Overview
Elizabeth Schorry is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Schorry is highly rated in 7 conditions, according to our data. Her top areas of expertise are Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Brittle Cornea Syndrome, and Vascular Ehlers-Danlos Syndrome (VEDS).
Her clinical research consists of co-authoring 44 peer reviewed articles and participating in 5 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- PPO
Locations
3333 Burnet Ave, Ml 5021, Cincinnati, OH 45229
Additional Areas of Focus
Dr. Schorry has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
5 Clinical Trials
Children's Hospital Medical Center
Robert Hopkin is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Hopkin is highly rated in 206 conditions, according to our data. His top areas of expertise are Fabry Disease, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Micrognathia, and Orchiectomy.
Howard Saal is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Saal is highly rated in 200 conditions, according to our data. His top areas of expertise are Achondroplasia, Acrofacial Dysostosis Rodriguez Type, Treacher Collins Syndrome, and Acrofacial Dysostosis Catania Type.
Kathryn Weaver is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Weaver is highly rated in 116 conditions, according to our data. Her top areas of expertise are Acrofacial Dysostosis Catania Type, RASopathies, Costello Syndrome, and Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- NeurofibromatosisDr. Schorry isElite. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)
- Advanced
- Brittle Cornea SyndromeDr. Schorry isAdvanced. Learn about Brittle Cornea Syndrome.
- Legius SyndromeDr. Schorry isAdvanced. Learn about Legius Syndrome.
- Musculocontractural Ehlers-Danlos Syndrome (mcEDS)
- Rubinstein-Taybi SyndromeDr. Schorry isAdvanced. Learn about Rubinstein-Taybi Syndrome.
- Vascular Ehlers-Danlos Syndrome (VEDS)
- Experienced
- Achalasia Microcephaly SyndromeDr. Schorry isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Aplasia Cutis CongenitaDr. Schorry isExperienced. Learn about Aplasia Cutis Congenita.
- Chromosome 11 Uniparental DisomyDr. Schorry isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 13q DeletionDr. Schorry isExperienced. Learn about Chromosome 13q Deletion.
- Chromosome 2 Uniparental DisomyDr. Schorry isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 6 Uniparental DisomyDr. Schorry isExperienced. Learn about Chromosome 6 Uniparental Disomy.