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About the journal
Human Molecular Genetics is a journal published by Oxford University Press in United Kingdom. It is listed in MEDLINE and PUBMED according to the sources read. Declared publication charge: 4,181 USD. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Oxford University Press
- ISSN
- 0964-6906 · 1460-2083
- Country
- United Kingdom
- Access
- Not open access / not declared
- Declared publication charge
- 4,181 USD
- Official website
- http://hmg.oxfordjournals.org/
Index listings
- MEDLINE · 1992-01-01
- PUBMED · 2000-01-01
- Indexing
- MEDLINE · PUBMED
- APC
- 4,181 USD
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 133 days received→accepted — computed from PubMed (n=95)
- 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
14271
Last recorded publication year
2026
Reported by OpenAlex in 1 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core
h-index
357
i10-index
11554
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2027
- Level 2 — top tier (~20% of the field's channels)
- Open references deposited at Crossref
- 90%
- ORCID iDs in current deposits
- 76%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9208958
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
- Genetic Associations and Epidemiology
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Genetics and Neurodevelopmental Disorders
- Genetic Neurodegenerative Diseases
- Genomics and Rare Diseases
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
Show all subjects (75)
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- RNA modifications and cancer
- RNA modifications and cancer
- Muscle Physiology and Disorders
- RNA Research and Splicing
- RNA Research and Splicing
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Hereditary Neurological Disorders
- Amyotrophic Lateral Sclerosis Research
- Muscle Physiology and Disorders
- Muscle Physiology and Disorders
- Genomic variations and chromosomal abnormalities
- Mitochondrial Function and Pathology
- Genomics and Chromatin Dynamics
- Metabolism and Genetic Disorders
- Retinal Development and Disorders
- Lysosomal Storage Disorders Research
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Alzheimer's disease research and treatments
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Epigenetics and DNA Methylation
- DNA Repair Mechanisms
- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
- Genetic factors in colorectal cancer
- Neurogenetic and Muscular Disorders Research
- RNA Research and Splicing
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Diverse Scientific and Economic Studies
- Diverse Scientific and Economic Studies
- Retinal Development and Disorders
- Retinal Development and Disorders
- Cellular transport and secretion
- Cellular transport and secretion
- RNA regulation and disease
- RNA regulation and disease
- Parkinson's Disease Mechanisms and Treatments
- Glycogen Storage Diseases and Myoclonus
- Human auditory perception and evaluation
- Human auditory perception and evaluation
- Parkinson's Disease Mechanisms and Treatments
- Parkinson's Disease Mechanisms and Treatments
- Genetic Mapping and Diversity in Plants and Animals
- RNA and protein synthesis mechanisms
- RNA and protein synthesis mechanisms
- Educational Robotics and Engineering
- Educational Robotics and Engineering
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- DNA Repair Mechanisms
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- Genetic Syndromes and Imprinting
- Developmental Biology and Gene Regulation
- Amyotrophic Lateral Sclerosis Research
- Amyotrophic Lateral Sclerosis Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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The journal's record in other sources:Web of Science MJLDOAJ