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Neurology. Genetics|June 3, 2021
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain, et al.
Neurology. Genetics|June 25, 2021
SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral SclerosisJeroen W Bos, Ewout J N Groen, Renske I Wadman, et al.
Neurology. Genetics|June 25, 2021
Adult-Onset Spinal Muscular Atrophy due to Mutations in the VRK1 GeneAngela Sung, Paolo Moretti, Aziz Shaibani
Neurology. Genetics|June 7, 2021
Association of HLA-DQA2 and HLA-B With Moyamoya Disease in the Chinese Han PopulationJiang Wan, Wei Ling, Zhang Zhengshan, et al.
Neurology. Genetics|March 17, 2021
MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
Neurology. Genetics|March 17, 2021
Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental DisorderJennifer M Bain, Olivia Thornburg, Cheryl Pan, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology. Genetics|December 20, 2021
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic FindingsDianalee McKnight, Sara L Bristow, Rebecca M Truty, et al.
Neurology. Genetics|November 17, 2021
Genetic Predisposition to Mosaic Chromosomal Loss Is Associated With Functional Outcome After Ischemic StrokeMalin Johansson, Annie Pedersen, John W Cole, et al.
Neurology. Genetics|November 29, 2021
Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore SequencingYa Wang, Jianxin Tan, Yan Wang, et al.
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