Overview
Robert Hopkin is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Hopkin and is rated as an Experienced provider by MediFind in the treatment of Plagiocephaly. His top areas of expertise are Fabry Disease, Micrognathia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, and Multiple Sulfatase Deficiency.
His clinical research consists of co-authoring 132 peer reviewed articles and participating in 4 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Plagiocephaly.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Medical Health
- CareSource
Locations
3333 Burnet Ave, Cincinnati, OH 45229
Additional Areas of Focus
Dr. Hopkin has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
4 Clinical Trials
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.
- Elite
- Fabry Disease
- Distinguished
- Crouzon Syndrome
- Fetal Akinesia Sequence
- Holoprosencephaly
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Micrognathia
- Multiple Sulfatase Deficiency
- Advanced
- 2q37 Deletion Syndrome
- 47 XYY Syndrome
- Aase Syndrome
- Abruzzo-Erickson Syndrome
- Achalasia Microcephaly Syndrome
- Acrodermatitis Enteropathica
- Experienced
- 3MC Syndrome
- Autism Spectrum Disorder
- Brachydactyly Mononen Type
- Cardiofaciocutaneous Syndrome
- Cardiomyopathic Lentiginosis
- Cerebellar Hypoplasia