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Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice

Overview of attention for article published in PLOS ONE, August 2012
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Title
Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice
Published in
PLOS ONE, August 2012
DOI 10.1371/journal.pone.0042422
Pubmed ID
Authors

Ozlem Bozdagi, Takeshi Sakurai, Nathan Dorr, Marion Pilorge, Nagahide Takahashi, Joseph D. Buxbaum

Abstract

Copy number variation (CNV) at the 15q11.2 region, which includes a gene that codes for CYFIP1 (cytoplasmic FMR1 interacting protein 1), has been implicated in autism, intellectual disability and additional neuropsychiatric phenotypes. In the current study we studied the function of Cyfip1 in synaptic physiology and behavior, using mice with a disruption of the Cyfip1 gene.

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Mendeley readers

The data shown below were compiled from readership statistics for 130 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 <1%
Germany 1 <1%
Netherlands 1 <1%
France 1 <1%
Brazil 1 <1%
Iran, Islamic Republic of 1 <1%
Spain 1 <1%
United States 1 <1%
Unknown 122 94%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 28 22%
Researcher 24 18%
Student > Bachelor 15 12%
Student > Master 10 8%
Professor 7 5%
Other 23 18%
Unknown 23 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 43 33%
Neuroscience 20 15%
Medicine and Dentistry 15 12%
Biochemistry, Genetics and Molecular Biology 12 9%
Psychology 8 6%
Other 10 8%
Unknown 22 17%