Detalhe da pesquisa
1.
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin ß-cluster genes in the developing brain.
Mol Psychiatry
; 26(12): 7550-7559, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34262135
2.
Differential genetic associations and expression of PAPST1/SLC35B2 in bipolar disorder and schizophrenia.
J Neural Transm (Vienna)
; 129(7): 913-924, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501530
3.
Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression.
Cereb Cortex
; 31(1): 448-462, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32924060
4.
Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation.
Proc Natl Acad Sci U S A
; 116(14): 7083-7088, 2019 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30890645
5.
Genetic risks of schizophrenia identified in a matched case-control study.
Eur Arch Psychiatry Clin Neurosci
; 271(4): 775-781, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32623490
6.
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
J Psychiatry Neurosci
; 43(3): 194-200, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29688875
7.
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
J Psychiatry Neurosci
; 43(2): 170053, 2018 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29402374
8.
Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val158Met Polymorphism on Language Function in Developing Children.
Cereb Cortex
; 27(1): 104-116, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27909011
9.
Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus.
Am J Med Genet B Neuropsychiatr Genet
; 174(8): 798-807, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28990294
10.
Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies.
Hum Mol Genet
; 23(24): 6495-511, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027319
11.
Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis.
J Biol Chem
; 289(15): 10785-10796, 2014 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24554717
12.
Association study of H2AFZ with schizophrenia in a Japanese case-control sample.
J Neural Transm (Vienna)
; 122(6): 915-23, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25392085
13.
Erratum to: Association study of H2AFZ with schizophrenia in a Japanese case-control sample.
J Neural Transm (Vienna)
; 122(11): 1619-20, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26259709
14.
Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia.
J Neural Transm (Vienna)
; 122(3): 477-85, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25005592
15.
Association of decreased prefrontal hemodynamic response during a verbal fluency task with EGR3 gene polymorphism in patients with schizophrenia and in healthy individuals.
Neuroimage
; 85 Pt 1: 527-34, 2014 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23962955
16.
Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population.
J Hum Genet
; 59(1): 54-6, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24196380
17.
Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.
J Psychiatry Neurosci
; 39(5): 294-303, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24866414
18.
Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.
Am J Med Genet B Neuropsychiatr Genet
; 165B(5): 421-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24888570
19.
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.
J Neurochem
; 124(5): 685-94, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23205734
20.
Protocadherin α (PCDHA) as a novel susceptibility gene for autism.
J Psychiatry Neurosci
; 38(3): 192-8, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23031252