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The Lancet. Neurology|November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studiesMike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.Nature Genetics|March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetranceAshley P L Marsh, Delphine Heron, Timothy J Edwards, et al.Neurology|October 19, 2014
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseJessie Theuns, Aline Verstraeten, Kristel Sleegers, et al.Science (New York, N.Y.)|February 1, 2014
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disordersGaia Novarino, Ali G Fenstermaker, Maha S Zaki, et al.Human Mutation|December 24, 2008
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletionPaola S Denora, David Schlesinger, Carlo Casali, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 11, 2019
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohortsHirotaka Iwaki, Cornelis Blauwendraat, Hampton L Leonard, et al.Neurology|July 13, 2012
Large-scale replication and heterogeneity in Parkinson disease genetic lociManu Sharma, John P A Ioannidis, Jan O Aasly, et al.Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.Neurology|September 11, 2015
Large-scale assessment of polyglutamine repeat expansions in Parkinson diseaseLisa Wang, Jan O Aasly, Grazia Annesi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2020
Differences in the Presentation and Progression of Parkinson's Disease by SexHirotaka Iwaki, Cornelis Blauwendraat, Hampton L Leonard, et al.Pageof 50