Overview
Janet Thomas is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Thomas is rated as an Advanced provider by MediFind in the treatment of Urea Cycle Disorders (UCD). Her top areas of expertise are Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Tyrosinemia Type 1.
Her clinical research consists of co-authoring 32 peer reviewed articles and participating in 4 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
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- OTHER COMMERCIAL
- POS
- PPO
- EPO
- HMO
- POS
- PPO
Locations
13123 E 16th Ave, Aurora, CO 80045
Additional Areas of Focus
Dr. Thomas has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
4 Clinical Trials
University Physicians Incorporated
Shawn Mccandless is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Mccandless is rated as a Distinguished provider by MediFind in the treatment of Urea Cycle Disorders (UCD). His top areas of expertise are Prader-Willi Syndrome, Urea Cycle Disorders (UCD), Pyruvate Decarboxylase Deficiency, and Pyruvate Dehydrogenase Deficiency. Dr. Mccandless is currently accepting new patients.
Farrah Rajabi is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Rajabi is rated as an Advanced provider by MediFind in the treatment of Urea Cycle Disorders (UCD). Her top areas of expertise are Miller-Dieker Syndrome, Smith-Magenis Syndrome, Oculocutaneous Albinism, and Ornithine Transcarbamylase Deficiency. Dr. Rajabi is currently accepting new patients.
Lauren Beard is a Neonatologist and a Pediatrics provider in Aurora, Colorado. Dr. Beard is rated as an Experienced provider by MediFind in the treatment of Urea Cycle Disorders (UCD). Her top areas of expertise are Urea Cycle Disorders (UCD) and Premature Infant. Dr. Beard 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
- Phenylketonuria (PKU)Dr. Thomas isElite. Learn about Phenylketonuria (PKU).
- Advanced
- Classic GalactosemiaDr. Thomas isAdvanced. Learn about Classic Galactosemia.
- Dihydropteridine Reductase Deficiency
- Galactose Epimerase DeficiencyDr. Thomas isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Thomas isAdvanced. Learn about Galactosemia.
- HomocystinuriaDr. Thomas isAdvanced. Learn about Homocystinuria.
- HypermethioninemiaDr. Thomas isAdvanced. Learn about Hypermethioninemia.
- Experienced
- Epilepsy in ChildrenDr. Thomas isExperienced. Learn about Epilepsy in Children.
- Galactokinase DeficiencyDr. Thomas isExperienced. Learn about Galactokinase Deficiency.
- Mucopolysaccharidoses (MPS)Dr. Thomas isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Pyruvate Decarboxylase DeficiencyDr. Thomas isExperienced. Learn about Pyruvate Decarboxylase Deficiency.