• Publications
  • Influence

Claim Your Author Page
Ensure your research is discoverable on Semantic Scholar. Claiming your author page allows you to personalize the information displayed and manage your publications. Semantic Scholar automatically creates author pages based on data aggregated from public sources and our publisher partners.
  • Ruth Gershoni-baruch, Ada Rosenmann, Sara Droetto, Stuart A. Holmes, R. K. Tripathi, Richard A. Spritz
  • Biology, Medicine
  • American journal of human genetics
  • 1994 (First Publication: 1 April 1994)
  • We have analyzed the tyrosinase (TYR) gene in 38 unrelated patients with oculocutaneous albinism (OCA), derived from several different ethnic groups of the diverse population of Israel. We detectedExpand
  • Richard A. Spritz, Lutz B. Giebel, Stuart A. Holmes
  • Biology, Medicine
  • American journal of human genetics
  • 1992 (First Publication: 1 February 1992)
  • Piebaldism is an autosomal dominant disorder of melanocyte development and is characterized by congenital white patches of skin and hair from which melanocytes are completely absent. A similarExpand
  • Rhonda E. Schnur, B T Sellinger, Stuart A. Holmes, P. A. Wick, Yvonne Tatsumura, Richard A. Spritz
  • Biology, Medicine
  • The Journal of investigative dermatology
  • 1996 (First Publication: 1 May 1996)
  • Type I oculocutaneous albinism is an autosomal recessive disorder in which the biosynthesis of melanin is reduced or absent in skin, hair, and eyes because of deficient activity of tyrosinase (ECExpand
  • Richard A. Spritz, Stuart A. Holmes, R. S. Ramesar, Jacquie Greenberg, David Curtis, Peter Beighton
  • Biology, Medicine
  • American journal of human genetics
  • 1992 (First Publication: 1 November 1992)
  • Piebaldism is a rare autosomal dominant disorder of pigmentation, characterized by congenital patches of white skin and hair from which melanocytes are absent. We have previously shown thatExpand