About the journal
Human Mutation is a journal published by Wiley in United States. It is listed in MEDLINE according to the sources read. Declared publication charge: 2,300 USD. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Wiley
- ISSN
- 1059-7794 · 1098-1004
- Country
- United States
- Access
- Not open access / not declared
- Declared publication charge
- 2,300 USD
- Declared peer-review model
- peer_review
- Official website
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004
Index listings
- MEDLINE · 1992-01-01
- Indexing
- MEDLINE
- APC
- 2,300 USD
- Declared review time (DOAJ)
- —
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
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
8084
Last recorded publication year
2026
h-index
218
i10-index
5226
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-09-21
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2027
- Level 2 — top tier (~20% of the field's channels)
- Open references deposited at Crossref
- 98%
- ORCID iDs in current deposits
- 98%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity3
- Source type
- journal
- NLM unique ID (PubMed)
- 9215429
- Society affiliations
- HUMAN GENOME VARIATION SOCIETY
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
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Cancer Genomics and Diagnostics
- Cancer Genomics and Diagnostics
Show all subjects (50)
- RNA modifications and cancer
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA and protein synthesis mechanisms
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- RNA Research and Splicing
- RNA Research and Splicing
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- DNA Repair Mechanisms
- DNA Repair Mechanisms
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Connective tissue disorders research
- Connective tissue disorders research
- Cystic Fibrosis Research Advances
- CRISPR and Genetic Engineering
- CRISPR and Genetic Engineering
- Cystic Fibrosis Research Advances
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- RNA regulation and disease
- RNA regulation and disease
- Cellular transport and secretion
- Cellular transport and secretion
- Biochemical and Molecular Research
- Biochemical and Molecular Research
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Carbohydrate Chemistry and Synthesis
- Carbohydrate Chemistry and Synthesis
- Retinal Development and Disorders
- Genomics and Phylogenetic Studies
- Genomics and Phylogenetic Studies
- Retinal Development and Disorders
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
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