Staci M Peron, Ph.D.
Rare Disease Specialist
National Cancer Institute (NCI)
Bethesda, Maryland
PI on 8 trials
ℹ
Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- Legius syndrome
- Multiple non-ossifying fibromatosis
- Rare genetic cardiac disease
- Rare hereditary neurologic disease with peripheral neuropathy
- Rare skin disease
- Rare genetic tumor
- Hemoglobinopathy
- Rare circulatory system disease
- Sickle cell disease
- Noonan syndrome
- Neurofibromatosis-Noonan syndrome
- Rare neurodegenerative disease
- Hereditary neurocutaneous malformation
- Sickle cell anemia
- Cardiofaciocutaneous syndrome
- Rare cardiac disease
- Diffuse astrocytoma
- Neurofibroma
- Genetic cardiac tumor
- Genetic neurodegenerative disease
- Genetic hemoglobinopathy
- Costello syndrome
- Rare genetic neurological disorder
- Young syndrome
- Rare tumor
- Rare hereditary connective tissue disease
- Rare cardiac tumor
- Neurofibromatosis type 1
- Rare hereditary disease with peripheral neuropathy
- Rare genetic skin disease
Clinical trials (8)
Verify independently
Other specialists for Legius syndrome
Peers ranked by clinical-trial PI role, publications, and verification quality.
- Federico ZaraIRCCS Giannina Gaslini Institute
- Eric LegiusKU Leuven and University Hospital
- Patrizia De MarcoIRCCS Giannina Gaslini Institute
- Valeria CapraGenomics and Clinical Genetics Unit
- Ludwine MessiaenUniversity of Alabama at Birmingham
- Marcello ScalaIRCCS Giannina Gaslini Institute
- Kathryn N Weaver, MDChildren's Hospital Medical Center, Cincinnati
- Douglas R Stewart, M.D.National Cancer Institute (NCI)Maryland