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Molecular Syndromology : Impact Factor & More

eISSN: 1661-8777pISSN: 1661-8769

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
LanguageEnglish
FrequencyBi-monthly
Publication Start Year2010
Publisher URLVisit website
Website URLVisit 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

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