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American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 105, Issue 6, 2001, Pages 507-517

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia

(7) Petryshen, Tracey L a Kaplan, Bonnie J a,b Liu, Ming Fu a De French, Norma Schmill a Tobias, Rose a Hughes, Martha L a Leigh Field, L a,c

a UNIVERSITY OF CALGARY (Canada)

b ALBERTA CHILDREN'S HOSPITAL (Canada)

c UNIVERSITY OF BRITISH COLUMBIA (Canada)

Author keywords

Dyslexia genetics; Human; Linkage; Qualitative trait; Quantitative trait

Indexed keywords

ARTICLE; CHROMOSOME 6Q; DYSLEXIA; GENE LOCUS; GENETIC LINKAGE; GENETIC MARKER; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; PHENOTYPE; PHONETICS; PRIORITY JOURNAL; QUANTITATIVE TRAIT; SIBLING;

ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 6; DYSLEXIA; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LINKAGE DISEQUILIBRIUM; LOD SCORE; MALE; MICROSATELLITE REPEATS; NUCLEAR FAMILY; PHENOTYPE;

EID: 0035828096 PISSN: 15524841 EISSN: 1552485X Source Type: Journal
DOI: 10.1002/ajmg.1475 Document Type: Article

Times cited : (77)

References (79)

1
- 0033358545
- Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure
- (1999) Am J Hum Genet , vol.65 , pp. 531-544
- Allison, D.B.¹ Neale, M.C.² Zannolli, R.³ Schork, N.J.⁴ Amos, C.I.⁵ Blangero, J.⁶

2
- 0015606171
- Reading disability in twins
- (1973) Dev Med Child Neurol , vol.15 , pp. 184-187
- Bakwin, H.¹

3
- 0023254230
- Dyslexia and chromosome 15 heteromorphisms: Negative lod score in a Danish material
- (1987) Clin Genet , vol.32 , pp. 118-119
- Bisgard, M.L.¹ Eiberg, H.² Møller, N.³ Niebuhr, E.⁴ Mohr, J.⁵

4
- 0026145027
- Naming speed deficits in reading disability: Multiple measures of a singular process
- (1991) J Exp Psychol , vol.51 , pp. 195-219
- Bowers, P.G.¹ Swanson, L.B.²

5
- 0028030006
- Quantitative trait locus for reading disability on chromosome 6
- (1994) Science , vol.266 , pp. 276-279
- Cardon, L.R.¹ Smith, S.D.² Fulker, D.W.³ Kimberling, W.J.⁴ Pennington, B.F.⁵ DeFries, J.C.⁶

6
- 0027366195
- Faster sequential genetic linkage computations
- (1993) Am J Hum Genet , vol.53 , pp. 252-263
- Cottingham R.W., Jr.¹ Idury, R.M.² Schaffer, A.A.³

7
- 0023179955
- Evidence for a genetic aetiology in reading disability of twins
- (1987) Nature , vol.329 , pp. 537-539
- DeFries, J.C.¹ Fulker, D.W.² LaBuda, M.C.³

8
- 0016150610
- Rapid "automatized" naming of pictured objects, colors, letters and numbers by normal children
- (1974) Cortex , vol.10 , pp. 186-202
- Denckla, M.B.¹ Rudel, R.G.²

9
- 0017140877
- Rapid automatized naming (R.A.N.): Dyslexia differentiated from other learning disabilities
- (1976) Neuropsychologia , vol.14 , pp. 471-479
- Denckla, M.B.¹ Rudel, R.G.²

10
- 84986754615
- Phases of development in learning to read words by sight
- (1995) J Res Read , vol.18 , pp. 116-125
- Ehri, L.¹

11
- 0024788805
- Man bites dog? The validity of maximizing led scores to determine mode of inheritance
- (1989) Am J Med Genet , vol.34 , pp. 487-488
- Elston, R.C.¹

12
- 0031066950
- Algorithms and inferences: The challenge of multifactorial diseases
- (1997) Am J Hum Genet , vol.60 , pp. 255-262
- Elston, R.C.¹

13
- 0032231299
- Methods of linkage analysis-and the assumptions underlying them
- (1998) Am J Hum Genet , vol.63 , pp. 931-934
- Elston, R.C.¹

14
- 0032877882
- A new gene (DYX3) for dyslexia is located on chromosome 2
- (1999) J Med Genet , vol.36 , pp. 664-669
- Fagerheim, T.¹ Raeymaekers, P.² Tonnessen, F.E.³ Pedersen, M.⁴ Tranebjaerg, L.⁵ Lubs, H.A.⁶

