Overview
Jamie Fraser is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Fraser is highly rated in 5 conditions, according to our data. Her top areas of expertise are Methylmalonic Acidemia, Pyruvate Decarboxylase Deficiency, Leukodystrophy, Pyruvate Dehydrogenase Deficiency, and Gastrostomy.
Her clinical research consists of co-authoring 58 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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.
1 Clinical Trials
William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl is highly rated in 31 conditions, according to our data. His top areas of expertise are Oculocutaneous Albinism Type 2, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism, and Deep Brain Stimulation.
Nancy Braverman is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Braverman is highly rated in 14 conditions, according to our data. Her top areas of expertise are Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.
Forbes Porter is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Porter is highly rated in 15 conditions, according to our data. His top areas of expertise are Smith-Lemli-Opitz Syndrome, Niemann-Pick Disease, Reticulohistiocytoma, and X-Linked Creatine Deficiency.
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
- Cockayne SyndromeDr. Fraser isAdvanced. Learn about Cockayne Syndrome.
- LeukodystrophyDr. Fraser isAdvanced. Learn about Leukodystrophy.
- Methylmalonic AcidemiaDr. Fraser isAdvanced. Learn about Methylmalonic Acidemia.
- Pyruvate Decarboxylase DeficiencyDr. Fraser isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Fraser isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Fraser isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Allan-Herndon-Dudley SyndromeDr. Fraser isExperienced. Learn about Allan-Herndon-Dudley Syndrome.
- Cockayne Syndrome Type 1Dr. Fraser isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Dr. Fraser isExperienced. Learn about Cockayne Syndrome Type 2.
- Corpus Callosum AgenesisDr. Fraser isExperienced. Learn about Corpus Callosum Agenesis.
- Dandy-Walker SyndromeDr. Fraser isExperienced. Learn about Dandy-Walker Syndrome.