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Nature Communications|June 19, 2021
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorderMasaki Nishioka, An-A Kazuno, Takumi Nakamura, et al.
Human Genome Variation|December 10, 2020
Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibilityYoshihiro Nawa, Hiroki Kimura, Daisuke Mori, et al.
Translational Psychiatry|August 29, 2019
The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studiesChenxing Liu, Tetsufumi Kanazawa, Ye Tian, et al.
Schizophrenia Research|October 30, 2012
Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibilityMing Li, Yi Wang, Xue-bin Zheng, et al.
Biological Psychiatry|September 14, 2010
Genome-wide association study of schizophrenia in a Japanese populationMasashi Ikeda, Branko Aleksic, Yoko Kinoshita, et al.
Schizophrenia Bulletin|October 22, 2014
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia SusceptibilityHiroki Kimura, Daisuke Tsuboi, Chenyao Wang, et al.
The International Journal of Neuropsychopharmacology|January 10, 2016
Catechol-O-Methyltransferase Val158Met Polymorphism and Clinical Response to Antipsychotic Treatment in Schizophrenia and Schizo-Affective Disorder Patients: a Meta-AnalysisEric Huang, Clement C Zai, Amanda Lisoway, et al.
Nature Genetics|October 3, 2024
Population-specific putative causal variants shape quantitative traitsSatoshi Koyama, Xiaoxi Liu, Yoshinao Koike, et al.
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