Muriel T. Davisson

15.6k citations

183 papers · 12.0k indexed · 3 hit papers · h-index 56

Ophthalmology top 0.2%
Genetics top 0.2%
- Animal Genetics and Reproduction 18
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 10
Developmental Neuroscience top 1%
Molecular Biology top 0.5%
- Retinal Development and Disorders 17
- RNA Research and Splicing 12
- CRISPR and Genetic Engineering 11
- Genomics and Chromatin Dynamics 11
Cellular and Molecular Neuroscience top 0.5%
Public Health, Environmental and Occupational Health
- Down syndrome and intellectual disability research 20

Co-authors: Bo Chang John R. Heckenlively Cecilia Schmidt Norman L. Hawes Ellen C. Akeson Thomas H. Roderick Hope O. Sweet Steven Nusinowitz
Cited by: Ophthalmology Genetics Developmental Neuroscience
Journals: Mammalian Genome (26 papers)Genomics (17 papers)Cytogenetic and Genome Research (12 papers)
Partner nations: United States United Kingdom Germany

In The Last Decade

Muriel T. Davisson

183 papers receiving 11.8k citations

Hit Papers

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Peers

Countries citing papers authored by Muriel T. Davisson

Since Specialization

Citations

This map shows the geographic impact of Muriel T. Davisson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Muriel T. Davisson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Muriel T. Davisson more than expected).

