Detalhe da pesquisa
1.
Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population.
Int Rev Psychiatry
; 34(2): 154-167, 2022 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35699097
2.
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization.
Psychiatry Clin Neurosci
; 76(12): 667-673, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36073611
3.
Clinical manifestations of schizophrenia in four patients with variants in voltage-gated calcium channel-encoding genes: a case series.
Psychiatry Clin Neurosci
; 77(1): 57-59, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36271890
4.
Case report of a female with bipolar disorder and MBD5 deletion.
Psychiatry Clin Neurosci
; 76(4): 127-128, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35088487
5.
Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders.
Transl Psychiatry
; 14(1): 236, 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38830862
6.
Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study.
Neuropsychopharmacol Rep
; 44(1): 42-50, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37915257
7.
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder.
Biol Psychiatry
; 92(5): 362-374, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35667888