Original Research
Accepted on 18 Aug 2026
Computational Prioritization of Candidate TCDD-Associated Targets in Retinoblastoma Using Network Toxicology and Transcriptomic Analysis
in Predictive Toxicology and Exposomics
Frontiers in Genetics
Type at least 3 characters
17,061 articles
articles
Original Research
Accepted on 18 Aug 2026
Loss of Lactate Dehydrogenase A disrupts R-loop homeostasis and induces DNA damage in breast cancer cells
in Epigenetics and Genome Architecture
Frontiers in Genetics
Original Research
Accepted on 18 Aug 2026
Transcriptional Signatures of Respiratory Syncytial Virus (RSV) Infection Using Relaxed Magnitude Altitude Score with Hub-Centric Network Analysis (RMAS-HCNA)
in Computational Genomics
Frontiers in Genetics
Mini Review
Accepted on 18 Aug 2026
Mechanisms for the formation and maintenance of microhabitat self-organization in the root system of orchid
in Genomics of Plants and Plant-Associated Organisms
Frontiers in Genetics
Correction
Accepted on 18 Aug 2026
Correction: Editorial: Hepatocellular carcinoma: from bench to bedside
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Original Research
Published on 18 Aug 2026
Comprehensive analysis of SYTL4 differential expression and clinical implications in DLBCL
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1908683
- 355 views
Opinion
Published on 18 Aug 2026
Repositioning candidate gene approaches in the post-GWAS era: a clinical perspective from psychiatric pharmacogenetics
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1828563
- 681 views
Original Research
Published on 18 Aug 2026
NLRP3 inflammasome pathway activation is associated with cardiac remodeling, gut microbiota dysbiosis, and dietary protein restriction in a rat heart failure model: an integrative exploratory analysis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1852819
- 341 views
Systematic Review
Published on 18 Aug 2026
Diagnostic accuracy of cell-free DNA-based non-invasive prenatal testing for fetal aneuploidies: a systematic review
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1886738
- 746 views
Original Research
Accepted on 17 Aug 2026
Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Case Report
Accepted on 17 Aug 2026
Presymptomatic Risdiplam in Preterm Monozygotic Twins with Co-occurring Spinal Muscular Atrophy and Tuberous Sclerosis Complex
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Case Report
Accepted on 17 Aug 2026
A Rare De Novo Contiguous 15q11.1-q13.3 Duplication with Tetrasomy (CN=4) and Adjacent Trisomy (CN=3) Associated with Severe Global Developmental Delay, Autism Spectrum Disorder, and Subclinical Epileptiform Discharges: A Case Report and Literature Review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
Yield of Actionable Variants From High-Risk Cancer Gene Panel Testing in Guideline-Eligible and Ineligible Individuals
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
A methodological framework for developing bioinformatics databases: A case study on the Boesenbergia rotunda genome database
in Computational Genomics
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
The Expressions and m⁶A Methylation Modification Patterns of mRNAs and lncRNAs in Major Depressive Disorder
in Epigenetics and Genome Architecture
Frontiers in Genetics
Case Report
Accepted on 17 Aug 2026
Adult presentation of SLC29A3-related disorder spectrum with marked hypogammaglobulinemia due to a recurrent homozygous pathogenic variant (G437R): a case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
Missingness-aware machine learning using routine laboratory data for distinguishing hepatitis from cirrhosis
in Computational Genomics
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
Integrating Single-Cell Multi-Omics for Precision Radiotherapy Stratification in Hypopharyngeal Squamous Cell Carcinoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
Genetic diversity, population structure, and linkage disequilibrium among tropical quality protein maize (QPM) lines assessed with high-density SNP markers
in Genomics of Plants and Plant-Associated Organisms
Frontiers in Genetics
Editorial
Accepted on 17 Aug 2026
Editorial: Nutrigenetics and Nutrigenomics in Livestock
in Livestock Genomics
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
Genomic Analysis Identifies Candidate Supergene Architecture for Host-Feeding Behavior in Wild Aedes aegypti Dengue Vector Mosquitoes
in Applied Genetic Epidemiology
Frontiers in Genetics
Original Research
Accepted on 17 Aug 2026
HSTXGB: a hyperparameter self-tuning XGBoost method integrating pre-and post-processing for gene regulatory network inference
in Computational Genomics
Frontiers in Genetics
Review
Published on 17 Aug 2026
Integrating single-cell transcriptomics with deep learning for glioblastoma treatment
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1813369
- 373 views
Original Research
Published on 17 Aug 2026
Cross-cancer transcriptomic analysis reveals conserved developmental, ferroptosis, and immune remodeling modules in Wilms tumor and oral cancer
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1861806
- 420 views