Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population-Reference-Cited by-同舟云学术

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Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population

Published:2023-10 Issue:5 Volume:16 Page:486-489
ISSN:2574-8300
Container-title:Circulation: Genomic and Precision Medicine
language:en
Short-container-title:Circ: Genomic and Precision Medicine

Author:

Muroke Valtteri¹^ORCID,Jalanko Mikko¹^ORCID,Ruotsalainen Sanni²,Perola Markus³^ORCID,Helle Emmi⁴⁵,Sinisalo Juha¹^ORCID

Affiliation:

1. Department of Cardiology, Helsinki University Hospital (V.M., M.J., J.S.), University of Helsinki, Finland.

2. Institute for Molecular Medicine Finland (FIMM), HiLIFE (S.R.), University of Helsinki, Finland.

3. Finnish Institute for Health and Welfare, Helsinki, Finland (M.P.).

4. Stem Cells and Metabolism Research Program, Faculty of Medicine (E.H.), University of Helsinki, Finland.

5. New Children’s Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Finland (E.H.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference5 articles.

1. Molecular genetics of congenital atrial septal defects

2. Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect

3. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

4. 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

5. Atrial Septal Defect (ASD) associated long non-coding RNA STX18-AS1 maintains time-course of in vitro cardiomyocyte differentiation

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