Original Research
Published on 17 Dec 2025
LRRC56 deficiency cause motile ciliopathies in humans and mice
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1658063
- 1,798 views
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16,574 articles
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Editorial
Published on 16 Dec 2025
Editorial: A year in review: discussions in RNA
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1752525
- 1,605 views
Original Research
Published on 16 Dec 2025
A transcriptomic atlas at bulk and single-cell levels identifies novel transcriptional and splicing regulators of ECM homeostasis in osteoarthritis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1690319
- 1,359 views
Original Research
Published on 16 Dec 2025
Identification and validation of biomarkers related to nicotinamide metabolic pathway activity in heart failure
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1673314
- 1,326 views
Original Research
Published on 16 Dec 2025
Structural heterogeneity and functional convergence of transposable elements
in Evolutionary, Population, and Conservation Genetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1605675
- 1,420 views
Case Report
Published on 16 Dec 2025
Neonatal-onset familial hemophagocytic lymphohistiocytosis: a case report with genetic confirmation of PRF1 mutations
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1690283
- 1,142 views
Editorial
Published on 15 Dec 2025
Editorial: Genetic modulation of gut microbiome: effects on neurological health and aging
in Genetics of Aging
Frontiers in Genetics
doi 10.3389/fgene.2025.1760164
- 1,172 views
Technology and Code
Published on 12 Dec 2025
Automatic detection of n-degree family members
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1708315
- 1,254 views
Original Research
Published on 11 Dec 2025
Adrenomedullin orchestrates treatment resistance in hepatocellular carcinoma via immune microenvironment remodeling
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1721263
- 1,603 views
Case Report
Published on 11 Dec 2025
Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1674158
- 1,232 views
Original Research
Published on 10 Dec 2025
Development and application of an updated haplotype reference panel for association analysis of spontaneous sex reversal in XX rainbow trout
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1692544
- 1,431 views
Original Research
Published on 10 Dec 2025
Hyperlipidemia-associated specific modules and hub genes revealed by integrative methods of WGCNA and MetaDE
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1592778
- 1,368 views
Review
Published on 08 Dec 2025
The risk factors for chemotherapy myelosuppression in breast cancer: a systematic review and meta-analysis
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1704489
- 1,886 views
Case Report
Published on 08 Dec 2025
Neuronal intranuclear inclusion disease presenting with recurrent dizziness and headache: a case report with 5-year follow-up
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1719182
- 1,418 views
Case Report
Published on 08 Dec 2025
Early onset Arboleda-Tham syndrome due to KAT6A variants: Case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1704725
- 1,484 views
Original Research
Published on 08 Dec 2025
Sex-specific circRNA–miRNA–mRNA networks in peripheral blood mononuclear cells of patients with idiopathic pulmonary arterial hypertension: a pilot study
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1674894
- 1,454 views
- 1 citation
Original Research
Published on 05 Dec 2025
Optical genome mapping uncovers clinically relevant structural variants in congenital heart disease with heterotaxy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1673539
- 1,355 views
Original Research
Published on 04 Dec 2025
Integrating GWAS and machine learning for disease risk prediction in the Taiwanese Hakka population
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1694084
- 1,861 views
Original Research
Published on 04 Dec 2025
Development of a prognostic model related to mitochondria and programmed cell death-related genes in bladder cancer
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1615167
- 1,623 views
Original Research
Published on 03 Dec 2025
Perspectives of parents receiving normal results from genomic newborn screening: a mixed-methods evaluation from the early check program
in ELSI in Science and Genetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1704364
- 1,960 views
Correction
Published on 01 Dec 2025
Correction: MAPT mutation-induced behavioral variant frontotemporal dementia in an Asian patient: a multimodal biomarker case report resolving diagnostic challenges with Alzheimer’s disease
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1749030
- 1,115 views
Original Research
Published on 01 Dec 2025
FusDRM-m5C: a hybrid model for accurate prediction of 5-methylcytosine modification sites based on feature fusion and attention mechanism
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1642286
- 1,285 views
Original Research
Published on 01 Dec 2025
Bulk RNA-seq deconvolution heterogeneity across paired pancreatic cancer human samples
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1662924
- 1,744 views
Case Report
Published on 01 Dec 2025
Case Report: Pitfalls in CF screening – targeted variant analysis can cause misleading results and therapy recommendations
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1693573
- 1,412 views