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  • Nahid Tayebi, Barbara K Stubblefield, +4 authors Ellen Sidransky
  • Medicine, Biology
  • American journal of human genetics
  • 2003 (First Publication: 1 March 2003)
  • Gaucher disease results from an autosomal recessive deficiency of the lysosomal enzyme glucocerebrosidase. The glucocerebrosidase gene is located in a gene-rich region of 1q21 that contains six genesContinue Reading
  • Ozlem Goker-Alpan, Raphael Schiffmann, Joseph K. Park, Barbara K Stubblefield, Nahid Tayebi, Ellen Sidransky
  • Medicine
  • The Journal of pediatrics
  • 2003 (First Publication: 1 August 2003)
  • Neuronopathic Gaucher disease, classically divided into two types, can have a continuum of phenotypes, often defying categorization. Nine children had an intermediate phenotype characterized by aContinue Reading
  • E. I. Ginns, Prabhakara V. Choudary, +5 authors J. A. Barranger
  • Biology, Medicine
  • Proceedings of the National Academy of Sciences…
  • 1985 (First Publication: 1 October 1985)
  • Analysis of immunologic cross-reacting material in Chinese hamster-human somatic cell hybrids allowed assignment of the structural gene for glucocerebrosidase (glucosylceramidase;Continue Reading
  • Zheng Yan Liu, Barry J. Richmond, +5 authors Edward I. Ginns
  • Biology, Medicine
  • Proceedings of the National Academy of Sciences…
  • 2004 (First Publication: 17 August 2004)
  • When schedules of several operant trials must be successfully completed to obtain a reward, monkeys quickly learn to adjust their behavioral performance by using visual cues that signal how manyContinue Reading