Absence of linkage of phonological coding dyslexia to chromosome 6p23- p21.3 in a large family data set

American Journal of Human Genetics

Volumn 63, Issue 5, 1998, Pages 1448-1456

  Field, L L ^a,b   Kaplan, B J ^a  

^a UNIVERSITY OF CALGARY   (Canada)

^b Health Sciences Centre Calgary   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 6P; CHROMOSOME MARKER; DYSLEXIA; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 0032231869     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302107     Document Type: Article

References (53)

1. Babron M-C, Martinez M, Bonaïti-Pellié C, Clerget-Darpoux F (1993) Linkage detection by the affected-pedigree-member method: what is really tested? Genet Epidemiol 10:389-394
2. Bakwin H (1973) Reading disability in twins. Dev Med Child Neurol 15:184-187
3. Bisgaard ML, Eiberg H, Moller N, Niebuhr E, Mohr J (1987) Dyslexia and chromosome 15 heteromorphism: negative lod score in Danish material. Clin Genet 32:118-119
4. Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276-279
5. Chase CH, Rosen GD, Sherman GF (eds) (1996) Developmental dyslexia: neural, cognitive, and genetic mechanisms. York Press, Baltimore
6. Cottingham RW, Idury RM, Schaffer AA (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252-263
7. Crawford SG, Kaplan BJ, Kinsbourne M (1992) The effects of parental immunoreactivity on pregnancy, birth, and cognitive development: maternal immune attack on the fetus? Cortex 28:483-491
8. Davis S, Schroeder M, Goldin LR, Weeks DE (1996) Nonparametric simulation-based statistics for detecting linkage in general pedigrees. Am J Hum Genet 58:867-880
9. DeFries JC, Fulker DW, LaBuda MC (1987) Evidence for a genetic aetiology in reading disability of twins. Nature 329:537-539
10. Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1380:152-154
11. Duara R, Kushch A, Gross-Glen K, Barker W, Jallad B, Pascal S, Loewenstein DA et al (1991) Neuroanatomic differences between dyslexic and normal readers on magnetic resonance imaging scans. Arch Neurol 48:410-416
12. Elston RC (1992) Statistical analysis for genetic epidemiology, release 2.1. Computer program package available from Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio
13. Field LL, Tobias R, Thomson G, Pion S (1996) Susceptibility ito insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31. Gen-omics 33:1-8
14. Finucci JM, Guthrie JT, Childs AL, Abbey H, Childs B (1976) The genetics of specific reading disability. Ann Hum Genet 40:1-23
15. Gilger JW, Pennington BF, DeFries JC (1991) Risk for reading disability as a function of parental history in three family studies. Reading & Writing 3:205-217
16. Gilger JW, Pennington BF, Green P, Smith SM, Smith SD (1992) Reading disability, immune disorders and non-right-hand-edness. Neuropsychologia 30:209-227
17. Goldin LR, Weeks DE (1993) Two-locus models of disease: comparison of likelihood and nonparametric linkage meth-ods. Am J Hum Genet 53:908-915
18. Greenberg DA, Hodge SE, Vieland VJ, Spence MA (1996) Affecteds-only linkage methods are not a panacea. Am J Hum Genet 58:892-895
19. Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, Pauls DL (1997) Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet 60:27-39
20. Hallgren B (1950) Specific dyslexia ("congenital word blind-ness"): a clinical and genetic study. Acta Psychiatr Scand 65: 1-287
21. Hynd G, Semrud-Clikeman M, Lorys AR, Novey ES, Eliopulos D (1990) Brain morphology in developmental syslexia and attention deficit disorder/hyperactivity. Arch Neurol 47: 919-926
22. Jastak S, Wilkinson GS (1984) The wide range achievement test - revised. Jastak Associates, Wilmington, Delaware
23. Kaplan BJ, Crawford SG (1994) The GBG model: is there more to consider than handedness? Brain Cogn 26:291-299
24. Lathrop GM, Lalouel M, Julier C, Ott J (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 37:482-498
