AmyFLewandaMD

PubMed

• 5 citations
  Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.
  Jonathan J. Rios, Kristin Denton, Jamie Russell, Julia Kozlitina, Carlos Ferreira, Amy F Lewanda, Joshua E. Mayfield, Eva Marie Y. Moresco, Sara Ludwig, Miao Tang, Xia...> ;Journal of Bone and Mineral Research. 2021 Aug 1
• 25 citations
  Opportunities, barriers, and recommendations in down syndrome research
  James A Hendrix, Angelika Amon, Leonard J Abbeduto, Stamatis Agiovlasitis, Tarek Alsaied, Heather A Anderson, Lisa J Bain, Nicole Bäumer, Anita Bhattacharyya, Dusan Bo...> ;Translational Science of Rare Diseases. 2021 Apr 15
• 14 citations
  Patterns of Dietary Supplement Use in Children with Down Syndrome
  Amy Feldman Lewanda, Margo Faust Gallegos, Marshall L. Summar> ;The Journal of Pediatrics. 2018 Oct 1
• 7 citations
  Intellectual disability and epilepsy due to the K/L-mediated Xq28 duplication: Further evidence of a distinct, dosage-dependent phenotype.
  David Isum Ward, Bethany A. Buckley, Eyby Leon, Jullianne Diaz, Margaret Faust Galegos, Sean E. Hofherr, Amy Feldman Lewanda> ;American Journal of Medical Genetics. Part A. 2018 Jan 17
• 35 citations
  Preoperative evaluation and comprehensive risk assessment for children with Down syndrome
  Amy Feldman Lewanda, Andrew J. Matisoff, Mary Revenis, Ashraf S Harahsheh, Craig Futterman, Gustavo Nino, Jay Greenberg, John S. Myseros, Kenneth N. Rosenbaum, Marshal...> ;Paediatric Anaesthesia. 2016 Apr 1
• 52 citations
  ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
  Lev Prasov, Tehmina Masud, Shagufta Khaliq, S. Qasim Mehdi, Aiysha Abid, Edward R. Oliver, Eduardo Silva, Amy Feldman Lewanda, Michael C. Brodsky, Mark Borchert, Danie...> ;Human Molecular Genetics. 2012 Aug 15
• 144 citations
  Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum
  Verena Matejas, Bernward B. Hinkes, Faisal F. Alkandari, Lihadh Al-Gazali, Ellen E. Annexstad, Mehmet Baha Aytac, Margaret Barrow, Květa Bláhová, Detlef Bockenhauer, H...> ;Human Mutation. 2010 Sep 1
• 29 citations
  Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctata
  Michelle C. Nino, Claudia Matos-Miranda, Momoe Maeda, Li Chen, Judith Allanson, Christine M. Armour, Carol L. Greene, Majeeda Kamaluddeen, Debra Rita, Livija Medne, El...> ;American Journal of Medical Genetics. Part A. 2008 Apr 15
• 225 citations
  Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation
  Mitsuhiro Kato, Soma Das, Kristin Petras, Kunio Kitamura, Ken Ichirou Morohashi, Diane Abuelo, Mason Barr, Dominique Bonneau, Angela F. Brady, Nancy J. Carpenter, Kare...> ;Human Mutation. 2004 Feb 1
• Phenotypic discordance in a family with monozygotic twins and nonsyndromic cleft lip and palate: follow-up.
  Diego F Wyszynski, Terri H Beaty> ;American Journal of Medical Genetics. 2002 Jun 15
• 53 citations
  Testing for Interaction between Maternal Smoking and TGFA Genotype among Oral Cleft Cases Born in Maryland 1992–1996
  Terri H. Beaty, Nancy E. Maestri, Jacqueline B. Hetmanski, Diego F. Wyszynski, Craig A. Vanderkolk, Jennifer C. Simpson, Iain McIntosh, E. Anne Smith, Joanna S. Zeiger...> ;The Cleft Palate-Craniofacial Journal. 1997 Sep 1
• 20 citations
  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.
  Diego F. Wyszynski, Nancy E. Maestri, Amy Feldman Lewanda, Iain McIntosh, E.A. Smith, C. Garcia-Delgado, E. Vinageras-Guarneros, Eric A. Wulfsberg, Terri H. Beaty> ;Human Heredity. 1997 Jul 1
• 50 citations
  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.
  Diego F. Wyszynski, Nancy E. Maestri, Iain McIntosh, E. Anne Smith, Amy Feldman Lewanda, Constanza Garcia-Delgado, Enrique Vinageras-Guarneros, Eric A. Wulfsberg, Terr...> ;Human Genetics. 1996 Dec 3
• 9 citations
  Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.
  Amy Feldman Lewanda, Gregory A. Meyers, Ethylin Wang Jabs> ;Proceedings of the Association of American Physicians. 1996 Jan 1
• 41 citations
  Two craniosynostotic patients with 11q deletions, and review of 48 cases
  Amy Feldman Lewanda, Susan Morsey, Cheryl S. Reid, Ethylin Wang Jabs> ;American Journal of Medical Genetics. 1995 Nov 6
• 21 citations
  Evidence That the Saethre-Chotzen Syndrome Locus Lies between D7S664 and D7S507, by Genetic Analysis and Detection of a Microdeletion in a Patient
  Amy Feldman Lewanda, Eric D. Green, Jean Weissenbach, Heather Jerald, Eugene W. Taylor, Marshall L. Summar, John A. Phillips, Melinda Cohen, Murray Feingold, Wendy E. ...> ;American Journal of Human Genetics. 1994 Dec 1
• 7 citations
  Genetics of craniofacial disorders.
  Amy Feldman Lewanda, Ethylin Wang Jabs> ;Current Opinion in Pediatrics. 1994 Dec 1
• 26 citations
  Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26.
  Xiang Li, Amy Feldman Lewanda, Fabian Eluma, Heather Jerald, Hoon Choi, Ihuoma Alozie, Christos Proukakis, C. Conover Talbot, Craig A. Vander Kolk, Lynne M. Bird, Mari...> ;Genomics. 1994 Jul 15
• 28 citations
  Genetic heterogeneity among craniosynostosis syndromes : mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzo...
  Amy Feldman Lewanda, M. Michael Cohen, Charles E. Jackson, Eugene W. Taylor, Xiang Li, Michelle Beloff, Donald Day, Sterling K. Clarren, Rosa Ortiz, Constanza Garcia, ...> ;Genomics. 1994 Jan 1
• 6 citations
  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.
  Amy Feldman Lewanda, M. Michael Cohen, Jean Hood, Susan Morsey, Melissa Walters, Joseph L. Kennedy, Ethylin Wang Jabs> ;American Journal of Diseases of Children. 1993 Dec 1
• Wake up, guys! Women doctors are here to stay.
  Lewanda, A. F.> ;Med Econ. 1995 Feb 27
• Phenotypic discordance in a family with monozygotic twins and non-syndromic cleft lip and palate.
  Wyszynski, D. F., Lewanda, A. F., Beaty, T. H.> ;Am J Med Genet. 1996 Dec 30
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