Alpha 2.0
Login Register
» Articles » PMID: 28473349

Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease

Overview
Journal Circ Cardiovasc Genet
Specialties Cardiology & Vascular Diseases
Genetics
Date 2017 May 6
PMID 28473349
Citations 9
Authors
Laura Zahavich
Sarah Bowdin
Seema Mital
Affiliations
Soon will be listed here.
Citing Articles

Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease.

Stanley K, Kalbfleisch K, Moran O, Chaturvedi R, Roifman M, Chen X Eur J Hum Genet. 2024; 32(7):795-803.

PMID: 38778082 PMC: 11219983. DOI: 10.1038/s41431-024-01629-4.

Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease.

Tambi R, Zehra B, Nandkishore S, Sharafat S, Kader F, Nassir N Physiol Genomics. 2023; 55(12):634-646.

PMID: 37811720 PMC: 11550899. DOI: 10.1152/physiolgenomics.00070.2023.

Molecular genetic mechanisms of congenital heart disease.

Choudhury T, Garg V Curr Opin Genet Dev. 2022; 75:101949.

PMID: 35816939 PMC: 9673038. DOI: 10.1016/j.gde.2022.101949.

Inherited and de novo variants extend the etiology of -associated neurodevelopmental disorder.

Hunter J, Massingham L, Manickam K, Bartholomew D, Williamson R, Schwab J Cold Spring Harb Mol Case Stud. 2022; 8(2).

PMID: 35091509 PMC: 8958914. DOI: 10.1101/mcs.a006180.

Genetics of congenital heart disease: a narrative review of recent advances and clinical implications.

Yasuhara J, Garg V Transl Pediatr. 2021; 10(9):2366-2386.

PMID: 34733677 PMC: 8506053. DOI: 10.21037/tp-21-297.