Overview
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 Urea Cycle Disorders (UCD), Prader-Willi Syndrome, Pyruvate Decarboxylase Deficiency, and Pyruvate Dehydrogenase Deficiency. Dr. Mccandless is currently accepting new patients.
His clinical research consists of co-authoring 58 peer reviewed articles and participating in 10 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Medica
Locations
13123 E 16th Ave, Children's Hospital Colorado, 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
University Physicians Incorporated
Matthew Taylor is a Medical Genetics specialist and a Cardiologist in Aurora, Colorado. Dr. Taylor is highly rated in 20 conditions, according to our data. His top areas of expertise are Danon Disease, Cardiomyopathy, Dilated Cardiomyopathy (DCM), Familial Dilated Cardiomyopathy, and Heart Transplant.
University Physicians Incorporated
Janet Thomas is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Thomas is highly rated in 8 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Tyrosinemia Type 1, Homocystinuria, and Tyrosinemia Type 3.
Jessica Duis is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Duis has been practicing medicine for over 14 years is highly rated in 4 conditions, according to our data. Her top areas of expertise are Angelman Syndrome, Prader-Willi Syndrome, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Hypotonia, and Gastrostomy. Dr. Duis is currently accepting new patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Prader-Willi Syndrome
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Advanced
- Aarskog Syndrome
- Campomelic Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Cockayne Syndrome
- Coffin-Siris Syndrome
- Experienced
- Argininosuccinic Aciduria
- Brachydactyly Mononen Type
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Chondrodystrophy
- Classic Galactosemia
- Dihydrolipoamide Dehydrogenase Deficiency