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Movement Disorders : Official Journal of the Movement Disorder Society|March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsyMax-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Scientific Reports|July 17, 2021
Multidisciplinary assessment of the Abbott BinaxNOW SARS-CoV-2 point-of-care antigen test in the context of emerging viral variants and self-administrationJennifer K Frediani, Joshua M Levy, Anuradha Rao, et al.
Cell Stem Cell|January 22, 2013
A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibitionDaniel J Goff, Angela Court Recart, Anil Sadarangani, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Nature Medicine|March 25, 2026
LRRK2-targeting antisense oligonucleotide in Parkinson's disease: a phase 1 randomized controlled trialOmar S Mabrouk, Ben Tichler, H Moore Arnold, et al.
JAMA Neurology|June 8, 2026
Pathology and Genetics in a Global Cohort of Parkinsonian DisordersLesley Y Wu, Tessa du Toit, Tatiana Georgiades, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
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