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JP20dm0107087

Funded outputs count: 20
Funder award ID: JP20dm0107087
OpenAlex ID: G8400387461
Treatment‐resistant schizophrenia with 22q11.2 deletion and additional genetic defects
2024 · Sawako Furukawa, Shusei Arafuka, et al. · Neuropsychopharmacology Reports · 4
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Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions
2023 · Sawako Furukawa, Itaru Kushima, et al. · Neuropsychopharmacology Reports · 9
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Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype
2022 · Akane Yoshikawa, Itaru Kushima, et al. · PLoS ONE · 9
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Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder.
2022 · Sho Furuta, Branko Aleksic, et al. · PubMed · 5
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Psychiatric patients with a de novo 17q12 deletion: Two case reports
2022 · Itaru Kushima, Mariko Uematsu, et al. · Psychiatry and Clinical Neurosciences · 8
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Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder
2022 · Chenyao Wang, Shin-ichiro Horigane, et al. · Translational Psychiatry · 8
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Case report of a female with bipolar disorder and MBD5 deletion
2022 · Itaru Kushima, Tzuyao Lo, et al. · Psychiatry and Clinical Neurosciences · 3
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Mice with exonic RELN deletion identified from a patient with schizophrenia have impaired visual discrimination learning and reversal learning in touchscreen operant tasks
2021 · Jingzhu Liao, Geyao Dong, et al. · Behavioural Brain Research · 14
Microinjection of Reelin into the mPFC prevents MK-801-induced recognition memory impairment in mice
2021 · Masahito Sawahata, Hiroki Asano, et al. · Pharmacological Research · 25
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Brain capillary structures of schizophrenia cases and controls show a correlation with their neuron structures
2021 · Rino Saiga, Masayuki Uesugi, et al. · Scientific Reports · 21
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Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress
2021 · Akane Yoshikawa, Itaru Kushima, et al. · Translational Psychiatry · 8
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Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders
2021 · Ryo Saito, Chika Miyoshi, et al. · Molecular Brain · 20
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Mice carrying a schizophrenia-associated mutation of the Arhgap10 gene are vulnerable to the effects of methamphetamine treatment on cognitive function: association with morphological abnormalities in striatal neurons
2021 · Kazuhiro Hada, Bolati Wulaer, et al. · Molecular Brain · 19
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Structural diverseness of neurons between brain areas and between cases
2021 · Ryuta Mizutani, Rino Saiga, et al. · Translational Psychiatry · 17
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Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons
2020 · Yuko Arioka, Emiko Shishido, et al. · EBioMedicine · 24
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Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder
2020 · Hidekazu Kato, Itaru Kushima, et al. · Translational Psychiatry · 17
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Overexpression of astroglial major histocompatibility complex class I in the medial prefrontal cortex impairs visual discrimination learning in mice
2020 · Bolati Wulaer, Kazuhiro Hada, et al. · Molecular Brain · 12
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Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
2020 · Kanako Ishizuka, Tomoyuki Yoshida, et al. · Journal of Neurodevelopmental Disorders · 45
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Reelin Supplementation Into the Hippocampus Rescues Abnormal Behavior in a Mouse Model of Neurodevelopmental Disorders
2020 · Daisuke Ibi, Genki Nakasai, et al. · Frontiers in Cellular Neuroscience · 31
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ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk
2020 · Mariko Sekiguchi, Akira Sobue, et al. · Translational Psychiatry · 76
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