About the journal
BMC Medical Genetics is an open-access journal published by BMC in United Kingdom, publishing in english. It is listed in DOAJ and PUBMED according to the sources read. Declared publication charge: 2,890 EUR. Declared review time at DOAJ: 22 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- BMC
- ISSN
- 1471-2350
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Declared publication charge
- 2,890 EUR
- Articles in DOAJ
- 1813
- Declared review time
- 22 weeks
- Declared peer-review model
- open_review
- Official website
- https://bmcmedgenet.biomedcentral.com
Index listings
- DOAJ · 2003-04-08
- PUBMED · 2002-05-16
- Indexing
- DOAJ · PUBMED
- APC
- 2,890 EUR
- Declared review time (DOAJ)
- 22 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Dormant — no works recorded since 2020
- 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.
Articles in DOAJ
1813
Most recent article
6 years ago
Average review time (journal-declared via DOAJ)
22weeks
Works in OpenAlex
2352
Last recorded publication year
2020
h-index
94
i10-index
1882
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2026-03-17
- Added to DOAJ
- 2003-04-08
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPMCPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2021
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 0%
- ORCID iDs in current deposits
- 0%
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity4
- Alternate titles
- Medical genetics
- Continued by
- 1755-8794
- Source type
- journal
- NLM unique ID (PubMed)
- 100968552
Classification4
Subjects (DOAJ)
LCC codes
Subject areas
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Adipokines, Inflammation, and Metabolic Diseases
- Adipokines, Inflammation, and Metabolic Diseases
Show all subjects (50)
- Connective tissue disorders research
- Connective tissue disorders research
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Genetic factors in colorectal cancer
- BRCA gene mutations in cancer
- Genetic factors in colorectal cancer
- Congenital heart defects research
- Congenital heart defects research
- Renin-Angiotensin System Studies
- Renin-Angiotensin System Studies
- Hearing, Cochlea, Tinnitus, Genetics
- Hearing, Cochlea, Tinnitus, Genetics
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Diabetes and associated disorders
- Diabetes and associated disorders
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Asthma and respiratory diseases
- Asthma and respiratory diseases
- Pancreatic function and diabetes
- Pancreatic function and diabetes
- Genetic and Kidney Cyst Diseases
- Genetic and Kidney Cyst Diseases
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Cardiomyopathy and Myosin Studies
- Cardiomyopathy and Myosin Studies
- Glycogen Storage Diseases and Myoclonus
- Immunodeficiency and Autoimmune Disorders
- Immunodeficiency and Autoimmune Disorders
- Glycogen Storage Diseases and Myoclonus
- Hemoglobinopathies and Related Disorders
- Hemoglobinopathies and Related Disorders
Keywords (DOAJ)
- medical genetics
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