Opinion
Accepted on 23 Dec 2025
Rethinking Parkinson's Disease Genetics in the Precision Medicine Era: Why Genomic Diversity Matters?
in Neurogenomics
Frontiers in Genetics
- 195 views
- Frontiers in Genetics
- Neurogenomics
- Articles
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231 articles
articles
Correction
Accepted on 17 Dec 2025
Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
in Neurogenomics
Frontiers in Genetics
Case Report
Published on 11 Dec 2025
Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1674158
- 482 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
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1719182
- 647 views
Original Research
Published on 20 Nov 2025
Five novel EP300 variants expand the genetic and phenotypic spectrum of Rubinstein–Taybi syndrome type 2 in Chinese patients
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1690693
- 966 views
Case Report
Published on 06 Nov 2025
Case Report: Co-occurring de novo SHANK3 and SRCAP variants in a patient with autoimmune encephalitis and exhibiting Phelan-McDermid syndrome features
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1699311
- 1,109 views
Case Report
Published on 14 Oct 2025
Ataxia, intentional tremor and hypotonia syndrome caused by a novel POU4F1 gene mutation: a case report
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1702803
- 1,518 views
Original Research
Published on 08 Oct 2025
Integrated transcriptomic and single-cell RNA sequencing identifies lysosomal ion channel genes as potential biomarkers for Alzheimer’s disease
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1676565
- 2,258 views
Original Research
Published on 29 Aug 2025
Affective phenotypes in heterozygous LRRK2 R1441G knock-in mice
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1629897
- 3,599 views
Case Report
Published on 14 Aug 2025
Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1613022
- 3,619 views
- 2 citations
Mini Review
Published on 30 Jul 2025
X chromosome-wide association studies in neurological disorders: uncovering the hidden influence of the X chromosome
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1650259
- 3,993 views
Case Report
Published on 04 Jul 2025
Case Report: The window that closed too soon: lessons from a late CLN2 diagnosis and death of a 9-year-old boy
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1622185
- 3,158 views
Original Research
Published on 18 Jun 2025
Epigenetic mechanisms linking atherosclerosis to ischemic stroke: insights from DNA methylation and transcriptome integration
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1567951
- 2,188 views
Original Research
Published on 25 Apr 2025
Correlation of tumor necrosis factor-α and interleukin-1 single-nucleotide polymorphisms with the risk of migraine development
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1556498
- 1,696 views
- 2 citations
Case Report
Published on 05 Mar 2025
A novel HMBS gene mutation in acute intermittent porphyria: a case report of abdominal pain, seizures, and reversible neuroimaging findings
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1551832
- 1,970 views
Correction
Published on 27 Jan 2025
Corrigendum: Codon usage is influenced by compositional constraints in genes associated with dementia
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1556255
- 1,372 views
Case Report
Published on 17 Jan 2025
Case Report: A 3’ splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1508922
- 2,497 views
Case Report
Published on 07 Jan 2025
Facioscapulohumeral muscular dystrophy type 1 combined with becker muscular dystrophy: a family case report
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1522203
- 2,684 views
Editorial
Published on 10 Dec 2024
Editorial: Multi-omic approaches decipher the pathogenesis of nervous system diseases and identify potential therapeutic drugs
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1520148
- 1,820 views
Editorial
Published on 29 Oct 2024
Editorial: Epigenetic modification in neurological diseases
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1506551
- 1,794 views
- 1 citation
Original Research
Published on 23 Sep 2024
Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1483574
- 4,410 views
- 1 citation
Editorial
Published on 11 Sep 2024
Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1481705
- 1,417 views
Case Report
Published on 21 Aug 2024
Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1421952
- 2,556 views
- 2 citations
Case Report
Published on 17 Jul 2024
Long-term clinical course of adult-onset refractory epilepsy in cardiofaciocutaneous syndrome with a pathogenic MAP2K1 variant: a case report
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1410979
- 2,842 views
- 2 citations