Professor of Pediatrics, New York Medical College
Medical Genetics
Dr. Lawrence E. Shapiro, MD
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Lawrence Shapiro practices Medical Genetics. He researched medicine at NYU School of Medicine. Lawrence Shapiro is a published doctor and has 26 publications published. The lastest was: 'Addditional features of the Aarskog syndrome.'
Publications
- Structures of aminoarabinose transferase ArnT suggest a molecular basis for lipid A glycosylation.
- Molecular Logic of Neuronal Self-Recognition through Protocadherin Domain Interactions.
- Structural and energetic determinants of adhesive binding specificity in type I cadherins.
- Single-Cell Identity Generated by Combinatorial Homophilic Interactions between α, β, and γ Protocadherins.
- FGF5 is a crucial regulator of hair length in humans.
- Mechanism of E-cadherin dimerization probed by NMR relaxation dispersion.
- Nectin ectodomain structures reveal a canonical adhesive interface.
- Thinking outside the cell: how cadherins drive adhesion.
- Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
- Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East.
- Structural basis for phosphatidylinositol-phosphate biosynthesis.
- Structural basis for catalysis in a CDP-alcohol phosphotransferase.
- Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair.
- Acrocallosal syndrome: additional manifestations.
- Interrelationships of the hemifacial microsomia-VATER, VATER, and sirenomelia phenotypes.
- Greig cephalopolysyndactyly syndrome.
- Three-generation dominant transmission of the Silver-Russell syndrome.
- Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?
- Addditional features of the Aarskog syndrome.
- The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia.
- Streamlining and implementing nutritional assessment: the dietary approach.
- The trajectory of cognitive development in males with fragile X syndrome.
- Linear growth patterns in patients with cleft lip or palate or both.
- Down''s syndrome in twins.
- Rare etiology of autosomal recessive disease in a child with noncarrier parents.
Schools
University of California At San Francisco
Kings County Hospital Center
La Co Harbor UCLA Med Center
Doctors Specialties
- Pulmonology
- Medical Genetics
Accepted Insurances
Education
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NYU School of Medicine -
Children's Hospital of Los Angeles
Hospital
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James J. Peters Veterans Affairs Medical Center -
Westchester Medical Center
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