Detalhe da pesquisa
1.
Complete nanopore repeat sequencing of SCA27B (GAA-FGF14 ataxia) in Japanese.
J Neurol Neurosurg Psychiatry
; 2024 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38816190
2.
Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation.
J Hum Genet
; 68(12): 875-878, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37592133
3.
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
4.
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
5.
Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.
Brain
; 144(4): 1103-1117, 2021 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33791773
6.
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
7.
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
8.
Detecting a long insertion variant in SAMD12 by SMRT sequencing: implications of long-read whole-genome sequencing for repeat expansion diseases.
J Hum Genet
; 64(3): 191-197, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30559482
9.
A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.
Psychiatry Clin Neurosci
; 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38646907
10.
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
11.
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
12.
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
13.
Erratum to: Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.
Brain
; 144(8): e67, 2021 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34037746
14.
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
15.
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
16.
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
17.
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
18.
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
19.
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
20.
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