Detalhe da pesquisa
1.
Risk Factors and Outcomes Associated with Gaps in Care in Children with Congenital Heart Disease.
Pediatr Cardiol
; 45(5): 976-985, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38485760
2.
Underrepresentation of Diverse Ancestries Drives Uncertainty in Genetic Variants Found in Cardiomyopathy-Associated Genes.
JACC Adv
; 3(2)2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38464909
3.
DiscoVari: A Web-Based Precision Medicine Tool for Predicting Variant Pathogenicity in Cardiomyopathy- and Channelopathy-Associated Genes.
Circ Genom Precis Med
; 16(4): 317-327, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37409478
4.
PRDM16 Deletion Is Associated With Sex-dependent Cardiomyopathy and Cardiac Mortality: A Translational, Multi-Institutional Cohort Study.
Circ Genom Precis Med
; 16(4): 390-400, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37395136
5.
Pathogenicity Assignment of Variants in Genes Associated With Cardiac Channelopathies Evolve Toward Diagnostic Uncertainty.
Circ Genom Precis Med
; 15(3): e003491, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35543671
6.
GENESIS: Gene-Specific Machine Learning Models for Variants of Uncertain Significance Found in Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome-Associated Genes.
Circ Arrhythm Electrophysiol
; 15(4): e010326, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35357185
7.
Risk Factors for Sudden Infant Death in North Carolina.
Front Pediatr
; 9: 770803, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34956982
8.
ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.
J Am Heart Assoc
; 10(17): e019887, 2021 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459253