Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects

عرض إصدارات أخرى (3)

Dyslexia (or reading disability) and specific language impairment (or SLI) are common childhood disorders that show considerable co-morbidity and diagnostic overlaps and have been suggested to share some genetic aetiology. Recently, genetic risk variants have been identified for SLI and dyslexia ena...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Newbury, D, Paracchini, S, Scerri, T, Winchester, L, Addis, L, Richardson, A, Walter, J, Stein, J, Talcott, J, Monaco, A
التنسيق:	Journal article
اللغة:	English
منشور في:	2011

مواد مشابهة

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)

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

PCSK6 is associated with handedness in individuals with dyslexia.
حسب: Scerri, T, وآخرون
منشور في: (2011)

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

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

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

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)

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

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

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)

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

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

Genome-wide screening for DNA variants associated with reading and language traits.
حسب: Gialluisi, A, وآخرون
منشور في: (2014)

Multivariate linkage analysis of specific language impairment (SLI).
حسب: Monaco, A
منشور في: (2007)

Multivariate linkage analysis of specific language impairment (SLI)
حسب: Monaco, A
منشور في: (2007)

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

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

Exome sequencing of an isolated Chilean population affected by Specific Language Impairment (SLI)
حسب: Newbury, D, وآخرون
منشور في: (2012)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits
حسب: Scerri, T, وآخرون
منشور في: (2011)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
حسب: Scerri, T, وآخرون
منشور في: (2011)

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

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

Reading and language disorders: the importance of both quantity and quality.
حسب: Newbury, D, وآخرون
منشور في: (2014)

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

Specific Language Impairment (SLI): The Internet Ralli Campaign to Raise Awareness of SLI
حسب: Conti-Ramsden Gina, وآخرون
منشور في: (2014-08-01)

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

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

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)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Megan Y Dennis, وآخرون
منشور في: (2009-03-01)

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

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)

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures
حسب: Martinelli, A, وآخرون
منشور في: (2021)

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

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
حسب: Fisher, S, وآخرون
منشور في: (2002)

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment
حسب: Newbury, D, وآخرون
منشور في: (2004)

A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).
حسب: Fisher, S, وآخرون
منشور في: (1999)