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DYX1C1 gene

Known as: dynein, axonemal, assembly factor 4, DYX1C1, dyslexia susceptibility 1 candidate 1 
 
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
DYX1C1 has been associated with dyslexia and neuronal migration in the developing neocortex. Unexpectedly, we found that deleting… Expand
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Highly Cited
2013
Highly Cited
2013
DYX1C1, a susceptibility gene for dyslexia, encodes a tetratricopeptide repeat domain containing protein that has been implicated… Expand
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Volume and integrity of white matter correlate with reading ability, but the underlying factors contributing to this… Expand
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Review
2009
Review
2009
Developmental dyslexia is a highly heritable disorder with a prevalence of at least 5% in school-aged children. Linkage studies… Expand
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Highly Cited
2007
Highly Cited
2007
Developmental malformations of cortex have been shown to co-occur with language, learning, and other cognitive deficits in humans… Expand
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Highly Cited
2006
Highly Cited
2006
Rodent homologues of two candidate dyslexia susceptibility genes, Kiaa0319 and Dcdc2, have been shown to play roles in neuronal… Expand
Highly Cited
2005
Highly Cited
2005
A candidate gene, EKN1, was recently described in a cohort from Finland for the dyslexia locus on chromosome 15q, DYX1. This… Expand
Highly Cited
2004
Highly Cited
2004
Dyslexia has been linked to a number of chromosomal regions including 15q. Recently a gene, EKN1, with unknown function in the… Expand
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Highly Cited
2004
Highly Cited
2004
Developmental dyslexia is diagnosed as a specific impairment in reading ability, despite adequate intelligence and educational… Expand
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Highly Cited
2003
Highly Cited
2003
Approximately 3–10% of people have specific difficulties in reading, despite adequate intelligence, education, and social… Expand
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