Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. (Q53658316)

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scientific article published in February 2003

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3–22

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English	Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.	scientific article published in February 2003	Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3–22

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31 October 2019

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22 (English)

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31 October 2019

reading disability

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based on heuristic

inferred from title

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based on heuristic

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linkage disequilibrium

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based on heuristic

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Derek W. Morris

4

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31 October 2019

Michael C O'Donovan

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31 October 2019

Marianne Bernadette van den Bree

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31 October 2019

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D Turic

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31 October 2019

L Robinson

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31 October 2019

M Duke

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31 October 2019

V Webb

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31 October 2019

M Hamshere

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31 October 2019

C Milham

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31 October 2019

E Hopkin

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31 October 2019

K Pound

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31 October 2019

S Fernando

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31 October 2019

A Grierson

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31 October 2019

M Easton

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31 October 2019

N Williams

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31 October 2019

R Chowdhury

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31 October 2019

J Gruen

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31 October 2019

J Stevenson

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31 October 2019

M Krawczak

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31 October 2019

M J Owen

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31 October 2019

J Williams

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31 October 2019

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1 February 2003

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31 October 2019

Molecular Psychiatry

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31 October 2019

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31 October 2019

2

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31 October 2019

176-185

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31 October 2019

Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

A twin study of genetic influences on reading and spelling ability and disability.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Evidence for a genetic aetiology in reading disability of twins.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Evidence for major gene transmission of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Commingling and segregation analysis of reading performance in families of normal reading probands

1 reference

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21 January 2018

Evidence for linkage of spelling disability to chromosome 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Two translocations of chromosome 15q associated with dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Quantitative trait locus for reading disability on chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

1 reference

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21 January 2018

Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Extent and distribution of linkage disequilibrium in three genomic regions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

21 January 2018

Linkage disequilibrium in the human genome

1 reference

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Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations

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Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.

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Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)

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Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.

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Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C gene

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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Localisation of a gene implicated in a severe speech and language disorder

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Normative data on revised Conners Parent and Teacher Rating Scales

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An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

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Model-free analysis and permutation tests for allelic associations.

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Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex

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The structure of genetic influences on general cognitive, language, phonological, and reading abilities

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7 January 2021

based on heuristic

inferred from DOI database lookup

Specific reading disability: identification of an inherited form through linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

7 January 2021

based on heuristic

inferred from DOI database lookup

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

7 January 2021

based on heuristic

inferred from DOI database lookup

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001216

7 January 2021

based on heuristic

inferred from DOI database lookup

Quantitative trait locus for reading disability: correction

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

1 reference

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The Children's Test of Nonword Repetition: a test of phonological working memory

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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