Case Report
Accepted on 24 Oct 2025
Case Report: Novel compound heterozygous mutations in PNPLA6 gene associated with Oliver-McFarlane syndrome
in Genetics of Common and Rare Diseases
Case Report
Accepted on 24 Oct 2025
in Genetics of Common and Rare Diseases
Original Research
Accepted on 24 Oct 2025
in Computational Genomics
Correction
Published on 24 Oct 2025
in Genomics of Plants and the Phytoecosystem
Case Report
Published on 24 Oct 2025
in Human and Medical Genomics
Review
Published on 24 Oct 2025
in RNA
Original Research
Published on 23 Oct 2025
in Computational Genomics
Original Research
Published on 23 Oct 2025
in Toxicogenomics
Review
Published on 23 Oct 2025
in Cancer Genetics and Oncogenomics
Case Report
Published on 23 Oct 2025
in Genetics of Common and Rare Diseases
Original Research
Published on 23 Oct 2025
in Pharmacogenetics and Pharmacogenomics
Correction
Published on 23 Oct 2025
in Systems Biology Archive
Original Research
Published on 23 Oct 2025
in Cancer Genetics and Oncogenomics
Original Research
Accepted on 22 Oct 2025
in Cancer Genetics and Oncogenomics
Brief Research Report
Accepted on 22 Oct 2025
in ELSI in Science and Genetics
Original Research
Accepted on 22 Oct 2025
in Evolutionary and Population Genetics
Case Report
Accepted on 22 Oct 2025
in Genetics of Common and Rare Diseases