Overview
Austin Larson is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Larson is rated as an Experienced provider by MediFind in the treatment of Cornelia De Lange Syndrome. His top areas of expertise are Leigh Syndrome, Proximal Symphalangism, MELAS Syndrome, and Marshall-Smith Syndrome. Dr. Larson is currently accepting new patients.
His clinical research consists of co-authoring 73 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Cornelia De Lange Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
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.
1 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 Cornelia De Lange Syndrome. 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.
Jessica Duis is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Duis is rated as a Distinguished provider by MediFind in the treatment of Cornelia De Lange Syndrome. Her top areas of expertise are Angelman Syndrome, Prader-Willi Syndrome, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Chondrodystrophy, and Gastrostomy.
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
- HypotoniaDr. Larson isAdvanced. Learn about Hypotonia.
- Leigh SyndromeDr. Larson isAdvanced. Learn about Leigh Syndrome.
- Marshall-Smith SyndromeDr. Larson isAdvanced. Learn about Marshall-Smith Syndrome.
- MELAS SyndromeDr. Larson isAdvanced. Learn about MELAS Syndrome.
- MicrognathiaDr. Larson isAdvanced. Learn about Micrognathia.
- Orotic Aciduria Type 1Dr. Larson isAdvanced. Learn about Orotic Aciduria Type 1.
- Experienced
- 2q37 Deletion SyndromeDr. Larson isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Larson isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Larson isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Larson isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Larson isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Larson isExperienced. Learn about Acrorenal Mandibular Syndrome.