Overview
Benjamin Cocanougher is a Medical Genetics provider practicing medicine in Cincinnati, Ohio.
Dr. Cocanougher is highly rated in 4 conditions, according to our data. His clinical expertise encompasses Galactosemia, Galactose Epimerase Deficiency, Classic Galactosemia, and Galactokinase Deficiency.
He is actively involved in clinical research, co-authoring 25 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. 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.
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Frequently Asked Questions about Dr. Benjamin T. Cocanougher
How do I make an appointment with Dr. Benjamin T. Cocanougher?
You can book an appointment with Dr. Benjamin T. Cocanougher by calling their office at 513-636-4760. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Benjamin T. Cocanougher a top-rated expert for Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Benjamin T. Cocanougher is classified as an Advanced expert for Galactosemia, 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. Benjamin T. Cocanougher specialize in?
While Dr. Benjamin T. Cocanougher is a Medical Genetics, they have specific expertise in Galactosemia, Galactose Epimerase Deficiency, and Classic Galactosemia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Benjamin T. Cocanougher participate in research or clinical trials?
Yes. Dr. Benjamin T. Cocanougher has published 25 articles and abstracts on conditions like Galactosemia. You can view a list of Dr. Benjamin T. Cocanougher'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
- Classic GalactosemiaDr. Cocanougher isAdvanced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Cocanougher isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Cocanougher isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Cocanougher isAdvanced. Learn about Galactosemia.
- Experienced
- AchondroplasiaDr. Cocanougher isExperienced. Learn about Achondroplasia.
- Congenital Fiber-Type DisproportionDr. Cocanougher isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Crouzon SyndromeDr. Cocanougher isExperienced. Learn about Crouzon Syndrome.
- Molybdenum Cofactor Deficiency (MoCD)Dr. Cocanougher isExperienced. Learn about Molybdenum Cofactor Deficiency (MoCD).
- MosaicismDr. Cocanougher isExperienced. Learn about Mosaicism.
- Tubular Aggregate MyopathyDr. Cocanougher isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyDr. Cocanougher isExperienced. Learn about X-Linked Myotubular Myopathy.