Fields of papers citing papers by Muriel T. Davisson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Muriel T. Davisson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Muriel T. Davisson. The network helps show where Muriel T. Davisson may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Muriel T. Davisson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Muriel T. Davisson Line = papers co-authored together Muriel T. Davisson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers Kidney International ·Ron Korstanje,L. Almandoz,Rosalinda Doty,Susan A. Cook,Roderick T. Bronson,Muriel T. Davisson,Jeffrey H. Miner	2014	37
2	Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse Genomics ·Dominique Simon‐Chazottes,Sylvie Tutois,Michael R. Kuehn,Martin Evans,Franck Bourgade,Bill Michael Nandwa Oloo,Muriel T. Davisson,Jean‐Louis Guénet	2006	62
3	Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). PubMed ·Khan Samim,Bo Chang,Norman L. Hawes,Ronald E. Hurd,Muriel T. Davisson,Jie Li,Syed M. Noorwez,Ritu Malhotra,J. Hugh McDowell,Shalesh Kaushal,William W. Hauswirth,Steven Nusinowitz,Debra A. Thompson,John R. Heckenlively	2005	182
4	Behavioral, cognitive and biochemical responses to different environmental conditions in male Ts65Dn mice, a model of Down syndrome Behavioural Brain Research ·Carmen Martínez‐Cué,Noemı́ Rueda,Eva María Pérez García,Muriel T. Davisson,Cecilia Schmidt,Jesús Flórez	2005	68
5	Selective Loss Of ERG b–Wave Caused By An Autosomal Recessive Mutation In Mice. Investigative Ophthalmology & Visual Science ·Bo Chang,Norman L. Hawes,R.E. Hurd,Birhanu Getie,Muriel T. Davisson,Steven Nusinowitz,John R. Heckenlively	2004	2
6	The effects of piracetam on cognitive performance in a mouse model of Down's syndrome Physiology & Behavior ·Timothy H. Moran,George T. Capone,Man-Sik Kim,Muriel T. Davisson,Roger H. Reeves,John D. Gearhart	2002	55
7	Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene Cytogenetic and Genome Research ·Susan A. Cook,Ellen C. Akeson,Yu. Yu. Ratovskii,Keith R. Johnson,Jessica B. Mandell,N. L. Hawes,Rod T. Bronson,Thomas H. Roderick,Muriel T. Davisson	2001	5
8	The Mouse Brain Transcriptome by SAGE: Differences in Gene Expression between P30 Brains of the Partial Trisomy 16 Mouse Model of Down Syndrome (Ts65Dn) and Normals Genome Research ·Roman Chrast,Hamish S. Scott,Daniella Isaacs,Colette Rossier,Emmanuel S. Antonarakis,Christine Barras,Muriel T. Davisson,Cecilia Schmidt,Xavier Estivill,Mara Dierssen,Melanie Pritchard,Stylianos E. Antonarakis	2000	13
9	The Mouse Gene Map ILAR Journal ·Muriel T. Davisson,Dirck Bradt,Jennifer Merriam,Tamera S. Jahnke,Janan T. Eppig	1998	10
10	Rules and guidelines for genetic nomenclature in mice: excerpted version Transgenic Research ·Muriel T. Davisson	1997	18
11	A new mouse mutation causing male sterility and histoincompatibility Mammalian Genome ·Patricia F. Ward‐Bailey,Keith R. Johnson,Mary Ann Handel,Belinda S. Harris,Muriel T. Davisson	1996	11
12	Effect of the mouse scid mutation on meiotic recombination Mammalian Genome ·(unknown),Ella Kipervasser,Vishal Patel,Leonard D. Shultz,Patricia F. Ward‐Bailey,Susan A. Cook,Muriel T. Davisson	1996	1
13	Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration Mammalian Genome ·Hope O. Sweet,Roderick T. Bronson,Keith R. Johnson,Susan A. Cook,Muriel T. Davisson	1996	129
14	RNA Expression and Chromosomal Location of the Mouse Long-Chain Acyl-CoA Dehydrogenase Gene Genomics ·Myron E. Hinsdale,Susan C. Farmer,Kenneth R. Johnson,Muriel T. Davisson,Doug A. Hamm,Ravi Tolwani,Philip A. Wood	1995	11
15	Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse Mammalian Genome ·Keith R. Johnson,Susan A. Cook,Muriel T. Davisson	1994	26
16	The stumbler mutation maps to proximal mouse Chromosome 2 Mammalian Genome ·Wayne N. Frankel,Hope O. Sweet,Muriel T. Davisson	1994	5
17	Rules and guidelines for nomenclature of mouse genes Gene ·Muriel T. Davisson	1994	40
18	Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins Genomics ·Kenneth R. Johnson,Bill Michael Nandwa Oloo,Muriel T. Davisson	1992	63
19	A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11 Genomics ·Joseph H. Nadeau,F G Berger,David R. Cox,Ana M. Geer,Muriel T. Davisson,Sumatah Christie Kumar,Elaine Fuchs,Elvis Castellon Acuña,Lisa Hunihan,P.A. Lalley,Oyshaxon Jurayeva,Gail R. Martin,Е.П. Ренкас,S J Phillips,Thomas H. Roderick,Dennis R. Roop,F.H. Ruddle,Loren C. Skow,John G. Compton	1989	47
20	A Survey of Neurological Mutant Mice. pp 110–122 Developmental Neuroscience ·A. Ganser,Ю. А. Гурин,А И Ерчак,Muriel T. Davisson,Daniel A. Kirschner	1988	1

About Muriel T. Davisson

Muriel T. Davisson is a scholar working on Genetics, Molecular Biology and Ophthalmology, having authored 183 papers that have together received 12.0k indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (20 papers), Animal Genetics and Reproduction (18 papers), Retinal Development and Disorders (17 papers), Genetics and Neurodevelopmental Disorders (12 papers), RNA Research and Splicing (12 papers), CRISPR and Genetic Engineering (11 papers), Genomics and Chromatin Dynamics (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). The work is most often cited by research in Ophthalmology (1.5k citations), Genetics (3.4k citations) and Developmental Neuroscience (472 citations). Muriel T. Davisson has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Bo Chang, John R. Heckenlively, Cecilia Schmidt, Norman L. Hawes, Ellen C. Akeson, Thomas H. Roderick, Hope O. Sweet, Steven Nusinowitz, Roderick T. Bronson and Susan A. Cook. Their work appears in journals such as Mammalian Genome, Genomics, Cytogenetic and Genome Research, Journal of Heredity and Proceedings of the National Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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