Overview
Erin Conboy is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Conboy and is rated as an Experienced provider by MediFind in the treatment of Imperforate Anus. Her top areas of expertise are Hereditary Multiple Osteochondromas, Chromosome 6q Deletion, Chromosome 6p Duplication, and Chromosome 6q Duplication. Dr. Conboy is currently accepting new patients.
Her clinical research consists of co-authoring 30 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Anthem
- CareSource
- Humana
Locations
550 University Blvd, Indianapolis, IN 46202
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.
Brett Graham is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Graham and is rated as a Distinguished provider by MediFind in the treatment of Imperforate Anus. His top areas of expertise are MELAS Syndrome, Mitochondrial Complex 1 Deficiency, Hypotonia, and Smith-Magenis Syndrome. Dr. Graham is currently accepting new patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Hereditary Multiple Osteochondromas
- Advanced
- Cardiomyopathic Lentiginosis
- Chromosome 6p Duplication
- Chromosome 6q Deletion
- Chromosome 6q Duplication
- Coenzyme Q Cytochrome C Reductase Deficiency
- Cortical Dysplasia
- Experienced
- Achalasia Microcephaly Syndrome
- Acromicric Dysplasia
- Angelman Syndrome
- Aplasia Cutis Congenita
- Autism Spectrum Disorder
- Chondrodystrophy