Review
Accepted on 03 Apr 2026
Epitranscriptomic Regulation of Endothelial Plasticity under Hemodynamic Forces: Insights from the KLF2/4–METTL3–H19 Pathway
in Epigenomics and Epigenetics
Frontiers in Genetics
Type at least 3 characters
16,691 articles
articles
Original Research
Accepted on 03 Apr 2026
Charting the Immune Terrain: A Novel Risk Model for Thyroid Cancer Prognosis
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Case Report
Accepted on 02 Apr 2026
Ochronotic Arthropathy Mimicking Spondyloarthritis: A Case-based Review of Diagnostic Pitfalls and a Novel Likely Pathogenic HGD Variant
in Human and Medical Genomics
Frontiers in Genetics
Original Research
Published on 02 Apr 2026
Single-cell sequencing reveals the functional heterogeneity of melanoma cells and their crosstalk with the tumor microenvironment
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1779213
- 142 views
Original Research
Published on 02 Apr 2026
Multi-omics analysis to identify the dynamic changes of immune cells and marker genes in renal fibrosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1767093
Brief Research Report
Published on 02 Apr 2026
Functional inactivation of MDR3 caused by a homozygous ABCB4 missense variant leading to liver failure
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1802238
Original Research
Published on 02 Apr 2026
BHLHE41–SLC7A11 transcriptional axis and chromatin remodeling signatures in osteogenic-lineage disulfidptosis-like stress in osteoporosis
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2026.1794298
Mini Review
Published on 01 Apr 2026
Federated, governed, and interoperable? The emerging architecture of public human genomic data infrastructures: a European perspective
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1819270
Original Research
Published on 01 Apr 2026
Serum tumor markers combined with HRCT for malignancy risk assessment of solitary pulmonary nodules: a retrospective study
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1731395
Original Research
Published on 01 Apr 2026
Genetic association of LOC100130476 rs80213143 with susceptibility and renal involvement in systemic lupus erythematosus
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1609849
Original Research
Published on 01 Apr 2026
TTN variants in pediatric cardiomyopathy: a retrospective cohort study
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1758524
- 129 views
Editorial
Accepted on 31 Mar 2026
Editorial: Chromatin Modifications and Gene Expression: From Mechanisms to Therapeutic Implications in Disease
in Epigenomics and Epigenetics
Frontiers in Genetics
Case Report
Accepted on 31 Mar 2026
X-linked Recessive Ichthyosis with X-linked Retinoschisis in Two Brothers: A Case Report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 31 Mar 2026
Clinical outcomes of preimplantation genetic testing for structural rearrangements in couples with chromosomal inversions: a retrospective analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 31 Mar 2026
Lipid metabolism-driven gene expression predicts prognostic outcomes in lung adenocarcinoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Case Report
Accepted on 31 Mar 2026
Case Report:Co-inheritance of Familial Lecithin-Cholesterol Acyltransferase Deficiency and α0-Thalassemia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Review
Accepted on 31 Mar 2026
Long noncoding RNAs, microRNAs, and circular RNAs landscape in hypertensive disorders of pregnancy: Progress, challenges, and perspectives
in Epigenomics and Epigenetics
Frontiers in Genetics
Brief Research Report
Accepted on 31 Mar 2026
Application of Integrated Nested Laplace Approximation to identify hotspots of methylation heterogeneity in healthy individuals from the MAMELI cohort
in Computational Genomics
Frontiers in Genetics
Original Research
Accepted on 31 Mar 2026
Evaluation of the contribution of trio-exome sequencing in selected prenatal indications
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Data Report
Published on 31 Mar 2026
A single-cell multi-omics atlas of human eyelid skin
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1780660
- 205 views
Original Research
Published on 31 Mar 2026
Genomic and transcriptomic insights into aflatoxin-induced intrahepatic cholangiocarcinoma: an integrated pathway and meta-analysis study
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1785259
Original Research
Accepted on 30 Mar 2026
Clinical variant interpretation comparing two saturation genome editing-based functional studies for BRCA2
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Original Research
Accepted on 30 Mar 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databases
in Behavioral and Psychiatric Genetics
Frontiers in Genetics
Original Research
Accepted on 30 Mar 2026
Sez6l promotes neuropathic pain via Wnt5a/Ca²⁺ pathways in dorsal root ganglion
in Neurogenomics
Frontiers in Genetics