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Genetic-Background Modulation of Core and Variable Autistic-Like Symptoms in Fmr1 Knock-Out Mice

Overview of attention for article published in PLOS ONE, February 2011
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Title
Genetic-Background Modulation of Core and Variable Autistic-Like Symptoms in Fmr1 Knock-Out Mice
Published in
PLOS ONE, February 2011
DOI 10.1371/journal.pone.0017073
Pubmed ID
Authors

Susanna Pietropaolo, Aurélie Guilleminot, Benoît Martin, Francesca R. D'Amato, Wim E. Crusio

Abstract

No animal models of autism spectrum disorders (ASD) with good construct validity are currently available; using genetic models of pathologies characterized by ASD-like deficits, but with known causes, may be therefore a promising strategy. The Fmr1-KO mouse is an example of this approach, modeling Fragile X syndrome, a well-known genetic disorder presenting ASD symptoms. The Fmr1-KO is available on different genetic backgrounds (FVB versus C57BL/6), which may explain some of the conflicting results that have been obtained with these mutants up till now.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 161 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 <1%
France 1 <1%
Brazil 1 <1%
United Kingdom 1 <1%
United States 1 <1%
Unknown 156 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 35 22%
Researcher 23 14%
Student > Bachelor 18 11%
Student > Master 12 7%
Student > Doctoral Student 10 6%
Other 30 19%
Unknown 33 20%
Readers by discipline Count As %
Neuroscience 42 26%
Agricultural and Biological Sciences 35 22%
Biochemistry, Genetics and Molecular Biology 18 11%
Medicine and Dentistry 10 6%
Psychology 9 6%
Other 7 4%
Unknown 40 25%