Muriel T. Davisson - Concepedia

Author

Muriel T. Davisson

Also Known As

M DAVISSON, M Davisson, M T Davisson, M. Davisson, M. T. Davisson, M.T. DAVISSON, M.T. Davisson, MURIEL DAVISSON, MURIEL T. DAVISSON, MURIEL T. Davisson

237

Publications

15.6K

Citations

H-Index

208

Concepts

All Affiliations

Jackson Laboratory Tufts University

About

Muriel T. Davisson is an author at Jackson Laboratory specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	94	10K
2	Natural Sciences	11	13	907
3	Engineering	6	6	860
4	Health Sciences	6	6	848
5	Language Studies	1	1	46

Muriel T. Davisson

143

Publications

13.6K

Citations

H-Index

Page 1

	Year	Citations
A mouse model for Down syndrome exhibits learning and behaviour deficits Roger H. Reeves, Nicholas G. Irving, Timothy H. Moran, Nature Genetics Down SyndromeBehavioral SciencesNeuropsychologyBehavioral NeuroscienceBehaviour Deficits	1995	906
Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice Elizabeth M. Simpson, C. Linder, Evelyn E. Sargent, Nature Genetics Knockout MouseEngineeringGenetic DisorderGeneticsGenetic Engineering	1997	696
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration Jeong-Woong Lee, Kirk Beebe, Leslie A. Nangle, Nature Neurodegenerative DiseasesMolecular BiologyProtein MisfoldingEditing-defective Trna SynthetaseMolecular Neurobiology	2006	587
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. Simon W. M. John, Richard S. Smith, Olga V. Savinova, PubMed	1998	558
Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene Bo Chang, Norman L. Hawes, Machelle T. Pardue, Vision Research Missense MutationsOcular DiseaseRetinaPhotoreceptor CellOphthalmology	2007	406
Segmental trisomy of murine chromosome 16: a new model system for studying Down syndrome. Muriel T. Davisson, Cecilia Schmidt, Ellen C. Akeson PubMed Down SyndromeChromatinChromosome DynamicsDevelopmental BiologyCytogenetics	1990	356
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, The American Journal of Human Genetics Knockout MouseOculocutaneous AlbinismAllelic VariantDevelopmental BiologyGenetic Disorder	2001	355
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Stewart D. Chipman, H O Sweet, David J. McBride, Proceedings of the National Academy of Sciences GeneticsBone RepairOsteogenesisRecessive MutationOrthopaedic Surgery	1993	343
Segmental trisomy as a mouse model for Down syndrome. Muriel T. Davisson, Cecilia Schmidt, Roger H. Reeves, PubMed Down SyndromeChromatinKnockout MouseDevelopmental BiologyCytogenetics	1993	305
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice Bo Chang, Richard S. Smith, Norman L. Hawes, Nature Genetics Ocular DiseaseOphthalmologyGeneticsGlaucomaOcular Pathology	1999	302

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