Original Research
Accepted on 20 Nov 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
Type at least 3 characters
16,377 articles
Correction
Accepted on 20 Nov 2025
Corrigendum to: Individual and combined effects of the GSTM1, GSTT1, and GSTP1 polymorphisms on type 2 diabetes mellitus risk: A systematic review and meta-analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 20 Nov 2025
Lorentz-Regularized Interpretable VAE for Multi-Scale Single-cell Transcriptomic and Epigenomic Embeddings
in Computational Genomics
Frontiers in Genetics
Original Research
Published on 20 Nov 2025
Benign mosaic chromosomal structural variants across generations: evidence for a developmental correction mechanism from clinical and computational models
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1710280
- 167 views
Methods
Published on 20 Nov 2025
A network-based discovery of prognostic markers in recurrent IDH wild-type gliomas
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1672015
- 155 views
Original Research
Published on 20 Nov 2025
Five novel EP300 variants expand the genetic and phenotypic spectrum of Rubinstein–Taybi syndrome type 2 in Chinese patients
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1690693
- 132 views
Review
Published on 20 Nov 2025
Bioinformatics identification of key genes and therapeutic targets for exercise intervention in polycystic ovary syndrome
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1634588
- 161 views
Opinion
Published on 20 Nov 2025
Why all MODY variants in transcription factor genes are dominantly inherited
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1690468
- 451 views
Original Research
Published on 20 Nov 2025
SHMT2 modulates the transcriptome and metabolism profiles to promote the tumor phenotypes of bladder cancer HT-1376 cells
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1694089
- 197 views
Case Report
Accepted on 19 Nov 2025
Type 1 Bartter Syndrome Presenting as Primary Diabetes Insipidus: a rare case report with 8-year follow-up
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 19 Nov 2025
Early genetic events in the colorectal carcinogenic pathway of familial adenomatous polyposis and sporadic polyp: Germline and somatic alterations in carcinogenesis
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
Original Research
Accepted on 19 Nov 2025
Integrating GWAS and Machine Learning for Disease Risk Prediction in the Taiwanese Hakka Population
in Computational Genomics
Frontiers in Genetics
Case Report
Accepted on 19 Nov 2025
Pitfalls in CF screening – targeted variant analysis can cause misleading results and therapy recommendations
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
Correction
Accepted on 19 Nov 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
Review
Published on 19 Nov 2025
Single-cell sequencing in molecular diagnostics: Transformative yet untapped potential
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2025.1621081
- 428 views
Original Research
Published on 19 Nov 2025
FTO rs9939609 and rs17817449 polymorphisms contribute to metabolic syndrome risk by increasing triglyceride and glucose levels
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1659460
- 359 views