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Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease

Overview of attention for article published in PLOS ONE, March 2013
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Title
Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease
Published in
PLOS ONE, March 2013
DOI 10.1371/journal.pone.0055429
Pubmed ID
Authors

Georgina Caruana, Peter G. Farlie, Adam H. Hart, Stefan Bagheri-Fam, Megan J. Wallace, Michael S. Dobbie, Christopher T. Gordon, Kerry A. Miller, Belinda Whittle, Helen E. Abud, Ruth M. Arkell, Timothy J. Cole, Vincent R. Harley, Ian M. Smyth, John F. Bertram

Abstract

Mice harbouring gene mutations that cause phenotypic abnormalities during organogenesis are invaluable tools for linking gene function to normal development and human disorders. To generate mouse models harbouring novel alleles that are involved in organogenesis we conducted a phenotype-driven, genome-wide mutagenesis screen in mice using the mutagen N-ethyl-N-nitrosourea (ENU).

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 3%
Italy 1 3%
Unknown 34 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 9 25%
Student > Ph. D. Student 7 19%
Student > Bachelor 4 11%
Student > Postgraduate 3 8%
Student > Master 3 8%
Other 6 17%
Unknown 4 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 16 44%
Biochemistry, Genetics and Molecular Biology 7 19%
Medicine and Dentistry 5 14%
Business, Management and Accounting 1 3%
Nursing and Health Professions 1 3%
Other 1 3%
Unknown 5 14%