Methods
Published on 19 Dec 2025
fastMETA: a fast and efficient tool for multivariate meta-analysis of GWAS
Frontiers in Genetics
doi 10.3389/fgene.2025.1718626
- 701 views
16,463 Publications
volumes
Volume 16 - 2025
Original Research
Published on 19 Dec 2025
Early genetic events in the colorectal carcinogenic pathway of familial adenomatous polyposis and sporadic polyp: germline and somatic alterations in carcinogenesis
Frontiers in Genetics
doi 10.3389/fgene.2025.1668133
- 718 views
Original Research
Accepted on 18 Dec 2025
Phenotype and Genotype of Hypophosphatasia Cases in Saudi Arabia: Multi-Center Case Cohort
Frontiers in Genetics
- 148 views
Original Research
Published on 18 Dec 2025
Transcriptomic profiling of human endothelial cells infected with venezuelan equine encephalitis virus reveals NRF2 driven host reprogramming mediated by omaveloxolone treatment
Frontiers in Genetics
doi 10.3389/fgene.2025.1722527
- 872 views
Original Research
Published on 18 Dec 2025
Copy number variants in fetuses with isolated and non-isolated increased nuchal translucency detected by chromosomal microarray analysis
Frontiers in Genetics
doi 10.3389/fgene.2025.1712025
- 577 views
Original Research
Published on 18 Dec 2025
Integrative linkage and recombination analysis of 25 X-STRs across 7 linkage groups using pedigree-based and SNP-based strategies
Frontiers in Genetics
doi 10.3389/fgene.2025.1727583
- 672 views
Original Research
Published on 18 Dec 2025
rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation
Frontiers in Genetics
doi 10.3389/fgene.2025.1721264
- 490 views
Case Report
Published on 18 Dec 2025
Case Report: Minigene assays reveal a novel DNAAF6 intronic variant as the key etiology for primary ciliary dyskinesia
Frontiers in Genetics
doi 10.3389/fgene.2025.1692658
- 610 views
Original Research
Published on 18 Dec 2025
Expanding the spectrum of NUS1-related progressive myoclonic epilepsy: a novel variant and exploratory use of metformin
Frontiers in Genetics
doi 10.3389/fgene.2025.1665623
- 706 views
Case Report
Published on 18 Dec 2025
Case Report: UMOD gene mutation and phenotypic overlap with REN in autosomal dominant tubulointerstitial kidney disease
Frontiers in Genetics
doi 10.3389/fgene.2025.1661377
- 540 views
Opinion
Published on 18 Dec 2025
Application of next-generation sequencing to determine mutations in candidate genes for congenital eye malformations in the Mexican indigenous population
Frontiers in Genetics
doi 10.3389/fgene.2025.1710953
- 673 views
Original Research
Published on 18 Dec 2025
Post-translational modification gene signatures implicate FBXW7 in immune and vascular dysregulation of Moyamoya disease
Frontiers in Genetics
doi 10.3389/fgene.2025.1723233
- 605 views
Original Research
Accepted on 17 Dec 2025
Time-series transcriptomic analysis of flower tissue during heat stress in heat-resilient and heat-sensitive Brassica napus L
Frontiers in Genetics
- 134 views
Original Research
Accepted on 17 Dec 2025
Identification of potentially deleterious mutations in gastric cancer using patient-derived xenograft models
Frontiers in Genetics
- 111 views
Correction
Accepted on 17 Dec 2025
Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
Frontiers in Genetics
Review
Accepted on 17 Dec 2025
Omics in mini-livestock: A genomic perspective on the future of sustainable food systems
Frontiers in Genetics
- 139 views
Brief Research Report
Published on 17 Dec 2025
Variance of Ks distribution corrects the bias in the divergence caused by the ancestral population size
Frontiers in Genetics
doi 10.3389/fgene.2025.1725551
- 786 views
Original Research
Published on 17 Dec 2025
Diagnostic and prognostic value of polygene methylation detection in ascites
Frontiers in Genetics
doi 10.3389/fgene.2025.1680036
- 565 views
Editorial
Published on 17 Dec 2025
Editorial: Genetics (SKINOMICS): new trends in skin aging research and clinical application
Frontiers in Genetics
doi 10.3389/fgene.2025.1764308
- 897 views
Original Research
Published on 17 Dec 2025
LRRC56 deficiency cause motile ciliopathies in humans and mice
Frontiers in Genetics
doi 10.3389/fgene.2025.1658063
- 674 views
Original Research
Accepted on 16 Dec 2025
Elective genomic screening: Results of the implementation of a whole genome sequencing program at a medical check-up unit in Spain
Frontiers in Genetics
Review
Accepted on 16 Dec 2025
Exploring the role and therapeutic potential of RNA N6-methyladenosine modification in abortion disease pathology: A comprehensive review
Frontiers in Genetics
- 152 views
Editorial
Published on 16 Dec 2025
Editorial: A year in review: discussions in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1752525
- 967 views
Original Research
Published on 16 Dec 2025
Identification and validation of biomarkers related to nicotinamide metabolic pathway activity in heart failure
Frontiers in Genetics
doi 10.3389/fgene.2025.1673314
- 620 views