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A Genome-Wide Investigation of Copy Number Variation in Patients with Sporadic Brain Arteriovenous Malformation

Overview of attention for article published in PLOS ONE, October 2013
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Title
A Genome-Wide Investigation of Copy Number Variation in Patients with Sporadic Brain Arteriovenous Malformation
Published in
PLOS ONE, October 2013
DOI 10.1371/journal.pone.0071434
Pubmed ID
Authors

Nasrine Bendjilali, Helen Kim, Shantel Weinsheimer, Diana E. Guo, Pui-Yan Kwok, Jonathan G. Zaroff, Stephen Sidney, Michael T. Lawton, Charles E. McCulloch, Bobby P. C. Koeleman, Catharina J. M. Klijn, William L. Young, Ludmila Pawlikowska

Abstract

Brain arteriovenous malformations (BAVM) are clusters of abnormal blood vessels, with shunting of blood from the arterial to venous circulation and a high risk of rupture and intracranial hemorrhage. Most BAVMs are sporadic, but also occur in patients with Hereditary Hemorrhagic Telangiectasia, a Mendelian disorder caused by mutations in genes in the transforming growth factor beta (TGFβ) signaling pathway.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Sweden 1 3%
Unknown 39 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 20%
Student > Ph. D. Student 5 13%
Other 4 10%
Student > Doctoral Student 4 10%
Student > Bachelor 4 10%
Other 11 28%
Unknown 4 10%
Readers by discipline Count As %
Medicine and Dentistry 14 35%
Biochemistry, Genetics and Molecular Biology 5 13%
Agricultural and Biological Sciences 5 13%
Neuroscience 2 5%
Computer Science 2 5%
Other 3 8%
Unknown 9 23%