset Alzheimer's disease in a Japanese populationAtsushi Hirano, Tomoyuki Ohara, Atsushi Takahashi, et al.Nature Genetics|September 12, 2017
Genome-wide association study identifies 112 new loci for body mass index in the Japanese populationMasato Akiyama, Yukinori Okada, Masahiro Kanai, et al.Biological Psychiatry|December 15, 2012
A population-specific uncommon variant in GRIN3A associated with schizophreniaAtsushi Takata, Yoshimi Iwayama, Yasuhisa Fukuo, et al.Molecular Brain|September 23, 2008
Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disordersNobuyuki Yamasaki, Motoko Maekawa, Katsunori Kobayashi, et al.Translational Psychiatry|February 27, 2022
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorderChenyao Wang, Shin-Ichiro Horigane, Minoru Wakamori, et al.Plos One|June 1, 2012
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patientsTakayoshi Koide, Masahiro Banno, Branko Aleksic, et al.Pageof 21