Detalhe da pesquisa
1.
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Circ Res
; 124(4): 553-563, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30582441
2.
Predicting congenital renal tract malformation genes using machine learning.
Sci Rep
; 13(1): 13204, 2023 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37580336
3.
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability.
Cell Rep Med
; 3(2): 100501, 2022 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35243414
4.
Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.
Circ Genom Precis Med
; 12(10): 442-451, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31613678
5.
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Nat Commun
; 10(1): 1951, 2019 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31028252
6.
Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage.
F1000Res
; 7: 1617, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30473780
7.
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.
J Clin Invest
; 126(8): 3080-8, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27400125
8.
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Nat Commun
; 6: 8085, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26333996