15
- 0025569408
- Neuropsychological profile of adult dyslexics
- (1990) Brain Lang , vol.39 , pp. 485-497
- Felton, R.H.¹ Naylor, C.E.² Wood, F.B.³

16
- 0038400472
- The endogenous cannabinoid system and brain development
- (2000) Trends Neurosci , vol.23 , pp. 14-20
- Fernández-Ruiz, J.¹ Berrendero, F.² Hernández, M.L.³ Ramos, J.A.⁴

17
- 0032231869
- Absence of linkage of phonological coding dyslexia to chromosome 6p23-21.3 in a large family data set
- (1998) Am J Hum Genet , vol.63 , pp. 1448-1456
- Field, L.L.¹ Kaplan, B.J.²

18
- 0029920402
- Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31
- (1996) Genomics , vol.33 , pp. 1-8
- Field, L.L.¹ Tobias, R.² Thomson, G.³ Plon, S.⁴

19
- 0017107298
- The genetics of specific reading disability
- (1976) Ann Hum Genet , vol.40 , pp. 1-23
- Finucci, J.M.¹ Guthrie, J.T.² Childs, A.L.³ Abbey, H.⁴ Childs, B.⁵

20
- 0033366739
- A quantitative-trait locus on chromosome 6p influence different aspects of developmental dyslexia
- (1999) Am J Hum Genet , vol.64 , pp. 146-156
- Fisher, S.E.¹ Marlow, A.J.² Lamb, J.³ Maestrini, E.⁴ Williams, D.F.⁵ Richardson, A.J.⁶ Weeks, D.E.⁷ Stein, J.F.⁸ Monaco, A.P.⁹

21
- 0344329866
- Predictors of cognitive test patterns in autism families
- (1999) J Child Psychol Psychiatry , vol.49 , pp. 1117-1128
- Folstein, S.E.¹ Santangelo, S.L.² Gilman, S.E.³ Piven, J.⁴ Landa, R.⁵ Lainhart, J.⁶ Hein, J.⁷ Wzorek, M.⁸

22
- 0027947017
- Digitized and differentially shaded human chromosome ideograms for genomic applications
- (1994) Cytogenet Cell Genet , vol.65 , pp. 206-219
- Francke, U.¹

23
- 0033364213
- Quantitative-trait locus for specific language and reading deficits on chromosome 6p
- (1999) Am J Hum Genet , vol.64 , pp. 157-164
- Gayán, J.¹ Smith, S.D.² Cherny, S.S.³ Cardon, L.R.⁴ Fulker, D.W.⁵ Brower, A.M.⁶ Olson, R.K.⁷ Pennington, B.F.⁸ DeFries, J.C.⁹

24
- 0000783911
- Risk for reading disability as a function of parental history in three family studies
- (1991) Reading Writing , vol.3 , pp. 205-217
- Gilger, J.W.¹ Pennington, B.F.² DeFries, J.C.³

25
- 0032231937
- The power to detect linkage in complex disease by means of simple LOD-score analyses
- (1998) Am J Hum Genet , vol.63 , pp. 870-879
- Greenberg, D.A.¹ Abreu, P.² Hodge, S.E.³

26
- 0031027824
- Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
- (1997) Am J Hum Genet , vol.60 , pp. 27-39
- Grigorenko, E.L.¹ Wood, F.B.² Meyer, M.S.³ Hart, L.A.⁴ Speed, W.C.⁵ Shuster, A.⁶ Pauls, D.L.⁷

27
- 0001762112
- Linkage studies suggest a possible locus for dyslexia near the Rh region on chromosome 1
- (1998) Behav Genet , vol.28 , pp. 470
- Grigorenko, E.L.¹ Wood, F.B.² Meyer, M.S.³ Pauls, J.E.D.⁴ Hart, L.A.⁵ Pauls, D.L.⁶

28
- 0033928210
- Chromosome 6p influence on different dyslexia-related cognitive processes: Further confirmation
- (2000) Am J Hum Genet , vol.66 , pp. 715-723
- Grigorenko, E.L.¹ Wood, F.B.² Meyer, M.S.³ Pauls, D.L.⁴

29
- 76549233000
- Specific dyslexia ("congenital word blindness"): A clinical and genetic study
- (1950) Acta Psychiatr Scand , vol.65 , pp. 1-287
- Hallgren, B.¹

