About the journal
Journal of Medical Genetics is a journal published by BMJ in United Kingdom. It is listed in MEDLINE and PUBMED according to the sources read. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- BMJ
- ISSN
- 0022-2593 · 1468-6244
- Country
- United Kingdom
- Access
- Not open access / not declared
- Official website
- http://jmg.bmj.com/
Index listings
- MEDLINE · 1965-01-01
- PUBMED · 2017-08-09
- Indexing
- MEDLINE · PUBMED
- APC
- —
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 107 days received→accepted — computed from PubMed (n=98)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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Methodology signals (dated facts from their sources)
Details of the evaluation under the published methodology are shown to signed-in users (free).
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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
11292
Last recorded publication year
2026
h-index
247
i10-index
7558
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- Portico
- Norwegian register (HK-dir)— 2027
- Level 2 — top tier (~20% of the field's channels)
- Open references deposited at Crossref
- 99%
- ORCID iDs in current deposits
- 99%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity3
- Alternate titles
- EJMGJMG onlineJMG
- Source type
- journal
- NLM unique ID (PubMed)
- 2985087R
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
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
Show all subjects (50)
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Connective tissue disorders research
- Genetic Neurodegenerative Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Neurodegenerative Diseases
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Congenital heart defects research
- Congenital heart defects research
- Congenital limb and hand anomalies
- Congenital limb and hand anomalies
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Sexual Differentiation and Disorders
- Sexual Differentiation and Disorders
- RNA modifications and cancer
- RNA modifications and cancer
- Muscle Physiology and Disorders
- Muscle Physiology and Disorders
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Congenital Anomalies and Fetal Surgery
- Nutrition, Genetics, and Disease
- Congenital Anomalies and Fetal Surgery
- Cystic Fibrosis Research Advances
- Cystic Fibrosis Research Advances
- Nutrition, Genetics, and Disease
- Genetic and Kidney Cyst Diseases
- Genetic and Kidney Cyst Diseases
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