Elizabeth F. Neufeld

Elizabeth F. Neufeld publication distribution in Molecular Biology in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Molecular Biology in 2026. The highlighted bar marks where Elizabeth F. Neufeld sits on this spectrum.

Elizabeth F. Neufeld D-index placement in Molecular Biology in 2026

The chart shows the D-index (discipline H-index) distribution of Molecular Biology scientists ranked by Research.com in 2026. The highlighted bar marks where Elizabeth F. Neufeld sits on this spectrum.

Research.com Recognitions

• 1994 - US President's National Medal of Science "For her contributions to the understanding of the lysosomal storage diseases, demonstrating the strong linkage between basic and applied scientific investigation.", Presented by Vice President Gore at Andrew W. Mellon Auditorium, Washington, DC on Monday, December 19, 1994.
• 1988 - Fellow of the American Association for the Advancement of Science (AAAS)
• 1982 - William Allan Award, the American Society of Human Genetics
• 1977 - Fellow of the American Academy of Arts and Sciences
• 1977 - Member of the National Academy of Sciences

Overview

Best Publications

• Lysosomal storage diseases

  Frances M Platt;Alessandra d'Azzo;Beverly L Davidson;Elizabeth F Neufeld

  1133
  Citations

• Enzyme-replacement therapy in mucopolysaccharidosis I.

  Emil D. Kakkis;Joseph Muenzer;George E. Tiller;Lewis Waber

  820
  Citations

• Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB.

  Kazuhiro Ohmi;David S. Greenberg;Kavitha S. Rajavel;Sergey Ryazantsev

  576
  Citations

• The Defect in the Hurler and Scheie Syndromes: Deficiency of α-L-Iduronidase

  Gideon Bach;Robert Friedman;Bernard Weissmann;Elizabeth F. Neufeld

  289
  Citations

• The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase

  Gideon Bach;Frank Eisenberg;Michael Cantz;Elizabeth F. Neufeld

  284
  Citations

• Inborn Errors of Mucopolysaccharide Metabolism

  Elizabeth F. Neufeld;Joseph C. Fratantoni

  282
  Citations

• Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis I

  Emil D. Kakkis;Michael F. McEntee;Artur Schmidtchen;Elizabeth F. Neufeld

  269
  Citations

• Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.

  C.w. Hall;Ingeborg Liebaers;P. Di Natale;E.f. Neufeld

  251
  Citations

• Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase.

  Hong Hua Li;Wei-Hong Yu;Nora Rozengurt;Hui-Zhi Zhao

  251
  Citations

• Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblasts.

  R L Proia;A d'Azzo;E F Neufeld

  219
  Citations

• Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain.

  Rachel Myerowitz;Richard Piekarz;Elizabeth F. Neufeld;Thomas B. Shows

  210
  Citations

• Natural History and Inherited Disorders of a Lysosomal Enzyme, β-Hexosaminidase

  E F Neufeld

  185
  Citations

• The molecular basis of Sanfilippo syndrome type B.

  Hong G. Zhao;Hong Hua Li;Gideon Bach;Artur Schmidtchen

  182
  Citations

• Direct demonstration of binding of a lysosomal enzyme, alpha-L-iduronidase, to receptors on cultured fibroblasts.

  Leonard H. Rome;Bernard Weissmann;Elizabeth F. Neufeld

  178
  Citations

• Morphologic study of the internalization of a lysosomal enzyme by the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells

  Mark C. Willingham;Ira H. Pastan;G. Gary Sahagian;George W. Jourdian

  175
  Citations

• Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy

  Kazuhiro Ohmi;Lili C. Kudo;Sergey Ryazantsev;Hui-Zhi Zhao

  161
  Citations

• METABOLISM OF MYO-INOSITOL IN PLANTS: CONVERSION TO PECTIN, HEMICELLULOSE, D-XYLOSE, AND SUGAR ACIDS

  Frank A. Loewus;Stanley Kelly;Elizabeth F. Neufeld

  155
  Citations

• Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease.

  Richard L. Proia;Elizabeth F. Neufeld

  154
  Citations

• Architecture of the canine IDUA gene and mutation underlying canine mucopolysaccharidosis I

  Kaushiki P. Menon;Phuong T. Tieu;Elizabeth F. Neufeld

  141
  Citations

• Delivery of an enzyme-IGFII fusion protein to the mouse brain is therapeutic for mucopolysaccharidosis type IIIB

  Shih-hsin Kan;Mika Aoyagi-Scharber;Steven Q. Le;Jon Vincelette

  133
  Citations