About the journal
Molecular Syndromology is a journal published by Karger Publishers in Switzerland. It is listed in PUBMED according to the sources read. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Karger Publishers
- ISSN
- 1661-8769 · 1661-8777
- Country
- Switzerland
- Access
- Not open access / not declared
- Official website
- http://content.karger.com/ProdukteDB/produkte.asp?ISSN=1661-8777
Index listings
- PUBMED · 2025-03-25
- Indexing
- PUBMED
- APC
- —
- Declared review time (DOAJ)
- —
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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Methodology signals (dated facts from their sources)
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Works in OpenAlex
1063
Last recorded publication year
2026
h-index
53
i10-index
294
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- Portico
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 79%
- ORCID iDs in current deposits
- 46%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 101525192
Classification(no data)
No data available to the platform for this group
No platform data for: Classification — absence is not a judgment about the journal.
Subject areas
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
Show all subjects (50)
- Congenital heart defects research
- Congenital heart defects research
- Human auditory perception and evaluation
- Human auditory perception and evaluation
- Physics and Engineering Research Articles
- Physics and Engineering Research Articles
- Connective tissue disorders research
- Connective tissue disorders research
- RNA modifications and cancer
- RNA modifications and cancer
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Congenital Ear and Nasal Anomalies
- Congenital Ear and Nasal Anomalies
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
- Craniofacial Disorders and Treatments
- Craniofacial Disorders and Treatments
- Genetic and Kidney Cyst Diseases
- Genetic and Kidney Cyst Diseases
- RNA regulation and disease
- RNA regulation and disease
- Autism Spectrum Disorder Research
- Autism Spectrum Disorder Research
- Fetal and Pediatric Neurological Disorders
- Fetal and Pediatric Neurological Disorders
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Protein Tyrosine Phosphatases
- Protein Tyrosine Phosphatases
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