Impact Factor
2.55
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.23
137 total citations
h5-index
14
h5 depth signal
Cited share
55.8%
67 of 120
Total citations
137
Citation footprint
Metric signal
0.98
External metric anchor
Self-citation
1.5%
2 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
China
464
United States
158
Iran
49
Turkey
49
India
38
Citing Fields of Research
Genetics & Genomics
369
Noncoding RNA
117
Oncology
92
Cancer & Development
76
Musculoskeletal Disorders
73
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
2,135
Articles tracked across the journal lifetime
Indexed publication set
120
67 cited publications
Last 12 months
45
4.1 publications/month
Open access share
2.2%
1 OA publications in the last year
Leading citing country
China
464 citing publications
Leading citing field
Genetics & Genomics
369 citing publications
Latest tracked publication
26 September 2026
10 recent records available
Coverage & Indexing History
v13n1, 2009-
v13n1, 2009-
Research Focus & Classification
Indexed Subjects
Genetics & Genomics
Noncoding RNA
Musculoskeletal Disorders
Immunology
Hematology
Auto-Inflammatory Disorders
Broad Categories
Genetics
Molecular Biology
Genetics & Genomics
Noncoding RNA
Cell Differentiation & Development
Hematology
Musculoskeletal Disorders
Cancer, Autophagy & Apoptosis
MeSH Descriptors
Biomarkers
Genetic Diseases, Inborn
Genetic Testing
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1177/19450265261493084
Open DOI
Biomarker-Guided Diagnosis of Riboflavin Transporter Deficiency Presenting as Seronegative Myasthenia Gravis: A Short Report from a Consanguineous Family
Background: Brown–Vialetto–Van Laere syndrome (BVVLS) is a rare, treatable neurodegenerative disorder caused by riboflavin transporter gene variants (SLC52A2, SLC52A3). Early symptoms can mimic neuromuscular junction disorders, causing d...
02
DOI 10.1177/19450265261491102
Open DOI
The Impacts of MTHFR C677T Variant (rs1801133) on Cardiometabolic Profiles and Early Onset Coronary Artery Disease: A Case–Control Study
Background: The MTHFR C677T polymorphism (rs1801133) is a well-documented genetic variant in cardiovascular research, yet its mechanistic role in early onset coronary artery disease (EOCAD) remains poorly characterized in East Asian popu...
03
DOI 10.1177/19450265261491098
Open DOI
Clinical Evaluation of miR-135b-5p and miR-21-5p Expression on Self-Collected Cervical Swab Samples for Triaging HR-HPV-Positive High-Grade Preneoplastic Lesions in India
Objective: This study aimed to evaluate the triage performance of microRNA (miRNA) biomarkers on self-collected, high-risk human papillomavirus (HR-HPV)-positive cervical swabs to discern cervical intraepithelial neoplasia II–III or high...
04
DOI 10.1177/19450265261491082
Open DOI
Association of Interleukin-27 Gene Variants with Susceptibility to Brucellosis Among Iranian Population: A Case–Control Study
Objectives: Brucellosis is recognized as one of the most widespread zoonotic diseases, caused by facultative intracellular coccobacilli of the genus Brucella . Interleukin-27 (IL-27) is a pleiotropic cytokine that serves a critical role ...
05
DOI 10.1177/19450265261488655
Open DOI
Integrative Genetic and Bioinformatic Analysis of Androgen Pathway Gene Polymorphisms, Testosterone, and PSA Levels in Prostate Cancer
Background: Prostate cancer (PCa) is genetically a complicated disease with mediation by variations in genes coding for androgen biosynthesis and signaling genes. In the current study, we investigate the associations of key polymorphisms...
06
DOI 10.1177/19450265261481765
Open DOI
Fat Mass and Obesity Associated (FTO) and Melanocortin 4 Receptor (MC4R) Gene Variants as Prognostic Markers of Obesity in Quetta City
Background: Obesity is a complex condition caused by environmental and hereditary factors. Single nucleotide polymorphisms (SNPs) in the FTO (rs9939609) and melanocortin-4-receptor (MC4R) (rs17782313) genes have been strongly linked to a...
07
DOI 10.1177/19450265261477354
Open DOI
TGFBI p.H626R Mutation in a Chinese Family with Lattice Corneal Dystrophy: A Short Report and Literature Review
Purpose: To report a Chinese family with lattice corneal dystrophy (LCD) caused by the TGFBI p.H626R mutation and summarize its clinical and genetic characteristics through a literature review. Methods: A three-generation Chinese family ...
08
DOI 10.1177/19450265261470709
Open DOI
The Expression Profile of microRNA Genes and NT-proBNP as Possible Predictors of One-Year Mortality in Egyptian Adults with Acute Heart Failure: A Prospective Biomarker Study
Background: Acute heart failure (AHF) is a prevalent and life-threatening condition that is associated with high morbidity and mortality, particularly in adults. MicroRNAs (miRNAs) have been identified as potential biomarkers in various ...
09
DOI 10.1177/19450265261469732
Open DOI
A Short Indel is Causing Biotinidase Deficiency in a 4-Month-Old Boy from Jammu and Kashmir
Background: Biotinidase is an enzyme recycling endogenous biotin by hydrolyzing ε- N -biotinyl lysine (biocytin) to lysine and biotin. Biotin acts as a coenzyme in various carboxylation reactions. Biotinidase deficiency is rare, with an ...
10
DOI 10.1177/19450265261469740
Open DOI
Association of Serum IL-17A Levels and IL-17/IL-17R Gene Variants with Community-Acquired Pneumonia in Iranian Children
Background: Because the IL-17/IL-17 receptor (IL-17R) axis is involved in lung inflammation and genetic variants, such as single nucleotide polymorphisms (SNPs), can affect its function, this study examined the associations between IL-17...
Bibliographical & Catalog Notes
Description based on: Vol. 13, no. 1 (Feb. 2009); title from cover.
Latest issue consulted: Vol. 13, no. 2 (Apr. 2009).
Also issued online.