Overview
William Craigen is a Pediatrics specialist and a Medical Genetics provider in Austin, Texas. Dr. Craigen and is rated as an Advanced provider by MediFind in the treatment of Andersen Disease. His top areas of expertise are MELAS Syndrome, Citrullinemia, Andersen Disease, and Mitochondrial Complex 1 Deficiency.
His clinical research consists of co-authoring 92 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 3 articles in the study of Andersen Disease.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Community Health
- Friday Health
- Humana
Locations
8611 N Mopac Expy, Austin, TX 78759
Additional Areas of Focus
Dr. Craigen 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.
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
- MELAS Syndrome
- Distinguished
- Citrullinemia
- Advanced
- Achalasia Microcephaly Syndrome
- Andersen Disease
- Inborn Amino Acid Metabolism Disorder
- Maple Syrup Urine Disease
- Microcephaly
- Mitochondrial Complex 1 Deficiency
- Experienced
- Aniridia
- Autism Spectrum Disorder
- Cerebral Hypoxia
- Childhood Pancreatitis
- Cortical Dysplasia
- Homocystinuria