Multivariate multipoint linkage analysis of QTL in dyslexia

Multivariate multipoint linkage analysis of QTL in dyslexia

Bibliografski detalji
Glavni autori:	Marlow, A, Fisher, S, Francks, C, Richardson, A, Talcott, J, Stein, J, Monaco, A, Cardon, L
Format:	Journal article
Izdano:	2002

Slični predmeti

Use of multivariate linkage analysis for dissection of a complex cognitive trait.
od: Marlow, A, i dr.
Izdano: (2003)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
od: MacPhie, I, i dr.
Izdano: (2001)

A genome-wide screen for quantitative trait loci involved in developmental dyslexia in a large sample of sib-pairs from the UK
od: Francks, C, i dr.
Izdano: (2000)

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.
od: Marlow, A, i dr.
Izdano: (2001)

Familial correlations between reading measures in a UK sib-pair cohort
od: Marlow, A, i dr.
Izdano: (2000)

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
od: Fisher, S, i dr.
Izdano: (2002)

A genomewide linkage screen for relative hand skill in sibling pairs.
od: Francks, C, i dr.
Izdano: (2002)

Association mapping of the 6p23-21.3 QTL for reading disability
od: Francks, C, i dr.
Izdano: (2004)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
od: Francks, C, i dr.
Izdano: (2004)

PCSK6 is associated with handedness in individuals with dyslexia
od: Richardson, A, i dr.
Izdano: (2011)

PCSK6 is associated with handedness in individuals with dyslexia.
od: Scerri, T, i dr.
Izdano: (2011)

The genetic basis of dyslexia.
od: Francks, C, i dr.
Izdano: (2002)

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
od: Scerri, T, i dr.
Izdano: (2004)

Genes, cognition and dyslexia: learning to read the genome.
od: Fisher, S, i dr.
Izdano: (2006)

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
od: Francks, C, i dr.
Izdano: (2000)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
od: Newbury, D, i dr.
Izdano: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
od: Newbury, D, i dr.
Izdano: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
od: Newbury, D, i dr.
Izdano: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
od: Richardson, A, i dr.
Izdano: (2011)

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
od: Fisher, S, i dr.
Izdano: (1999)

Molecular genetic analysis of a quantitative measure of relative hand skill
od: Francks, C, i dr.
Izdano: (2002)

The perception of "sine-wave speech" by adults with developmental dyslexia.
od: Rosner, B, i dr.
Izdano: (2003)

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
od: Francks, C, i dr.
Izdano: (2003)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
od: Scerri, T, i dr.
Izdano: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
od: Richardson, A, i dr.
Izdano: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
od: Scerri, T, i dr.
Izdano: (2010)

Cerebellar morphology in developmental dyslexia.
od: Rae, C, i dr.
Izdano: (2002)

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder
od: Gayan, J, i dr.
Izdano: (2004)

Bivariate linkage analyses for reading difficulties and rapid naming
od: Davis, C, i dr.
Izdano: (2002)

Multivariate linkage analysis of specific language impairment (SLI).
od: Monaco, A
Izdano: (2007)

Multivariate linkage analysis of specific language impairment (SLI)
od: Monaco, A
Izdano: (2007)

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
od: Gayán, J, i dr.
Izdano: (2005)

Quantitative trait analysis of the entire genome in large samples of dyslexic sib-pairs from the UK and US.
od: Fisher, S, i dr.
Izdano: (2002)

Lack of asymmetry characterises the cerebellum in developmental dyslexia
od: Harasty, J, i dr.
Izdano: (2001)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
od: Harold, D, i dr.
Izdano: (2006)

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
od: Francks, C, i dr.
Izdano: (2002)

Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneity.
od: Morris, A, i dr.
Izdano: (2003)

A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).
od: Fisher, S, i dr.
Izdano: (1999)

Handedness and schizophrenia susceptibility are paternally linked to a locus on chromosome 2p12-q11.
od: Francks, C, i dr.
Izdano: (2003)

Familial and genetic effects on motor coordination, laterality, and reading-related cognition.
od: Francks, C, i dr.
Izdano: (2003)