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Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders.
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- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02962-4
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- Publication type:
- Article
Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature.
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- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02952-6
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- Article
Study of the genetic association between selected 3q29 region genes and schizophrenia and autism spectrum disorder in the Japanese population.
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- Nagoya Journal of Medical Science, 2024, v. 86, n. 2, p. 216, doi. 10.18999/nagjms.86.2.216
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- Article
Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice.
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- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-023-02679-w
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- Article
Indoleamine 2,3-dioxygenase 2 deficiency associates with autism-like behavior via dopaminergic neuronal dysfunction.
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- FEBS Journal, 2024, v. 291, n. 5, p. 945, doi. 10.1111/febs.17019
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- Article
Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study.
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- Neuropsychopharmacology Reports, 2024, v. 44, n. 1, p. 42, doi. 10.1002/npr2.12370
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- Article
Mesenchymal stem/stromal cells generated from induced pluripotent stem cells are highly resistant to senescence.
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- Nagoya Journal of Medical Science, 2023, v. 85, n. 4, p. 682, doi. 10.18999/nagjms.85.4.682
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- Article
Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions.
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- 2023
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- Publication type:
- Case Study
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues.
- Published in:
- Human Genetics, 2023, v. 142, n. 7, p. 949, doi. 10.1007/s00439-023-02569-7
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- Article
Structural aging of human neurons is opposite of the changes in schizophrenia.
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- PLoS ONE, 2023, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0287646
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- Article
Clinical characterization of patients with schizophrenia and 16p13.11 duplication: A case series.
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- 2023
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- Publication type:
- Case Study
Astrotactin 2 (ASTN2) regulates emotional and cognitive functions by affecting neuronal morphogenesis and monoaminergic systems.
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- Journal of Neurochemistry, 2023, v. 165, n. 2, p. 211, doi. 10.1111/jnc.15790
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- Article
A case of bipolar disorder with AIF1 (coding gene of Iba‐1) deletion: A pilot in vitro analysis using blood‐derived microglia‐like cells.
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- Psychiatry & Clinical Neurosciences, 2023, v. 77, n. 2, p. 128, doi. 10.1111/pcn.13505
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- Publication type:
- Article
Clinical manifestations of schizophrenia in four patients with variants in voltage‐gated calcium channel‐encoding genes: a case series.
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- Psychiatry & Clinical Neurosciences, 2023, v. 77, n. 1, p. 57, doi. 10.1111/pcn.13494
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- Article
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 12, p. 667, doi. 10.1111/pcn.13474
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- Article
Turner syndrome presenting with idiopathic regression: A case report.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 12, p. 680, doi. 10.1111/pcn.13483
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- Article
Contribution of copy number variations to the risk of severe eating disorders.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 9, p. 423, doi. 10.1111/pcn.13430
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- Article
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02033-6
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- Publication type:
- Article
Exonic deletions in IMMP2L in schizophrenia with enhanced glycation stress subtype.
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- PLoS ONE, 2022, v. 17, n. 7, p. 1, doi. 10.1371/journal.pone.0270506
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- Article
Treatment‐resistant schizophrenia in patients with 3q29 deletion: A case series of four patients.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 7, p. 338, doi. 10.1111/pcn.13361
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- Publication type:
- Article
Psychiatric patients with a de novo 17q12 deletion: Two case reports.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 7, p. 345, doi. 10.1111/pcn.13367
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- Article
Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels.
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- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268321
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- Article
Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder.
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- Nagoya Journal of Medical Science, 2022, v. 84, n. 2, p. 260, doi. 10.18999/nagjms.84.2.260
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- Publication type:
- Article
Case report of a female with bipolar disorder and MBD5 deletion.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 4, p. 127, doi. 10.1111/pcn.13329
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- Publication type:
- Article
Variable psychiatric manifestations in patients with 16p11.2 duplication: a case series of 4 patients.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 3, p. 86, doi. 10.1111/pcn.13324
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- Publication type:
- Article
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01851-y
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- Publication type:
- Article
Effect of a novel nasal oxytocin spray with enhanced bioavailability on autism: a randomized trial.
- Published in:
- 2022
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- Publication type:
- journal article
Trends in big data analyses by multicenter collaborative translational research in psychiatry.
- Published in:
- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 1, p. 1, doi. 10.1111/pcn.13311
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- Publication type:
- Article
Autism spectrum disorder comorbid with obsessive compulsive disorder and eating disorder in a woman with NBEA deletion.
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- Psychiatry & Clinical Neurosciences, 2022, v. 76, n. 1, p. 36, doi. 10.1111/pcn.13309
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- Article
AKR1A1 Variant Associated With Schizophrenia Causes Exon Skipping, Leading to Loss of Enzymatic Activity.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.762999
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- Article
Brain capillary structures of schizophrenia cases and controls show a correlation with their neuron structures.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91233-z
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- Publication type:
- Article
Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01460-1
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- Publication type:
- Article
Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders.
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- Molecular Brain, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13041-021-00778-7
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- Publication type:
- Article
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.
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- Molecular Brain, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13041-021-00735-4
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- Publication type:
- Article
Structural diverseness of neurons between brain areas and between cases.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01173-x
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- Article
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-01107-7
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- Publication type:
- Article
Support vector machine-based classification of schizophrenia patients and healthy controls using structural magnetic resonance imaging from two independent sites.
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- PLoS ONE, 2020, v. 15, n. 11, p. 1, doi. 10.1371/journal.pone.0239615
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- Publication type:
- Article
Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility.
- Published in:
- Human Genome Variation, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1038/s41439-020-00125-7
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- Publication type:
- Article
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
- Published in:
- Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s11689-020-09325-2
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- Publication type:
- Article
ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00917-z
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- Publication type:
- Article
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders.
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- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 7, p. 1117, doi. 10.1002/acn3.51093
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- Article
Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia.
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- Psychiatry & Clinical Neurosciences, 2020, v. 74, n. 5, p. 318, doi. 10.1111/pcn.12993
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- Publication type:
- Article
Cell body shape and directional movement stability in human-induced pluripotent stem cell-derived dopaminergic neurons.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-62598-4
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- Publication type:
- Article
Cutting‐edge morphological studies of post‐mortem brains of patients with schizophrenia and potential applications of X‐ray nanotomography (nano‐CT).
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- Psychiatry & Clinical Neurosciences, 2020, v. 74, n. 3, p. 176, doi. 10.1111/pcn.12957
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- Publication type:
- Article
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0723-z
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- Publication type:
- Article
Polygenic risk scores in schizophrenia with clinically significant copy number variants.
- Published in:
- Psychiatry & Clinical Neurosciences, 2020, v. 74, n. 1, p. 35, doi. 10.1111/pcn.12926
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- Publication type:
- Article
A network of networks approach for modeling interconnected brain tissue-specific networks.
- Published in:
- Bioinformatics, 2019, v. 35, n. 17, p. 3092, doi. 10.1093/bioinformatics/btz032
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- Publication type:
- Article
Quantitative facial expression analysis revealed the efficacy and time course of oxytocin in autism.
- Published in:
- 2019
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- Publication type:
- journal article
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
- Published in:
- Schizophrenia Bulletin, 2019, v. 45, n. 4, p. 824, doi. 10.1093/schbul/sby140
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- Publication type:
- Article
Author Correction: Proteomic analysis of lymphoblastoid cell lines from schizophrenic patients.
- Published in:
- 2019
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- Publication type:
- Correction Notice