Physician

Medical Genetics

Doctor Robert M. Greenstein, MD works in the field of Medical Genetics. He went to Albert Einstein College of Medicine at Jacobi Medical Center. Robert Greenstein is also a published MD. He has 27 paper published. The most recent paper is: Maternal serum screening for birth defects: results of a Connecticut regional program.

Publications

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• A Mosaic Activating Mutation in AKT1 Associated with the Proteus Syndrome.
• Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
• Improved pulmonary and growth outcomes in cystic fibrosis by newborn screening.
• Motion analysis of a child with Niemann-Pick disease type C treated with miglustat.
• When is enlargement of the subarachnoid spaces not benign? A genetic perspective.
• Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
• The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.
• Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions.
• Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
• Newborn screening compared to clinical identification of biochemical genetic disorders.
• Maternal serum screening for birth defects: results of a Connecticut regional program.
• Developing a role for genetics within a cancer program.
• Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome.
• New syndrome of hydrocephalus, endocardial fibroelastosis, and cataracts (HEC syndrome).
• Long-term follow-up of a patient transplanted for Hunter''s disease type IIB: a case report and literature review.
• Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman synd...
• Jarcho-Levin syndrome: unusual survival in a classical case.
• Variable clinical expression of mosaic trisomy 16 in the newborn infant.
• Analysis of skull anthropometric measurements in patients with neurofibromatosis type-1.
• Neurofibromatosis type 1: magnetic resonance imaging findings.
• Calculated risk of chromosomal abnormalities in twin gestations.
• Malignant osteoporosis and defective immunoregulation.
• Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
• Screening for fetal Down's syndrome in pregnancy by measuring maternal serum alpha-fetoprotein levels.
• Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members.
• Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndrome.

Schools

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• Albert Einstein College of Medicine of Yeshiva University

• Albert Einstein College Med

• Stanford University

Doctors Specialties

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• Clinical Cytogenetics
• Clinical Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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• Aetna HMO
• Choice Plus POS II
• Cigna HMO
• Cigna PPO
• Great West Healthcare-Cigna PPO
• Open Access Plus
• Commercial Insurance Company
• Connecticare
• GHI PPO
• Harvard Pilgrim Health Care PPO
• HealthPartners
• Choice Care PPO
• Medicaid
• Medicare MCR
• Meritain Health
• MVP Health Care
• United Healthcare

Education

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• Albert Einstein College of Medicine at Jacobi Medical Center
• Albert Einstein College of Medicine of Yeshiva University

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