Original Research
Published on 27 Jan 2025
The role of SPINK5 mutation distribution in phenotypes of Netherton syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1475054
- 356 views
Type at least 3 characters
15,627 articles
Articles
Brief Research Report
Published on 27 Jan 2025
Characterization of novel human endogenous retrovirus structures on chromosomes 6 and 7
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1498978
- 491 views
Original Research
Published on 24 Jan 2025
Identification of key genes underlying radiosensitivity and radioresistance in endometrial cancer through integrated bioinformatics analysis
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1469610
- 433 views
Original Research
Accepted on 23 Jan 2025
Exploring the Underlying Molecular Connections: A Bioinformatics Approach to Link Melanoma and Parkinson's Disease
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1526018
Original Research
Published on 23 Jan 2025
Transgenerational epigenetic heritability for growth, body composition, and reproductive traits in Landrace pigs
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1526473
- 770 views
Review
Published on 23 Jan 2025
Genetic ancestry and the colonial legacies of race in genomics: a cross-disciplinary dialogue
in ELSI in Science and Genetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1523406
- 801 views
Original Research
Published on 22 Jan 2025
In silico design of an epitope-based vaccine ensemble for fasliolopsiasis
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1451853
- 647 views
Original Research
Published on 22 Jan 2025
DEmiRNA-mRNA regulatory network reveals miR‐122-5p as a regulatory factor of arginine metabolism in necrotizing enterocolitis
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2024.1480431
- 588 views
Original Research
Published on 22 Jan 2025
Machine learning potential predictor of idiopathic pulmonary fibrosis
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1464471
- 949 views
Original Research
Accepted on 21 Jan 2025
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1514610
Correction
Published on 21 Jan 2025
Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2025.1553186
- 402 views
Original Research
Published on 21 Jan 2025
Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1496411
- 613 views
Original Research
Published on 20 Jan 2025
Mutation in the COL2A1 gene is associated with acetabular dysplasia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1521412
- 516 views
Case Report
Published on 20 Jan 2025
Tell me y: anticipation of sex discrepancies in cell-free DNA testing due to maternal genetic abnormalities: a case report
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1502287
- 529 views
Case Report
Published on 20 Jan 2025
Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1491870
- 461 views
Original Research
Published on 20 Jan 2025
Therapeutic target genes and regulatory networks of gallic acid in cervical cancer
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1508869
- 794 views