Detalhe da pesquisa
1.
The Family Game to support parents with intellectual disability in managing challenging behaviours: A replication.
J Appl Res Intellect Disabil
; 37(2): e13207, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332447
2.
Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
Mol Psychiatry
; 26(6): 2663-2676, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33414497
3.
Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
J Med Genet
; 56(10): 701-710, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31451536
4.
Clinical correlates of diagnostic certainty in children and youths with Autistic Disorder.
Mol Autism
; 15(1): 15, 2024 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38570867
5.
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Front Psychiatry
; 15: 1369767, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751416
6.
Using rare genetic mutations to revisit structural brain asymmetry.
Nat Commun
; 15(1): 2639, 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531844
7.
Brief Report: Virtual Reality to Raise Awareness About Autism.
J Autism Dev Disord
; 2023 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38079034
8.
Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank.
Biol Psychiatry
; 94(7): 591-600, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36764568
9.
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age.
Adv Genet (Hoboken)
; 4(1): 2200012, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36910592
10.
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
medRxiv
; 2023 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38076919
11.
Phenotypic effects of genetic variants associated with autism.
Nat Med
; 29(7): 1671-1680, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37365347
12.
Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry.
Biol Psychiatry
; 93(1): 45-58, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36372570
13.
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence.
Nat Hum Behav
; 7(6): 1001-1017, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36864136
14.
Using rare genetic mutations to revisit structural brain asymmetry.
bioRxiv
; 2023 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37131672
15.
Subcortical brain alterations in carriers of genomic copy number variants.
medRxiv
; 2023 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36865328
16.
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
Am J Psychiatry
; 180(9): 685-698, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37434504
17.
Using developmental regression to reorganize the clinical importance of autistic atypicalities.
Transl Psychiatry
; 12(1): 498, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36456542
18.
Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.
Transl Psychiatry
; 12(1): 424, 2022 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36192372
19.
Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum Disorder.
Am J Psychiatry
; 179(11): 853-861, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36000218
20.
Bayonet-shaped language development in autism with regression: a retrospective study.
Mol Autism
; 12(1): 35, 2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33985558