Overview
Bryan Hainline is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Hainline is rated as an Advanced 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.
His clinical research consists of co-authoring 12 peer reviewed articles and participating in 2 clinical trials. 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
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- 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
- 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
975 W Walnut St, 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.
2 Clinical Trials
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.
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 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.
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
- Adrenoleukodystrophy (ALD)Dr. Hainline isDistinguished. Learn about Adrenoleukodystrophy (ALD).
- Inborn Amino Acid Metabolism DisorderDr. Hainline isDistinguished. Learn about Inborn Amino Acid Metabolism Disorder.
- Phenylketonuria (PKU)Dr. Hainline isDistinguished. Learn about Phenylketonuria (PKU).
- Pyruvate Carboxylase DeficiencyDr. Hainline isDistinguished. Learn about Pyruvate Carboxylase Deficiency.
- Urea Cycle Disorders (UCD)Dr. Hainline isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Aarskog SyndromeDr. Hainline isAdvanced. Learn about Aarskog Syndrome.
- Arginase DeficiencyDr. Hainline isAdvanced. Learn about Arginase Deficiency.
- Argininosuccinic AciduriaDr. Hainline isAdvanced. Learn about Argininosuccinic Aciduria.
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Hainline isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Experienced
- 2q37 Deletion SyndromeDr. Hainline isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Hainline isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Hainline isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Hainline isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Hainline isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Hainline isExperienced. Learn about Acrorenal Mandibular Syndrome.