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Joseph R. Mazzulli

Northwestern University · US
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Area of research
Neurology · Physiology
Research interest
Research interests include Parkinson's Disease Mechanisms and Treatments, Lysosomal Storage Disorders Research, Cellular transport and secretion, and Neurological disorders and treatments.
h-index
36
citations
12,087
works
69
NIH funding
primary concept
email

Recent publications

CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry
iScience 2022cited by 2position: middledoi
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease
New England Journal of Medicine 2019cited by 798position: middledoi
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease
Science 2017cited by 855position: middledoi
Dopamine induces soluble α-synuclein oligomers and nigrostriatal degeneration
Nature Neuroscience 2017cited by 220position: middledoi
α-Synuclein–induced lysosomal dysfunction occurs through disruptions in protein trafficking in human midbrain synucleinopathy models
Proceedings of the National Academy of Sciences 2016cited by 385position: firstdoi
Activation of  -Glucocerebrosidase Reduces Pathological  -Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons
Journal of Neuroscience 2016cited by 275position: firstdoi
Parkin and PINK1 Patient iPSC-Derived Midbrain Dopamine Neurons Exhibit Mitochondrial Dysfunction and α-Synuclein Accumulation
Stem Cell Reports 2016cited by 206position: middledoi
The Glycolytic Enzyme, GPI, Is a Functionally Conserved Modifier of Dopaminergic Neurodegeneration in Parkinson’s Models
Cell Metabolism 2014cited by 104position: middledoi
Identification and Rescue of α-Synuclein Toxicity in Parkinson Patient–Derived Neurons
Science 2013cited by 460position: middledoi
Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease
Science Translational Medicine 2012cited by 505position: middledoi
Sirt1 Mediates Neuroprotection from Mutant Huntingtin by Activation of TORC1 and CREB Transcriptional Pathway
Digital Access to Scholarship at Harvard (DASH) (Harvard University) 2012cited by 368position: middledoi
Deficiency of ATP13A2 Leads to Lysosomal Dysfunction, α-Synuclein Accumulation, and Neurotoxicity
Journal of Neuroscience 2012cited by 288position: middledoi
<i>Glucocerebrosidase</i> mutations in a <scp>S</scp>erbian <scp>P</scp>arkinson's disease population
European Journal of Neurology 2012cited by 55position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Dimitri Krainc · Saint Thomas - Rutherford Hospital9 papers (2012–2017)Guy A. Caldwell · University of Alabama2 papers (2014–2017)Carolyn M. Sue · Research and Design and Technological Institute of Rolling Stock2 papers (2012–2016)Jeffrey N. Savas · Northwestern University2 papers (2012–2017)Lena F. Burbulla · German Center for Neurodegenerative Diseases2 papers (2016–2017)Friederike Zunke · Johannes Gutenberg University Mainz2 papers (2016–2016)Lorenz Studer · Cornell University2 papers (2016–2016) · 1 papers (2017–2017) · 1 papers (2016–2016)Sarah Kishinevsky · Memorial Sloan Kettering Cancer Center1 papers (2016–2016)Michael D. Pluth · Massachusetts Institute of Technology1 papers (2013–2013)Andrea Supinski · Massachusetts Institute of Technology1 papers (2012–2012)Bárbara Schmidt · University Hospital Regensburg1 papers (2022–2022)Chelsee Strojny · Northwestern University1 papers (2017–2017)Rudolf Jaenisch · Massachusetts Institute of Technology1 papers (2013–2013)Judith Blanz · Northwestern University1 papers (2017–2017)Siyuan Zhang · University of Notre Dame1 papers (2014–2014)Hanna Kim · Jeonbuk National University1 papers (2017–2017)Pingping Song · Chinese Academy of Sciences1 papers (2017–2017) · 1 papers (2012–2012)
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