PCSK6 is associated with handedness in individuals with dyslexia.

PCSK6 is associated with handedness in individuals with dyslexia.

عرض إصدارات أخرى (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...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Scerri, T, Brandler, W, Paracchini, S, Morris, A, Ring, S, Richardson, A, Talcott, J, Stein, J, Monaco, A
التنسيق:	Journal article
اللغة:	English
منشور في:	Oxford University Press 2011

مواد مشابهة

PCSK6 is associated with handedness in individuals with dyslexia
حسب: Richardson, A, وآخرون
منشور في: (2011)

The genetics of handedness and dyslexia
حسب: Brandler, W
منشور في: (2014)

The genetic lexicon of dyslexia.
حسب: Paracchini, S, وآخرون
منشور في: (2007)

The genetic relationship between handedness and neurodevelopmental disorders
حسب: Brandler, W, وآخرون
منشور في: (2014)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
حسب: Scerri, T, وآخرون
منشور في: (2010)

PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness.
حسب: Larissa Arning, وآخرون
منشور في: (2013-01-01)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
حسب: Newbury, D, وآخرون
منشور في: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
حسب: Newbury, D, وآخرون
منشور في: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
حسب: Newbury, D, وآخرون
منشور في: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
حسب: Richardson, A, وآخرون
منشور في: (2011)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
حسب: Richardson, A, وآخرون
منشور في: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
حسب: Scerri, T, وآخرون
منشور في: (2010)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
حسب: Paracchini, S, وآخرون
منشور في: (2008)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
حسب: Scerri, T, وآخرون
منشور في: (2012)

Dyslexia, Handedness, and Immune Disorders
حسب: J Gordon Millichap
منشور في: (1993-04-01)

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
حسب: Scerri, T, وآخرون
منشور في: (2004)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
حسب: Thomas S Scerri, وآخرون
منشور في: (2010-10-01)

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
حسب: Brandler, WM, وآخرون
منشور في: (2013)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
حسب: Thomas S. Scerri, وآخرون
منشور في: (2010-01-01)

The DCDC2 deletion is not a risk factor for dyslexia
حسب: Scerri, T, وآخرون
منشور في: (2017)

Multivariate multipoint linkage analysis of QTL in dyslexia
حسب: Marlow, A, وآخرون
منشور في: (2002)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
حسب: Francks, C, وآخرون
منشور في: (2004)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
حسب: Thomas S Scerri, وآخرون
منشور في: (2012-01-01)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
حسب: Simpson, N, وآخرون
منشور في: (2014)

Further evidence that KIAA0319 is associated with developmental dyslexia
حسب: Harold, D, وآخرون
منشور في: (2006)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
حسب: Paracchini, S, وآخرون
منشور في: (2006)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
حسب: Simpson, N, وآخرون
منشور في: (2014)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
حسب: Paracchini, S, وآخرون
منشور في: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Dennis, M, وآخرون
منشور في: (2009)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
حسب: Harold, D, وآخرون
منشور في: (2006)

Alternative splicing in the dyslexia-associated gene KIAA0319.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2007)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
حسب: MacPhie, I, وآخرون
منشور في: (2001)

The perception of "sine-wave speech" by adults with developmental dyslexia.
حسب: Rosner, B, وآخرون
منشور في: (2003)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
حسب: Harold, D, وآخرون
منشور في: (2006)

Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
حسب: Francks, C, وآخرون
منشور في: (2003)

Cerebellar morphology in developmental dyslexia.
حسب: Rae, C, وآخرون
منشور في: (2002)

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
حسب: Francks, C, وآخرون
منشور في: (2003)

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2008)

Handedness in twins: meta-analyses
حسب: Lena Sophie Pfeifer, وآخرون
منشور في: (2022-01-01)

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
حسب: Gialluisi, A, وآخرون
منشور في: (2019)