Muriel T. Davisson

Muriel T. Davisson publication distribution in Biology and Biochemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Biology and Biochemistry in 2026. The highlighted bar marks where Muriel T. Davisson sits on this spectrum.

Muriel T. Davisson D-index placement in Biology and Biochemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Biology and Biochemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Muriel T. Davisson sits on this spectrum.

Overview

Best Publications

• Retinal degeneration mutants in the mouse.

  B. Chang;N.L. Hawes;R.E. Hurd;M.T. Davisson

  1082
  Citations

• Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

  Elizabeth M. Simpson;Carol C. Linder;Evelyn E. Sargent;Muriel T. Davisson

  847
  Citations

• Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

  Jeong Woong Lee;Kirk Beebe;Leslie A. Nangle;Jaeseon Jang

  718
  Citations

• Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.

  Simon W M John;Richard S. Smith;Olga V. Savinova;Norman L. Hawes

  639
  Citations

• Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

  B. Chang;N.L. Hawes;M.T. Pardue;M.T. Pardue;A.M. German

  474
  Citations

• Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta.

  Stewart D. Chipman;Hope O. Sweet;Daniel J. McBride;Muriel T. Davisson

  452
  Citations

• Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

  J.M. Newton;Orit Cohen-Barak;Nobuko Hagiwara;John M. Gardner

  448
  Citations

• Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage.

  E J Michaud;M J van Vugt;S J Bultman;H O Sweet

  390
  Citations

• Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

  Bo Chang;Richard S Smith;Norman L Hawes;Michael G Anderson

  321
  Citations

• Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions.

  Katheleen Gardiner;Andrew Fortna;Lawrence Bechtel;Muriel T Davisson

  301
  Citations

• VAC14 Nucleates a Protein Complex Essential for the Acute Interconversion of PI3P and PI(3,5)P2 in Yeast and Mouse

  Natsuko Jin;Clement Y Chow;Li Liu;Sergey N Zolov

  297
  Citations

• Report of the committee on comparative mapping

  P. L. Pearson;T. H. Roderick;M. T. Davisson;J. J. Garver

  296
  Citations

• A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

  Novrouz B. Akhmedov;Natik I. Piriev;Bo Chang;Ana Lia Rapoport

  295
  Citations

• Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)

  Ji Jing Pang;Bo Chang;Norman L. Hawes;Ronald E. Hurd

  284
  Citations

• The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.

  Bo Chang;John R. Heckenlively;Philippa R. Bayley;Nicholas C. Brecha

  238
  Citations

• Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

  H. O. Sweet;R. T. Bronson;K. R. Johnson;S. A. Cook

  222
  Citations

• Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

  Carmen Martı́nez-Cué;Carmela Baamonde;Marian Lumbreras;Jesús Paz

  214
  Citations

• Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease).

  Roderick T. Bronson;Brian D. Lake;Susan Cook;Susanne Taylor

  211
  Citations

• The fatty liver dystrophy (fld) mutation: A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

  C A Langner;E H Birkenmeier;O Ben-Zeev;M C Schotz

  205
  Citations

• Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn

  Laura G. Reinholdt;Yueming Ding;Griffith T. Gilbert;Anne Czechanski

  196
  Citations