Overview
Cary Harding is a Medical Genetics specialist and a Pediatrics provider in Portland, Oregon. Dr. Harding is highly rated in 17 conditions, according to our data. His top areas of expertise are Phenylketonuria (PKU), Urea Cycle Disorders (UCD), Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Mitochondrial Trifunctional Protein Deficiency, and Hepatectomy. Dr. Harding is currently accepting new patients.
His clinical research consists of co-authoring 103 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
MediFind strives to display the most accurate insurance information for every doctor. Please contact your provider to confirm if they accept your insurance.
Dr. Cary O. Harding accepts the following insurance:
- BridgeSpan
- PacificSource
- Moda Health
- Regence
- Prominence Health
- Humana
Locations
707 Sw Gaines St, Portland, OR 97239
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.
3 Clinical Trials
University Professional Services
Markus Grompe is a Pediatrics specialist and a Medical Genetics provider in Portland, Oregon. Dr. Grompe is highly rated in 8 conditions, according to our data. His top areas of expertise are Congenital Aplastic Anemia, Tyrosinemia Type 1, Phenylketonuria (PKU), Islet Cell Transplantation, and Hepatectomy.
David Koeller is a Medical Genetics specialist and a Pediatrics provider in Portland, Oregon. Dr. Koeller is highly rated in 12 conditions, according to our data. His top areas of expertise are Glutaric Acidemia Type 1, Glycogen Storage Disease Type 0, Phosphoglycerate Mutase Deficiency, and Andersen Disease. Dr. Koeller is currently accepting new patients.
University Professional Services
Susan Hayflick is a Medical Genetics specialist and a Pediatrics provider in Portland, Oregon. Dr. Hayflick is highly rated in 17 conditions, according to our data. Her top areas of expertise are Mosaic Monosomy 22, Chromosome 13q Duplication, Cat Eye Syndrome, and 15q11.2 Microdeletion. Dr. Hayflick 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
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maternal Hyperphenylalaninemia
- Mitochondrial Trifunctional Protein Deficiency
- Tyrosinemia Type 1
- Advanced
- Gaucher Disease
- Gaucher Disease Type 1
- Gaucher Disease Type 2
- Gaucher Disease Type 3
- Infantile Refsum Disease
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Experienced
- Argininosuccinic Aciduria
- Fabry Disease
- Hepatectomy
- Homocystinuria
- Inborn Amino Acid Metabolism Disorder
- MELAS Syndrome