
Academic Journal
Q2European Journal of Medical Genetics
About European Journal of Medical Genetics
About European Journal of Medical Genetics
European Journal of Medical Genetics is a peer-reviewed scholarly journal published by Elsevier Masson s.r.l. (France). It focuses on Q2. Publication coverage spans 2005-2026.
Key indicators: ISSN 1878-0849, 1769-7212; H-index 71.
Understanding This Journal's Metrics
Journal metrics help researchers assess fit, but they must be interpreted in context:
- H-index (71): Strong citation impact — 71 articles cited at least 71 times each, reflecting solid influence.
Publishing in European Journal of Medical Genetics
An established venue in its field. The journal welcomes solid, well-executed research. Ensure your manuscript fits the stated scope and follows author guidelines carefully.
- Scope fit: Confirm your research aligns with Q2. Off-scope manuscripts are typically desk-rejected quickly.
- Author guidelines: Follow formatting, reference style, and article-type requirements exactly — non-compliant manuscripts may be returned without review.
- Submission: Submit via the official journal website.
Is This Journal Right for Your Paper?
- Audience match: Will the journal's readers cite and build on your findings?
- Timeline: Higher-tier journals mean longer review and higher rejection risk. Balance prestige against your schedule.
- Indexing: Confirm indexing in Web of Science, Scopus, and PubMed (if biomedical) meets your institutional requirements.
- Open access needs: Check funder mandates and whether the journal offers compliant OA options.
Frequently Asked Questions
What is the ISSN of European Journal of Medical Genetics?
1878-0849, 1769-7212.
Who publishes European Journal of Medical Genetics?
Elsevier Masson s.r.l..
What are European Journal of Medical Genetics's metrics?
H-index 71.
Where do I submit to European Journal of Medical Genetics?
Via the official website.
Is European Journal of Medical Genetics peer-reviewed?
Yes — it is a peer-reviewed scholarly journal indexed in major academic databases.
Source-backed journal facts
Topics in published research
Genomic variations and chromosomal abnormalities; Genetics and Neurodevelopmental Disorders; Genomics and Rare Diseases; Congenital heart defects research; Prenatal Screening and Diagnostics; Connective tissue disorders research.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Reported open-access list prices
3,330.00 USD; 3,120.00 EUR; 2,670.00 GBP; 413,020.00 JPY
APC list prices reported by OpenAlex, which obtains this information from DOAJ. Confirm current charges, taxes, waivers and eligibility with the publisher; this is not a fee quotation.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
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Version History
October 9, 2026 at 10:14 pm
October 2, 2026