(Q34660700)

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Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children

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scholarly article

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Europe PubMed Central

3 August 2017

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children (English)

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Europe PubMed Central

3 August 2017

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reading disability

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based on heuristic

inferred from title

quantitative trait locus

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3

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Europe PubMed Central

3 August 2017

5

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Europe PubMed Central

3 August 2017

Leonard C. Schalkwyk

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object named as

L C Schalkwyk

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Europe PubMed Central

3 August 2017

author name string

E L Meaburn

1

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Europe PubMed Central

3 August 2017

N Harlaar

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Europe PubMed Central

3 August 2017

language of work or name

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publication date

7 August 2007

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Europe PubMed Central

3 August 2017

Molecular Psychiatry

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Europe PubMed Central

3 August 2017

13

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Europe PubMed Central

3 August 2017

7

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Europe PubMed Central

3 August 2017

729-740

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Europe PubMed Central

3 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4002063

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Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins

1 reference

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Generalist genes and learning disabilities

1 reference

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The genetic basis of complex human behaviors

1 reference

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Genes, cognition and dyslexia: learning to read the genome

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The genetics of developmental dyslexia

1 reference

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Breakthroughs in the search for dyslexia candidate genes

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Genetics of dyslexia: the evolving landscape

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Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

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Searching for genetic determinants in the new millennium

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Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

1 reference

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The complex interplay among factors that influence allelic association.

1 reference

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Association study designs for complex diseases

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Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

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Toward genome-wide SNP genotyping

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Genome-wide association studies for common diseases and complex traits

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Mapping complex disease loci in whole-genome association studies

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Genetic association studies of complex traits: design and analysis issues

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Recent developments in genomewide association scans: a workshop summary and review

1 reference

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Genome-wide association studies: theoretical and practical concerns

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DNA pooling as a tool for large-scale association studies in complex traits

1 reference

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Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

1 reference

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21 January 2018

Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs

1 reference

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21 January 2018

Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

21 January 2018

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

1 reference

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21 January 2018

Pooled DNA genotyping on Affymetrix SNP genotyping arrays

1 reference

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21 January 2018

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

1 reference

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21 January 2018

Genotype prediction using a dense map of SNPs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

21 January 2018

The impact of SNP density on fine-scale patterns of linkage disequilibrium

1 reference

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21 January 2018

Twins' Early Development Study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems from childhood through adolescence

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

21 January 2018

DNA Pooling: a tool for large-scale association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

21 January 2018

Telephone Testing and Teacher Assessment of Reading Skills in 7-year-olds: I. Substantial Correspondence for a Sample of 5544 Children and for Extremes

1 reference

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21 January 2018

Telephone Testing and Teacher Assessment of Reading Skills in 7-year-olds: II. Strong Genetic Overlap

1 reference

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Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

1 reference

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Complement factor H polymorphism in age-related macular degeneration

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

1 reference

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Mining for SNPs: putting the common variants--common disease hypothesis to the test

1 reference

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21 January 2018

Identification of disease causing loci using an array-based genotyping approach on pooled DNA.

1 reference

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21 January 2018

Global variation in copy number in the human genome

1 reference

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A comprehensive analysis of common copy-number variations in the human genome

1 reference

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DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping

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21 January 2018

1 reference

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7 January 2021

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Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

7 January 2021

based on heuristic

inferred from DOI database lookup

The genetic lexicon of dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

7 January 2021

based on heuristic

inferred from DOI database lookup

Design and Analysis of Association Studies using Pooled DNA from Large Twin Samples

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

7 January 2021

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Exploiting large scale computing to construct high resolution linkage disequilibrium maps of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002063

7 January 2021

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10.1038/SJ.MP.4002063

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Europe PubMed Central

3 August 2017

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https://api.fatcat.wiki/v0/release/qzyl7g6qrffarj5h5iewfcwe7u

24 November 2022

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Europe PubMed Central

3 August 2017

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