About the journal
European Journal of Medical Genetics is a journal published by Elsevier BV in France. It is listed in MEDLINE according to the sources read. Declared publication charge: 3,190 USD. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier BV
- ISSN
- 1878-0849 · 1769-7212
- Country
- France
- Access
- Not open access / not declared
- Declared publication charge
- 3,190 USD
- Declared peer-review model
- peer_review
Index listings
- MEDLINE · 2005-01-01
- Indexing
- MEDLINE
- APC
- 3,190 USD
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 131 days received→accepted — computed from PubMed (n=99)
- 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
2937
Last recorded publication year
2026
h-index
85
i10-index
1614
From OpenAlex open data (CC0).
Editorial & policy4
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 99%
- ORCID iDs in current deposits
- 73%
- Deposits licence metadata at Crossref
- ✓
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 101247089
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
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Congenital heart defects research
- Congenital heart defects research
Show all subjects (50)
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Connective tissue disorders research
- Connective tissue disorders research
- RNA modifications and cancer
- Genetic Syndromes and Imprinting
- RNA modifications and cancer
- Genetic Syndromes and Imprinting
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Congenital Ear and Nasal Anomalies
- Congenital Ear and Nasal Anomalies
- Educational Robotics and Engineering
- Educational Robotics and Engineering
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Fetal and Pediatric Neurological Disorders
- Fetal and Pediatric Neurological Disorders
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Human auditory perception and evaluation
- Human auditory perception and evaluation
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- RNA regulation and disease
- RNA regulation and disease
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Renal and related cancers
- Renal and related cancers
- Congenital limb and hand anomalies
- Congenital limb and hand anomalies
- Immunodeficiency and Autoimmune Disorders
- Immunodeficiency and Autoimmune Disorders
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