Detalhe da pesquisa
1.
Rare copy number variation in posttraumatic stress disorder.
Mol Psychiatry
; 27(12): 5062-5069, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36131047
2.
HOTAIR lncRNA promotes epithelial-mesenchymal transition by redistributing LSD1 at regulatory chromatin regions.
EMBO Rep
; 22(7): e50193, 2021 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33960111
3.
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
4.
A Dual Model for Prioritizing Cancer Mutations in the Non-coding Genome Based on Germline and Somatic Events.
PLoS Comput Biol
; 11(11): e1004583, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26588488
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.
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
8.
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
9.
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
10.
Using rare genetic mutations to revisit structural brain asymmetry.
bioRxiv
; 2023 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37131672
11.
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
12.
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
13.
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.
JAMA Psychiatry
; 79(7): 699-709, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35544191
14.
Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.
Am J Psychiatry
; 178(1): 87-98, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32911998
15.
Reference-free transcriptome exploration reveals novel RNAs for prostate cancer diagnosis.
Life Sci Alliance
; 2(6)2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31732695
16.
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry.
Nat Commun
; 15(1): 3098, 2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38600109