LisaLouiseBraileyMD

PubMed

• 181 citations
  Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation
  Agatino Battaglia, H. Eugene Hoyme, Bruno Dallapiccola, Elaine H. Zackai, Louanne Hudgins, Donna M. McDonald-McGinn, Nadia Bahi-Buisson, Corrado Romano, Charles A. Wil...> ;Pediatrics. 2008 Feb 1
• 167 citations
  Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
  Saori Yamaguchi, Lisa L Brailey, Hiroki Morizono, Allen E Bale, Mendel Tuchman> ;Human Mutation. 2006 Jul 1
• 151 citations
  Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused.
  Ayanna F. Cooper, Kuan Ping Yu, Martina Brueckner, Lisa L. Brailey, Linda K Johnson, James L. McGrath, Allen E. Bale> ;Development. 2005 Oct 1
• 13 citations
  Mutations and polymorphisms in the human ornithine transcarbamylase gene.
  Mendel Tuchman, Naser Jaleel, Hiroki Morizono, Lisa Sheehy, Michael G Lynch> ;Human Mutation. 2002 Feb 1
• 80 citations
  Integrin-mediated signaling regulates AP-1 transcription factors and proliferation in osteoblasts.
  Elizabeth A. Cowles, Lisa L. Brailey, Gloria Gronowicz> ;Journal of Biomedical Materials Research. 2000 Dec 15
• 10 citations
  Apheresis and the thrombotic thrombocytopenic purpura syndrome: current advances in diagnosis, pathophysiology, and management.
  Lisa Louise Brailey, Mark E. Brecher, Nicholas Bandarenko> ;Therapeutic Apheresis. 1999 Feb 1
• Mineralization and the expression of matrix proteins during in vivo bone development.
  Cowles, E. A., DeRome, M. E., Pastizzo, G., Brailey, L. L., Gronowicz, G. A.> ;Calcif Tissue Int. 1998 Jan
• Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studies.
  Brailey, L. L., Davis, T., Kolker, S. E., Murry, T. C., Thomas, D., Bale, A. E., Ruhoy, S. M.> ;J Cutan Pathol. 2007 Jan
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