Dr. Jessica R. Priestley
Overview
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years is highly rated in 21 conditions, according to our data. Her top areas of expertise are Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Graduate Institution
Residency
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- 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
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
35 Michigan Street Northeast, Suite 3003, Grand Rapids, MI 49503
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
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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Stacie Adams is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Adams is highly rated in 20 conditions, according to our data. Her top areas of expertise are Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactosemia. Dr. Adams is currently accepting new patients.
Frequently Asked Questions about Dr. Jessica R. Priestley
How do I make an appointment with Dr. Jessica R. Priestley?
You can book an appointment with Dr. Jessica R. Priestley by calling their office at 616-486-9830. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Jessica R. Priestley a top-rated expert for Fabry Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Jessica R. Priestley is classified as an Advanced expert for Fabry Disease, 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. Jessica R. Priestley specialize in?
While Dr. Jessica R. Priestley is a Pediatrics, they have specific expertise in Fabry Disease, Biotinidase Deficiency, and Ornithine Transcarbamylase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Jessica R. Priestley participate in research or clinical trials?
Yes. Dr. Jessica R. Priestley has published 12 articles and abstracts on conditions like Fabry Disease. You can view a list of Dr. Jessica R. Priestley's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Jessica R. Priestley accept my insurance?
Dr. Jessica R. Priestley accepts most major insurance plans, including Alignment Health Plan and Blue Cross Blue Shield. We recommend calling the office directly at 616-486-9830 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
- Autosomal Recessive Congenital Methemoglobinemia
- Biotinidase DeficiencyDr. Priestley isAdvanced. Learn about Biotinidase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Classic GalactosemiaDr. Priestley isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Priestley isAdvanced. Learn about Danon Disease.
- Experienced
- 15q11.2 MicrodeletionDr. Priestley isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Priestley isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Priestley isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Priestley isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Priestley isExperienced. Learn about 47 XYY Syndrome.