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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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  • Target Advancement Program, 2020
    Identification of ASC as a Disease-modifying Therapeutic Target in Parkinson’s Disease

    Study Rationale:
    Inflammasomes are large multiprotein complexes that play a central role in the innate immune system, the body’s first line of defense against microbes. Inflammasomes are key drivers...

  • Research Grant, 2020
    Targeting of the Raphe-Cortical Pathway to Reduce Levodopa-Induced Psychosis

    Study Rationale:
    Parkinson’s disease is best known as a movement disorder, yet non-motor symptoms such as anxiety, depression and psychosis afflict over 50 percent of patients and severely impact...

  • Biosample Use Program, 2020
    CSF RT-QuIC Alpha-Synuclein Amplification in LRRK2-Parkinson’s Disease

    Study Rationale:
    Parkinson’s disease caused by genetic mutations in the gene called leucine rich repeat kinase 2 (LRRK2) is clinically indistinguishable from idiopathic Parkinson’s disease, in which...

  • Aligning Science Across Parkinson's, 2020
    Impaired Integration of Organelle Function in Parkinson’s Disease
    ASAP logo

    Study Rationale:
    Geneticists have made great progress in identifying gene mutations that either cause Parkinson’s or increase disease risk. The critical next step is to determine how some of these...

  • Aligning Science Across Parkinson's, 2020
    Dissecting the Mechanisms Underlying Disease Progression
    ASAP logo

    Study Rationale:
    The progression of Parkinson’s disease is very variable, with some individuals having a rapid course and others having a longer and more benign course. We believe that by...

  • Aligning Science Across Parkinson's, 2020
    Mapping the LRRK2 Signaling Pathway and Its Interplay with Other Parkinson’s Disease Components
    ASAP logo

    Study Rationale:
    Genetic mutations that lead to the activation of the enzyme LRRK2 are a major cause of inherited Parkinson's disease. We aim to combine the complementary expertise of our four...

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