Literature DB >> 11708534

Familial aggregation in specific language impairment.

P Tallal1, L S Hirsch, T Realpe-Bonilla, S Miller, L M Brzustowicz, C Bartlett, J F Flax.   

Abstract

A case-control family study design, in which the current language-related abilities of all biological, primary relatives (mother, father, siblings) of probands with specific language impairment (SLI) and matched controls were assessed, was used to investigate familial aggregation for language disorders. Current test data from each family member showed the rate of language impairment for mothers, fathers, sisters, and brothers of the SLI probands to be significantly higher than for members of control families. Impairment rates for fathers and mothers were approximately equal, whereas rates for brothers were significantly higher than for sisters. In SLI proband families, Language Impairment (LI) occurred in 13.0% of offspring (excluding proband) with neither parent affected, 40% of offspring with one parent affected, and 71.4% of offspring in families in which both parents were language impaired. Rates of impairment as determined in current testing were compared directly to impairment rates estimated from family-history questionnaires collected from the same families. Group data showed impairment rates estimated from the family-history questionnaires to be similar to the rates based on actual testing. Furthermore, both appeared in line with rates based primarily on questionnaire data as reported previously in the literature. However, case-by-case analyses showed poor intrasubject agreement on classification as language impaired on the basis of current testing as compared to history information.

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Year:  2001        PMID: 11708534     DOI: 10.1044/1092-4388(2001/091)

Source DB:  PubMed          Journal:  J Speech Lang Hear Res        ISSN: 1092-4388            Impact factor:   2.297


  12 in total

1.  A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).

Authors:  Erin M Andres; Huma Hafeez; Adnan Yousaf; Sheikh Riazuddin; Mabel L Rice; Muhammad Asim Raza Basra; Muhammad Hashim Raza
Journal:  Eur J Hum Genet       Date:  2019-04-11       Impact factor: 4.246

2.  The infant as a prelinguistic model for language learning impairments: predicting from event-related potentials to behavior.

Authors:  April A Benasich; Naseem Choudhury; Jennifer T Friedman; Teresa Realpe-Bonilla; Cecylia Chojnowska; Zhenkun Gou
Journal:  Neuropsychologia       Date:  2005-07-28       Impact factor: 3.139

3.  A major susceptibility locus for specific language impairment is located on 13q21.

Authors:  Christopher W Bartlett; Judy F Flax; Mark W Logue; Veronica J Vieland; Anne S Bassett; Paula Tallal; Linda M Brzustowicz
Journal:  Am J Hum Genet       Date:  2002-06-04       Impact factor: 11.025

4.  Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.

Authors:  Tabatha R Simmons; Judy F Flax; Marco A Azaro; Jared E Hayter; Laura M Justice; Stephen A Petrill; Anne S Bassett; Paula Tallal; Linda M Brzustowicz; Christopher W Bartlett
Journal:  Hum Hered       Date:  2010-10-14       Impact factor: 0.444

5.  Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.

Authors:  Mabel L Rice; Shelley D Smith; Javier Gayán
Journal:  J Neurodev Disord       Date:  2009-08-26       Impact factor: 4.025

6.  Infant information processing and family history of specific language impairment: converging evidence for RAP deficits from two paradigms.

Authors:  Naseem Choudhury; Paavo H T Leppanen; Hilary J Leevers; April A Benasich
Journal:  Dev Sci       Date:  2007-03

7.  A family aggregation study: the influence of family history and other risk factors on language development.

Authors:  Naseem Choudhury; April Ann Benasich
Journal:  J Speech Lang Hear Res       Date:  2003-04       Impact factor: 2.297

8.  Heritable risk factors associated with language impairments.

Authors:  J G Barry; I Yasin; D V M Bishop
Journal:  Genes Brain Behav       Date:  2007-02       Impact factor: 3.449

9.  Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Authors:  Pía Villanueva; Ron Nudel; Alexander Hoischen; María Angélica Fernández; Nuala H Simpson; Christian Gilissen; Rose H Reader; Lillian Jara; María Magdalena Echeverry; Maria Magdalena Echeverry; Clyde Francks; Gillian Baird; Gina Conti-Ramsden; Anne O'Hare; Patrick F Bolton; Elizabeth R Hennessy; Hernán Palomino; Luis Carvajal-Carmona; Joris A Veltman; Jean-Baptiste Cazier; Zulema De Barbieri; Simon E Fisher; Dianne F Newbury
Journal:  PLoS Genet       Date:  2015-03-17       Impact factor: 5.917

10.  The genetics of reading disabilities: from phenotypes to candidate genes.

Authors:  Wendy H Raskind; Beate Peter; Todd Richards; Mark M Eckert; Virginia W Berninger
Journal:  Front Psychol       Date:  2013-01-07
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