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Neurology. Genetics|April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Neurology. Genetics|April 26, 2021
Interactive Effects of HLA and GM Alleles on the Development of Alzheimer DiseaseJanardan P Pandey, Paul J Nietert, Ronald T Kothera, et al.
Neurology. Genetics|April 26, 2021
Novel Cysteine-Sparing Hypomorphic NOTCH3 A1604T Mutation Observed in a Family With Migraine and White Matter LesionsSnjolaug Arnardottir, Francesca Del Gaudio, Stefanos Klironomos, et al.
Neurology. Genetics|April 15, 2021
Progressive Ataxia and Neurologic Regression in RFXANK-Associated Bare Lymphocyte SyndromeEssa Alharby, Mona Obaid, Mohammed A O Elamin, et al.
Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.
Neurology. Genetics|August 22, 2020
Erratum: Neuraxial dysraphism in EPAS1-associated syndrome due to improper mesenchymal transition
Neurology. Genetics|May 1, 2023
Identifying Aging and Alzheimer Disease-Associated Somatic Variations in Excitatory Neurons From the Human Frontal CortexMeng Zhang, Gerard A Bouland, Henne Holstege, et al.
Neurology. Genetics|May 8, 2023
CircPDS5B Reduction Improves Angiogenesis Following Ischemic Stroke by Regulating MicroRNA-223-3p/NOTCH2 AxisLing Kui, Zongyu Li, Guoyun Wang, et al.
Neurology. Genetics|May 8, 2023
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic DisordersNika Schuermans, Hannah Verdin, Jody Ghijsels, et al.
Neurology. Genetics|May 18, 2023
Complex 4q35 and 10q26 Rearrangements: A Challenge for Molecular Diagnosis of Patients With Facioscapulohumeral DystrophyMegane Delourme, Chaix Charlene, Laurene Gerard, et al.
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