Overview
Wendy Smith is a Medical Genetics specialist and a Pediatrics provider in Portland, Maine. Dr. Smith is highly rated in 14 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and MELAS Syndrome.
Her clinical research consists of co-authoring 2 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Hospital Affiliations
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
- PPO
- PPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- MANAGED MEDICAID PLAN
- EPO
- HMO
- POS
- PPO
- MEDICARE DISCOUNT CARD
- MEDICARE PDP
- OTHER MEDICARE
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
22 Bramhall St, Portland, ME 04102
1577 Congress St, Portland, ME 04102
Additional Areas of Focus
Dr. Smith 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.
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Rosemarie Smith is a Medical Genetics specialist and a Pediatrics provider in Portland, Maine. Dr. Smith is highly rated in 85 conditions, according to our data. Her top areas of expertise are Cardiomyopathic Lentiginosis, Costello Syndrome, Leber Hereditary Optic Neuropathy (LHON), and RASopathies.
Frequently Asked Questions about Dr. Wendy Smith
How do I make an appointment with Dr. Wendy Smith?
You can book an appointment with Dr. Wendy Smith by calling their office at 207-885-9905. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Wendy Smith a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Wendy Smith is classified as an Distinguished expert for Phenylketonuria (PKU), 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. Wendy Smith specialize in?
While Dr. Wendy Smith is a Medical Genetics, they have specific expertise in Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Wendy Smith participate in research or clinical trials?
Yes. Dr. Wendy Smith has published 2 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Dr. Wendy Smith's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Wendy Smith accept my insurance?
Dr. Wendy Smith accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 207-885-9905 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
- Distinguished
- Phenylketonuria (PKU)Dr. Smith isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Chromosome 13q DeletionDr. Smith isAdvanced. Learn about Chromosome 13q Deletion.
- Danon DiseaseDr. Smith isAdvanced. Learn about Danon Disease.
- Dihydropteridine Reductase Deficiency
- Fabry DiseaseDr. Smith isAdvanced. Learn about Fabry Disease.
- Galactokinase DeficiencyDr. Smith isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Smith isAdvanced. Learn about Galactose Epimerase Deficiency.
- Experienced
- 15q11.2 MicrodeletionDr. Smith isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Smith isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Smith isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Smith isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Smith isExperienced. Learn about 47 XYY Syndrome.