RH
Highly rated in
116
conditions

Dr. Robert J. Hopkin

Burnet Campus
Cincinnati, OH
Highly rated in
116
conditions
Specialties:Pediatrics | Medical Genetics
Experience:33 Years
Clinical Trials:Currently Recruiting for 1 Trial
Accepts:New PatientsMedicare
Highly rated in
116
conditions
About|Expertise|Insurance|Location|Research
Areas of Expertise

Many doctors have expertise treating multiple conditions. MediFind uses a variety of data sources to determine what conditions a doctor treats and their level of experience.

    View 160 More Conditions +
    Check Dr. Robert J. Hopkin's experience treating your condition:
    About Dr. Robert J. Hopkin

    Robert Hopkin is a Pediatrics specialist and a Medical Genetics expert in Cincinnati, Ohio. Hopkin has been practicing medicine for over 33 years and is highly rated in 116 conditions, according to our data. His top areas of expertise are Fabry Disease, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Neurofibromatosis Type 1 (NF1), and Micrognathia. He is licensed to treat patients in Ohio. Hopkin is currently accepting new patients.

    His clinical research consists of co-authoring 124 peer reviewed articles and participating in 4 clinical trials in the past 15 years.

    Insurance

    MediFind strives to display the most accurate insurance information for every doctor. If you do not see your insurance listed for Dr. Robert J. Hopkin it is best to call his office and ask if your insurance is accepted.

    Accepts Medicare

    Dr. Robert J. Hopkin accepts the following insurance:

    •  Ambetter
    •  CareSource
    •  Buckeye Health
    Call to see if your plan is accepted.
    Locations
    3333 Burnet Ave, Cincinnati, OH 45229
    Other Locations
    7777 Yankee Rd, Liberty Township, OH 45044
    Background & Education
    Graduate Institution
    University Of Nevada School Of Medicine, 1990
    Specialties
    Pediatrics
    Medical Genetics
    Licenses
    Clinical Genetics in OH
    Hospital Affiliations
    Cincinnati Childrens Burnet Campus
    University Of Cincinnati Medical Center
    Languages Spoken
    English
    French
    Gender
    Male
    Clinical Research

    Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Doctors 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
    A Phase I/II, Multicenter, Open-Label, Single-Dose, Dose-Ranging Study to Assess the Safety and Tolerability of ST-920, an AAV2/6 Human Alpha Galactosidase A Gene Therapy, in Subjects With Fabry Disease
    Enrollment Status: Recruiting
    Publish Date: November 03, 2022
    Intervention Type: Biological
    Study Drug: ST-920
    Study Phase: Phase 1/Phase 2
    A Phase 2/3, Randomized, Double-Blind, Placebo-Controlled Study of RAD011 (Cannabidiol Oral Solution) for the Treatment of Patients With Prader- Willi Syndrome
    Enrollment Status: Terminated
    Publish Date: December 07, 2022
    Intervention Type: Drug
    Study Drug: RAD011
    Study Phase: Phase 2/Phase 3
    A Randomized, Double Blind, Active Control Study of the Safety and Efficacy of PRX-102 Compared to Agalsidase Beta on Renal Function in Patients With Fabry Disease Previously Treated With Agalsidase Beta
    Enrollment Status: Completed
    Publish Date: October 13, 2022
    Intervention Type: Biological
    Study Drugs: PRX-102 (Pegunigalsidase Alfa)Agalsidase Beta
    Study Phase: Phase 3
    Phase 3, Open-Label, Switch Over Study to Assess Safety, Efficacy & PK of Pegunigalsidase Alfa 2 mg/kg Administered Every 4 Weeks for 52 Weeks in Fabry Disease Patients Currently Treated With Enzyme Replacement Therapy: Fabrazyme® (Agalsidase Beta) or Replagal™ (Agalsidase Alfa)
    Enrollment Status: Completed
    Publish Date: April 07, 2022
    Intervention Type: Biological
    Study Drug: Pegunigalsidase Alfa
    Study Phase: Phase 3
    View 3 Less Clinical Trials -
    124 Total Publications
    Arrhythmia Burden and Heart Rate Response During Exercise in Anderson-Fabry Disease.
    Journal: Texas Heart Institute journal
    Published: September 07, 2022
    Save this doctor for later
    Sign Up
    Looking for the best doctor for you?
    Start Here
    Is this your doctor?
    Find a second opinion
    Not sure about your diagnosis?
    Check Your Symptoms
     
     
     
     
    Learn about our expert tiers
    Learn more
    Similar Doctors
    GG
    Dr. Gregory A. Grabowski
    Medical Genetics
    Highly rated in
    11
    conditions
    Medical Genetics

    3333 Burnet Ave, 
    Cincinnati, OH 
     0.1 mi

    Gregory Grabowski is a Medical Genetics expert in Cincinnati, Ohio. Grabowski has been practicing medicine for over 49 years and is highly rated in 11 conditions, according to our data. His top areas of expertise are Gaucher Disease, Gaucher Disease Type 1, Gaucher Disease Type 2, Spinal Fusion, and Bone Graft. He is licensed to treat patients in Ohio.

    KW
    Dr. Kathryn N. Weaver
    Pediatrics | Medical Genetics
    Highly rated in
    19
    conditions
    Pediatrics
    Medical Genetics

    Cincinnati Childrens Hospital Medical Center

    3333 Burnet Ave, 
    Cincinnati, OH 
     0.1 mi

    Kathryn Weaver is a Pediatrics specialist and a Medical Genetics expert in Cincinnati, Ohio. Weaver has been practicing medicine for over 14 years and is highly rated in 19 conditions, according to our data. Her top areas of expertise are Acrofacial Dysostosis Catania Type, Micrognathia, RASopathies, and Acrofacial Dysostosis Rodriguez Type. She is licensed to treat patients in Ohio. Weaver is currently accepting new patients.

    ES
    Dr. Elizabeth K. Schorry
    Pediatrics | Medical Genetics
    Highly rated in
    10
    conditions
    Pediatrics
    Medical Genetics

    Cincinnati Childrens Hospital Medical Center

    Burnet Campus

    3333 Burnet Ave, 
    Cincinnati, OH 

    Elizabeth Schorry is a Pediatrics specialist and a Medical Genetics expert in Cincinnati, Ohio. Schorry has been practicing medicine for over 41 years and is highly rated in 10 conditions, according to our data. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Malignant Peripheral Nerve Sheath Tumor, and Ehlers-Danlos Syndrome (EDS). She is licensed to treat patients in Ohio. Schorry is currently accepting new patients.