Overview
Shay Ben-Shachar is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Ben-Shachar is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Neurofibromatosis, Neurofibromatosis Type 1 (NF1), Viral Gastroenteritis, and Oculofaciocardiodental Syndrome.
His clinical research consists of co-authoring 85 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 Chromosome 13q Duplication.
Insurance
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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.
UT Physicians
Hope Northrup is a Medical Genetics specialist and a Pediatrics provider in Houston, Texas. Dr. Northrup is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Cortical Dysplasia, Epilepsy in Children, Phenylketonuria (PKU), and Spasmus Nutans. Dr. Northrup is currently accepting new patients.
Daryl Scott is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Scott is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are 1p36 Deletion Syndrome, Hernia, Coffin-Siris Syndrome, and Hypotonia. Dr. Scott is currently accepting new patients.
Utmb Faculty Group Practice
Joseph Ray is a Medical Genetics specialist and a Pediatrics provider in Galveston, Texas. Dr. Ray has been practicing medicine for over 16 years and is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, Phenylketonuria (PKU), and Fabry Disease.
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
- Advanced
- Mosaic Monosomy 22Dr. Ben-Shachar isAdvanced. Learn about Mosaic Monosomy 22.
- NeurofibromatosisDr. Ben-Shachar isAdvanced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Dr. Ben-Shachar isAdvanced. Learn about Neurofibromatosis Type 1 (NF1).
- Oculofaciocardiodental SyndromeDr. Ben-Shachar isAdvanced. Learn about Oculofaciocardiodental Syndrome.
- Viral GastroenteritisDr. Ben-Shachar isAdvanced. Learn about Viral Gastroenteritis.
- Experienced
- Achalasia Microcephaly SyndromeDr. Ben-Shachar isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Aplasia Cutis CongenitaDr. Ben-Shachar isExperienced. Learn about Aplasia Cutis Congenita.
- Chromosome 13q DuplicationDr. Ben-Shachar isExperienced. Learn about Chromosome 13q Duplication.
- Clouston SyndromeDr. Ben-Shachar isExperienced. Learn about Clouston Syndrome.
- Congenital Fiber-Type DisproportionDr. Ben-Shachar isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Cortical DysplasiaDr. Ben-Shachar isExperienced. Learn about Cortical Dysplasia.