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Cooperation of LIM domain‐binding 2 (LDB2) with EGR in the pathogenesis of schizophrenia.
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- EMBO Molecular Medicine, 2021, v. 13, n. 4, p. 1, doi. 10.15252/emmm.202012574
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- Article
Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology.
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- EMBO Molecular Medicine, 2019, v. 11, n. 12, p. N.PAG, doi. 10.15252/emmm.201910695
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- Article
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia.
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- Schizophrenia Bulletin, 2021, v. 47, n. 4, p. 1190, doi. 10.1093/schbul/sbab007
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- Article
Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia.
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- Schizophrenia Bulletin, 2020, v. 46, n. 5, p. 1172, doi. 10.1093/schbul/sbaa052
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- Article
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
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- Schizophrenia Bulletin, 2019, v. 45, n. 4, p. 824, doi. 10.1093/schbul/sby140
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- Article
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
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- Schizophrenia Bulletin, 2015, v. 41, n. 3, p. 744, doi. 10.1093/schbul/sbu147
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- Article
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.
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- Journal of Clinical Investigation, 2007, v. 117, n. 4, p. 931, doi. 10.1172/JCI29031
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- Article
Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01392-w
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- Article
Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population.
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- Journal of Human Genetics, 2014, v. 59, n. 1, p. 54, doi. 10.1038/jhg.2013.116
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- Article
Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects.
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- Journal of Human Genetics, 2010, v. 55, n. 2, p. 127, doi. 10.1038/jhg.2009.133
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- Article
Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population.
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- Journal of Human Genetics, 2009, v. 54, n. 9, p. 538, doi. 10.1038/jhg.2009.76
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- Article
Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia.
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- Journal of Human Genetics, 2009, v. 54, n. 7, p. 386, doi. 10.1038/jhg.2009.47
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- Article
Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics.
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- Journal of Human Genetics, 2007, v. 52, n. 1, p. 86, doi. 10.1007/s10038-006-0084-3
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- Article
Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 8, p. 798, doi. 10.1002/ajmg.b.32595
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- Article
Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: Support for association of MHC region with psychosis.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 5, p. 421, doi. 10.1002/ajmg.b.32246
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- Article
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
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- Scientific Reports, 2016, p. 33311, doi. 10.1038/srep33311
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- Article
Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism.
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- Scientific Reports, 2016, p. 20268, doi. 10.1038/srep20268
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- Article
Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism.
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- Scientific Reports, 2015, p. 16239, doi. 10.1038/srep16239
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- Article
Single-cell transcriptomics uncovers EGFR signaling-mediated gastric progenitor cell differentiation in stomach homeostasis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39113-0
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- Article
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
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- Autism Research: Official Journal of the International Society for Autism Research, 2016, v. 9, n. 3, p. 340, doi. 10.1002/aur.1536
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- Article
Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (<i>SP8</i>) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070964
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- Article
Population-Specific Haplotype Association of the Postsynaptic Density Gene <i>DLG4</i> with Schizophrenia, in Family-Based Association Studies.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0070302
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- Article
Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029499
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- Article
Association of Transcription Factor Gene LMX1B with Autism.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023738
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- Article
Genome-Wide Association Study of Schizophrenia in Japanese Population.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020468
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- Article
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
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- Journal of Psychiatry & Neuroscience, 2018, v. 43, n. 3, p. 194, doi. 10.1503/jpn.170053
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- Article
Research Paper. Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.
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- Journal of Psychiatry & Neuroscience, 2014, v. 39, n. 5, p. 294, doi. 10.1503/jpn.130126
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- Article
Protocadherin α (PCDHA) as a novel susceptibility gene for autism.
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- 2013
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- Journal Article
Protocadherin α (PCDHA) as a novel susceptibility gene for autism.
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- Journal of Psychiatry & Neuroscience, 2013, v. 38, n. 3, p. 192, doi. 10.1503/jpn.120058
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- Article
Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population.
