Overview
Shay Ben-Shachar is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Ben-Shachar and is rated as an Experienced provider by MediFind in the treatment of Legius Syndrome. His top areas of expertise are Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Viral Gastroenteritis, and Oculofaciocardiodental Syndrome.
His clinical research consists of co-authoring 78 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 Legius Syndrome.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Locations
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.
MD Anderson
John Slopis is a Pediatric Neurologist and a Pediatrics provider in Houston, Texas. Dr. Slopis and is rated as a Distinguished provider by MediFind in the treatment of Legius Syndrome. His top areas of expertise are Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Neurofibromatosis Type 2 (NF2), and Schwannomatosis.
Christian Schaaf is a Pediatrics provider in Houston, Texas. Dr. Schaaf and is rated as an Advanced provider by MediFind in the treatment of Legius Syndrome. His top areas of expertise are Autism Spectrum Disorder, Hypotonia, Fountain Syndrome, and Arthrogryposis Multiplex Congenita.
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
- Mosaic Monosomy 22
- Neurofibromatosis
- Neurofibromatosis Type 1 (NF1)
- Oculofaciocardiodental Syndrome
- Viral Gastroenteritis
- Experienced
- Achalasia Microcephaly Syndrome
- Aplasia Cutis Congenita
- Chromosome 13q Duplication
- Clouston Syndrome
- Congenital Fiber-Type Disproportion
- Cortical Dysplasia