Overview
Brett Graham is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Graham is rated as an Experienced provider by MediFind in the treatment of Dihydropteridine Reductase 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.
His clinical research consists of co-authoring 89 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
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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 Dihydropteridine Reductase 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.
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 Dihydropteridine Reductase Deficiency. Her top areas of expertise are Pompe Disease, Danon Disease, Phenylketonuria (PKU), and Maternal Hyperphenylalaninemia. Dr. Mcpheron is currently accepting new patients.
University Family Physicians, Inc.
Melissa Lah is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Lah is rated as a Distinguished provider by MediFind in the treatment of Dihydropteridine Reductase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Prader-Willi Syndrome, Maternal Hyperphenylalaninemia, and Miller-Dieker Syndrome. Dr. Lah 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
- Elite
- MELAS SyndromeDr. Graham isElite. Learn about MELAS Syndrome.
- Distinguished
- HypotoniaDr. Graham isDistinguished. Learn about Hypotonia.
- Mitochondrial Complex 1 DeficiencyDr. Graham isDistinguished. Learn about Mitochondrial Complex 1 Deficiency.
- Smith-Magenis SyndromeDr. Graham isDistinguished. Learn about Smith-Magenis Syndrome.
- Advanced
- Argininosuccinic AciduriaDr. Graham isAdvanced. Learn about Argininosuccinic Aciduria.
- Cerebellar HypoplasiaDr. Graham isAdvanced. Learn about Cerebellar Hypoplasia.
- Chondrodysplasia Punctata Syndrome
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- CitrullinemiaDr. Graham isAdvanced. Learn about Citrullinemia.
- Coffin-Lowry SyndromeDr. Graham isAdvanced. Learn about Coffin-Lowry Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Graham isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Graham isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Graham isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Graham isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Graham isExperienced. Learn about 47 XYY Syndrome.