About the journal
Human Genome Variation is an open-access journal published by Nature Publishing Group in United Kingdom, publishing in english. It is listed in DOAJ and PUBMED according to the sources read. Declared publication charge: 2,790 EUR. Declared review time at DOAJ: 13 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Nature Publishing Group
- ISSN
- 2054-345X
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Declared publication charge
- 2,790 EUR
- Articles in DOAJ
- 222
- Declared review time
- 13 weeks
- Declared peer-review model
- peer_review
- Official website
- https://www.nature.com/hgv/
Index listings
- DOAJ · 2015-10-22
- PUBMED · 2020-11-10
- Indexing
- DOAJ · PUBMED
- APC
- 2,790 EUR
- Declared review time (DOAJ)
- 13 weeks — journal-declared only (not measured)
- 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.
Articles in DOAJ
222
Most recent article
last month
Average review time (journal-declared via DOAJ)
13weeks
Works in OpenAlex
534
Last recorded publication year
2026
h-index
32
i10-index
180
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2026-03-17
- Added to DOAJ
- 2015-10-22
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- PMC
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 95%
- ORCID iDs in current deposits
- 93%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity3
- Source type
- journal
- NLM unique ID (PubMed)
- 101652445
- Society affiliations
- Zhejiang UniversityZhejiang University Press
Classification4
Subjects (DOAJ)
LCC codes
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Connective tissue disorders research
Show all subjects (50)
- RNA regulation and disease
- RNA modifications and cancer
- RNA regulation and disease
- RNA modifications and cancer
- Congenital heart defects research
- Congenital heart defects research
- Cell Adhesion Molecules Research
- Cell Adhesion Molecules Research
- RNA Research and Splicing
- RNA Research and Splicing
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Mitochondrial Function and Pathology
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Mitochondrial Function and Pathology
- RNA and protein synthesis mechanisms
- Genetic and Kidney Cyst Diseases
- Genetic and Kidney Cyst Diseases
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Retinal Development and Disorders
- Retinal Development and Disorders
- Prenatal Screening and Diagnostics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Prenatal Screening and Diagnostics
- Neurogenetic and Muscular Disorders Research
- Ubiquitin and proteasome pathways
- Neurogenetic and Muscular Disorders Research
- Ubiquitin and proteasome pathways
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Cancer Genomics and Diagnostics
- Neurological diseases and metabolism
- Cancer Genomics and Diagnostics
- Neurological diseases and metabolism
Keywords (DOAJ)
- genomevariation
- gene mutation
- rare diseases
- disease-associated genes
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