
Overview
Chester Whitley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota.
Dr. Whitley is highly rated in 33 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome).
Dr. Whitley is board certified in Clinical Biochemical Genetics: American Board Of Medical Genetics And Genomics, 1984 and Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 1984. He is actively involved in clinical research, co-authoring 108 peer reviewed articles and participating in 11 clinical trials. Dr. Whitley is currently accepting new patients.
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:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- POS
- PPO
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MANAGED MEDICAID
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE PDP
- HMO
- OTHER COMMERCIAL
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- HMO
- PPO
- EPO
- HMO
- INDEMNITY
- POS
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- EPO
- HMO
- POS
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
12th Flr, East Bld 2450 Riverside Ave, Minneapolis, MN 55454
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.
11 Clinical Trials
M Health Fairview Explorer Pediatric Specialty Clinic
William Dobyns is a Pediatrics specialist and a Neurologist practicing medicine in Minneapolis, Minnesota. He has been practicing medicine for over 48 years. Dr. Dobyns is highly rated in 46 conditions, according to our data. His clinical expertise encompasses Increased Head Circumference, Lissencephaly, Cerebellar Hypoplasia, and Cortical Dysplasia. Dr. Dobyns is board certified in Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 1987. Dr. Dobyns is currently accepting new patients.
M Health Fairview Metabolic Disorders Clinic Minneapolis
Susan Berry is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Minneapolis, Minnesota. Dr. Berry is highly rated in 23 conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Propionic Acidemia, Argininosuccinic Aciduria, and Inborn Amino Acid Metabolism Disorder. Dr. Berry is board certified in Clinical Genetics And Genomics: American Board Of Medical Genetics And Genomics, 1984 and Pediatrics: American Board Of Pediatrics, 1983. Dr. Berry is currently accepting new patients.
M Health Fairview Center For Pediatric Blood And Marrow Transplant And Celluar Therapy
Margaret Macmillan is a Pediatrics specialist and a Pediatric Hematologist Oncology provider practicing medicine in Minneapolis, Minnesota. Dr. Macmillan is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Congenital Aplastic Anemia, Fanconi Anemia, Graft Versus Host Disease (GvHD), Aplastic Anemia, and Bone Marrow Transplant. Dr. Macmillan is currently accepting new patients.
Frequently Asked Questions about Dr. Chester Whitley
How do I make an appointment with Dr. Chester Whitley?
You can book an appointment with Dr. Chester Whitley by calling their office at 612-365-6777. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Chester Whitley a top-rated expert for Mucopolysaccharidoses (MPS)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Chester Whitley is classified as an Elite expert for Mucopolysaccharidoses (MPS), 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. Chester Whitley specialize in?
While Dr. Chester Whitley is a Pediatrics, they have specific expertise in Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Chester Whitley participate in research or clinical trials?
Yes. Dr. Chester Whitley has published 108 articles and abstracts on conditions like Mucopolysaccharidoses (MPS). You can view a list of Dr. Chester Whitley's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Chester Whitley accept my insurance?
Dr. Chester Whitley accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 612-365-6777 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
- Elite
- GangliosidosisDr. Whitley isElite. Learn about Gangliosidosis.
- GM1 GangliosidosisDr. Whitley isElite. Learn about GM1 Gangliosidosis.
- Mucopolysaccharidoses (MPS)Dr. Whitley isElite. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Distinguished
- Cholesteryl Ester Storage DiseaseDr. Whitley isDistinguished. Learn about Cholesteryl Ester Storage Disease.
- Fabry DiseaseDr. Whitley isDistinguished. Learn about Fabry Disease.
- Lysosomal Acid Lipase DeficiencyDr. Whitley isDistinguished. Learn about Lysosomal Acid Lipase Deficiency.
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Multiple Sulfatase DeficiencyDr. Whitley isDistinguished. Learn about Multiple Sulfatase Deficiency.
- Pompe DiseaseDr. Whitley isDistinguished. Learn about Pompe Disease.
- Advanced
- Danon DiseaseDr. Whitley isAdvanced. Learn about Danon Disease.
- Delayed GrowthDr. Whitley isAdvanced. Learn about Delayed Growth.
- Dihydropteridine Reductase Deficiency
- Gaucher DiseaseDr. Whitley isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Whitley isAdvanced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Whitley isAdvanced. Learn about Gaucher Disease Type 2.
- Experienced
- Aarskog SyndromeDr. Whitley isExperienced. Learn about Aarskog Syndrome.
- Antigen-Peptide-Transporter 2 DeficiencyDr. Whitley isExperienced. Learn about Antigen-Peptide-Transporter 2 Deficiency.
- AspartylglucosaminuriaDr. Whitley isExperienced. Learn about Aspartylglucosaminuria.
- Brachydactyly Mononen TypeDr. Whitley isExperienced. Learn about Brachydactyly Mononen Type.
- Brittle Cornea SyndromeDr. Whitley isExperienced. Learn about Brittle Cornea Syndrome.
- Campomelic DysplasiaDr. Whitley isExperienced. Learn about Campomelic Dysplasia.


