About the journal
European Journal of Human Genetics is a journal published by Springer Nature in United Kingdom. It is listed in MEDLINE and PUBMED according to the sources read. Declared publication charge: 3,690 EUR. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Springer Nature
- ISSN
- 1018-4813 · 1476-5438
- Country
- United Kingdom
- Access
- Not open access / not declared
- Declared publication charge
- 3,690 EUR
- Declared peer-review model
- peer_review
- Official website
- http://www.nature.com/ejhg/
Index listings
- MEDLINE · 1993-01-01
- PUBMED · 2013-02-27
- Indexing
- MEDLINE · PUBMED
- APC
- 3,690 EUR
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 149 days received→accepted — computed from PubMed (n=96)
- 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
7270
Last recorded publication year
2026
h-index
178
i10-index
4868
From OpenAlex open data (CC0).
Editorial & policy5
- 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
- 95%
- ORCID iDs in current deposits
- 93%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity3
- Alternate titles
- EJHG
- Source type
- journal
- NLM unique ID (PubMed)
- 9302235
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
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
Show all subjects (50)
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- RNA modifications and cancer
- RNA modifications and cancer
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Ethics in Clinical Research
- Ethics in Clinical Research
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Cancer Genomics and Diagnostics
- Cancer Genomics and Diagnostics
- Congenital heart defects research
- Congenital heart defects research
- Forensic and Genetic Research
- Forensic and Genetic Research
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- RNA Research and Splicing
- RNA Research and Splicing
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Connective tissue disorders research
- Connective tissue disorders research
- Genetic Mapping and Diversity in Plants and Animals
- Genetic Mapping and Diversity in Plants and Animals
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- RNA regulation and disease
- RNA regulation and disease
- Autism Spectrum Disorder Research
- Autism Spectrum Disorder Research
- Biomedical Ethics and Regulation
- Biomedical Ethics and Regulation
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