Overview
Janet Thomas is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Thomas is highly rated in 9 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Urea Cycle Disorders (UCD).
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
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.
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Matthew Taylor is a Medical Genetics provider in Aurora, Colorado. Dr. Taylor is highly rated in 13 conditions, according to our data. His top areas of expertise are Danon Disease, Gaucher Disease Type 1, Gaucher Disease, and Fabry Disease.
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Shawn Mccandless is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Mccandless is highly rated in 25 conditions, according to our data. 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.
University Physicians Incorporated
Ellen Elias is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Elias is highly rated in 17 conditions, according to our data. Her top areas of expertise are Smith-Lemli-Opitz Syndrome, Ehlers-Danlos Syndrome (EDS), Musculocontractural Ehlers-Danlos Syndrome (mcEDS), and Delayed Growth. Dr. Elias is currently accepting new patients.
Frequently Asked Questions about Dr. Janet Thomas
How do I make an appointment with Dr. Janet Thomas?
You can book an appointment with Dr. Janet Thomas by calling their office at 720-777-1234. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Janet Thomas a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Janet Thomas is classified as an Advanced expert for Phenylketonuria (PKU), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Janet Thomas specialize in?
While Dr. Janet Thomas is a Medical Genetics, they have specific expertise in Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Janet Thomas accept my insurance?
Dr. Janet Thomas accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 720-777-1234 to verify that your specific plan is currently accepted before your visit.
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
- Advanced
- Dihydropteridine Reductase Deficiency
- Galactose Epimerase DeficiencyDr. Thomas isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Thomas isAdvanced. Learn about Galactosemia.
- Maternal HyperphenylalaninemiaDr. Thomas isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Dr. Thomas isAdvanced. Learn about Phenylketonuria (PKU).
- Tyrosinemia Type 1Dr. Thomas isAdvanced. Learn about Tyrosinemia Type 1.
- Experienced
- Classic GalactosemiaDr. Thomas isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Thomas isExperienced. Learn about Galactokinase Deficiency.
- Mucopolysaccharidoses (MPS)Dr. Thomas isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency