Original Research
Published on 27 May 2025
MultiV_Nm: a prediction method for 2′-O-methylation sites based on multi-view features
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1608490
- 1,861 views
- 3 citations
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16,617 articles
articles
Original Research
Published on 26 May 2025
Genetic association of ACE2 rs2285666 (C>T) and rs2106809 (A>G) and susceptibility to SARS-CoV-2 infection among the Ghanaian population
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2025.1555515
- 3,240 views
- 2 citations
Original Research
Published on 26 May 2025
Uncovering codon usage patterns during murine embryogenesis and tissue-specific developmental diseases
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1554773
- 2,227 views
Case Report
Published on 26 May 2025
Case Report: Multiple cerebral infarctions in a patient with hereditary hemorrhagic telangiectasia following a fall
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1581625
- 2,308 views
Original Research
Published on 26 May 2025
Prediction of mild cognitive impairment using blood multi-omics data
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1552063
- 2,818 views
Case Report
Published on 26 May 2025
Case Report: A neurodevelopmental disorder with global developmental delay, microcephaly, eye anomalies, sweat dysregulation, and skeletal implications due to an ultra-rare de novo 5q14.3q15 copy number gain
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1549685
- 2,148 views
Original Research
Published on 23 May 2025
The role of E2F1 in promoting EIF4EBP1 transcription in cryptorchid mice: association with autophagy in germ cells
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2025.1536672
- 2,096 views
Brief Research Report
Published on 23 May 2025
Molecular variants of multiple genes were revealed by whole-exome sequencing in PCOS patients with diabetes
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1541946
- 3,285 views
Brief Research Report
Published on 23 May 2025
Distinct germ-line genetic mutation patterns correlate with reproductive outcomes in ICSI patients: a pilot study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1610943
- 2,541 views
Original Research
Published on 23 May 2025
Global, regional, and national burden of glucose-6-phosphate dehydrogenase (G6PD) deficiency from 1990 to 2021: a systematic analysis of the global burden of disease study 2021
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2025.1593728
- 7,849 views
- 11 citations
Case Report
Published on 22 May 2025
Autosomal recessive primary microcephaly in sibs in time of Zika epidemic: a Case Report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1565296
- 2,232 views
- 2 citations
Case Report
Published on 22 May 2025
Case Report: Optical genome mapping enables identification of complex balanced chromosomal rearrangements
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1555485
- 3,056 views
- 1 citation
Original Research
Published on 22 May 2025
Outcomes of cochlear implants in patients with PCDH15 mutations: a clinical study
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1541333
- 2,281 views
- 1 citation
Methods
Published on 22 May 2025
stGuide advances label transfer in spatial transcriptomics through attention-based supervised graph representation learning
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1566675
- 2,852 views
- 1 citation
Original Research
Published on 22 May 2025
Whole exome sequencing and bioinformatics reveal PMAIP1 and PDGFRL as immune-related gene markers in follicular thyroid carcinoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1509245
- 2,496 views
- 2 citations
Original Research
Published on 21 May 2025
IGF-1 secreted by mesenchymal stem cells affects the function of lymphatic endothelial progenitor cells: a potential strategy for the treatment of lymphedema
in Stem Cell Research
Frontiers in Genetics
doi 10.3389/fgene.2025.1584095
- 3,322 views
- 2 citations
Original Research
Published on 20 May 2025
IFI35 and IFIT3 are potentially important biomarkers for early diagnosis and treatment of esophageal squamous cell carcinoma: based on WGCNA and machine learning analysis
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1583202
- 2,438 views
Editorial
Published on 20 May 2025
Editorial: A year in review: discussions in human and medical genomics
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1618183
- 1,752 views
Original Research
Published on 20 May 2025
Impact of ITH on PRAD patients and feasibility analysis of the positive correlation gene MYLK2 applied to PRAD treatment
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1589259
- 3,118 views
Original Research
Published on 20 May 2025
Lack of association between genetic variations in CYP3A5 and blood pressure or hypertension risk in the UK biobank
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1490863
- 2,312 views
Original Research
Published on 19 May 2025
Normal hearing function genetics: have you heard all about it? An integrated approach of genome-wide association studies and transcriptome-wide association studies in three Italian cohorts
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1522338
- 3,248 views
- 1 citation
Original Research
Published on 19 May 2025
Evaluating the therapeutic potential of BSA-reduced mussel-derived selenium nanoparticles to mitigate copper sulfate-induced hepatic damage and neurodegeneration in a zebrafish model
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1522370
- 2,378 views
- 3 citations
Case Report
Published on 19 May 2025
Cognitive decline in an adult with ATR-16 syndrome due to an unbalanced translocation between 11p15.5 and 16p13.3: a case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1595298
- 2,003 views
Original Research
Published on 19 May 2025
Analysis of the correlation between RFC4 expression and tumor immune microenvironment and prognosis in patients with cervical cancer
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1514383
- 2,976 views
- 3 citations