A genome-wide screen for quantitative trait loci involved in developmental dyslexia in a large sample of sib-pairs from the UK

A genome-wide screen for quantitative trait loci involved in developmental dyslexia in a large sample of sib-pairs from the UK

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Francks, C, Fisher, S, Marlow, A, Williams, D, Ishikawa-Brush, Y, Talcott, J, Weeks, D, Cardon, L, Richardson, A, Stein, J, Monaco, A
التنسيق:	Journal article
منشور في:	2000

مواد مشابهة

Familial correlations between reading measures in a UK sib-pair cohort
حسب: Marlow, A, وآخرون
منشور في: (2000)

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.
حسب: Marlow, A, وآخرون
منشور في: (2001)

Quantitative trait analysis of the entire genome in large samples of dyslexic sib-pairs from the UK and US.
حسب: Fisher, S, وآخرون
منشور في: (2002)

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

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

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
حسب: Francks, C, وآخرون
منشور في: (2000)

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)

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

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
حسب: Fisher, S, وآخرون
منشور في: (1999)

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)

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

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

A genomewide linkage screen for relative hand skill in sibling pairs.
حسب: Francks, C, وآخرون
منشور في: (2002)

Lack of asymmetry characterises the cerebellum in developmental dyslexia
حسب: Harasty, J, وآخرون
منشور في: (2001)

Use of multivariate linkage analysis for dissection of a complex cognitive trait.
حسب: Marlow, A, وآخرون
منشور في: (2003)

Discovery of 42 genome-wide significant loci associated with dyslexia
حسب: Doust, C, وآخرون
منشور في: (2022)

Design considerations in a sib-pair study of linkage for susceptibility loci in cancer
حسب: Finkelstein Dianne M, وآخرون
منشور في: (2008-07-01)

The genetic basis of dyslexia.
حسب: Francks, C, وآخرون
منشور في: (2002)

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)

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)

What is Developmental Dyslexia?
حسب: Stein, J
منشور في: (2018)

What is Developmental Dyslexia?
حسب: John Stein
منشور في: (2018-02-01)

A population-based study of personality in 34,000 sib-pairs.
حسب: Martin, N, وآخرون
منشور في: (2000)

Genes, cognition and dyslexia: learning to read the genome.
حسب: Fisher, S, وآخرون
منشور في: (2006)

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)

The magnocellular theory of developmental dyslexia.
حسب: Stein, J
منشور في: (2001)

Theories about Developmental Dyslexia
حسب: John Stein
منشور في: (2023-01-01)

Could platelet activating factor play a role in developmental dyslexia?
حسب: Taylor, K, وآخرون
منشور في: (2001)

Cerebellar function in developmental dyslexia.
حسب: Stoodley, C, وآخرون
منشور في: (2013)

Cerebellar Function in Developmental Dyslexia
حسب: Stoodley, C, وآخرون
منشور في: (2012)

Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs.
حسب: Vipin Gupta, وآخرون
منشور في: (2013-01-01)

Developmental Dyslexia
حسب: Guinevere F. Eden, وآخرون
منشور في: (2019-08-01)

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

Multisensory integration and attention in developmental dyslexia
حسب: Harrar, V, وآخرون
منشور في: (2014)

Multisensory integration and attention in developmental dyslexia.
حسب: Harrar, V, وآخرون
منشور في: (2014)

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