Impact Factor
3.77
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
3.35
1,879 total citations
h5-index
34
h5 depth signal
Cited share
82.4%
518 of 629
Total citations
1,879
Citation footprint
Metric signal
3.50
External metric anchor
Self-citation
0.8%
15 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
1,184
United States
421
Iran
100
South Korea
88
United Kingdom
79
Citing Fields of Research
Genetics & Genomics
1,049
Cytogenetics
317
Noncoding RNA
275
Oncology
204
Immunology
190
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
2,960
Articles tracked across the journal lifetime
Indexed publication set
629
518 cited publications
Last 12 months
263
21.9 publications/month
Open access share
100.0%
263 OA publications in the last year
Leading citing country
China
1,184 citing publications
Leading citing field
Genetics & Genomics
1,049 citing publications
Latest tracked publication
15 October 2026
10 recent records available
Coverage & Indexing History
v1, 2008-
v1, 2008-
Active Coverage
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Cytogenetics
Noncoding RNA
Auditory Loss
Immunology
Musculoskeletal Disorders
Issuing & Sponsoring Bodies
Contributor
BioMed Central Ltd
Broad Categories
Genetics, Medical
Genetics & Genomics
Cytogenetics
Noncoding RNA
Cancer, Autophagy & Apoptosis
Hematology
Musculoskeletal Disorders
MeSH Descriptors
Genetics, Medical
Genomics
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1186/s12920-026-02482-8
Open DOI
Patient perspectives on gene therapies and gene editing for familial cardiomyopathies
02
DOI 10.1186/s12920-026-02481-9
Open DOI
FOXO1 modulates proliferation and apoptosis of chondrocytes isolated from developmental dysplastic hips
03
04
05
DOI 10.1186/s12920-026-02467-7
Open DOI
Multi-omics signatures of endometrial receptivity in recurrent implantation failure: a systematic review
06
DOI 10.1186/s12920-026-02488-2
Open DOI
Insensitivity to skin pain, tickling, and spicy food in a woman with a pathogenic NAA10 variant: a case report
Background: The NAA10 gene on the X chromosome encodes NAA10, the catalytic subunit of the N-terminal acetyltransferase complex NatA, which co-translationally acetylates nearly half the human proteome. From the variety of NAA10 substrate...
07
DOI 10.1186/s12920-026-02493-5
Open DOI
A novel splice-site variant in CNKSR2 causes exon 16 skipping and X-linked syndromic intellectual developmental disorder
08
DOI 10.1186/s12920-026-02485-5
Open DOI
Pan-cancer and experimental analyses reveal TTC39B as a suppressor of cell proliferation in clear cell renal cell carcinoma
Background: Tetratricopeptide repeat domain protein 39B (TTC39B) is a lipid metabolism–related gene recently implicated in cholesterol regulation. However, its clinical and biological relevance in human cancers remains undefined. Methods...
09
DOI 10.1186/s12920-026-02492-6
Open DOI
Mutation-specific correction of SOD1 in familial ALS using prime and base editing in human induced pluripotent stem cells
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive motor neuron degeneration and respiratory failure. Approximately 10% of ALS cases are familial, with mutations in SOD1 rep...
10
Bibliographical & Catalog Notes
Description based on first issue; title from journal home page (publisher's Web site, viewed Feb. 23, 2008).
Latest issue consulted: 1:6 (14 Feb. 2008) (viewed Feb. 23, 2008).
Volume numbering corresponds to a calendar year, and articles are numbered sequentially as they are published.