Lisa L. Brailey

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 et al. · PEDIATRICS · 2008 · 310 citations

Life Sciences, Genetics, Pediatrics +17

Mutations and polymorphisms in the human ornithine transcarbamylase (<i>OTC</i>) gene

Saori Yamaguchi, Lisa L. Brailey, Hiroki Morizono et al. · Human Mutation · 2006 · 275 citations

Life Sciences, Genetics, Molecular Genetics +16

Mineralization and the Expression of Matrix Proteins During In Vivo Bone Development

Elizabeth Cowles, Mary DeRome, G. Pastizzo et al. · Calcified Tissue International · 1998 · 211 citations

Medicine, Developmental Biology, Orthopaedic Surgery +14

Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused

Ayanna F. Cooper, Kuan Ping Yu, Martina Brueckner et al. · Development · 2005 · 196 citations

Life Sciences, Developmental Biology, Genetics +17

Integrin-mediated signaling regulates AP-1 transcription factors and proliferation in osteoblasts

Elizabeth Cowles, Lisa L. Brailey, Gloria Gronowicz · Journal of Biomedical Materials Research · 2000 · 114 citations

Life Sciences, Cell Biology, Developmental Biology +13