Overview
Cary Harding is a Medical Genetics specialist and a Pediatrics provider in Portland, Oregon. Dr. Harding is highly rated in 16 conditions, according to our data. His top areas of expertise are Phenylketonuria (PKU), Urea Cycle Disorders (UCD), Mitochondrial Trifunctional Protein Deficiency, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, and Hepatectomy. Dr. Harding is currently accepting new patients.
His clinical research consists of co-authoring 105 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- PPO
- PPO
- EPO
- PPO
- EPO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
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
Wojciech Wiszniewski is a Medical Genetics specialist and a Pediatrics provider in Portland, Oregon. Dr. Wiszniewski is highly rated in 5 conditions, according to our data. His top areas of expertise are Microcephaly, Achalasia Microcephaly Syndrome, Cortical Dysplasia, and Focal or Multifocal Malformations in Neuronal Migration.
University Professional Services
Markus Grompe is a Pediatrics specialist and a Medical Genetics provider in Portland, Oregon. Dr. Grompe is highly rated in 7 conditions, according to our data. His top areas of expertise are Congenital Aplastic Anemia, Tyrosinemia Type 1, Phenylketonuria (PKU), Islet Cell Transplantation, and Hepatectomy.
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, Gastrostomy, and Deep Brain Stimulation. Dr. Hayflick is currently accepting new patients.
Frequently Asked Questions about Dr. Cary O. Harding
How do I make an appointment with Dr. Cary O. Harding?
You can book an appointment with Dr. Cary O. Harding by calling their office at 503-494-8905. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Cary O. Harding a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Cary O. Harding is classified as an Elite 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. Cary O. Harding specialize in?
While Dr. Cary O. Harding is a Medical Genetics, they have specific expertise in Phenylketonuria (PKU), Urea Cycle Disorders (UCD), and Mitochondrial Trifunctional Protein Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Cary O. Harding participate in research or clinical trials?
Yes. Dr. Cary O. Harding has published 105 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Dr. Cary O. Harding's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Cary O. Harding accept my insurance?
Dr. Cary O. Harding accepts most major insurance plans, including BridgeSpan and Cambia Health Solutions. We recommend calling the office directly at 503-494-8905 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
- Elite
- Phenylketonuria (PKU)Dr. Harding isElite. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Dr. Harding isElite. Learn about Urea Cycle Disorders (UCD).
- Distinguished
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maternal HyperphenylalaninemiaDr. Harding isDistinguished. Learn about Maternal Hyperphenylalaninemia.
- Mitochondrial Trifunctional Protein Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Advanced
- Gaucher DiseaseDr. Harding isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Harding isAdvanced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Harding isAdvanced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Harding isAdvanced. Learn about Gaucher Disease Type 3.
- Infantile Refsum DiseaseDr. Harding isAdvanced. Learn about Infantile Refsum Disease.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Experienced
- Argininosuccinic AciduriaDr. Harding isExperienced. Learn about Argininosuccinic Aciduria.
- Fabry DiseaseDr. Harding isExperienced. Learn about Fabry Disease.
- HepatectomyDr. Harding isExperienced. Learn about Hepatectomy.
- HomocystinuriaDr. Harding isExperienced. Learn about Homocystinuria.
- Inborn Amino Acid Metabolism DisorderDr. Harding isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Infantile NeutropeniaDr. Harding isExperienced. Learn about Infantile Neutropenia.