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Journal of the Neurological Sciences|October 25, 2016
Neuropsychiatric characteristics of GBA-associated Parkinson diseaseMatthew Swan, Nancy Doan, Robert A Ortega, et al.
Neurology|February 27, 2020
Defining research priorities in dystoniaCodrin Lungu, Laurie Ozelius, David Standaert, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.
Brain Communications|June 2, 2023
Establishing a natural history of X-linked dystonia parkinsonismPatrick Acuna, Melanie Leigh Supnet-Wells, Neil A Spencer, et al.
Neurology. Genetics|March 16, 2017
Research conference summary from the 2014 International Task Force on ATP1A3-Related DisordersHendrik Rosewich, Matthew T Sweney, Suzanne DeBrosse, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2020
TAF1 Transcripts and Neurofilament Light Chain as Biomarkers for X-linked Dystonia-ParkinsonismJamal Al Ali, Christine A Vaine, Shivangi Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonismRachita Yadav, Christine A Vaine, Aloysius Domingo, et al.
Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 19, 2013
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutationsRoy N Alcalay, Anat Mirelman, Rachel Saunders-Pullman, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
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