John T Horan, MD
Rare Disease / Clinical Research
Children's Healthcare of Atlanta/Emory University
PI on 1 trial
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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
- Leukocyte adhesion deficiency type I
- Primary hemophagocytic lymphohistiocytosis
- Ocular albinism
- Hurler syndrome
- Shwachman-Diamond syndrome
- Kostmann syndrome
- Autosomal anomaly syndrome
- Aplasia cutis congenita
- X-linked recessive ocular albinism
- Sickle cell-beta-thalassemia disease
- Multiple symmetric lipomatosis
- Severe congenital neutropenia
- Glanzmann thrombasthenia
- Congenital neutropenia
- Leukocyte adhesion deficiency
- Autosomal recessive severe congenital neutropenia
- Neonatal neutropenia
- Hemophagocytic syndrome
- X-linked severe congenital neutropenia
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