Overview
Shawn Mccandless is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Mccandless is rated as an Elite provider by MediFind in the treatment of Prader-Willi 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.
His clinical research consists of co-authoring 57 peer reviewed articles and participating in 10 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 9 articles and participated in 6 clinical trials in the study of Prader-Willi Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
13123 E 16th Ave, Aurora, CO 80045
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.
9 Clinical Trials
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 Prader-Willi Syndrome. Her top areas of expertise are Angelman Syndrome, Prader-Willi Syndrome, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Chondrodystrophy, and Gastrostomy.
Daniel Pique is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Pique is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are 15q11.2 Microdeletion and Prader-Willi Syndrome.
University Physicians Incorporated
Matthew Taylor is a Medical Genetics provider in Aurora, Colorado. Dr. Taylor is rated as a Distinguished provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Danon Disease, Gaucher Disease Type 1, Gaucher Disease, and Fabry Disease.
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
- Prader-Willi SyndromeDr. Mccandless isElite. Learn about Prader-Willi Syndrome.
- Urea Cycle Disorders (UCD)Dr. Mccandless isElite. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Aarskog SyndromeDr. Mccandless isAdvanced. Learn about Aarskog Syndrome.
- Campomelic DysplasiaDr. Mccandless isAdvanced. Learn about Campomelic Dysplasia.
- Camptodactyly Syndrome Guadalajara Type 1Dr. Mccandless isAdvanced. Learn about Camptodactyly Syndrome Guadalajara Type 1.
- Camptodactyly Syndrome Guadalajara Type 2Dr. Mccandless isAdvanced. Learn about Camptodactyly Syndrome Guadalajara Type 2.
- Cockayne SyndromeDr. Mccandless isAdvanced. Learn about Cockayne Syndrome.
- Coffin-Siris SyndromeDr. Mccandless isAdvanced. Learn about Coffin-Siris Syndrome.
- Experienced
- Argininosuccinic AciduriaDr. Mccandless isExperienced. Learn about Argininosuccinic Aciduria.
- Brachydactyly Mononen TypeDr. Mccandless isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 DeficiencyDr. Mccandless isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- ChondrodystrophyDr. Mccandless isExperienced. Learn about Chondrodystrophy.
- Classic GalactosemiaDr. Mccandless isExperienced. Learn about Classic Galactosemia.
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Mccandless isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.