30
- 0028029930
- Lods wrods, and mods: The interpretation of lod scores calculated under different models
- (1994) Genet Epidemiol , vol.11 , pp. 329-342
- Hodge, S.E.¹ Elston, R.C.²

31
- 0003455561
- Wilmington: DE: Jastak Associates
- (1984) The wide range achievement test, revised
- Jastak, S.¹ Wilkinson, G.S.²

32
- 0029046177
- Complete multipoint sib-pair analysis of qualitative and quantitative traits
- (1995) Am J Hum Genet , vol.57 , pp. 439-454
- Kruglyak, L.¹ Lander, E.S.²

33
- 0029886532
- Parametric and nonparametric linkage analysis: A unified multipoint approach
- (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
- Kruglyak, L.¹ Daly, M.J.² Reeve-Daly, M.P.³ Lander, E.S.⁴

34
- 0000803318
- Construction of multilocus genetic linkage maps in humans
- (1987) Proc Natl Acad Sci USA , vol.84 , pp. 2363-2367
- Lander, E.S.¹ Green, P.²

35
- 0028877463
- Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
- (1995) Nat Genet , vol.11 , pp. 241-247
- Lander, E.S.¹ Kruglyak, L.²

36
- 0021344005
- Easy calculations of LOD scores and genetic risks on small computers
- (1984) Am J Hum Genet , vol.36 , pp. 460-465
- Lathrop, G.M.¹ Lalouel, J.M.²

37
- 0342499587
- Strategies for multilocus analysis in humans
- (1984) Proc Natl Acad Sci USA , vol.81 , pp. 3443-3446
- Lathrop, G.M.¹ Lalouel, J.M.² Julier, C.³ Ott, J.⁴

38
- 0022646961
- Construction of human genetic linkage maps: Likelihood calculations for multilocus analysis
- (1986) Genet Epidemiol , vol.3 , pp. 39-52
- Lathrop, G.M.¹ Lalouel, J.M.² White, R.L.³

39
- 0024364215
- Educational interventions in learning disabilities
- (1989) J Am Acad Child Adolesc Psychiatry , vol.28 , pp. 326-331
- Lerner, J.W.¹

40
- 0031172430
- New evidence for neurotransmitter influences on brain development
- (1997) Trends Neurosci , vol.20 , pp. 269-274
- Levitt, P.¹ Harvey, J.A.² Friedman, E.³ Simansky, K.⁴ Murphy, E.H.⁵

41
- 0018900809
- Genetic models of reading disability
- (1980) Behav Genet , vol.10 , pp. 9-30
- Lewitter, F.I.¹ DeFries, J.C.² Elston, R.C.³

42
- 0028343233
- Automated construction of genetic linkage maps using an expert system (MultiMap): A human genome linkage map
- (1994) Nat Genet , vol.6 , pp. 384-390
- Matise, T.C.¹ Perlin, M.² Chakravarti, A.³

43
- 0034701254
- Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
- (2000) Hum Mol Genet , vol.9 , pp. 843-848
- Morris, D.W.¹ Robinson, L.² Turic, D.³ Duke, M.⁴ Webb, V.⁵ Milham, C.⁶ Hopkin, E.⁷ Pound, K.⁸ Fernando, S.⁹ Easton, M.¹⁰ Hamshere, M.¹¹ Williams, N.¹² McGuffin, P.¹³ Stevenson, J.¹⁴ Krawczak, M.¹⁵ Owen, M.J.¹⁶ O'Donovan, M.C.¹⁷ Williams, J.¹⁸

44
- 0004454620
- Linkage disequilibrium and positional candidate gene analyses of a susceptibility locus for reading disability of chromosome 15q
- (2000) Am J Med Genet (Neuropsychiatr Genet) , vol.96 , pp. 471
- Morris, D.W.¹ Robinson, L.² Turic, D.³ Duke, M.⁴ Webb, V.⁵ Southgate, L.⁶ Hamshere, M.⁷ Williams, N.⁸ McGuffin, P.⁹ Rowen, L.¹⁰ Stevenson, J.¹¹ Krawczak, M.¹² Owen, M.J.¹³ Williams, J.¹⁴ O'Donovan, M.C.¹⁵

45
- 0344496507
- Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
- (1999) Eur Child Adolesc Psychiatry , vol.8 , Issue.SUPPL. 3 , pp. 56-59
- Nothen, M.M.¹ Schulte-Korne, G.² Grimm, T.³ Cichon, S.⁴ Vogt, I.R.⁵ Muller-Myhsok, B.⁶ Propping, P.⁷ Remschmidt, H.⁸

