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Funded Studies

The Foundation supports research across basic, translational and clinical science to speed breakthroughs that can lead to the creation of new treatments and a better quality of life for people with Parkinson's disease.

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Previously funded studies appear chronologically, with the most recent appearing first.

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  • Bridge Funding for Disrupted Neurodegenerative Research Grant Program, 2026
    Region-specific Effects of Pathology and Vocal Training

    Study Rationale:                   

    Voice and communication deficits are common in Parkinson’s disease. They occur early in the disease process, are progressive in nature, and significantly impact...

  • Research Grant, 2026
    Disease Modeling for Neuronal Alpha-synuclein Diseases

    Neuronal alpha-synuclein diseases (NSD), such as Parkinson’s disease, progress slowly and affect people differently, making it hard to predict when symptoms will appear or worsen. Current methods for...

  • Summer 2023 RFP: Accelerating Biological Understanding and Therapeutic Translation for Parkinson’s Disease Program - Biology, 2026
    Characterization of Constrained Peptides Targeting LRRK2 and Downstream Signaling

    Study Rationale:                   

    Genetic mutations in LRRK2 are linked to familial Parkinson’s, however, there are currently no clinically approved inhibitors for LRRK2. In this study, we will...

  • Accelerating Biological Understanding and Therapeutic Translation for Parkinson’s Disease Program, 2023
    Characterization of a Novel Strategy to Target LRRK2 and Its Downstream Signaling Pathway

    Study Rationale: Genetic mutations that activate LRRK2 are linked to familial Parkinson’s disease (PD). However, no clinically approved inhibitors for LRRK2 currently exist. In this study, we will...

  • Fall 2022 RFP: Accelerating Biological Understanding and Therapeutic Translation for Parkinson’s Disease Program - Biology, 2026
    Biomarker Discovery by Interrogating LRRK2 Signaling in Parkinson’s Biosamples with the Asian LRRK2 G2385R and R1628P Variants

    Study Rationale:                   

    Mutations in the LRRK2 gene are the most common genetic cause of Parkinson's disease (PD). Most research has focused on the LRRK2 G2019S mutation seen in Caucasians...

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