Overview
Andrea Yu practices practicing medicine in Ottawa, Canada.
Her clinical expertise encompasses Chromosome 7p Deletion, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Ornithine Transcarbamylase Deficiency, and Inborn Amino Acid Metabolism Disorder.
She is actively involved in clinical research, co-authoring 16 peer reviewed articles.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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.
Frequently Asked Questions about Andrea C. Yu
Is Andrea C. Yu a top-rated expert for Chromosome 7p Deletion?
MediFind is an objective health platform that identifies experts based on real-world data. Andrea C. Yu is classified as an Experienced expert for Chromosome 7p Deletion, 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.
Does Andrea C. Yu participate in research or clinical trials?
Yes. Andrea C. Yu has published 16 articles and abstracts on conditions like Chromosome 7p Deletion. You can view a list of Andrea C. Yu's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Autosomal Dominant Hyper IgE Syndrome
- Chromosome 7p DeletionMs. Yu isExperienced. Learn about Chromosome 7p Deletion.
- Classic GalactosemiaMs. Yu isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Yu isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Yu isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Yu isExperienced. Learn about Galactosemia.
- Hyper IgE SyndromeMs. Yu isExperienced. Learn about Hyper IgE Syndrome.
- Inborn Amino Acid Metabolism Disorder
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaMs. Yu isExperienced. Learn about Methylmalonic Acidemia.
- Ornithine Transcarbamylase Deficiency
- Phenylketonuria (PKU)Ms. Yu isExperienced. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Ms. Yu isExperienced. Learn about Urea Cycle Disorders (UCD).