Publications by authors named "Stanley Fahn"

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in untreated Parkinson's disease in sub-Saharan Africa: A 12-month, multicenter, randomized, controlled trial.
Roberto Cilia, Momodou Cham, Vida Obese, Albert Akpalu, Emanuele Cereda, Stanley Fahn

J Parkinsons Dis· November 2025

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Genome-Wide Association Study of Glucocerebrosidase Activity Modifiers.
Emma N Somerville, Lynne Krohn, Konstantin Senkevich, Eric Yu, Jamil Ahmad, Stanley Fahn

Mol Neurobiol· September 2025

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Parkinson's Disease, Second Edition.
Serge Przedborski, Stanley Fahn

Cold Spring Harb Perspect Med· September 2025

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Correction: The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.
Jace Jones-Tabah, Kathy He, Nathan Karpilovsky, Konstantin Senkevich, Ghislaine Deyab, Stanley Fahn

Mol Neurodegener· December 2024

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The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.
Jace Jones-Tabah, Kathy He, Nathan Karpilovsky, Konstantin Senkevich, Ghislaine Deyab, Stanley Fahn

Mol Neurodegener· November 2024

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Genome-wide association study of glucocerebrosidase activity modifiers.
Emma N Somerville, Lynne Krohn, Konstanin Senkevich, Eric Yu, Jamil Ahmad, Stanley Fahn

Res Sq· June 2024

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Intrinsic auricular muscle zone stimulation for Parkinson disease: The EARSTIM-PD Phase II multi-center pilot study results.
Hubert H Fernandez, Eric A Macklin, Robert A Hauser, Kelvin L Chou, Yusuf O Cakmak, Stanley Fahn

Parkinsonism Relat Disord· April 2024

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Association of Rare Variants in ARSA with Parkinson's Disease.
Konstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, Eric Yu, Jamil Ahmad, Stanley Fahn

Mov Disord· October 2023

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Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations.
Julian Agin-Liebes, Richard A Hickman, Jean Paul Vonsattel, Phyllis L Faust, Xena Flowers, Stanley Fahn

Mov Disord· August 2023

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Treatment of strabismus and blepharospasm with Botox (onabotulinumtoxinA): Development, insights, and impact.
Alan B Scott, Stanley Fahn, Mitchell F Brin

Medicine (Baltimore)· July 2023

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GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease.
Konstantin Senkevich, Cornelia E Zorca, Aliza Dworkind, Uladzislau Rudakou, Emma Somerville, Stanley Fahn

Brain· May 2023

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Association of rare variants in with Parkinson's disease.
Konstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, Eric Yu, Jamil Ahmad, Stanley Fahn

medRxiv· March 2023

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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Stanley Fahn

Mov Disord· February 2023

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Baseline Differences in Long-term Survivors and Nonsurvivors of the Colorado/Columbia Fetal Implant Trial.
Cynthia McRae, Michelle Dunk, Dan Russell, Heiner Ellgring, Yaakov Stern, Stanley Fahn

J Int Neuropsychol Soc· May 2022

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COVID-19 manifestations in people with Parkinson's disease: a USA cohort.
Yaqian Xu, Matthew Surface, Amanda K Chan, Joshua Halpern, Nora Vanegas-Arroyave, Stanley Fahn

J Neurol· March 2022

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Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1.
Sarah A O'Shea, Richard A Hickman, Etty Cortes, Jean Paul Vonsattel, Stanley Fahn

Mov Disord· November 2021

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Neuropathological correlation supports automated image-based differential diagnosis in parkinsonism.
Katharina A Schindlbeck, Deepak K Gupta, Chris C Tang, Sarah A O'Shea, Kathleen L Poston, Stanley Fahn

Eur J Nucl Med Mol Imaging· October 2021

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What Is the Most Important and Impactful Paper Related to Movement Disorder Therapy Published in the 20th Century?
Stanley Fahn

Mov Disord Clin Pract· October 2021

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Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, Enrico Mingardo, Haktan B Erdem, Stanley Fahn

Genet Med· September 2021

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Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants.
Laura Williams, Diana A Olszewska, Conor Fearon, Brian Magennis, Allan McCarthy, Stanley Fahn

Mov Disord Clin Pract· August 2021

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LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease.
Yuri L Sosero, Eric Yu, Lynne Krohn, Uladzislau Rudakou, Kheireddin Mufti, Stanley Fahn

Neurobiol Aging· July 2021

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Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease.
Jasmin Galper, Manisha Balwani, Stanley Fahn, Cheryl Waters, Lynne Krohn

Mov Disord· June 2021

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Persistent dyskinesias in patients with fetal tissue transplantation for Parkinson disease.
Paul E Greene, Stanley Fahn, David Eidelberg, Kimberly B Bjugstad, Robert E Breeze

NPJ Parkinsons Dis· April 2021

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Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations.
Uladzislau Rudakou, Eric Yu, Lynne Krohn, Jennifer A Ruskey, Farnaz Asayesh, Stanley Fahn

Brain· March 2021

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Oleh Hornykiewicz, a giant in the understanding and treatment of Parkinson disease.
Luigi Zecca, Christian Pifl, Stanley Fahn, David Sulzer, Ruggero G Fariello

NPJ Parkinsons Dis· January 2021

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