The Neurodegeneration cluster portfolio consists of research on adult onset neurodegenerative diseases of all types, broadly focusing on pathogenesis, treatment and prevention. Research on the normal structure and function of neural systems is also included to enable identification of intervention strategies. The role of the programmatic team is to develop, implement and manage these research programs and to promote the translation of research findings into clinical practice. Included in the portfolio are topics such as neuronal cell death, protein misfolding, aggregation, and processing, mitochondrial pathologies, epidemiological studies, genetic studies including genome-wide association studies (GWAS), biomarker studies, clinical studies including deep brain stimulation and gene therapy and translational projects that will accelerate bench-to-bedside therapies for neurodegenerative disorders.
| Scientific Staff | Research Area |
| Roderick Corriveau, Ph.D. Program Director Point of contact: AD, vascular dementias, hereditary spastic paraplegia |
Alzheimer’s disease, vascular dementias, and hereditary spastic paraplesia. For Alzheimer’s disease research, studies focused on molecular mechanisms of disease pathophysiology with areas of emphasis including but not limited to: (1) APP, beta-amyloid, presenilins, tau, neurotrophins and synaptic proteins; (2) animal models; (3) neuroinflammation; (4) post-translational protein modifications; (5) protein trafficking and clearance. |
| Amelie Gubitz, Ph.D. Program Director Point of contact: ALS, SBMA (Kennedy's Disease) |
Basic, translational, and clinical research studies of amyotrophic lateral sclerosis (ALS) and X-linked spinal and bulbar muscular atrophy (SBMA, Kennedy's Disease). |
| Beth-Anne Sieber, Ph.D. Program Director Point of contact: PD, parkinsonism, ET, dystonia |
Parkinson’s disease (PD), including molecular biology, cell biology, neurochemistry, deep brain stimulation (DBS), gene therapy, motor and non-motor manifestations. Parkinsonian disorders including multiple system atrophy (MSA) and progressive supranuclear palsy (PSP); essential tremor; dystonia. |
| Margaret Sutherland, Ph.D. Program Director Point of contact: HD, FTD |
Huntington’s Disease (HD), Frontotemporal dementia (FTD), Parkinson’s Disease (PD), genome-wide association (GWA) studies, genetics, biomarkers, stem cells, protein and mitochondrial dynamics, translational research, clinical trials |
| Andrey Kuzmichev Ph.D. Health Program Specialist |
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| Pamela Wernett, Ph.D. Health Program Specialist |
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Neuroscience Center
6001 Executive Blvd.
Bethesda, Maryland 20892