Overview
Stephen Braddock is a Medical Genetics specialist and a Pediatrics provider in Saint Louis, Missouri. Dr. Braddock is highly rated in 8 conditions, according to our data. His top areas of expertise are Chromosome 20 Trisomy, Cerebellar Hypoplasia, Maple Syrup Urine Disease, and Micrognathia. Dr. Braddock is currently accepting new patients.
His clinical research consists of co-authoring 44 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Oscar
- Humana
Locations
10101 Woodfield Ln, Saint Louis, MO 63132
1465 S Grand Blvd, Saint Louis, MO 63104
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.
Washington University
Dorothy Grange is a Medical Genetics specialist and a Pediatrics provider in Saint Louis, Missouri. Dr. Grange is highly rated in 20 conditions, according to our data. Her top areas of expertise are Phenylketonuria (PKU), Aplasia Cutis Congenita, Clouston Syndrome, and Ectodermal Dysplasias. Dr. Grange is currently accepting new patients.
Washington University
Gary Gottesman is a Medical Genetics specialist and an Endocrinologist in Saint Louis, Missouri. Dr. Gottesman is highly rated in 12 conditions, according to our data. His top areas of expertise are X-Linked Hypophosphatemia, Hypophosphatemia, Juvenile Paget's Disease, Rickets, and Leg or Foot Amputation. Dr. Gottesman is currently accepting new patients.
Patricia Dickson is a Medical Genetics specialist and a Pediatrics provider in Saint Louis, Missouri. Dr. Dickson is highly rated in 6 conditions, according to our data. Her top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). Dr. Dickson is currently accepting new 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.
- Advanced
- Cerebellar Hypoplasia
- CHARGE Syndrome
- Chromosome 20 Trisomy
- Coloboma
- Maple Syrup Urine Disease
- Micrognathia
- Experienced
- Aplasia Cutis Congenita
- Brachydactyly Mononen Type
- Chromosome 13q Duplication
- Clouston Syndrome
- Coffin-Siris Syndrome
- Corpus Callosum Agenesis