Original Research
Published on 07 Nov 2025
ST8SIA6-AS1 serves as a prognostic biomarker in cancer and exhibits oncogenic properties in prostate cancer
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1648077
- 1,503 views
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16,578 articles
articles
Correction
Published on 07 Nov 2025
Correction: A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1722189
- 814 views
Original Research
Published on 07 Nov 2025
Precision genomic profiling in Gaucher disease: insights from atypical presentations
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1553036
- 1,960 views
Case Report
Published on 06 Nov 2025
Case Report: autosomal dominant distal motor neuropathy as a new phenotype of KIF21A-related disorders
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1699834
- 1,379 views
Original Research
Published on 06 Nov 2025
Clarifying species boundaries between bocachico (Prochilodus magdalenae) and bocachico de Maracaibo (Prochilodus reticulatus) (characiformes: Prochilodontidae) using complete mitochondrial genomes
in Evolutionary and Population Genetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1661527
- 1,678 views
Case Report
Published on 06 Nov 2025
Case Report: D-bifunctional protein deficiency caused by novel compound heterozygote HSD17B4 variants in a neonate in China
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1631767
- 1,626 views
Case Report
Published on 06 Nov 2025
Case Report: Co-occurring de novo SHANK3 and SRCAP variants in a patient with autoimmune encephalitis and exhibiting Phelan-McDermid syndrome features
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1699311
- 1,560 views
Case Report
Published on 06 Nov 2025
Case Report: Novel compound heterozygous mutations in PNPLA6 gene associated with Oliver-McFarlane syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1660243
- 1,311 views
Original Research
Published on 06 Nov 2025
Systems biology and experimental validation indicate DDIT4, FOXO1, and STAT3 as shared key genes linking osteoporosis and sarcopenia
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1630705
- 1,852 views
Case Report
Published on 06 Nov 2025
A rare case of de novo 20p12.3 microdeletion syndrome in a nine-year-old female: case report and literature review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1669947
- 1,482 views
Original Research
Published on 06 Nov 2025
Functional analysis of a novel variant in the COL5A1 gene in a Polish patient with the classical type of Ehlers–Danlos syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1689587
- 1,999 views
Review
Published on 06 Nov 2025
Non-coding RNAs in heart failure: epigenetic regulatory mechanisms and therapeutic potential
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1677797
- 2,575 views
- 1 citation
Case Report
Published on 05 Nov 2025
Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencing
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1669814
- 1,097 views
Original Research
Published on 05 Nov 2025
Downregulation of aquaporin 3 promotes hyperosmolarity-induced apoptosis of nucleus pulposus cells through PI3K/Akt/mTOR pathway suppression
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1665899
- 1,528 views
Original Research
Published on 03 Nov 2025
Family-based NGS panel testing of cardiopathies and arrhythmic syndromes
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1677311
- 1,944 views
Case Report
Published on 31 Oct 2025
“Case report”: Whole-exome sequencing reveals compound heterozygous variants in the EIF2B5 gene in a familial case of vanishing white matter
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1688885
- 1,865 views
Original Research
Published on 30 Oct 2025
Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1664424
- 1,738 views
Original Research
Published on 30 Oct 2025
Prenatal diagnosis of Prader–Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1675663
- 2,432 views
- 1 citation
Original Research
Published on 29 Oct 2025
LDLRAD4 is a potential diagnostic and prognostic biomarker correlated with immune infiltration in myelodysplastic syndromes
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1540161
- 1,713 views
Original Research
Published on 28 Oct 2025
Comparative RNA-seq and functional assays identify L-arginine transporter SLC7A2 as a potential regulator of osteogenesis in maxillary sinus mucosal stem cells
in Stem Cell Research
Frontiers in Genetics
doi 10.3389/fgene.2025.1701001
- 2,006 views
Review
Published on 28 Oct 2025
From bench to bytes: a practical guide to RNA sequencing data analysis
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1697922
- 5,278 views
Review
Published on 28 Oct 2025
Computational models for pan-cancer classification based on multi-omics data
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1667325
- 3,124 views
- 1 citation
Review
Published on 28 Oct 2025
Gene therapy for disorders of sex development: current applications and future challenges
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1661127
- 3,712 views
Data Report
Published on 28 Oct 2025
De novo assembly and functional annotation of Henbit (Lamium amplexicaule) transcriptome
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2025.1612607
- 2,878 views