Case Report
Accepted on 02 Apr 2025
CEBPA-associated familial acute myeloid leukemia mimicking Werner syndrome: a case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1575651
Type at least 3 characters
15,733 articles
Original Research
Accepted on 02 Apr 2025
Identification of a novel homozygous SLC13A5 nonstop mutation in a Chinese family with epileptic encephalopathy and developmental delay
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1474390
Correction
Accepted on 02 Apr 2025
Corrigendum: Genetic parameters and genome-wide association for milk production traits and somatic cell score in different lactation stages of Shanghai Holstein population
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1604082
Editorial
Accepted on 02 Apr 2025
Editorial: Recent Advancements in RNA-based and targeted Therapeutics
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1603498
Original Research
Published on 02 Apr 2025
Enhanced renal ischemia/reperfusion injury repair potential of exosomes derived from B7-H1high mesenchymal stem cells
in Stem Cell Research
Frontiers in Genetics
doi 10.3389/fgene.2025.1516626
- 188 views
Original Research
Published on 02 Apr 2025
Thyroid function and hepatic fibrosis/cirrhosis: a two-sample Mendelian randomization study
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1399353
- 167 views
Original Research
Published on 02 Apr 2025
Improving accuracy and precision of heritability estimation in twin studies through hierarchical modeling: reassessing the measurement error assumption
in Behavioral and Psychiatric Genetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1522729
- 207 views
Brief Research Report
Published on 02 Apr 2025
Optical genome mapping with whole genome sequencing identifies complex chromosomal structural variations in acute leukemia
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2025.1496847
- 176 views
Original Research
Published on 02 Apr 2025
Exploration of folate and its derivatives in grains of wheat with different colors
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2025.1549122
- 124 views
Review
Published on 02 Apr 2025
Life destiny of erythrocyte in high altitude erythrocytosis: mechanisms underlying the progression from physiological (moderate) to pathological (excessive) high-altitude erythrocytosis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1528935
- 152 views
Original Research
Accepted on 01 Apr 2025
A novel synonymous variant in the NF1 gene disrupting splicing contributes to Neurofibromatosis pathogenesis
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1572487
Original Research
Accepted on 01 Apr 2025
Identification of Cellular Senescence-related genes as biomarkers for lupus nephritis based on bioinformatics
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1551450
Original Research
Published on 01 Apr 2025
Endoplasmic reticulum stress-related prognosis signature characterizes the immune landscape and predicts the prognosis of colon adenocarcinoma
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1516232
- 283 views
Case Report
Accepted on 31 Mar 2025
A novel SIGMAR1 missense mutation leads to distal hereditary motor neuropathy phenotype mimicking juvenile ALS: a case report of China
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1477518
Case Report
Accepted on 31 Mar 2025
A case of hypoparathyroidismsensorineural deafness-renal dysplasia syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1501427
Case Report
Accepted on 31 Mar 2025
A Novel nonsense mutation in SCAF4 associated with Fliedner-Zweier syndrome: a case report and review of the literature
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1487352