Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
Overview
Overview
Journal
Circ Genom Precis Med
Specialties
Cardiology & Vascular Diseases
Genetics
Genetics
Date
2023 Aug 14
PMID
37577800
Authors
Affiliations
Affiliations
Soon will be listed here.
References
1.
Zhao L, Li B, Dian K, Ying B, Lu X, Hu X
. Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis. PLoS One. 2015; 10(4):e0123959.
PMC: 4395394.
DOI: 10.1371/journal.pone.0123959.
View
2.
Posch M, Perrot A, Berger F, Ozcelik C
. Molecular genetics of congenital atrial septal defects. Clin Res Cardiol. 2009; 99(3):137-47.
PMC: 2830584.
DOI: 10.1007/s00392-009-0095-0.
View
3.
Liu Y, Choy M, Abraham S, Tenin G, Black G, Keavney B
. Atrial Septal Defect (ASD) associated long non-coding RNA maintains time-course of cardiomyocyte differentiation. Genes Dis. 2023; 10(4):1150-1153.
PMC: 10311013.
DOI: 10.1016/j.gendis.2022.07.010.
View
4.
Caputo S, Capozzi G, Russo M, Esposito T, Martina L, Cardaropoli D
. Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect. Eur Heart J. 2005; 26(20):2179-84.
DOI: 10.1093/eurheartj/ehi378.
View
5.
Cordell H, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C
. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Nat Genet. 2013; 45(7):822-4.
PMC: 3793630.
DOI: 10.1038/ng.2637.
View