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Aging and Disease|December 16, 2025
Phosphorylated Ubiquitin as a Clinical Biomarker for Mitochondrial Damage in Neurodegenerative DiseasesFabienne C Fiesel, Jens O Watzlawik, Michael G Heckman, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2024
An integrative systems-biology approach defines mechanisms of Alzheimer's disease neurodegenerationMatthew J Leventhal, Camila A Zanella, Byunguk Kang, et al.
Autophagy|October 28, 2020
Sensitive ELISA-based detection method for the mitophagy marker p-S65-Ub in human cells, autopsy brain, and blood samplesJens O Watzlawik, Xu Hou, Dominika Fricova, et al.
Human Molecular Genetics|July 13, 2016
Identification of genetic modifiers of age-at-onset for familial Parkinson's diseaseErin M Hill-Burns, Owen A Ross, William T Wissemann, et al.
Annals of Neurology|October 8, 2016
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson'sGanqiang Liu, Brendon Boot, Joseph J Locascio, et al.
Archives of Neurology|June 16, 2005
Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonismMichael A Hauser, Yi-Ju Li, Hong Xu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 2, 2022
GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based StudyAleksandra A Szwedo, Ingvild Dalen, Kenn Freddy Pedersen, et al.
Biorxiv : the Preprint Server for Biology|May 4, 2026
Single cell eQTL mapping reveals convergent glial-neuronal risk architecture in Parkinson's diseaseZechuan Lin, Jacob Parker, Vanitha Nithianandam, et al.
BMJ Open|February 26, 2022
Australian Parkinson's Genetics Study (APGS): pilot (n=1532)Svetlana Bivol, George D Mellick, Jacob Gratten, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2021
Accelerating Medicines Partnership: Parkinson's Disease. Genetic ResourceHirotaka Iwaki, Hampton L Leonard, Mary B Makarious, et al.
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