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
- 236 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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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
- 233 views
ORIGINAL RESEARCH
Accepted on 19 Dec 2024
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
- 101 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
- 376 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
- 629 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
- 843 views
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
- 599 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
- 756 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
- 688 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
- 1,052 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
- 535 views
ORIGINAL RESEARCH
Published on 20 May 2024
Keratin 19 (Krt19) is a novel marker gene for epicardial cells
doi 10.3389/fgene.2024.1385867
- 1,149 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
- 12kTopic views
- 8,193Article views
- 3,180Article downloads