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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, 2018
    Studying Monocyte Entry into the Brain in Alpha-synuclein-induced Parkinson's Disease (supplement)

    Study Rationale:
    In the past, we demonstrated that entry of CCR2-positive monocytes into the brain is required for alpha-synuclein-induced inflammation and neurodegeneration in a model of Parkinson's...

  • Research Grant, 2018
    Measuring Protein Modifications to Monitor the Efficacy of LRRK2 Inhibitors

    Study Rationale:
    Leucine-rich repeat kinase 2 (LRRK2) is the greatest known genetic contributor to Parkinson's disease (PD). One important function of LRRK2 is to modify itself and proteins called Rab...

  • Target Advancement Program, 2018
    Interactions Between Alpha-synuclein and Glycoproteins as a Therapeutic Target

    Study Rationale:
    In Parkinson's disease (PD), the sticky protein alpha-synuclein clumps in the brain, causing cell death. Such toxic alpha-synuclein clumps can spread from cell to cell and multiply. It...

  • Target Advancement Program, 2018
    Investigating Alpha-synuclein Clumping in the Organoid Model of Parkinson's Disease

    Study Rationale:
    Alpha-synuclein -- a sticky protein that clumps in the brains of people with Parkinson's disease (PD) -- is a major target for the development of therapies for PD. Alpha-synuclein...

  • Inflammation Biomarkers Program, 2018
    The Role of Inflammation and Risk of Parkinson's Disease in People with GBA1 Mutations

    Study Rationale:
    Mutations (changes) in GBA1, the gene that directs the production of the glucocerebrosidase (GBA) protein, can increase the risk of Parkinson's disease (PD) in some people, but not in...

  • Mitochondrial Biomarkers Program, 2018
    Searching for Signs of Mitochondrial Breakdown in People with Parkinson’s Disease with an Unknown Cause

    Study Rationale:
    Some inherited forms of Parkinson's disease (PD) are caused by mutations (genetic changes) that lead to the breakdown of mitochondria, cell's energy generators. In some cases of...

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