A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability

Prostaglandins Leukotrienes and Essential Fatty Acids

Volumn 63, Issue 1-2, 2000, Pages 27-31

  Francks, C ^a   Fisher, S E ^a   Marlow, A J ^a   Richardson, A J ^b,c   Stein, J F ^b   Monaco, A P ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c MRC CLINICAL SCIENCES CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 6P; DYSLEXIA; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC LINKAGE; GENOTYPE; HUMAN; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE TRAIT; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 0033799726     PISSN: 09523278     EISSN: None     Source Type: Journal    
DOI: 10.1054/plef.2000.0187     Document Type: Article

References (44)

1. Prevalence of reading disability in boys and girls
2. Very early language deficits in dyslexic children
3. Functional disruption in the organization of the brain for reading in dyslexia
4. Developmental dyslexia, neural timing, and hemispheric lateralisation
5. To see but not to read: The magnocellular theory of dyslexia
6. Abnormal processing of visual motion in dyslexia revealed by functional brain imaging
7. Psychophysical evidence for a magnocellular pathway deficit in dyslexia
8. Impaired neuronal timing in developmental dyslexia-the magnocellular hypothesis
9. Metabolic abnormalities in developmental dyslexia detected by 1(H) magnetic resonance spectroscopy
10. Dyslexia and other specific learning disorders
11. Varieties of developmental dyslexia
12. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
13. Congenital 'word-blindness' and its treatment
14. Specific dyslexia (congenital word blindness): A clinical and genetic study
15. Genetic models of reading disabilities
16. Evidence for major gene transmission of developmental dyslexia
17. Familial dyslexia: Genetic and medical findings in eleven three-generation families
18. Evidence for a genetic aetiology in reading disability of twins
19. Linkage strategies for complex traits. I. Multilocus models. II. The power of affected relative pairs. III. The effect of marker polymorphism on analysis of affected relative pairs
20. Genetics of specific reading disability
21. Genetics of reading disability
22. Specific reading disability: Identification of an inherited form through linkage analysis
23. Dyslexia and chromosome 15 heteromorphism: Negative LOD score in a Danish sample
24. Cosegregation of a balanced translocation (1:2) with retarded speech development and dyslexia
25. Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
26. A new gene (DYX3) for dyslexia is located on chromosome 2
27. Quantitative trait locus for reading disability on chromosome 6
28. Quantitative trait locus for reading disability: Correction
29. Multiple regression analysis of twin data
30. Left-handedness and immune disorders in familial dyslexics
31. Immune and autoimmune disorders in dyslexic children
32. The affected-pedigree-member method of linkage analysis
33. Quantitative-trait locus for specific language and reading deficits on chromosome 6p
34. A quantitative trait locus on chromosome 6p influences different aspects of developmental dyslexia
35. The investigation of linkage between a quantitative trait and a marker locus
36. Complete multipoint sib-pair analysis of qualitative and quantitative traits
37. Robust variance components approach for assessing genetic linkage in pedigrees
38. Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set
39. Prospects for whole-genome linkage disequilibrium mapping of common disease genes
40. The future of genetic studies of complex human diseases
41. A genome wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia)