Detalhe da pesquisa
1.
Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function.
Hum Mol Genet
; 31(18): 3095-3106, 2022 09 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35531971
2.
Genomic findings in schizophrenia and their implications.
Mol Psychiatry
; 28(9): 3638-3647, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37853064
3.
Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia.
Mol Psychiatry
; 28(5): 2081-2087, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36914811
4.
The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis.
Int J Mol Sci
; 25(2)2024 Jan 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38256020
5.
A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia.
Hum Mol Genet
; 29(1): 159-167, 2020 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31691811
6.
Genetic association of FMRP targets with psychiatric disorders.
Mol Psychiatry
; 26(7): 2977-2990, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33077856
7.
Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank.
Br J Psychiatry
; 218(2): 104-111, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32792019
8.
Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank.
Mol Psychiatry
; 25(4): 854-862, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30679740
9.
Clinical indicators of treatment-resistant psychosis.
Br J Psychiatry
; 216(5): 259-266, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31155017
10.
De novo mutations in schizophrenia implicate synaptic networks.
Nature
; 506(7487): 179-84, 2014 Feb 13.
Artigo
Inglês
| MEDLINE | ID: mdl-24463507
11.
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
J Med Genet
; 56(3): 131-138, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30343275
12.
Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
Br J Psychiatry
; 214(5): 297-304, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30767844
13.
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
PLoS Genet
; 12(5): e1005993, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27153221
14.
Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.
BMC Genomics
; 19(1): 867, 2018 Dec 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30509170
15.
De novo CNVs in bipolar affective disorder and schizophrenia.
Hum Mol Genet
; 23(24): 6677-83, 2014 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25055870
16.
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Hum Mol Genet
; 23(6): 1669-76, 2014 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24163246
17.
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
Hum Mol Genet
; 23(12): 3316-26, 2014 Jun 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24474471
18.
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
BMC Med Genet
; 17(1): 34, 2016 04 26.
Artigo
Inglês
| MEDLINE | ID: mdl-27113213
19.
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
Hum Mol Genet
; 22(4): 816-24, 2013 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23148125
20.
Analysis of copy number variations at 15 schizophrenia-associated loci.
Br J Psychiatry
; 204(2): 108-14, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24311552