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Office
3333 Burnet Ave
# ML4006
Cincinnati, OH 45229Phone+1 513-636-4760Fax+1 513-636-7297
Education & Training
Cincinnati Children's Hospital Medical CenterResidency, Pediatrics, 1984 - 1985- Cincinnati Childrens Hospital Medical CenterInternship, Transitional Year, 1982 - 1983
University of Michigan Medical SchoolClass of 1982
Certifications & Licensure
OH State Medical License 1985 - 2026
American Board of Medical Genetics and Genomics Clinical Genetics
American Board of Pediatrics Pediatrics
Clinical Trials
- A Randomized Placebo-Controlled Study of Lovastatin in Children With Neurofibromatosis Type 1 Start of enrollment: 2009 Jul 01
- Everolimus for Children With NF1 Chemotherapy-Refractory Radiographic Progressive Low Grade Gliomas Start of enrollment: 2010 Jul 10
- Phase 2 Study of Bevacizumab in Children and Young Adults With NF 2 and Progressive Vestibular Schwannomas Start of enrollment: 2013 May 15
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Publications & Presentations
PubMed
- Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome.Jenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith, Dima Qu'd, Geraldine Kelly-Mancuso
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2024-12-01 - Compound Heterozygous Variants ofAssociated With Congenital Muscular Dystrophy and Progressive Myoclonus Epilepsy: A Case Report.Monica S Arroyo, Christine Fuller, Elizabeth K Schorry, Elizabeth Ulm, Cuixia Tian
Neurology. Genetics. 2024-08-01 - 1 citationsConsensus-Based Best Practice Guidelines for the Management of Spinal Deformity and Associated Tumors in Pediatric Neurofibromatosis Type 1: Screening and Surveillance...Amy L Xu, Krishna V Suresh, Jaime A Gomez, John B Emans, A Noelle Larson
Journal of Pediatric Orthopedics. 2023-08-01
Journal Articles
- Expanding the Clinical Phenotype of Individuals with a 3-Bp in-Frame Deletion of the NF1 Gene (c.2970_2972del): An Update of Genotype–Phenotype CorrelationRachel K Hachen, Elizabeth K Schorry, Arthur S Aylsworth, Katherine A Rauen, Ashraf Syed, Daryl A Scott, Lois J Starr, Donald G Basel, Lynne M Bird, Leah W Burke, Mari..., Nature
- Copb2 Is Essential for Embryogenesis and Hypomorphic Mutations Cause Human MicrocephalyElizabeth Schorry, Kristen Sund, Cynthia A Prows, Human Molecular Genetics
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