Skip to main content

Animations

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.

Search or browse funded studies

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

Filters
From
To
  • ${value}

Filter Results (2615${count})

  • Fall 2025 RFP: Data Advice To Action - DATA-PD, 2026
    Blood-based Signatures of CSF Synuclein SAA Positivity

    Study Rationale:                   

    The ability to identify people during life, who are likely to have underlying Lewy body pathology has been a game-changer. However, the current test (SAA) is limited...

  • Research Grant, 2026
    From Functional Maps to Clinical Outcomes: Interpreting GBA1 Variant Effects in Parkinson's Disease

    Study Rationale:                   

    Genetic variants in the GBA1 gene are among the most important risk factors for Parkinson’s disease. GBA1 encodes an enzyme that breaks down waste inside lysosomes...

  • 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...

Two female doctors talking in the lab.

Apply for a Grant

Our funding programs support basic, translational and clinical research from academia and industry.

See Funding Opportunities
We use cookies to ensure that you get the best experience. By continuing to use this website, you indicate that you have read our Terms of Service and Privacy Policy.