Literature DB >> 11235984

Familial aggregation of dyslexia phenotypes.

W H Raskind1, L Hsu, V W Berninger, J B Thomson, E M Wijsman.   

Abstract

There is evidence for genetic contributions to reading disability, but the phenotypic heterogeneity associated with the clinical diagnosis may make identification of the underlying genetic basis difficult. In order to elucidate distinct phenotypic features that may be contributing to the genotypic heterogeneity, we assessed the familial aggregation patterns of Verbal IQ and 24 phenotypic measures associated with dyslexia in 102 nuclear families ascertained through probands in grades 1 through 6 who met the criteria for this disorder. Correlations between relatives were computed for all diagnostic phenotypes, using a generalized estimating equation (GEE) approach. GEE is a recently developed semiparametric method for handling correlated data. The method is robust to model misspecification and flexible in adjusting for the subjects' characteristics and pedigree sizes as well as for the ascertainment process, while estimating the correlations between related subjects. The Nonword Memory (NWM) subtest of a prepublication version of the Comprehensive Test of Phonological Processing (CTOPP) and Phonemic Decoding Efficiency (PDE) subtest of a prepublication version of the Test of Word Reading Efficiency (TOWRE) showed correlation patterns in relatives that are strongly supportive of a genetic basis. The Wechsler Scale Digit Span, the Word Attack subtest of the Woodcock Reading Mastery Test--Revised, and the Spelling subtest of the Wide Range Achievement Test--Third Edition had slightly weaker evidence of a genetic basis. Five additional phenotypes (the Spelling subtest of the Wechsler Individual Achievement Test, the Accuracy, Rate, and Comprehension subtests of the Gray Oral Reading Test--Third Edition, and Rapid Automatized Naming of Letters and Numbers) gave suggestive evidence of such a pattern. The results cross-validate in that evidence for a pattern consistent with a genetic basis was obtained for two measures of phonological short-term memory (CTOPP Nonword Memory and WISCIII or WAIS-R Digit Span), for two measures of phonological decoding (WRMT-R Word Attack and TOWRE Phonemic Decoding Efficiency), and for two measures of spelling from dictation (WRAT-3 Spelling and, to a lesser extent, WIAT Spelling). These measures are thus good candidates for more sophisticated segregation analyses that can formulate models for incorporation into linkage analyses.

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Year:  2000        PMID: 11235984     DOI: 10.1023/a:1002700605187

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  18 in total

1.  Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes.

Authors:  Barbara A Lewis; Allison A Avrich; Lisa A Freebairn; Amy J Hansen; Lara E Sucheston; Iris Kuo; H Gerry Taylor; Sudha K Iyengar; Catherine M Stein
Journal:  J Speech Lang Hear Res       Date:  2011-09-19       Impact factor: 2.297

2.  Tract-based spatial statistics of diffusion tensor imaging in adults with dyslexia.

Authors:  T Richards; J Stevenson; J Crouch; L C Johnson; K Maravilla; P Stock; R Abbott; V Berninger
Journal:  AJNR Am J Neuroradiol       Date:  2008-05-08       Impact factor: 3.825

3.  Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.

Authors:  Beate Peter; Wendy H Raskind; Mark Matsushita; Mark Lisowski; Tiffany Vu; Virginia W Berninger; Ellen M Wijsman; Zoran Brkanac
Journal:  J Neurodev Disord       Date:  2010-11-09       Impact factor: 4.025

4.  Gene × gene interaction in shared etiology of autism and specific language impairment.

Authors:  Christopher W Bartlett; Judy F Flax; Zena Fermano; Abby Hare; Liping Hou; Stephen A Petrill; Steven Buyske; Linda M Brzustowicz
Journal:  Biol Psychiatry       Date:  2012-06-15       Impact factor: 13.382

5.  Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.

Authors:  Robert P Igo; Nicola H Chapman; Virginia W Berninger; Mark Matsushita; Zoran Brkanac; Joseph H Rothstein; Ted Holzman; Kathleen Nielsen; Wendy H Raskind; Ellen M Wijsman
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2006-01-05       Impact factor: 3.568

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

Authors:  E M Wijsman; D Peterson; A L Leutenegger; J B Thomson; K A Goddard; L Hsu; V W Berninger; W H Raskind
Journal:  Am J Hum Genet       Date:  2000-07-31       Impact factor: 11.025

7.  Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.

Authors:  Kevin Rubenstein; Mark Matsushita; Virginia W Berninger; Wendy H Raskind; Ellen M Wijsman
Journal:  Behav Genet       Date:  2010-09-18       Impact factor: 2.805

8.  Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.

Authors:  Kevin B Rubenstein; Wendy H Raskind; Virginia W Berninger; Mark M Matsushita; Ellen M Wijsman
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2014-05-08       Impact factor: 3.568

9.  PDD symptoms in ADHD, an independent familial trait?

Authors:  J S Nijmeijer; P J Hoekstra; R B Minderaa; J K Buitelaar; M E Altink; C J M Buschgens; E A Fliers; N N J Rommelse; J A Sergeant; C A Hartman
Journal:  J Abnorm Child Psychol       Date:  2009-04

10.  Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.

Authors:  Zoran Brkanac; Nicola H Chapman; Robert P Igo; Mark M Matsushita; Kathleen Nielsen; Virginia W Berninger; Ellen M Wijsman; Wendy H Raskind
Journal:  Behav Genet       Date:  2008-07-08       Impact factor: 2.805

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