Overview
Mari Mori is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Atlanta, Georgia.
Dr. Mori is highly rated in 5 conditions, according to our data. Her clinical expertise encompasses FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Von Gierke Disease, and Ornithine Transcarbamylase Deficiency.
She is actively involved in clinical research, co-authoring 36 peer reviewed articles. Dr. Mori is currently accepting new patients.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- HMO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
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. 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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The Emory Clinic Inc
Jaime Vengoechea-Barrios is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Atlanta, Georgia. Dr. Vengoechea-Barrios is highly rated in 9 conditions, according to our data. His clinical expertise encompasses Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, Fabry Disease, and Gaucher Disease Type 3. Dr. Vengoechea-Barrios is currently accepting new patients.
Frequently Asked Questions about Dr. Mari A. Mori
Is Dr. Mari A. Mori a top-rated expert for FG Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Mari A. Mori is classified as an Advanced expert for FG Syndrome, 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. Mari A. Mori specialize in?
While Dr. Mari A. Mori is a Medical Genetics, they have specific expertise in FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Von Gierke Disease. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Mari A. Mori participate in research or clinical trials?
Yes. Dr. Mari A. Mori has published 36 articles and abstracts on conditions like FG Syndrome. You can view a list of Dr. Mari A. Mori's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Mari A. Mori accept my insurance?
Dr. Mari A. Mori accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly to verify that your specific plan is currently accepted before your visit.
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
- Andersen DiseaseDr. Mori isAdvanced. Learn about Andersen Disease.
- FG SyndromeDr. Mori isAdvanced. Learn about FG Syndrome.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Ornithine Transcarbamylase Deficiency
- Von Gierke DiseaseDr. Mori isAdvanced. Learn about Von Gierke Disease.
- Experienced
- 3MC SyndromeDr. Mori isExperienced. Learn about 3MC Syndrome.
- Acromicric DysplasiaDr. Mori isExperienced. Learn about Acromicric Dysplasia.
- Alpha ThalassemiaDr. Mori isExperienced. Learn about Alpha Thalassemia.
- Arginase DeficiencyDr. Mori isExperienced. Learn about Arginase Deficiency.
- Atypical Hemolytic Uremic Syndrome (aHUS)
- Beta-Ketothiolase DeficiencyDr. Mori isExperienced. Learn about Beta-Ketothiolase Deficiency.