Overview
Gerard Berry is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Berry is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. His top areas of expertise are Classic Galactosemia, Galactose Epimerase Deficiency, Galactosemia, and Maple Syrup Urine Disease. Dr. Berry is currently accepting new patients.
His clinical research consists of co-authoring 1 peer reviewed article. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
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.
Children's Hospital Pediatric Associates, Inc
Melinda Peters is a Medical Genetics provider in Boston, Massachusetts. Dr. Peters is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
Children's Hospital Pediatric Associates, Inc
Amy Kritzer is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Kritzer is rated as a Distinguished provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome. Dr. Kritzer is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.
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
- Classic GalactosemiaDr. Berry isAdvanced. Learn about Classic Galactosemia.
- Galactose Epimerase DeficiencyDr. Berry isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Berry isAdvanced. Learn about Galactosemia.
- Maple Syrup Urine DiseaseDr. Berry isAdvanced. Learn about Maple Syrup Urine Disease.
- Experienced
- Arginase DeficiencyDr. Berry isExperienced. Learn about Arginase Deficiency.
- Autism Spectrum DisorderDr. Berry isExperienced. Learn about Autism Spectrum Disorder.
- Branchio-Oculo-Facial Syndrome (BOFS)Dr. Berry isExperienced. Learn about Branchio-Oculo-Facial Syndrome (BOFS).
- Camptodactyly TaurinuriaDr. Berry isExperienced. Learn about Camptodactyly Taurinuria.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency