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Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2018
Suggestive association between OPRM1 and impulse control disorders in Parkinson's diseaseFlorence Cormier-Dequaire, Samir Bekadar, Mathieu Anheim, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 19, 2019
Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar AtaxiaAlhassane Diallo, Heike Jacobi, Arron Cook, et al.Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.Nature Genetics|April 22, 2014
De novo mutations in HCN1 cause early infantile epileptic encephalopathyCaroline Nava, Carine Dalle, Agnès Rastetter, et al.Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.NPJ Parkinson'S Disease|August 10, 2022
Reduced synaptic activity and dysregulated extracellular matrix pathways in midbrain neurons from Parkinson's disease patientsShani Stern, Shong Lau, Andreea Manole, et al.Journal of Medical Genetics|May 1, 2014
Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6Sophie Tezenas du Montcel, Alexandra Durr, Maria Rakowicz, et al.Neurology|May 13, 2021
Primary Progressive Aphasia Associated With GRN Mutations: New Insights Into the Nonamyloid Logopenic VariantDario Saracino, Sophie Ferrieux, Marie Noguès-Lassiaille, et al.Journal of Neurology|July 1, 2018
Long-term evolution of patient-reported outcome measures in spinocerebellar ataxiasHeike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, et al.Neurology|May 10, 2019
Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7Giulia Coarelli, Rebecca Schule, Bart P C van de Warrenburg, et al.Pageof 50