Physician
Medical Genetics
Dr. Amy F. Lewanda, MD
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Dr. Amy F. Lewanda is an expert in the field of Medical Genetics. She went to medical school at Icahn School of Medicine at Mount Sinai. Icahn School of Medicine at Mount Sinai is ranked 20 in research and 62 in primary care medicine She has 1 awards "Top MD". Amy F. Lewanda is a published doctor and has 16 publications published. The lastest was: 'Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996.'
Publications
- Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.
- Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.
- Wake up, guys! Women doctors are here to stay.
- Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996.
- No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populations.
- Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families.
- Phenotypic discordance in a family with monozygotic twins and non-syndromic cleft lip and palate.
- Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.
- Two craniosynostotic patients with 11q deletions, and review of 48 cases.
- Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder.
- Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon...
- Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient.
- Genetics of craniofacial disorders.
- Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26.
- Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctata.
Schools
Mount Sinai School Of Medicine Of New York University
Mount Sinai Hospital
Johns Hopkins Hospital
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
Awards
- Top MD
Education
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Johns Hopkins University -
Mount Sinai School of Medicine -
Icahn School of Medicine at Mount Sinai
Hospital
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Inova Fairfax Hospital -
Holy Cross Hospital
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