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.
Specialties
Licenses
Languages Spoken
Gender
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
Kathryn Weaver is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Weaver has been practicing medicine for over 17 years is highly rated in 117 conditions, according to our data. Her top areas of expertise are Acrofacial Dysostosis Catania Type, RASopathies, Costello Syndrome, and Noonan Syndrome.
Howard Saal is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Saal is highly rated in 201 conditions, according to our data. His top areas of expertise are Achondroplasia, Acrofacial Dysostosis Rodriguez Type, Treacher Collins Syndrome, and Acrofacial Dysostosis Catania Type.
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 208 conditions, according to our data. His top areas of expertise are Fabry Disease, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Micrognathia, and Orchiectomy.
Frequently Asked Questions about Dr. Elizabeth Schorry
Is Dr. Elizabeth Schorry a top-rated expert for Neurofibromatosis?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Elizabeth Schorry is classified as an Elite expert for Neurofibromatosis, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Elizabeth Schorry specialize in?
While Dr. Elizabeth Schorry is a Medical Genetics, they have specific expertise in Neurofibromatosis, Neurofibromatosis Type 1 (NF1), and Brittle Cornea Syndrome. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Elizabeth Schorry participate in research or clinical trials?
Yes. Dr. Elizabeth Schorry has published 44 articles and abstracts on conditions like Neurofibromatosis. You can view a list of Dr. Elizabeth Schorry's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Elizabeth Schorry accept my insurance?
Dr. Elizabeth Schorry accepts most major insurance plans, including Aetna and CareSource. We recommend calling the office directly to verify that your specific plan is currently accepted before your visit.
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.