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Jun Egawa

Showing results (41-50 of 55) with videos related to

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Neuropsychiatric Disease and Treatment|February 3, 2021
Factor Structure and Measurement Invariance of the Hospital Anxiety and Depression Scale Across the Peripartum Period Among Pregnant Japanese WomenMaki Ogawa, Yuichiro Watanabe, Takaharu Motegi, et al.
Neuropsychiatric Disease and Treatment|December 28, 2020
Depression, Anxiety and Primiparity are Negatively Associated with Mother-Infant Bonding in Japanese MothersTakaharu Motegi, Yuichiro Watanabe, Naoki Fukui, 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.
Psychiatry and Clinical Neurosciences|June 29, 2017
Rare PDCD11 variations are not associated with risk of schizophrenia in JapanSatoshi Hoya, Yuichiro Watanabe, Akitoyo Hishimoto, et al.
Plos One|March 26, 2015
Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese populationJun Egawa, Yuichiro Watanabe, Chenyao Wang, et al.
Plos One|December 15, 2015
Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese PopulationEmiko Inoue, Yuichiro Watanabe, Jingrui Xing, et al.
Journal of Neurodevelopmental Disorders|September 18, 2020
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophreniaKanako Ishizuka, Tomoyuki Yoshida, Takeshi Kawabata, et al.
Psychiatry Research|December 27, 2015
Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese populationYuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, 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|January 11, 2018
Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibilityYanjie Yu, Yingni Lin, Yuto Takasaki, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Neuropsychiatric Disease and Treatment|February 3, 2021
Factor Structure and Measurement Invariance of the Hospital Anxiety and Depression Scale Across the Peripartum Period Among Pregnant Japanese WomenMaki Ogawa, Yuichiro Watanabe, Takaharu Motegi, et al.
Neuropsychiatric Disease and Treatment|December 28, 2020
Depression, Anxiety and Primiparity are Negatively Associated with Mother-Infant Bonding in Japanese MothersTakaharu Motegi, Yuichiro Watanabe, Naoki Fukui, 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.
Psychiatry and Clinical Neurosciences|June 29, 2017
Rare PDCD11 variations are not associated with risk of schizophrenia in JapanSatoshi Hoya, Yuichiro Watanabe, Akitoyo Hishimoto, et al.
Plos One|March 26, 2015
Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese populationJun Egawa, Yuichiro Watanabe, Chenyao Wang, et al.
Plos One|December 15, 2015
Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese PopulationEmiko Inoue, Yuichiro Watanabe, Jingrui Xing, et al.
Journal of Neurodevelopmental Disorders|September 18, 2020
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophreniaKanako Ishizuka, Tomoyuki Yoshida, Takeshi Kawabata, et al.
Psychiatry Research|December 27, 2015
Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese populationYuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, 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|January 11, 2018
Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibilityYanjie Yu, Yingni Lin, Yuto Takasaki, et al.
Pageof 6