Review
Published on 12 Feb 2026
Research progress in SYNGAP1-related neurodevelopmental disorders: from pathogenesis to therapeutic strategies
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1773363
- 221 views
- Frontiers in Neurology
- Neurogenetics
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344 articles
articles
Brief Research Report
Published on 11 Feb 2026
Recurrent migraine with visual aura as the primary phenotype of familial neuronal intranuclear inclusion disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1747202
- 283 views
Original Research
Published on 05 Feb 2026
Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: optimizing genetic diagnosis and molecular subregional effects
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1772239
- 418 views
Original Research
Published on 04 Feb 2026
Identification of novel FOXP1 variants in four unrelated patients with intellectual disability and speech impairment
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1743089
- 347 views
General Commentary
Accepted on 29 Jan 2026
Before stroke-like episodes are diagnosed, their definition should be clarified
in Neurogenetics
Frontiers in Neurology
- 118 views
Original Research
Published on 28 Jan 2026
KCNB1 mutation impairs neuronal differentiation by disrupting gene expression temporal regulation and neuron-specific pathways
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1739214
- 487 views
Review
Published on 20 Jan 2026
Disease-modifying therapies for Rett syndrome: a review for neurologists
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2026.1766679
- 1,393 views
Original Research
Accepted on 15 Jan 2026
Unmasking Genetic Etiologies in Neurodevelopmental Disorders Characterized by Cerebral Palsy: Insights from Integrative Genomic Approaches
in Neurogenetics
Frontiers in Neurology
- 282 views
Original Research
Published on 06 Jan 2026
LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1728652
- 728 views
Review
Published on 01 Dec 2025
IDEDNIK syndrome: a newly recognized rare genetic disorder caused by AP1S1 and AP1B1 mutations
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1695128
- 1,175 views
Brief Research Report
Published on 27 Nov 2025
Retropseudogene insertion generated through retrotransposition in the ATP7A gene results in premature stop codons and a case of Menkes disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1680208
- 877 views
Original Research
Published on 26 Nov 2025
Epilepsy-associated CHD2 missense variants and optimization strategies for genetic diagnosis: a comparative analysis of algorithms
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1729387
- 1,253 views
- 1 citation
Correction
Published on 10 Nov 2025
Correction: Exploring the causal relationship between plasma proteins and postherpetic neuralgia: a Mendelian randomization study
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1726757
- 708 views
Systematic Review
Published on 06 Nov 2025
Accelerated biological aging based on DNA methylation clocks is a predictor of stroke occurrence: a systematic review and meta-analysis
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1640853
- 2,020 views
Original Research
Published on 31 Oct 2025
Expanding the spectrum of white matter abnormalities in Wolfram syndrome: a retrospective review
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1623314
- 2,481 views
Editorial
Published on 21 Oct 2025
Editorial: Genetic insights and diagnostic innovations in cerebrovascular and cerebrospinal fluid disorders
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1691759
- 1,792 views
Original Research
Published on 15 Oct 2025
The genotypic and family characteristics and clinical intervention of neurofibromatosis type 1 gene are associated with dystrophic scoliosis by whole-exome sequencing
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1641665
- 2,616 views
Original Research
Published on 15 Oct 2025
Establishment and validation of a phenotype-driven predictive model for the diagnostic efficacy of trio-based whole exome sequencing (trio-WES) in children with genetic neurodevelopmental disorders (g-NDDs)
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1574021
- 1,367 views
Original Research
Published on 09 Oct 2025
Exploring the causal relationship between plasma proteins and postherpetic neuralgia: a Mendelian randomization study
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1575941
- 2,382 views
Review
Published on 02 Oct 2025
Clinical characteristics, molecular mechanisms, and exploration of association with gastrointestinal symptoms in CHAMP1 gene variation-related neurodevelopmental disorders
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1664776
- 2,892 views
Review
Published on 22 Sep 2025
Evaluation of the synapse adhesion molecule Kirrel3 in neurological disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1662931
- 2,996 views
- 2 citations
Review
Published on 12 Sep 2025
CADASIL or NOTCH3 mutaion spectrum diseases? Interpretation of NOTCH3 mutations and clinical heterogeneity in CADASIL
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1662012
- 3,969 views
Original Research
Published on 10 Sep 2025
Spinocerebellar ataxias masquerading as movement disorders: clinical and genetic characterization
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1661707
- 3,151 views
Review
Published on 02 Sep 2025
Riboflavin in neurological diseases: therapeutic advances, metabolic insights, and emerging genetic strategies
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2025.1663136
- 7,610 views
- 4 citations