PCSK6 is associated with handedness in individuals with dyslexia.

PCSK6 is associated with handedness in individuals with dyslexia.

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Approximately 90% of humans are right-handed. Handedness is a heritable trait, yet the genetic basis is not well understood. Here we report a genome-wide association study for a quantitative measure of relative hand skill in individuals with dyslexia [reading disability (RD)]. The most highly associ...

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Xehetasun bibliografikoak
Egile Nagusiak:	Scerri, T, Brandler, W, Paracchini, S, Morris, A, Ring, S, Richardson, A, Talcott, J, Stein, J, Monaco, A
Formatua:	Journal article
Hizkuntza:	English
Argitaratua:	Oxford University Press 2011

Antzeko izenburuak

PCSK6 is associated with handedness in individuals with dyslexia
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The genetics of handedness and dyslexia
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The genetic lexicon of dyslexia.
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The genetic relationship between handedness and neurodevelopmental disorders
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Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
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PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness.
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Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
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Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
nork: Newbury, D, et al.
Argitaratua: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
nork: Newbury, D, et al.
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Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
nork: Richardson, A, et al.
Argitaratua: (2011)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
nork: Richardson, A, et al.
Argitaratua: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
nork: Scerri, T, et al.
Argitaratua: (2010)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
nork: Paracchini, S, et al.
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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
nork: Scerri, T, et al.
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Dyslexia, Handedness, and Immune Disorders
nork: J Gordon Millichap
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Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
nork: Scerri, T, et al.
Argitaratua: (2004)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
nork: Thomas S Scerri, et al.
Argitaratua: (2010-10-01)

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
nork: Brandler, WM, et al.
Argitaratua: (2013)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
nork: Thomas S. Scerri, et al.
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The DCDC2 deletion is not a risk factor for dyslexia
nork: Scerri, T, et al.
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Multivariate multipoint linkage analysis of QTL in dyslexia
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A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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Further evidence that KIAA0319 is associated with developmental dyslexia
nork: Harold, D, et al.
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
nork: Paracchini, S, et al.
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
nork: Simpson, N, et al.
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
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A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
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Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
nork: Harold, D, et al.
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Alternative splicing in the dyslexia-associated gene KIAA0319.
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Characterisation of a major locus for developmental dyslexia on 18p11.2.
nork: MacPhie, I, et al.
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The perception of "sine-wave speech" by adults with developmental dyslexia.
nork: Rosner, B, et al.
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Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
nork: Harold, D, et al.
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Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
nork: Francks, C, et al.
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Cerebellar morphology in developmental dyslexia.
nork: Rae, C, et al.
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Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
nork: Francks, C, et al.
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The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
nork: Velayos-Baeza, A, et al.
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Handedness in twins: meta-analyses
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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
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