Overview
William Dobyns is a Medical Genetics specialist and a Pediatrics provider in Minneapolis, Minnesota. Dr. Dobyns has been practicing medicine for over 47 years and is rated as an Experienced provider by MediFind in the treatment of FOXG1 Syndrome. His top areas of expertise are Increased Head Circumference, Lissencephaly, Polymicrogyria, and Cortical Dysplasia. Dr. Dobyns is currently accepting new patients.
His clinical research consists of co-authoring 233 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of FOXG1 Syndrome.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Sanford Health
- Medica
Locations
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.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Achalasia Microcephaly Syndrome
- Agyria Pachygyria Polymicrogyria
- Bilateral Perisylvian Polymicrogyria
- Cerebellar Hypoplasia
- Cortical Dysplasia
- Focal or Multifocal Malformations in Neuronal Migration
- Distinguished
- Aplasia Cutis Congenita
- Cerebellar Agenesis
- Clouston Syndrome
- Corpus Callosum Agenesis
- Dandy-Walker Syndrome
- Ectodermal Dysplasias
- Advanced
- Acromicric Dysplasia
- Arthrogryposis Multiplex Congenita
- Autism Spectrum Disorder
- Chromosome 6q Deletion
- Coloboma
- Congenital Contractures
- Experienced
- Absence Seizure
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Adrenoleukodystrophy (ALD)
- Alpha Thalassemia
- Brachydactyly Mononen Type