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- Human Genetics, 2012, v. 131, n. 3, p. 443, doi. 10.1007/s00439-011-1089-3
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- Article
Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson’s disease.
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- Human Genetics, 2005, v. 117, n. 6, p. 520, doi. 10.1007/s00439-005-1342-8
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- Article
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01851-y
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- Article
Genetic risks of schizophrenia identified in a matched case–control study.
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- European Archives of Psychiatry & Clinical Neuroscience, 2021, v. 271, n. 4, p. 775, doi. 10.1007/s00406-020-01158-3
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- Article
Variable number of tandem repeat polymorphisms of DRD4: re-evaluation of selection hypothesis and analysis of association with schizophrenia.
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- European Journal of Human Genetics, 2009, v. 17, n. 6, p. 793, doi. 10.1038/ejhg.2008.247
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- Article
DNA Methylation Status of SOX10 Correlates with Its Downregulation and Oligodendrocyte Dysfunction in Schizophrenia.
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- Journal of Neuroscience, 2005, v. 25, n. 22, p. 5376, doi. 10.1523/JNEUROSCI.0766-05.2005
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- Article
A Promoter Haplotype of the Inositol Monophosphatase 2 Gene (IMPA2) at 18p11.2 Confers a Possible Risk for Bipolar Disorder by Enhancing Transcription.
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- Neuropsychopharmacology, 2007, v. 32, n. 8, p. 1727, doi. 10.1038/sj.npp.1301307
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- Article
Brain region-specific altered expression and association of mitochondria-related genes in autism.
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- Molecular Autism, 2012, v. 3, n. 1, p. 12, doi. 10.1186/2040-2392-3-12
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- 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
Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice.
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- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15800
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- Article
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures.
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- Nature Communications, 2014, v. 5, n. 7, p. 4501, doi. 10.1038/ncomms5501
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- Article
Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta-analysis of East Asian case-control samples.
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- Psychiatry & Clinical Neurosciences, 2011, v. 65, n. 3, p. 280, doi. 10.1111/j.1440-1819.2011.02193.x
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- Article
Giant Subependymoma Developed in a Patient with Aniridia: Analyses of PAX6 and Tumor-relevant Genes.
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- Brain Pathology, 2010, v. 20, n. 6, p. 1033, doi. 10.1111/j.1750-3639.2010.00406.x
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- Article
Human myo-inositol monophosphatase 2 rescues the nematode thermotaxis mutant ttx-7 more efficiently than IMPA1: functional and evolutionary considerations of the two mammalian myo-inositol monophosphatase genes.
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- Journal of Neurochemistry, 2013, v. 124, n. 5, p. 685, doi. 10.1111/jnc.12112
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- Article
Analysis of strain-dependent prepulse inhibition points to a role for Shmt1 ( SHMT1) in mice and in schizophrenia.
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- Journal of Neurochemistry, 2010, v. 115, n. 6, p. 1374, doi. 10.1111/j.1471-4159.2010.07039.x
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- Article
LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder.
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- Human Genome Variation, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1038/s41439-020-00117-7
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- Article
Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies.
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- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6495, doi. 10.1093/hmg/ddu369
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- Article
Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression.
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- Cerebral Cortex, 2021, v. 31, n. 1, p. 448, doi. 10.1093/cercor/bhaa236
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- Article
Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val<sup>158</sup>Met Polymorphism on Language Function in Developing Children.
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- Cerebral Cortex, 2017, v. 27, n. 1, p. 104, doi. 10.1093/cercor/bhw371
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- Article
Fabp7 Maps to a Quantitative Trait Locus for a Schizophrenia Endophenotype.
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- PLoS Biology, 2007, v. 5, n. 11, p. e297, doi. 10.1371/journal.pbio.0050297
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- Article
Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation.
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- Human Molecular Genetics, 2006, v. 15, n. 12, p. 1949, doi. 10.1093/hmg/ddl118
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- Article