EDITORIAL
Published on 18 Feb 2025
Editorial: Recent advances in causes, diagnosis, and therapeutics for congenital heart defects
doi 10.3389/fgene.2025.1564492
- 124 views
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Recent Advances in Causes, Diagnosis, and Therapeutics for Congenital Heart Defects
Recent Advances in Causes, Diagnosis, and Therapeutics for Congenital Heart Defects
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Articles
ORIGINAL RESEARCH
Published on 15 Jan 2025
Increased cardiac macrophages in Sorbs2-deficient hearts: revealing a potential role for macrophage in responding to embryonic myocardial abnormalities
doi 10.3389/fgene.2024.1525931
- 480 views
CASE REPORT
Published on 03 Jan 2025
Case Report: Efficacy and safety of recombinant growth hormone therapy in a girl with Loeys–Dietz syndrome
doi 10.3389/fcvm.2024.1377510
- 463 views
CASE REPORT
Published on 24 Dec 2024
Cleft palate, congenital heart disease, and developmental delay involving MEIS2 heterozygous mutations found in the patient with attention deficit hyperactivity disorder: a case report
doi 10.3389/fped.2024.1500152
- 430 views
CASE REPORT
Published on 18 Oct 2024
Case Report: An association of left ventricular outflow tract obstruction with 5p deletions
doi 10.3389/fgene.2024.1451746
- 453 views
ORIGINAL RESEARCH
Published on 09 Oct 2024
Genetic investigation and diagnosis in adults with congenital heart disease with or without structural or neurodevelopmental comorbidity: a retrospective chart review
doi 10.3389/fgene.2024.1412806
- 701 views
ORIGINAL RESEARCH
Published on 11 Sep 2024
Autoantibody profiling of patients with immune checkpoint inhibitor-associated myocarditis: a pilot study
doi 10.3389/fimmu.2024.1423622
- 979 views
- 1 citation
BRIEF RESEARCH REPORT
Published on 09 Sep 2024
De novo and inherited micro-CNV at 16p13.11 in 21 Chinese patients with defective cardiac left-right patterning
doi 10.3389/fgene.2024.1458953
- 734 views
MINI REVIEW
Published on 08 Aug 2024
The role of primary cilia in congenital heart defect-associated neurological impairments
doi 10.3389/fgene.2024.1460228
- 872 views
ORIGINAL RESEARCH
Published on 06 Aug 2024
Genetic testing and human leukocyte antigen in patients with hypertrophic cardiomyopathy and connective tissue diseases
doi 10.3389/fgene.2024.1432670
- 750 views
ORIGINAL RESEARCH
Published on 30 May 2024
Exploring the impact of a KCNH2 missense variant on Long QT syndrome: insights into a novel gender-selective, incomplete penetrance inheritance mode
doi 10.3389/fgene.2024.1409459
- 1,118 views
ORIGINAL RESEARCH
Published on 27 May 2024
Clinical characteristics and follow-up of complex arrhythmias associated with RYR2 gene mutations in children
doi 10.3389/fgene.2024.1405437
- 576 views
Published in
Frontiers in Genetics
- Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore
Impact
- 15kTopic views
- 9,952Article views
- 4,001Article downloads