Overview
Molly Mcpheron is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Mcpheron is highly rated in 135 conditions, according to our data. Her top areas of expertise are Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), Pompe Disease, and Danon Disease. Dr. Mcpheron is currently accepting new patients.
Her clinical research consists of co-authoring 13 peer reviewed articles and participating in 1 clinical trial. 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
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MANAGED MEDICAID
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- OTHER MEDICAID
- STATE MEDICAID
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1701 N Senate Ave, 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.
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Stephanie Ware is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Ware is highly rated in 89 conditions, according to our data. Her top areas of expertise are Arachnodactyly, KBG Syndrome, Costello Syndrome, and Isolated Ectopia Lentis. Dr. Ware 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
- Distinguished
- Ornithine Transcarbamylase DeficiencyDr. Mcpheron isDistinguished. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Dr. Mcpheron isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- 15q11.2 MicrodeletionDr. Mcpheron isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Mcpheron isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Mcpheron isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Mcpheron isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Mcpheron isAdvanced. Learn about 47 XYY Syndrome.
- Experienced
- 5-Alpha Reductase DeficiencyDr. Mcpheron isExperienced. Learn about 5-Alpha Reductase Deficiency.
- AchondroplasiaDr. Mcpheron isExperienced. Learn about Achondroplasia.
- Acro-Pectoro-Renal Field DefectDr. Mcpheron isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- AcrocephalopolydactylyDr. Mcpheron isExperienced. Learn about Acrocephalopolydactyly.
- Acromegaloid Facial Appearance SyndromeDr. Mcpheron isExperienced. Learn about Acromegaloid Facial Appearance Syndrome.
- Acromicric DysplasiaDr. Mcpheron isExperienced. Learn about Acromicric Dysplasia.