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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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  • Research Grant, 2019
    Pathogenesis of the Virome in Parkinson’s Disease

    Study Rationale:
    Numerous studies have implicated viruses as causal factors or potential triggers for Parkinson’s disease (PD). Our study will provide a comprehensive understanding of all the viral...

  • Aligning Science Across Parkinson's, 2019
    Global Parkinson’s Genetics Program (GP2)
    GP2 Logo

    GP2 is a resource of the Aligning Science Across Parkinson's (ASAP) InitiativeIt is an ambitious five-year program to genotype >150,000 volunteers around the world to further understand the genetic...

  • Therapeutic Pipeline Program, 2019
    Identification of Novel Compounds that Improve Mitochondrial Quality Control

    Study Rationale:
    Dysfunction of mitochondria, the powerhouses of the cell, has been linked to degeneration in nerve cells in Parkinson’s disease. When mitochondria can’t function properly, cellular...

  • Improved Biomarkers and Clinical Outcome Measures, 2019
    Applying Artificial Intelligence for Early Identification of Parkinson’s Disease

    Study Rationale:
    The nervous system regulates heart rate in response to situations such as stress and emergencies. Dysfunction of part of the nervous system controlling the heart can cause changes in...

  • Research Grant, 2019
    Enhancing the Clinical Utility of Data-Driven Parkinson’s Subtypes with Knowledge Distillation and Visualization

    Study Rationale:
    Data-driven analytics, such as machine learning methods, have been applied to discover comprehensive Parkinson’s disease (PD) subtypes from observational patient data. However, many...

  • Research Grant, 2019
    Measurement of BMP and NAG Activity in CSF Samples

    Study Rationale:
    Mutations in the LRRK2 gene are a common cause of dominantly inherited Parkinson’s disease (PD). Previous studies showed that urine levels of a lipid [di-22:6-bis(monoacylglycerol...

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

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