Overview
Melissa Wasserstein is a Medical Genetics specialist and a Pediatrics provider in Bronx, New York. Dr. Wasserstein is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Reticulohistiocytoma, and Splenomegaly.
Her clinical research consists of co-authoring 83 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Homocystinuria.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- PPO
- EPO
- HMO
- POS
- PPO
Locations
111 E 210th St, Bronx, NY 10467
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.
1 Clinical Trials
Icahn School Of Medicine At Mount Sinai
Jaya Ganesh is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Ganesh is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Fabry Disease.
Kimihiko Oishi is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Oishi is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. His top areas of expertise are Micrognathia, Citrullinemia, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia with Homocystinuria.
Icahn School Of Medicine At Mount Sinai
Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Lopiccolo is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Glutaric Acidemia Type 2, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Carnitine Palmitoyltransferase 1 Deficiency.
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
- Elite
- Acid Sphingomyelinase Deficiency (ASMD)
- Niemann-Pick DiseaseDr. Wasserstein isElite. Learn about Niemann-Pick Disease.
- ReticulohistiocytomaDr. Wasserstein isElite. Learn about Reticulohistiocytoma.
- Distinguished
- Phenylketonuria (PKU)Dr. Wasserstein isDistinguished. Learn about Phenylketonuria (PKU).
- SplenomegalyDr. Wasserstein isDistinguished. Learn about Splenomegaly.
- Advanced
- Adrenoleukodystrophy (ALD)Dr. Wasserstein isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Krabbe DiseaseDr. Wasserstein isAdvanced. Learn about Krabbe Disease.
- Experienced
- Carnitine Palmitoyltransferase 1 DeficiencyDr. Wasserstein isExperienced. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyDr. Wasserstein isExperienced. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Danon DiseaseDr. Wasserstein isExperienced. Learn about Danon Disease.
- Gaucher DiseaseDr. Wasserstein isExperienced. Learn about Gaucher Disease.
- HomocystinuriaDr. Wasserstein isExperienced. Learn about Homocystinuria.
- LeukodystrophyDr. Wasserstein isExperienced. Learn about Leukodystrophy.