25. Leonard CM, Voeller KK, Lombardino LJ, Morris MK, Hynd GW, Alexander AW, Andersen HG, et al (1993) Anomalous cerebral structure in dyslexia revealed with magnetic resonance imaging. Arch Neurol 50:461-469
26. Lerner JW (1989) Educational interventions in learning disabilities. J Am Acad Child Adolesc Psychiatry 28:326-331
27. Lewitter FI, DeFries JC, Elston RC (1980) Genetic models of reading disability. Behav Genet 10:9-30
28. Litt M, Luty JA (1990) Dinucleotide repeat polymorphism at the D6S89 locus. Nucleic Acids Res 18:4301
29. Miller SA, Dykes DD, Polesky HF (1988) A simple salting out prodedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215
30. Nedospasov SA, Udalova IA, Kuprash DV, Turetskaya RL (1991) DNA sequence polymorphism at the human tumour necrosis factor (TNF) locus: numerous TNF/lymphotoxin alleles tagged by two closely linked microsatellites in the upstream region of the lymphotoxin (TNF-B) gene. J Immunol 147:1053-1059
31. Olson R, Wise B, Gonners F, Rack J, Fulker D (1989) Specific deficits in component reading and language skills: genetic and environmental influences. J Learn Disabil 22:339-348
32. Pennington BF, Lefly DL, Van Orden GC, Bookman MO, Smith SD (1987) Is phonology bypassed in normal or dyslexic development? Ann Dyslexia 37:62-89
33. Ploughman L, Boehnke M (1989) Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet 44:543-551
34. Polymeropoulos MH, Rath DS, Xiao H, Merril CR (1991) Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1). Nucleic Acids Res 19:4306
35. Rosner J, Simon DP (1971) The auditory analysis test: an initial report. J Learn Disabil 4:384-392
36. Smith SD, Kimberling WJ, Pennington BF (1991) Screening for multiple genes influencing dyslexia. Reading & Writing 3:285-298
37. Smith SD, Kimberling WJ, Pennington BF, Lubs HA (1983) Specific reading disability: identification of an inherited form through linkage anlysis. Science 219:1345-1347
38. Smith SD, Pennington BF, Kimberling WJ, Ing PS (1990) Familial dyslexia: use of genetic linkage data to define subtypes. J Am Acad Child Adolesc Psychiatry 29:204-213
39. Spreen O (1988) Learning disabled children growing up: a follow-up into adulthood. Oxford University Press, Oxford
40. Stevenson J, Graham P, Fredman G, McLoughlin V (1987) A twin study of genetic influences on reading and spelling ability and disability. J Child Psychol Psychiatry 28:229-247
41. Stoffel M, Espinosa R III, Le Beau MM, Bell GI (1993) A human glucagon-like peptide 1 receptor: localization to chromosome band 6q21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6. Diabetes 42:1215-1218
42. Thomson G (1995) Mapping disease genes: family-based association studies. Am J Hum Genet 57:487-498
43. Van Eerderwegh P, Hampe CE, Suarez BK, Reich T (1993) Alzheimer's disease: a piscatorial trek. Genet Epidemiol 10:395-400
44. Van Orden GC, Goldinger SD (1996) Phonologic mediation in skilled and dyslexic reading. In: Chase CH, Rosen GD, Sherman GF (eds) Developmental dyslexia: neural, cognitive, and genetic mechanisms. York Press, Baltimore, pp 185-223
45. Vieland VJ, Greenberg DA, Hodge SE (1993) Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures. Hum Hered 43:329-336
46. Weber JL, May PE (1989) Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet 44:388-396
47. Weber JL, Kwitek AE, May PE, Zoghbi HY (1991) Dinucleotide repeat polymorphism at the D6S105 locus. Nucleic Acids Res 19:968
48. Wechsler D (1974) Manual for the Wechsler intelligence scale for children - revised. Psychological Corp., New York
49. _ (1981) Wechsler adult intelligence scale - revised. Psychological Corp., New York
50. Weeks DE, Lange K (1988) The affected-pedigree-member method of linkage analysis. Am J Hum Genet 42:315-326
51. Woodcock RW (1987) Woodcock reading mastery tests. American Guidance Service, Circle Pines, Minnesota
52. Woodcock RW, Johnson MB (1989) Woodcock-Johnson psychoeducational battery - revised. DLM Teaching Resources, Allen, Texas
53. Zahalkova M, Vrzal V, Kloboukova E (1972) Genetical investigations in dyslexia. J Med Genet 9:48-52