46
- 0024689078
- Specific deficits in component reading and language skills: Genetic and environmental influences
- (1989) J Learning Disabil , vol.22 , pp. 339-348
- Olson, R.¹ Wise, V.² Conners, F.³ Rack, J.⁴ Fulker, D.⁵

47
- 0003408936
- Baltimore: Johns Hopkins University Press
- (1991) Analysis of human genetic linkage, 2nd ed.
- Ott, J.¹

48
- 0003408936
- Baltimore: Johns Hopkins University Press
- (1999) Analysis of human genetic linkage, rev.
- Ott, J.¹

49
- 0031038237
- Using genetics to dissect cognition
- (1997) Am J Hum Genet , vol.60 , pp. 13-16
- Pennington, B.F.¹

50
- 0025992157
- Evidence for major gene transmission of developmental dyslexia
- (1991) JAMA , vol.266 , pp. 1527-1534
- Pennington, B.F.¹ Gilger, J.W.² Pauls, D.³ Smith, S.A.⁴ Smith, S.D.⁵ DeFries, J.C.⁶

51
- 0000768465
- Evidence for the chromosome 2p15-p16 dyslexia susceptibility locus (DYX3) in a large Canadian data set
- (2000) Am J Med Genet (Neuropsychiatr Genet) , vol.96 , pp. 472
- Petryshen, T.L.¹ Kaplan, B.J.² Hughes, M.L.³ Field, L.L.⁴

52
- 0033912869
- Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative trait methods: Confirmation of qualitative analyses
- (2000) Am J Hum Genet , vol.66 , pp. 708-714
- Petryshen, T.L.¹ Kaplan, B.J.² Liu, M.F.³ Field, L.L.⁴

53
- 0032945941
- Genome-wide scan for autism susceptibility genes
- (1999) Hum Mol Genet , vol.8 , pp. 805-812
- Philippe, A.¹ Martinez, M.² Guilloud-Bataille, M.³ Gillberg, C.⁴ Rastam, M.⁵ Sponheim, E.⁶ Coleman, M.⁷ Zappella, M.⁸ Aschauer, H.⁹ Van Maldergem, L.¹⁰ Penet, C.¹¹ Feingold, J.¹² Brice, A.¹³ Leboyer, M.¹⁴

54
- 0033928381
- Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components
- (2000) Am J Hum Genet , vol.66 , pp. 1153-1157
- Pratt, S.C.¹ Daly, M.J.² Kruglyak, L.³

55
- 0027213075
- Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
- (1993) Lancet , vol.342 , pp. 178
- Rabin, M.¹ Wen, X.L.² Hepburn, M.³ Lubs, H.A.⁴ Feldman, E.⁵ Duara, R.⁶

56
- 0002229514
- The auditory analysis test: An initial report
- (1971) J Learn Dis , vol.4 , pp. 382-392
- Rosner, J.¹ Simon, D.P.²

57
- 0003463528
- Cary NC: SAS Institute
- (1990) SAS release 6.4

58
- 0004417194
- Genetic analysis of phonologic core deficit (PCDD)
- (1998) Am J Hum Genet , vol.63
- Sawyer, D.L.¹ Krishnamani, R.S.² Hannig, V.L.³ Farcia, M.⁴ Kim, J.K.⁵ Haines, J.L.⁶ Phillips III, J.A.⁷

59
- 0028260703
- Avoiding recomputation in genetic linkage analysis
- (1994) Hum Hered , vol.44 , pp. 225-237
- Schaffer, A.A.¹ Gupta, S.K.² Shriram, K.³ Cottingham R.W., Jr.⁴

60
- 0032231443
- Evidence for linkage of spelling disability to chromosome 15
- (1998) Am J Hum Genet , vol.63 , pp. 279-282
- Schulte-Körne, G.¹ Grimm, T.² Nöthen, M.M.³ Müller-Myhsok, B.⁴ Cichon, S.⁵ Vogt, I.R.⁶ Propping, P.⁷ Remschmidt, H.⁸

61
- 0020622130
- Specific reading disability: Identification of an inherited form through linkage analysis
- (1983) Science , vol.219 , pp. 1345-1347
- Smith, S.D.¹ Kimberling, W.J.² Pennington, B.F.³ Lubs, H.A.⁴

