Overview
Theodore Wilson is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Wilson is rated as an Experienced provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. His top areas of expertise are EEC Syndrome, Zlotogora-Ogur Syndrome, Clouston Syndrome, and AEC Syndrome. Dr. Wilson is currently accepting new patients.
His clinical research consists of co-authoring 17 peer reviewed articles. 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
- EPO
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
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.
University Family Physicians, Inc.
Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Hainline is rated as a Distinguished provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. His top areas of expertise are Phenylketonuria (PKU), Pyruvate Carboxylase Deficiency, Urea Cycle Disorders (UCD), and Inborn Amino Acid Metabolism Disorder. Dr. Hainline is currently accepting new patients.
Brett Graham is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Graham is rated as a Distinguished provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. His top areas of expertise are MELAS Syndrome, Mitochondrial Complex 1 Deficiency, Smith-Magenis Syndrome, and Hypotonia. Dr. Graham is currently accepting new patients.
University Family Physicians, Inc.
Molly Mcpheron is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Mcpheron is rated as an Advanced provider by MediFind in the treatment of Phosphoglycerate Mutase Deficiency. Her top areas of expertise are Pompe Disease, Danon Disease, Phenylketonuria (PKU), and Maternal Hyperphenylalaninemia. Dr. Mcpheron is currently accepting new patients.
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
- Advanced
- 15q11.2 MicrodeletionDr. Wilson isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Wilson isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Wilson isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Wilson isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Wilson isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Wilson isAdvanced. Learn about Aase Syndrome.
- Experienced
- AchondroplasiaDr. Wilson isExperienced. Learn about Achondroplasia.
- Acro-Pectoro-Renal Field DefectDr. Wilson isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- Acrofrontofacionasal Dysostosis Syndrome
- Acropectoral SyndromeDr. Wilson isExperienced. Learn about Acropectoral Syndrome.
- Adams-Oliver SyndromeDr. Wilson isExperienced. Learn about Adams-Oliver Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Wilson isExperienced. Learn about Adrenoleukodystrophy (ALD).