Overview
Jennifer Mackenzie practices practicing medicine in Kingston, Canada.
Ms. Mackenzie is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Medium-Chain Acyl-CoA Dehydrogenase Deficiency, 1p36 Deletion Syndrome, Ornithine Translocase Deficiency, and Gaucher Disease Type 3.
She is actively involved in clinical research, co-authoring 33 peer reviewed articles and participating in 1 clinical trial.
Gender
Locations
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.
1 Clinical Trials
Frequently Asked Questions about Jennifer J. Mackenzie
Is Jennifer J. Mackenzie a top-rated expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Jennifer J. Mackenzie is classified as an Advanced expert for Medium-Chain Acyl-CoA Dehydrogenase Deficiency, 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 Jennifer J. Mackenzie participate in research or clinical trials?
Yes. Jennifer J. Mackenzie has published 33 articles and abstracts on conditions like Medium-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Jennifer J. Mackenzie'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
- Advanced
- 1p36 Deletion SyndromeMs. Mackenzie isAdvanced. Learn about 1p36 Deletion Syndrome.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- Classic GalactosemiaMs. Mackenzie isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Mackenzie isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Mackenzie isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Mackenzie isExperienced. Learn about Galactosemia.
- Gaucher Disease Type 3Ms. Mackenzie isExperienced. Learn about Gaucher Disease Type 3.
- HypotoniaMs. Mackenzie isExperienced. Learn about Hypotonia.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Obstructive UropathyMs. Mackenzie isExperienced. Learn about Obstructive Uropathy.
- Ornithine Translocase DeficiencyMs. Mackenzie isExperienced. Learn about Ornithine Translocase Deficiency.
- Phenylketonuria (PKU)Ms. Mackenzie isExperienced. Learn about Phenylketonuria (PKU).
- PhocomeliaMs. Mackenzie isExperienced. Learn about Phocomelia.
- SirenomeliaMs. Mackenzie isExperienced. Learn about Sirenomelia.
- Urea Cycle Disorders (UCD)Ms. Mackenzie isExperienced. Learn about Urea Cycle Disorders (UCD).