(Q52040525)

20 April 2018

title

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. (English)

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Haiying Meng

1

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20 April 2018

Karl Hager

2

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Matthew Held

3

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Grier P Page

4

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Richard K Olson

5

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Bruce F Pennington

6

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20 April 2018

John C DeFries

7

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Shelley D Smith

8

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Jeffrey R Gruen

9

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20 April 2018

publication date

28 October 2005

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20 April 2018

published in

Human Genetics

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20 April 2018

volume

118

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20 April 2018

page(s)

87-90

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20 April 2018

issue

1

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20 April 2018

https://scigraph.springernature.com/pub.10.1007/s00439-005-0017-9

exact match

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cites work

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia

1 reference

12 December 2020

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

1 reference

12 December 2020

Two translocations of chromosome 15q associated with dyslexia

1 reference

12 December 2020

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

1 reference

12 December 2020

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

1 reference

12 December 2020

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

1 reference

12 December 2020

Evidence for a genetic aetiology in reading disability of twins.

1 reference

12 December 2020

Evidence for linkage of spelling disability to chromosome 15

1 reference

12 December 2020

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

1 reference

12 December 2020

Specific deficits in component reading and language skills: genetic and environmental influences.

1 reference

12 December 2020

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

1 reference

12 December 2020

Comprehensive human genome amplification using multiple displacement amplification

1 reference

12 December 2020

Pedigree tests of transmission disequilibrium

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12 December 2020

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

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12 December 2020

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

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12 December 2020

Multiple regression analysis of twin data

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12 December 2020

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

1 reference

12 December 2020

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

1 reference

12 December 2020

Transmission-disequilibrium tests for quantitative traits

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12 December 2020

Dyslexia (Specific Reading Disability)

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12 December 2020

10.1007/S00439-005-0017-9

Identifiers

DOI

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20 April 2018

PubMed ID

16133186

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20 April 2018