Detalhe da pesquisa
1.
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Am J Hum Genet
; 110(9): 1454-1469, 2023 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595579
2.
Functional annotation of rare structural variation in the human brain.
Nat Commun
; 11(1): 2990, 2020 06 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32533064
3.
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
Science
; 362(6420)2018 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30545852
4.
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
Nat Genet
; 50(5): 727-736, 2018 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29700473
5.
Potential involvement of the interleukin-18 pathway in schizophrenia.
J Psychiatr Res
; 74: 10-6, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26736035
6.
Family-based tests applied to extended pedigrees identify rare variants related to hypertension.
BMC Proc
; 8(Suppl 1): S31, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25519318
7.
New insights into the genetic mechanism of IQ in autism spectrum disorders.
Front Genet
; 4: 195, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24151499