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The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

Overview of attention for article published in PLOS ONE, July 2012
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Title
The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy
Published in
PLOS ONE, July 2012
DOI 10.1371/journal.pone.0040696
Pubmed ID
Authors

Lisa J. Strug, Laura Addis, Theodore Chiang, Zeynep Baskurt, Weili Li, Tara Clarke, Huntley Hardison, Steven L. Kugler, David E. Mandelbaum, Edward J. Novotny, Steven M. Wolf, Deb K. Pal

Abstract

Reading disability (RD) is a common neurodevelopmental disorder with genetic basis established in families segregating "pure" dyslexia. RD commonly occurs in neurodevelopmental disorders including Rolandic Epilepsy (RE), a complex genetic disorder. We performed genomewide linkage analysis of RD in RE families, testing the hypotheses that RD in RE families is genetically heterogenenous to pure dyslexia, and shares genetic influences with other sub-phenotypes of RE.

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Geographical breakdown

Country Count As %
United Kingdom 2 5%
Japan 1 2%
Unknown 40 93%

Demographic breakdown

Readers by professional status Count As %
Student > Master 8 19%
Researcher 6 14%
Professor > Associate Professor 6 14%
Professor 5 12%
Student > Ph. D. Student 5 12%
Other 7 16%
Unknown 6 14%
Readers by discipline Count As %
Medicine and Dentistry 11 26%
Neuroscience 6 14%
Social Sciences 3 7%
Agricultural and Biological Sciences 3 7%
Psychology 3 7%
Other 8 19%
Unknown 9 21%