Lauri M. Burroughs, MD
Rare Disease / Clinical Research
Fred Hutch/University of Washington Cancer Consortium
SEATTLE, WA
PI on 1 trial 3 publicationsNPI: 1609090737
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.
- Dyskeratosis congenita
- Primary hemophagocytic lymphohistiocytosis
- Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
- Shwachman-Diamond syndrome
- Immune dysregulation disease with immunodeficiency
- Aplasia cutis congenita
- Genetic polyendocrinopathy
- Multiple symmetric lipomatosis
- Polyendocrinopathy
Clinical trials (1)
Verify independently
Other specialists for Dyskeratosis congenita
Peers ranked by clinical-trial PI role, publications, and verification quality.
- Tom VulliamyCentre for Genomics and Child Health
- Nikolas PontikosInstitute of Ophthalmology
- Jenna AlnajarCentre for Genomics and Child Health
- Manthan PatelCentre for Genomics and Child Health
- Hemanth TummalaCentre for Genomics and Child Health
- Sharon A Savage, MDClinical Genetics BranchMD
- Inderjeet DokalCentre for Genomics and Child Health
- Amanda WalneCentre for Genomics and Child Health