62
- 84878751729
- Genetic linkage analysis of 20 families with specific reading disability
- (1989) Am J Hum Genet , vol.45
- Smith, S.D.¹ Kimberling, W.J.² Shugart, Y.Y.³ Ing, P.S.⁴ Pennington, B.F.⁵

63
- 0000157151
- Screening for multiple genes influencing dyslexia
- (1991) Read Writ Interdisc , vol.3 , pp. 285-298
- Smith, S.D.¹ Kimberling, W.J.² Pennington, B.F.³

64
- 0032055976
- Molecular approaches to the genetic analysis of specific reading disability
- (1998) Hum Biol , vol.70 , pp. 239-256
- Smith, S.D.¹ Kelley, P.M.² Brower, A.M.³

65
- 0029945706
- Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
- (1996) Am J Hum Genet , vol.58 , pp. 1323-1337
- Sobel, E.¹ Lange, K.²

66
- 0007288062
- Oxford: Oxford University Press
- (1998) Learning disabled children growing up: a follow-up into adulthood
- Spreen, O.¹

67
- 0023299180
- A twin study of genetic influences on reading and spelling ability and disability
- (1987) J Child Psychol Psychiatry , vol.28 , pp. 229-247
- Stevenson, J.¹ Graham, P.² Fredman, G.³ McLoughlin, V.⁴

68
- 0030851777
- True and false positive peaks in genomewide scans: Applications of length-biased sampling to linkage mapping
- (1997) Am J Hum Genet , vol.61 , pp. 430-438
- Terwilliger, J.D.¹ Shannon, W.D.² Lathrop, G.M.³ Nolan, J.P.⁴ Goldin, L.R.⁵ Chase, G.A.⁶ Weeks, D.E.⁷

69
- 0029064537
- Mapping disease genes: Family-based association studies
- (1995) Am J Hum Genet , vol.57 , pp. 487-498
- Thomson, G.¹

70
- 0004454341
- Linkage disequilibrium mapping provides evidence for a susceptibility gene for reading disability on chromosome 6p
- (2000) Am J Med Genet (Neuropsychiatr Genet) , vol.96 , pp. 556
- Turic, D.¹ Morris, D.W.² Robinson, L.³ Duke, M.⁴ Grierson, A.⁵ Raha-Chowdhury, R.⁶ Southgate, L.⁷ Webb, V.⁸ Hamshere, M.⁹ Williams, B.¹⁰ McGuffin, P.¹¹ Stevenson, J.¹² Krawczak, M.¹³ Owen, M.J.¹⁴ O'Donovan, M.C.¹⁵ Williams, J.¹⁶

71
- 0002552955
- Phonologic mediation in skilled and dyslexic reading
- Chase CH, Rosen GD, Sherman GF, editors. Developmental dyslexia. Baltimore: York Press
- (1996) , pp. 185-223
- Van Orden, G.C.¹ Goldinger, S.D.²

72
- 0003664194
- New York: Psychological
- (1974) Manual for the Wechsler intelligence scale for children-revised
- Wechsler, D.¹

73
- 0003441705
- New York: Psychological
- (1981) Wechsler adult intelligence scale-revised
- Wechsler, D.¹

74
- 0031469587
- Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: Summary of GAW10 contributions
- (1997) Genet Epidemiol , vol.14 , pp. 719-735
- Wijsman, E.M.¹ Amos, C.I.²

75
- 24744443962
- What time may tell: Towards a new conceptualization of developmental dyslexia
- (1999) Ann Dyslexia , vol.49 , pp. 3-28
- Wolf, M.¹

76
- 0003422263
- Circle Pines, Minnesota: American Guidance Service
- (1987) Woodcock reading mastery tests
- Woodcock, R.W.¹

77
- 0003459924
- Allen, TX: DLM Teaching Resources
- (1989) Woodcock-Johnson psychoeducational battery-revised
- Woodcock, R.W.¹ Johnson, M.B.²

78
- 0001722772
- Lord score analysis
- Haines JL, Pericak-Vance MA, editors. Approaches to gene mapping in complex human diseases, New York: Wiley-Liss
- (1998) , pp. 253-272
- Xu, J.¹ Meyers, D.A.² Pericak-Vance, M.A.³

79
- 0015312276
- Genetical investigations in dyslexia
- (1972) J Med Genet , vol.9 , pp. 48-52
- Zahalkova, M.¹ Vrzal, V.² Kloboukova, E.³

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