Literature DB >> 16188486

Genetic influences on language impairment and phonological short-term memory.

Dianne F Newbury1, Dorothy V M Bishop, Anthony P Monaco.   

Abstract

It has been known for some years that specific language impairment (SLI), an unexpected failure to acquire age-appropriate language skills, is highly heritable. However, molecular genetic studies have been hampered by the heterogeneity of the disorder and the predominant lack of clear genotype-phenotype relationships. We review recent studies suggesting that a better understanding of the genetics of SLI might emerge if we move away from clinical criteria for diagnosis to look instead at a theoretically based quantitative and cognitive measure of the phenotype: a test of phonological short-term memory (STM). Deficient phonological STM has been linked to specific genetic loci, and might play a role in determining some types of reading impairment as well as SLI. Identifying those cognitive deficits that work best as indices of heritable phenotypes will help us to uncover the aetiology of developmental disorders.

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Year:  2005        PMID: 16188486     DOI: 10.1016/j.tics.2005.09.002

Source DB:  PubMed          Journal:  Trends Cogn Sci        ISSN: 1364-6613            Impact factor:   20.229


  28 in total

1.  A specific cognitive deficit within semantic cognition across a multi-generational family.

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Journal:  Proc Biol Sci       Date:  2012-06-20       Impact factor: 5.349

2.  12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

Authors:  Julien Thevenon; Patrick Callier; Joris Andrieux; Bruno Delobel; Albert David; Sylvie Sukno; Delphine Minot; Laure Mosca Anne; Nathalie Marle; Damien Sanlaville; Marlène Bonnet; Alice Masurel-Paulet; Fabienne Levy; Lorraine Gaunt; Sandra Farrell; Cédric Le Caignec; Annick Toutain; Virginie Carmignac; Francine Mugneret; Jill Clayton-Smith; Christel Thauvin-Robinet; Laurence Faivre
Journal:  Eur J Hum Genet       Date:  2012-06-20       Impact factor: 4.246

3.  Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

Authors:  Steven W Threlkeld; Melissa M McClure; Jilin Bai; Yu Wang; Joe J LoTurco; Glenn D Rosen; R Holly Fitch
Journal:  Brain Res Bull       Date:  2006-12-05       Impact factor: 4.077

4.  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

Review 5.  The interface between genetics and psychology: lessons from developmental dyslexia.

Authors:  D V M Bishop
Journal:  Proc Biol Sci       Date:  2015-05-07       Impact factor: 5.349

6.  Etiological Distinction of Working Memory Components in Relation to Mathematics.

Authors:  Sarah L Lukowski; Brooke Soden; Sara A Hart; Lee A Thompson; Yulia Kovas; Stephen A Petrill
Journal:  Intelligence       Date:  2014-11

7.  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

8.  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

9.  [Norms for the Mottier-Test from 4- to 6-year old children].

Authors:  C Kiese-Himmel; T Risse
Journal:  HNO       Date:  2009-09       Impact factor: 1.284

10.  A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.

Authors:  Julian E Asher; Janine A Lamb; Denise Brocklebank; Jean-Baptiste Cazier; Elena Maestrini; Laura Addis; Mallika Sen; Simon Baron-Cohen; Anthony P Monaco
Journal:  Am J Hum Genet       Date:  2009-02-05       Impact factor: 11.025

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