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X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia

Overview of attention for article published in PLOS ONE, June 2012
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Title
X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia
Published in
PLOS ONE, June 2012
DOI 10.1371/journal.pone.0039240
Pubmed ID
Authors

Astanand Jugessur, Øivind Skare, Rolv T. Lie, Allen J. Wilcox, Kaare Christensen, Lene Christiansen, Truc Trung Nguyen, Jeffrey C. Murray, Håkon K. Gjessing

Abstract

Orofacial clefts are common birth defects of complex etiology, with an excess of males among babies with cleft lip and palate, and an excess of females among those with cleft palate only. Although genes on the X chromosome have been implicated in clefting, there has been no association analysis of X-linked markers.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 28 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 1 4%
Unknown 27 96%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 18%
Student > Ph. D. Student 5 18%
Student > Bachelor 4 14%
Student > Doctoral Student 3 11%
Professor > Associate Professor 3 11%
Other 3 11%
Unknown 5 18%
Readers by discipline Count As %
Medicine and Dentistry 8 29%
Agricultural and Biological Sciences 4 14%
Biochemistry, Genetics and Molecular Biology 3 11%
Mathematics 2 7%
Immunology and Microbiology 2 7%
Other 4 14%
Unknown 5 18%