BMC Medical Genomics

BMC

Journal websitePeer review: Open review
Evaluation status available after sign-in

About the journal

BMC Medical Genomics is an open-access journal published by BMC in United Kingdom, publishing in english. It is listed in DOAJ and MEDLINE 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
1755-8794
Country
United Kingdom
Languages
english
Access
Open access
Declared publication charge
2,890 EUR
Articles in DOAJ
2502
Declared review time
22 weeks
Declared peer-review model
open_review

Index listings

  • DOAJ · 2008-02-08
  • MEDLINE · 2008-01-01
  • PUBMED · 2008-01-31
Indexing
DOAJ · MEDLINE · PUBMED
APC
2,890 EUR
Declared review time (DOAJ)
22 weeks
Actual review time (measured)
143 days received→accepted — computed from PubMed (n=99)
Activity (OpenAlex)
Active — latest works 2026
PublishLens list status
Shown after sign-in
Counts for promotion at your university?
Choose your university and rank below ↓

Methodology signals (dated facts from their sources)

Details of the evaluation under the published methodology are shown to signed-in users (free).

Create a free account to view the evaluation

Journal profile

Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.

Articles in DOAJ

2502

Most recent article

last month

Average review time (journal-declared via DOAJ)

22weeks

Works in OpenAlex

2914

Last recorded publication year

2026

Reported by OpenAlex in 2 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core

h-index

104

i10-index

1434

From OpenAlex open data (CC0).

Editorial & policy13
Last DOAJ review date
2026-03-17
Added to DOAJ
2008-02-08
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)— 2026
Level 1 — approved scholarly channel
Open references deposited at Crossref
90%
ORCID iDs in current deposits
12%
Enrolled in Crossref Similarity Check
✓
Deposits licence metadata at Crossref
✓
APC waiver policy
View policy
Peer-review policy
View policy
Identity & continuity3
Alternate titles
Medical genomics
Source type
journal
NLM unique ID (PubMed)
101319628
Classification4

Subjects (DOAJ)

Medicine: Internal medicineScience: Biology (General): Genetics

LCC codes

RC31-1245QH426-470

Subject areas

  • Genomics and Rare Diseases
  • Genomics and Rare Diseases
  • Ferroptosis and cancer prognosis
  • Ferroptosis and cancer prognosis
  • Genetic Associations and Epidemiology
  • Genetic Associations and Epidemiology
  • Bioinformatics and Genomic Networks
  • Bioinformatics and Genomic Networks
Show all subjects (50)
  • Genomic variations and chromosomal abnormalities
  • Genomic variations and chromosomal abnormalities
  • Gene expression and cancer classification
  • Gene expression and cancer classification
  • Cancer Genomics and Diagnostics
  • Cancer Genomics and Diagnostics
  • Cancer-related molecular mechanisms research
  • Cancer-related molecular mechanisms research
  • MicroRNA in disease regulation
  • MicroRNA in disease regulation
  • Epigenetics and DNA Methylation
  • Epigenetics and DNA Methylation
  • BRCA gene mutations in cancer
  • BRCA gene mutations in cancer
  • Prenatal Screening and Diagnostics
  • Prenatal Screening and Diagnostics
  • Single-cell and spatial transcriptomics
  • Single-cell and spatial transcriptomics
  • Genetic factors in colorectal cancer
  • Genetic factors in colorectal cancer
  • Connective tissue disorders research
  • Connective tissue disorders research
  • Cancer Immunotherapy and Biomarkers
  • Cancer Immunotherapy and Biomarkers
  • RNA modifications and cancer
  • RNA modifications and cancer
  • Congenital heart defects research
  • Congenital heart defects research
  • Genetic Syndromes and Imprinting
  • Acute Myeloid Leukemia Research
  • Acute Myeloid Leukemia Research
  • Genetic Syndromes and Imprinting
  • Breast Cancer Treatment Studies
  • Breast Cancer Treatment Studies
  • RNA Research and Splicing
  • RNA Research and Splicing
  • Machine Learning in Bioinformatics
  • Circular RNAs in diseases
  • Hearing, Cochlea, Tinnitus, Genetics
  • Machine Learning in Bioinformatics
  • Circular RNAs in diseases
  • Hearing, Cochlea, Tinnitus, Genetics

Keywords (DOAJ)

  • functional genomics
  • epigenomics
  • proteomics
  • pharmacogenomics

Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.

Loading community confirmations…
How do we evaluate?Publisher of this journal? Appeal a derived assessment or request a factual correction

The journal's record in other sources:Web of Science MJLDOAJ

Everything shown here is produced automatically from named sources (DOAJ, OpenAlex, Crossref, PubMed, the Norwegian register) as of its capture date, with no human editing. Facts appear as recorded at the source; derived scores (PCI, PTD, PublishLens score) follow a published methodology. Not a judgement on the journal, not an official accreditation, not advice.

Wrong items are corrected automatically by re-reading the source (24 h for daily sources, 7 days for weekly ones) with a dated change log, and each item links to its source record. PublishLens-derived assessments are contested through the appeals mechanism (15 working days). Appeals · Indicator guide

Norwegian register data: Kanalregisteret (HK-dir, Norway) — CC BY 4.0 / NLOD — adapted: level extracted per year · OASPA member list — CC BY

Last automated source read: