Perspective
Accepted on 09 Dec 2025
Monitoring diversity in genome-wide association studies requires measuring and reporting on immigration-related factors
Frontiers in Genetics
- 139 views
962 Publications
volumes
Original Research
Accepted on 08 Dec 2025
(Not) "Just Your Nature". Diagnostic Journeys of Adults with Neurofibromatosis Type 1 in Poland
Frontiers in Genetics
- 160 views
Original Research
Accepted on 08 Dec 2025
Biobanking as a Research Accelerator: Perspectives of Medical Students and interns in a Saudi University
Frontiers in Genetics
- 198 views
Original Research
Accepted on 08 Dec 2025
Systematic analysis of anoikis-related genes identifies SRPX2-FAK/AKT-IL-6 axis in the progression and peritoneal metastasis of gastric cancer
Frontiers in Genetics
- 242 views
Original Research
Accepted on 08 Dec 2025
Identification of major QTLs for seed vigor and growth-related traits using a bi-parental population in soybean
Frontiers in Genetics
- 132 views
Original Research
Accepted on 08 Dec 2025
scVAR: integrating genomics and transcriptomics from single-cell RNA-seq — insights from leukemia case studies
Frontiers in Genetics
- 166 views
Mini Review
Accepted on 08 Dec 2025
Metabolic Reprogramming in Clear Cell Renal Cell Carcinoma: Core Pathways and Targeted Therapeutic Strategies
Frontiers in Genetics
- 149 views
Systematic Review
Accepted on 08 Dec 2025
A Systematic Review on the Generative AI Applications in Human Medical Genetics
Frontiers in Genetics
- 162 views
Review
Published on 08 Dec 2025
The risk factors for chemotherapy myelosuppression in breast cancer: a systematic review and meta-analysis
Frontiers in Genetics
doi 10.3389/fgene.2025.1704489
- 908 views
Case Report
Published on 08 Dec 2025
Early onset Arboleda-Tham syndrome due to KAT6A variants: Case report
Frontiers in Genetics
doi 10.3389/fgene.2025.1704725
- 836 views
Original Research
Published on 08 Dec 2025
Sex-specific circRNA–miRNA–mRNA networks in peripheral blood mononuclear cells of patients with idiopathic pulmonary arterial hypertension: a pilot study
Frontiers in Genetics
doi 10.3389/fgene.2025.1674894
- 863 views
Case Report
Published on 08 Dec 2025
Neuronal intranuclear inclusion disease presenting with recurrent dizziness and headache: a case report with 5-year follow-up
Frontiers in Genetics
doi 10.3389/fgene.2025.1719182
- 738 views
Original Research
Published on 05 Dec 2025
Optical genome mapping uncovers clinically relevant structural variants in congenital heart disease with heterotaxy
Frontiers in Genetics
doi 10.3389/fgene.2025.1673539
- 949 views
Case Report
Accepted on 04 Dec 2025
Genotype–Phenotype Correlations in FLNA Mutations: Insights from a Case of Multisystem Dysfunction
Frontiers in Genetics
- 179 views
Original Research
Published on 04 Dec 2025
Integrating GWAS and machine learning for disease risk prediction in the Taiwanese Hakka population
Frontiers in Genetics
doi 10.3389/fgene.2025.1694084
- 1,233 views
Original Research
Published on 04 Dec 2025
Development of a prognostic model related to mitochondria and programmed cell death-related genes in bladder cancer
Frontiers in Genetics
doi 10.3389/fgene.2025.1615167
- 1,083 views
Original Research
Published on 03 Dec 2025
Perspectives of parents receiving normal results from genomic newborn screening: a mixed-methods evaluation from the early check program
Frontiers in Genetics
doi 10.3389/fgene.2025.1704364
- 1,283 views
Original Research
Accepted on 02 Dec 2025
Expanding the Mutational Spectrum of Congenital Microcephaly in Pakistani Families
Frontiers in Genetics
- 378 views
Review
Accepted on 02 Dec 2025
The power and the promise of epigenetic drugs in oncology
Frontiers in Genetics
- 197 views
Original Research
Accepted on 01 Dec 2025
Conditional Trust as a Driver of Public Engagement in Korea's National Project of Bio-Big Data
Frontiers in Genetics
- 245 views
Case Report
Accepted on 01 Dec 2025
Familial Multiple Fetal Cerebral Arteriovenous Malformations: A Case Report of Maternal Genetic Susceptibility and Fetal Manifestation
Frontiers in Genetics
- 109 views
Correction
Published on 01 Dec 2025
Correction: MAPT mutation-induced behavioral variant frontotemporal dementia in an Asian patient: a multimodal biomarker case report resolving diagnostic challenges with Alzheimer’s disease
Frontiers in Genetics
doi 10.3389/fgene.2025.1749030
- 889 views
Original Research
Published on 01 Dec 2025
FusDRM-m5C: a hybrid model for accurate prediction of 5-methylcytosine modification sites based on feature fusion and attention mechanism
Frontiers in Genetics
doi 10.3389/fgene.2025.1642286
- 1,017 views
Original Research
Published on 01 Dec 2025
Bulk RNA-seq deconvolution heterogeneity across paired pancreatic cancer human samples
Frontiers in Genetics
doi 10.3389/fgene.2025.1662924
- 1,154 views