Detalhe da pesquisa
1.
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome.
Hum Brain Mapp
; 45(1): e26553, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38224541
2.
Genomic findings in schizophrenia and their implications.
Mol Psychiatry
; 28(9): 3638-3647, 2023 Sep.
Artigo
em 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
em Inglês
| MEDLINE | ID: mdl-36914811
4.
Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study.
Mol Psychiatry
; 28(5): 1995-2006, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33981004
5.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
; 28(5): 2071-2080, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869225
6.
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
Brain
; 146(4): 1686-1696, 2023 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36059063
7.
Psychopathology in mothers of children with pathogenic Copy Number Variants.
J Med Genet
; 60(7): 706-711, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36446581
8.
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.
Neurobiol Dis
; 180: 106082, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36925053
9.
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Am J Hum Genet
; 106(1): 26-40, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31870554
10.
Psychopathology in adults with copy number variants.
Psychol Med
; 53(7): 3142-3149, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35144709
11.
Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome.
Mol Psychiatry
; 27(2): 819-830, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34112971
12.
The Duffy-null genotype and risk of infection.
Hum Mol Genet
; 29(20): 3341-3349, 2020 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32959868
13.
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
em Inglês
| MEDLINE | ID: mdl-31691811
14.
Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs.
Psychol Med
; 52(3): 574-586, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32643597
15.
Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence.
Psychol Med
; 52(1): 132-139, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32515721
16.
Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder.
Brain Behav Immun
; 99: 70-82, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34543680
17.
Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders.
Mol Psychiatry
; 26(6): 2082-2088, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32366953
18.
Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c.
Mol Psychiatry
; 26(6): 1748-1760, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33597718
19.
Genetic association of FMRP targets with psychiatric disorders.
Mol Psychiatry
; 26(7): 2977-2990, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33077856
20.
Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.
Mol Psychiatry
; 26(6): 2070-2081, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32398722