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  • Kenneth A. Pass, Peter A. Lane, +8 authors Louis J. Elsas
  • Medicine
  • The Journal of pediatrics
  • 2000 (First Publication: 1 October 2000)
  • implemented nationwide. Currently, each state, the District of Columbia, Puerto Rico, and the Virgin Islands screen all newborns for PKU and congenital hypothyroidism, and most include otherContinue Reading
  • Bronya J. B. Keats, Nassim Nouri, Mary Z. Pelias, Prescott L Deininger, Michael Litt
  • Biology, Medicine
  • American journal of human genetics
  • 1994 (First Publication: 1 April 1994)
  • Usher syndrome type I is an autosomal recessive disease characterized by profound congenital hearing impairment and vestibular dysfunction followed by the onset of progressive pigmentary retinopathyContinue Reading
  • Nicolas G Bazan, B. L. Scott, T. Sanjeeva Reddy, Mary Z. Pelias
  • Biology, Medicine
  • Biochemical and biophysical research…
  • 1986 (First Publication: 1 December 1986)
  • Docosahexaenoate and arachidonate were found to be significantly decreased in plasma phospholipids from Usher's syndrome patients. The fatty acid content of plasma triacylglycerols was not changed inContinue Reading
  • Stephanie L. Sherman, John C. Defries, +5 authors Irwin D. Waldman
  • Biology, Medicine
  • American journal of human genetics
  • 1997 (First Publication: 1 June 1997)
  • The field of behavioral genetics has enormous potential to uncover both genetic and environmental influences on normal and deviant behavior. Behavioral-genetic methods are based on a solid foundationContinue Reading
  • Richard J H Smith, Mary Z. Pelias, Stephen P. Daiger, Bronya J. B. Keats, William J. Kimberling, J Fielding Hejtmancik
  • Biology, Medicine
  • American journal of medical genetics
  • 1992 (First Publication: 1 August 1992)
  • A number of Usher syndrome (USH) families are found among the French-Acadians living in southwestern Louisiana. These families are descended from a few common ancestors, suggesting that USH may beContinue Reading