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Neurology. Genetics|May 8, 2026
Stratification of Phenotypes in Childhood-Onset COL4A1/COL4A2-Related Disorders Based on Age of PresentationGiulia S Porcari, Rudmila N Rashid, Caitlyn A Mulvihill, et al.Neurology. Genetics|April 27, 2026
Expanding the Clinical Spectrum of Arboleda-Tham Syndrome: Neuroimaging Findings and Hematologic ManifestationsJee Min Kim, Yoon Sunwoo, Haeryung Kim, et al.Neurology. Genetics|April 16, 2026
Parkinson Disease Pathogenic Variants: Cross-Ancestry Analysis and Microarray Data ValidationSamantha Hong, Mathew J Koretsky, Jens Lichtenberg, et al.Neurology. Genetics|April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function SCN1A Variants and Responsiveness to Sodium Channel BlockersSandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.Neurology. Genetics|February 19, 2026
Investigating the Genetic Relationship Between Vitamin B12 Metabolism and Parkinson DiseaseRaphael Dering, Margarita Onvumere, Lang Liu, et al.Neurology. Genetics|March 3, 2026
Genetically Simulated GLP-1 Receptor Agonism and Cerebral Small Vessel DiseasePanagiotis Zangas, Murad Omarov, Marios K GeorgakisNeurology. Genetics|October 27, 2016
Erratum: Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)Neurology. Genetics|October 30, 2016
Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.Neurology. Genetics|November 11, 2016
Novel HSPB1 mutation causes both motor neuronopathy and distal myopathyD J Lewis-Smith, J Duff, A Pyle, et al.Neurology. Genetics|November 11, 2016
Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsyRikke S Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.Pageof 88