(Q52055647)

English

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

scientific article published in July 2005

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. (English)

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

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author name string

Raskind WH

1

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Igo RP

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Chapman NH

3

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Berninger VW

4

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Thomson JB

5

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Matsushita M

6

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Brkanac Z

7

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Holzman T

8

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Brown M

9

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Wijsman EM

10

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Europe PubMed Central

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20 April 2018

http://europepmc.org/abstract/MED/15753956

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publication date

1 July 2005

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Molecular Psychiatry

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

10

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

7

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

699-711

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

Incidence of reading disability in a population-based birth cohort, 1976-1982, Rochester, Minn.

1 reference

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Phonological processing skills and deficits in adult dyslexics.

1 reference

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Persistence of phonological processing deficits in college students with dyslexia who have age-appropriate reading skills.

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From language to reading and dyslexia.

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Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

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Developmental dyslexia: genetic dissection of a complex cognitive trait

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A dominant gene for developmental dyslexia on chromosome 3

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Evidence for major gene transmission of developmental dyslexia

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Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span

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Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.

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

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Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

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A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

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Quantitative trait locus for reading disability on chromosome 6

1 reference

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

1 reference

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

1 reference

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

1 reference

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A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.

1 reference

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Familial dyslexia: use of genetic linkage data to define subtypes

1 reference

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Evidence for linkage of spelling disability to chromosome 15

1 reference

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Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

1 reference

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Familial aggregation of dyslexia phenotypes.

1 reference

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Neurobehavioral phenotype of Klinefelter syndrome

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Neuropsychological profiles of adults with Klinefelter syndrome

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A high-resolution recombination map of the human genome

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Exploring genetic analysis of complex traits through the paradigm of alcohol dependence: summary of GAW11 contributions

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Genome scans for Q1 and Q2 on general population replicates using Loki.

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Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees.

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Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure

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Composite statistics for QTL mapping with moderately discordant sibling pairs

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Ascertainment adjustment in complex diseases

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Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees

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Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

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Guess LOD approach: Sufficient conditions for robustness

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Effects of misspecifying genetic parameters in lod score analysis.

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The power to detect linkage in complex disease by means of simple LOD-score analyses

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Complex segregation analyses: uses and limitations

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Regressive logistic models for familial disease and other binary traits

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

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Multipoint quantitative-trait linkage analysis in general pedigrees

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Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

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Joint linkage and segregation analysis using Markov chain Monte Carlo methods.

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The nonword reading deficit in developmental dyslexia: evidence from children learning to read German

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Word recognition deficits in German: more evidence from a representative sample.

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Developmentally impaired processing speed decreases more than normally with age.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait

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Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families

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Prevalence of Reading Disability in Boys and Girls

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Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence

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Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p

1 reference

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inferred from DOI database lookup

Quantitative trait locus for reading disability: correction

1 reference

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inferred from DOI database lookup

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001657

7 January 2021

based on heuristic

inferred from DOI database lookup

Comment on "Ascertainment adjustment in complex diseases"

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001657

7 January 2021

based on heuristic

inferred from DOI database lookup

Model misspecification and multipoint linkage analysis

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.MP.4001657

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/15753956

ResearchGate publication ID

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