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Neurology. Genetics|August 7, 2023
Genomic Diagnoses for Ectopic Intracerebral CalcificationsChangrui Xiao, Thomas Cassini, Daniel Benavides, et al.Neurology. Genetics|August 30, 2023
Cerebral Aneurysms and Recurrent TIAs in a 42-Year-Old Patient With DADA2 Mutation: A Case ReportNetta Agajany, Liran Horev, Netanel Agajany, et al.Neurology. Genetics|June 22, 2023
Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in AfricansNomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, et al.Neurology. Genetics|March 6, 2026
Precision Diagnosis of Wilson Disease Using a MultiGene Panel: Insights From a Prospective Cohort StudyJie Lin, You-Liang Wang, Yongqiang Qu, et al.Neurology. Genetics|March 13, 2026
Plasma isomiRs as Candidate Biomarkers for Amyotrophic Lateral SclerosisRogan G Magee, Vivianna M Van Deerlin, Corey T McMillan, et al.Neurology. Genetics|March 16, 2026
Genetic Landscape and Diagnostic Outcomes of UK Patients With Congenital Myopathies and Muscular Dystrophies Over a 10-Year PeriodGianpaolo Cicala, Jo Mccauley, Rahul Phadke, et al.Neurology. Genetics|March 5, 2026
Utility of Targeted RNA Analysis in Neurogenetic DisordersShoji Ichikawa, Katie Yergert, Brooklynn Gasser, et al.Neurology. Genetics|March 13, 2026
Sex-Based Differences in Disease Burden and Phenotype in CADASIL: A Multicenter Study of 368 Korean PatientsJoong-Goo Kim, Jay Chol Choi, Chul-Hoo Kang, et al.Neurology. Genetics|March 30, 2026
Expanding the Clinicoradiologic Phenotype of the CTSA-Associated Small Vessel Disease CARASAL: A Comparison With CADASILMinne N Cerfontaine, Gido Gravesteijn, Remco J Hack, et al.Neurology. Genetics|April 6, 2026
Toward Trial Readiness in Congenital Myotonic Dystrophy: A Longitudinal Cohort Study of Predictors of Motor Function in ChildhoodMichael Kiefer, Julia M Hartman, Kiera N Berggren, et al.Pageof 88