PCSK6 is associated with handedness in individuals with dyslexia.

PCSK6 is associated with handedness in individuals with dyslexia.

Εμφάνιση άλλων εκδόσεων (1)

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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Scerri, T, Brandler, W, Paracchini, S, Morris, A, Ring, S, Richardson, A, Talcott, J, Stein, J, Monaco, A
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	Oxford University Press 2011

Παρόμοια τεκμήρια

PCSK6 is associated with handedness in individuals with dyslexia
ανά: Richardson, A, κ.ά.
Έκδοση: (2011)

The genetics of handedness and dyslexia
ανά: Brandler, W
Έκδοση: (2014)

The genetic lexicon of dyslexia.
ανά: Paracchini, S, κ.ά.
Έκδοση: (2007)

The genetic relationship between handedness and neurodevelopmental disorders
ανά: Brandler, W, κ.ά.
Έκδοση: (2014)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
ανά: Scerri, T, κ.ά.
Έκδοση: (2010)

PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness.
ανά: Larissa Arning, κ.ά.
Έκδοση: (2013-01-01)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
ανά: Newbury, D, κ.ά.
Έκδοση: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
ανά: Newbury, D, κ.ά.
Έκδοση: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
ανά: Newbury, D, κ.ά.
Έκδοση: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
ανά: Richardson, A, κ.ά.
Έκδοση: (2011)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
ανά: Richardson, A, κ.ά.
Έκδοση: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
ανά: Scerri, T, κ.ά.
Έκδοση: (2010)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
ανά: Paracchini, S, κ.ά.
Έκδοση: (2008)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
ανά: Scerri, T, κ.ά.
Έκδοση: (2012)

Dyslexia, Handedness, and Immune Disorders
ανά: J Gordon Millichap
Έκδοση: (1993-04-01)

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
ανά: Scerri, T, κ.ά.
Έκδοση: (2004)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
ανά: Thomas S Scerri, κ.ά.
Έκδοση: (2010-10-01)

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
ανά: Brandler, WM, κ.ά.
Έκδοση: (2013)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
ανά: Thomas S. Scerri, κ.ά.
Έκδοση: (2010-01-01)

The DCDC2 deletion is not a risk factor for dyslexia
ανά: Scerri, T, κ.ά.
Έκδοση: (2017)

Multivariate multipoint linkage analysis of QTL in dyslexia
ανά: Marlow, A, κ.ά.
Έκδοση: (2002)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
ανά: Francks, C, κ.ά.
Έκδοση: (2004)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
ανά: Thomas S Scerri, κ.ά.
Έκδοση: (2012-01-01)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
ανά: Simpson, N, κ.ά.
Έκδοση: (2014)

Further evidence that KIAA0319 is associated with developmental dyslexia
ανά: Harold, D, κ.ά.
Έκδοση: (2006)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
ανά: Paracchini, S, κ.ά.
Έκδοση: (2006)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
ανά: Simpson, N, κ.ά.
Έκδοση: (2014)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
ανά: Paracchini, S, κ.ά.
Έκδοση: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
ανά: Dennis, M, κ.ά.
Έκδοση: (2009)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
ανά: Harold, D, κ.ά.
Έκδοση: (2006)

Alternative splicing in the dyslexia-associated gene KIAA0319.
ανά: Velayos-Baeza, A, κ.ά.
Έκδοση: (2007)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
ανά: MacPhie, I, κ.ά.
Έκδοση: (2001)

The perception of "sine-wave speech" by adults with developmental dyslexia.
ανά: Rosner, B, κ.ά.
Έκδοση: (2003)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
ανά: Harold, D, κ.ά.
Έκδοση: (2006)

Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
ανά: Francks, C, κ.ά.
Έκδοση: (2003)

Cerebellar morphology in developmental dyslexia.
ανά: Rae, C, κ.ά.
Έκδοση: (2002)

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
ανά: Francks, C, κ.ά.
Έκδοση: (2003)

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
ανά: Velayos-Baeza, A, κ.ά.
Έκδοση: (2008)

Handedness in twins: meta-analyses
ανά: Lena Sophie Pfeifer, κ.ά.
Έκδοση: (2022-01-01)

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
ανά: Gialluisi, A, κ.ά.
Έκδοση: (2019)