Familial dyslexia: Neurocognitive and genetic correlation in a large Finnish family

Developmental Medicine and Child Neurology

Volumn 44, Issue 9, 2002, Pages 580-586

  Nopola Hemmi, Jaana ^a,c   Myllyluoma, Birgitta ^a   Voutilainen, Arja ^a   Leinonen, Seija ^b   Kere, Juha ^a   Ahonen, Timo ^b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b UNIVERSITY OF JYVÄSKYLÄ   (Finland)

^c JORVI HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGE; AGED; AMNESIA; ARTICLE; CHILD; CHROMOSOME; COGNITION; COMPARATIVE STUDY; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE CLASSIFICATION; DISEASE SEVERITY; DYSLEXIA; FAMILIAL DISEASE; FAMILY; FEMALE; FINLAND; GENE LOCUS; GENE SEGREGATION; GENETIC ASSOCIATION; HUMAN; HUMAN GENOME; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; NEUROPSYCHOLOGY; PHONETICS; PRIORITY JOURNAL; READING; SHORT TERM MEMORY; SKILL; VERBALIZATION;

ADULT; CHILD; COGNITION DISORDERS; DYSLEXIA; FEMALE; FINLAND; HUMANS; LANGUAGE DISORDERS; MALE; MEMORY; NEUROPSYCHOLOGICAL TESTS; PEDIGREE;

EID: 0036727070     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0012162201002614     Document Type: Article

References (37)

1. Defining disease phenotypes
2. Language phenotype for reading and writing disability: A family approach
3. Quantitative trait locus for reading disability on chromosome 6
4. The relationship between phonological awareness, rapid naming and verbal memory to severe reading and spelling disability
5. Converging evidence for multiple genetic forms of reading disability
6. Rapid automatized naming (R.A.N.): Dyslexia differentiated from other learning disabilities
7. A new gene (DYX3) for dyslexia is located on chromosome 2
8. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
9. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
10. Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia
11. Quantitative-trait locus for specific language and reading deficits on chromosome 6p
12. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
13. Practitioner review: Verbal working memory development and its disorders
14. The persistence of rapid naming problems in children with reading disabilities: A nine-year follow-up
15. Heterogeneity in adult dyslexic readers: Relating processing skills to the speed and accuracy of oral text reading
16. Dyslexia subtypes: Genetics, behavior, and brain imaging
17. In search of the core features of dyslexia: Observations concerning dyslexia in the highly orthographically regular Finnish language
18. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
19. Two translocations of chromosome 15q associated with dyslexia
20. A dominant gene for developmental dyslexia on chromosome 3
21. Specific deficits in component reading and language skills: Genetic and environmental influences
22. Phonological processing skills and deficits in adult dyslexics
23. Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
24. The nonword reading deficit in developmental dyslexia: A review
25. Evidence for linkage of spelling disability to chromosome 15
26. Dyslexia
27. Specific reading disability: Identification of an inherited form through linkage analysis
28. Alternative diagnostic approaches for specific developmental reading disabilities
29. Rapid alternating stimulus naming in the developmental dyslexias
30. Early naming deficits, developmental dyslexia and a specific deficit hypothesis