Original Research
Published on 07 Nov 2025
BRMS1L promotes chemotherapy sensitivity by inhibiting autophagy in breast cancer
Frontiers in Genetics
doi 10.3389/fgene.2025.1670001
- 1,415 views
963 Publications
volumes
Original Research
Published on 07 Nov 2025
Identifying gene-environment interactions across genome-wide, twin, and polygenic risk score approaches
Frontiers in Genetics
doi 10.3389/fgene.2025.1698381
- 1,284 views
Case Report
Published on 07 Nov 2025
Case Report: Whole-exome sequencing revealed a de novo variant in SETBP1 gene in a Chinese family with developmental delay
Frontiers in Genetics
doi 10.3389/fgene.2025.1637931
- 1,306 views
Correction
Published on 07 Nov 2025
Correction: Identification of shared diagnostic genes between osteoporosis and Crohn’s disease through integrated transcriptomic analysis and machine learning
Frontiers in Genetics
doi 10.3389/fgene.2025.1722642
- 716 views
Correction
Published on 07 Nov 2025
Correction: A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2
Frontiers in Genetics
doi 10.3389/fgene.2025.1722189
- 713 views
Original Research
Published on 07 Nov 2025
ST8SIA6-AS1 serves as a prognostic biomarker in cancer and exhibits oncogenic properties in prostate cancer
Frontiers in Genetics
doi 10.3389/fgene.2025.1648077
- 1,284 views
Original Research
Published on 07 Nov 2025
Precision genomic profiling in Gaucher disease: insights from atypical presentations
Frontiers in Genetics
doi 10.3389/fgene.2025.1553036
- 1,464 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1631767
- 1,111 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1661527
- 1,405 views
Case Report
Published on 06 Nov 2025
Case Report: autosomal dominant distal motor neuropathy as a new phenotype of KIF21A-related disorders
Frontiers in Genetics
doi 10.3389/fgene.2025.1699834
- 1,061 views
Case Report
Published on 06 Nov 2025
Case Report: Novel compound heterozygous mutations in PNPLA6 gene associated with Oliver-McFarlane syndrome
Frontiers in Genetics
doi 10.3389/fgene.2025.1660243
- 1,087 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1699311
- 1,116 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1669947
- 1,147 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1630705
- 1,418 views
Review
Published on 06 Nov 2025
Non-coding RNAs in heart failure: epigenetic regulatory mechanisms and therapeutic potential
Frontiers in Genetics
doi 10.3389/fgene.2025.1677797
- 1,964 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1689587
- 1,333 views
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
Frontiers in Genetics
doi 10.3389/fgene.2025.1669814
- 913 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1665899
- 1,165 views
Original Research
Published on 03 Nov 2025
Family-based NGS panel testing of cardiopathies and arrhythmic syndromes
Frontiers in Genetics
doi 10.3389/fgene.2025.1677311
- 1,574 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1688885
- 1,463 views
Original Research
Published on 30 Oct 2025
Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis
Frontiers in Genetics
doi 10.3389/fgene.2025.1664424
- 1,420 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1675663
- 1,960 views
Original Research
Published on 29 Oct 2025
LDLRAD4 is a potential diagnostic and prognostic biomarker correlated with immune infiltration in myelodysplastic syndromes
Frontiers in Genetics
doi 10.3389/fgene.2025.1540161
- 1,459 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
Frontiers in Genetics
doi 10.3389/fgene.2025.1701001
- 1,545 views