Original Research
Accepted on 13 Nov 2026
Survival-supervised network fusion for clinically relevant multi-omic cancer subtyping
in Computational Genomics
Frontiers in Genetics
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17,333 articles
articles
Perspective
Accepted on 13 Nov 2026
A genetic mutation does not equate to a confirmed diagnosis—Uncertainty in the interpretation of ATP7B gene variants
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Accepted on 13 Nov 2026
Identification of a Novel EYA1 Frameshift Variant (c.449delG) and Update of EYA1 Variants in Branchio-otorenal Spectrum Disorder
in Applied Genetic Epidemiology
Frontiers in Genetics
Perspective
Published on 13 Nov 2026
Addressing the diagnostic odyssey beyond variant calling: a perspective on long-read sequencing and context-aware genome interpretation
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2026.1965842
- 504 views
Original Research
Published on 13 Nov 2026
Family-based whole-genome and mitochondrial DNA analysis in fatal infantile cardiomyopathy: findings from blood and myocardium
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1998325
- 380 views
Original Research
Published on 13 Nov 2026
Unraveling the causal web between rheumatoid arthritis and fatigue: from genetic causality to therapeutic targets
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2026.1921117
- 408 views
Review
Published on 13 Nov 2026
Governing genomic AI in the era of agentic systems
in ELSI in Science and Genetics
Frontiers in Genetics
doi 10.3389/fgene.2026.1996700
- 345 views
Case Report
Published on 13 Nov 2026
Peripheral nerve involvement in a family with neuronal intranuclear inclusion disease: a case report
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1929909
- 330 views
Brief Research Report
Accepted on 12 Nov 2026
Exploratory joint modeling of genomic and exposure data for type 2 diabetes with BMI and height comparisons in PEGS
in Applied Genetic Epidemiology
Frontiers in Genetics
Case Report
Accepted on 12 Nov 2026
Multistage orthodontic and prosthodontic management of selective tooth agenesis type 4 associated with WNT10A mutation: A case report with literature review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Case Report
Accepted on 12 Nov 2026
Case Report: Co-occurrence of NOTCH2NLC-related neuronal intranuclear inclusion disease and CYP4V2-related Bietti crystalline dystrophy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Editorial
Published on 12 Nov 2026
Editorial: RNA viruses: from molecular mechanisms to novel therapeutic targeting strategies
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2026.2051642
- 240 views
Case Report
Published on 12 Nov 2026
Different phenotypic presentations of congenital insensitivity to pain with anhidrosis in siblings with identical NTRK1 mutations: a case report and literature review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1962821
- 421 views
Case Report
Published on 12 Nov 2026
Case report and literature review of spastic paraplegia type 5: a patient with two heterozygous CYP7B1 nonsense variants
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1955699
- 429 views
Original Research
Published on 12 Nov 2026
Shared molecular and immune signatures of tic disorders and allergic diseases: a cross-disease transcriptomic analysis
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.2031856
- 343 views
Original Research
Published on 12 Nov 2026
A compound genetic family with a maternal pathogenic Xp22.2-p21.3 deletion and an inherited 5q15 duplication classified as a VUS: prenatal diagnosis, genetic counseling, and retrospective clinical analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2026.1920571
- 397 views
Review
Published on 12 Nov 2026
Resolving previously unresolved regions to advance genetic improvement of domesticated animals: technological foundations, breakthroughs, research directions, and current challenges of T2T assemblies
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1995121
- 491 views
Original Research
Accepted on 11 Nov 2026
GIMWAF: A genetically informed microbiome-wide association framework identifies microbial features associated with renal cell carcinoma
in Computational Genomics
Frontiers in Genetics
- 740 views
Review
Accepted on 11 Nov 2026
Integrative Multi-Omics of Metabolic Reprogramming in Gallbladder Cancer: Mechanisms, Tumor Microenvironment Interactions, Diagnostics, and Therapeutic Opportunities
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
- 107 views
Case Report
Accepted on 11 Nov 2026
A Case Report: orofaciodigital syndrome type 1 – maxillofacial signs leading to the diagnosis of previously undetected polycystic kidney disease
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Case Report
Accepted on 11 Nov 2026
Case Report: When Quality Control Goes Wrong — An Incidental Finding of Hb E Compound Heterozygosity with Filipino β⁰-Thalassemia Deletion in a Commercial EQA Material Mistaken as Hb E Homozygote
in Genetics of Common and Rare Diseases
Frontiers in Genetics
- 101 views
Brief Research Report
Accepted on 11 Nov 2026
Case Report: Prenatal Interpretation of Variants of Uncertain Significance Using Integrated Multi-Modal Evidence
in Genetics of Common and Rare Diseases
Frontiers in Genetics
Original Research
Published on 11 Nov 2026
Explainable machine learning identifies a one-carbon–epigenetic axis associated with sperm DNA fragmentation in reproductive-age men with cancer: a retrospective translational cohort study
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.2011975
- 596 views
Data Report
Published on 11 Nov 2026
Chromosome-level genome assembly and annotation of female Acrossocheilus kreyenbergii
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1996339
- 575 views