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DCDC2 gene

Known as: DCDC2A, DOUBLECORTIN DOMAIN-CONTAINING PROTEIN 2, RU2 
 
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Hearing loss is the most common sensory deficit in humans. We show that a point mutation in DCDC2 (DCDC2a), a member of… 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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Highly Cited
2012
Highly Cited
2012
OBJECTIVE(S) Developmental dyslexia is a heritable condition, with genetic factors accounting for 44-75% of the variance in… Expand
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Highly Cited
2011
Highly Cited
2011
Background Several susceptibility genes have been proposed for dyslexia (reading disability; RD) and specific language impairment… Expand
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Highly Cited
2011
Highly Cited
2011
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of doublecortin domain containing… Expand
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Highly Cited
2011
Highly Cited
2011
Dyslexia (or reading disability) and specific language impairment (or SLI) are common childhood disorders that show considerable… Expand
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Highly Cited
2010
Highly Cited
2010
The 6p21-p22 chromosomal region has been identified as a developmental dyslexia locus both in linkage and association studies… Expand
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Highly Cited
2009
Highly Cited
2009
Dyslexia is a complex reading and writing disorder with a strong genetic component. In a German case-control cohort, we studied… Expand
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Highly Cited
2006
Highly Cited
2006
We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the most-replicated dyslexia… Expand
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Highly Cited
2005
Highly Cited
2005
DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with… Expand
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