Case Report
Published on 08 Dec 2025
Early onset Arboleda-Tham syndrome due to KAT6A variants: Case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1704725
- 1,490 views
Type at least 3 characters
16,584 articles
articles
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
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1719182
- 1,428 views
Original Research
Published on 05 Dec 2025
Optical genome mapping uncovers clinically relevant structural variants in congenital heart disease with heterotaxy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1673539
- 1,362 views
Original Research
Published on 04 Dec 2025
Integrating GWAS and machine learning for disease risk prediction in the Taiwanese Hakka population
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1694084
- 1,872 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
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1615167
- 1,700 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
in ELSI in Science and Genetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1704364
- 1,968 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
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1749030
- 1,122 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
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2025.1642286
- 1,301 views
Original Research
Published on 01 Dec 2025
Bulk RNA-seq deconvolution heterogeneity across paired pancreatic cancer human samples
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1662924
- 1,763 views
Case Report
Published on 01 Dec 2025
Case Report: Pitfalls in CF screening – targeted variant analysis can cause misleading results and therapy recommendations
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1693573
- 1,422 views
Correction
Published on 01 Dec 2025
Correction: Computational models for pan-cancer classification based on multi-omics data
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1743847
- 941 views
Original Research
Published on 01 Dec 2025
Potential prognostic biomarkers in restenosis of peripheral arteries identified through comprehensive ceRNA network analysis
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1597644
- 1,469 views
Correction
Published on 01 Dec 2025
Correction: Individual and combined effects of the GSTM1, GSTT1, and GSTP1 polymorphisms on type 2 diabetes mellitus risk: a systematic review and meta-analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1749934
- 1,161 views
Case Report
Published on 01 Dec 2025
Case Report: Novel mutations in two patients with MED13L-related intellectual disability highlighting the importance of genetic counseling
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1669849
- 1,425 views
Case Report
Published on 28 Nov 2025
Type 1 Bartter syndrome presenting as primary diabetes insipidus: a rare Case Report with 8-year follow-up
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1672214
- 1,472 views
Case Report
Published on 27 Nov 2025
Case Report: developmental delay and intellectual disability linked to a maternally inherited derivative chromosome 3 from a t(3;8) translocation
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1662915
- 1,369 views
Review
Published on 27 Nov 2025
Biogenesis and function of circular RNAs and their implications in the Down syndrome brain
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1708015
- 2,013 views
Original Research
Published on 27 Nov 2025
Development of a senescence-related lncRNA signature in endometrial cancer based on multiple machine learning models
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1687922
- 1,884 views
Correction
Published on 27 Nov 2025
Correction: Validation of a genome-wide polygenic score for body mass index in South Asians
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1708353
- 1,384 views
Original Research
Published on 26 Nov 2025
BAG3-related myofibrillar myopathy: focus on its cardiac involvement
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2025.1636999
- 1,806 views
Original Research
Published on 26 Nov 2025
Molecular mechanisms of TTC21B gene mutations in nephronophthisis type 12 and genetic prevention through PGT
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2025.1710252
- 1,538 views
Methods
Published on 26 Nov 2025
OFGPMA: Optimal frequency graph representation learning for pseudogene and miRNA association prediction
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1643921
- 1,088 views
Original Research
Published on 26 Nov 2025
DMAGCL: A dual-masked adaptive graph contrastive learning framework for predicting circRNA-drug sensitivity
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1721716
- 1,549 views
- 1 citation
Original Research
Published on 26 Nov 2025
Identification and experimental validation of demethylation-related genes in diabetic nephropathy
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2025.1675592
- 1,896 views