(Q53658316)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference

1 reference

linkage disequilibrium

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Michael C O'Donovan

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

Marianne Bernadette van den Bree

31 October 2019

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

author name string

D Turic

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

L Robinson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

M Duke

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

V Webb

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

M Hamshere

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

C Milham

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

E Hopkin

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

K Pound

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

S Fernando

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

A Grierson

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

M Easton

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

N Williams

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

R Chowdhury

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

J Gruen

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

J Stevenson

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

M Krawczak

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

M J Owen

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

J Williams

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 February 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

176-185

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610650%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001216

31 October 2019

exact match

0 references

cites work

Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning

1 reference

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

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

21 January 2018

1 reference

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

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

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

Evidence for major gene transmission of developmental dyslexia

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

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

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

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

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Extent and distribution of linkage disequilibrium in three genomic regions

21 January 2018

1 reference

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

Linkage disequilibrium in the human genome

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Normative data on revised Conners Parent and Teacher Rating Scales

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Model-free analysis and permutation tests for allelic associations.

21 January 2018

1 reference

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

Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

7 January 2021

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

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

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

Quantitative trait locus for reading disability: correction

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021