SCIESCOPUS
MOLECULAR SYNDROMOLOGY
Karger, Switzerland
MOLECULAR SYNDROMOLOGY is an academic journal published by Karger (Switzerland). Identifiers: ISSN 1661-8769, eISSN 1661-8777. Indexed in SCIE, SCOPUS. Metrics: CiteScore 1.8, SJR 0.437, SNIP 0.70. Subject areas: GENETICS & HEREDITY. tlooto lists 1,082 papers from this journal.
CiteScore
1.80
Scopus citation metric
SJR
0.437
SCImago rank
SNIP
0.70
Source normalized impact
Percentage rank
-
JIF percentile rank
Journal profile
- ISSN
- 1661-8769
- eISSN
- 1661-8777
- Abbreviation
- -
- Publisher
- Karger
- Country
- Switzerland
Web of Science categories
SCIEGENETICS & HEREDITY
Scopus ASJC categories
1311 Genetics2716 Genetics (clinical)
Keywords
Genetics & Heredity
Papers in this journal
Recent papers
- Diets-Jongmans Syndrome due to a Novel KDM3B Variant: The First Molecularly Confirmed Case from Turkey.
2026
- Whole Genome Sequence Identifies the Second Allele: An Intronic Variant in RYR1 Contributes to Early-Onset Fetal Akinesia Deformation Sequence
2026
- Complimentary Episignature Testing for Variant Reclassification: Case Reports with Variant Classification Guideline Consideration
2026
- Cytomolecular Analysis of a Ring X Chromosome in a Patient with Turner Syndrome: A Case Report.
2026
- Severe Thrombocytopenia and Facial Asymmetry in a Mexican Patient with Noonan Syndrome-Like Disorder with Loose Anagen Hair: Clinical Observations and Diagnostic Considerations
2026
Most cited papers
- The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)
2011 · 445 citations
- Noonan Syndrome: Clinical Aspects and Molecular Pathogenesis
2010 · 236 citations
- Bloom's Syndrome: Clinical Spectrum, Molecular Pathogenesis, and Cancer Predisposition
2016 · 232 citations
- Osteogenesis Imperfecta: A Review with Clinical Examples
2011 · 215 citations
- Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment
2016 · 208 citations