Key Metrics
CiteScore 

2.1
Impact Factor 

< 5
SJR 

Q4Genetics

SNIP 

0.69
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Topics Covered on Molecular Syndromology
Molecular Syndromology Journal Specifications
| Overview | |
| Publisher | KARGER |
| Language | English |
| Frequency | Bi-monthly |
| General Details | |
| Language | English |
| Frequency | Bi-monthly |
| Publication Start Year | 2010 |
| Publisher URL | Visit website |
| Website URL | Visit website |
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Recently Published Papers in Molecular Syndromology
CHOPS Syndrome: A Rare Malformation Syndrome with De Novo AFF4 Gene Variant
- 30 Mar 2026
- Molecular Syndromology
Role of hyperlipidemia-related PCSK9, APOE, and LRP8 variants in restenosis after stent implantation in male patients: a case-control study
- 27 Mar 2026
- Molecular Syndromology
Erratum
- 18 Mar 2026
- Molecular Syndromology
An Atypical Neurosensory-Predominant Presentation Associated with a Homozygous NDUFS3 Variant: A Diagnostic Challenge Involving Retinal and Hearing Phenotypes
- 11 Mar 2026
- Molecular Syndromology
A Systematic Bioinformatic Analysis of the miRNA Pathway in Inborn Errors of Amino Acid Metabolism Disorders.
- 11 Mar 2026
- Molecular syndromology
Cytomolecular Analysis of a Ring X Chromosome in a Patient with Turner Syndrome: A Case Report
- 3 Mar 2026
- Molecular Syndromology
CHOPS Syndrome: A Rare Malformation Syndrome with De Novo AFF4 Gene Variant
- 30 Mar 2026
- Molecular Syndromology
Role of hyperlipidemia-related PCSK9, APOE, and LRP8 variants in restenosis after stent implantation in male patients: a case-control study
- 27 Mar 2026
- Molecular Syndromology
Erratum
- 18 Mar 2026
- Molecular Syndromology
An Atypical Neurosensory-Predominant Presentation Associated with a Homozygous NDUFS3 Variant: A Diagnostic Challenge Involving Retinal and Hearing Phenotypes
- 11 Mar 2026
- Molecular Syndromology
A Systematic Bioinformatic Analysis of the miRNA Pathway in Inborn Errors of Amino Acid Metabolism Disorders.
- 11 Mar 2026
- Molecular syndromology
Cytomolecular Analysis of a Ring X Chromosome in a Patient with Turner Syndrome: A Case Report
- 3 Mar 2026
- Molecular Syndromology