Literature DB >> 27198479

Evaluation of results from genome-wide studies of language and reading in a novel independent dataset.

A Carrion-Castillo1, E van Bergen2,3, A Vino1, T van Zuijen4, P F de Jong4, C Francks1,5, S E Fisher1,5.   

Abstract

Recent genome-wide association scans (GWAS) for reading and language abilities have pin-pointed promising new candidate loci. However, the potential contributions of these loci remain to be validated. In this study, we tested 17 of the most significantly associated single nucleotide polymorphisms (SNPs) from these GWAS studies (P < 10(-6) in the original studies) in a new independent population dataset from the Netherlands: known as Familial Influences on Literacy Abilities. This dataset comprised 483 children from 307 nuclear families and 505 adults (including parents of participating children), and provided adequate statistical power to detect the effects that were previously reported. The following measures of reading and language performance were collected: word reading fluency, nonword reading fluency, phonological awareness and rapid automatized naming. Two SNPs (rs12636438 and rs7187223) were associated with performance in multivariate and univariate testing, but these did not remain significant after correction for multiple testing. Another SNP (rs482700) was only nominally associated in the multivariate test. For the rest of the SNPs, we did not find supportive evidence of association. The findings may reflect differences between our study and the previous investigations with respect to the language of testing, the exact tests used and the recruitment criteria. Alternatively, most of the prior reported associations may have been false positives. A larger scale GWAS meta-analysis than those previously performed will likely be required to obtain robust insights into the genomic architecture underlying reading and language.
© 2016 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society.

Entities:  

Keywords:  Association study; candidate SNPs; language; reading

Mesh:

Year:  2016        PMID: 27198479     DOI: 10.1111/gbb.12299

Source DB:  PubMed          Journal:  Genes Brain Behav        ISSN: 1601-183X            Impact factor:   3.449


  7 in total

1.  Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.

Authors:  Nicole Landi; Meaghan Perdue
Journal:  Lang Linguist Compass       Date:  2019-09-05

2.  Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.

Authors:  Alessandro Gialluisi; Till F M Andlauer; Nazanin Mirza-Schreiber; Kristina Moll; Jessica Becker; Per Hoffmann; Kerstin U Ludwig; Darina Czamara; Beate St Pourcain; William Brandler; Ferenc Honbolygó; Dénes Tóth; Valéria Csépe; Guillaume Huguet; Andrew P Morris; Jacqueline Hulslander; Erik G Willcutt; John C DeFries; Richard K Olson; Shelley D Smith; Bruce F Pennington; Anniek Vaessen; Urs Maurer; Heikki Lyytinen; Myriam Peyrard-Janvid; Paavo H T Leppänen; Daniel Brandeis; Milene Bonte; John F Stein; Joel B Talcott; Fabien Fauchereau; Arndt Wilcke; Clyde Francks; Thomas Bourgeron; Anthony P Monaco; Franck Ramus; Karin Landerl; Juha Kere; Thomas S Scerri; Silvia Paracchini; Simon E Fisher; Johannes Schumacher; Markus M Nöthen; Bertram Müller-Myhsok; Gerd Schulte-Körne
Journal:  Transl Psychiatry       Date:  2019-02-11       Impact factor: 6.222

3.  Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.

Authors:  Dongnhu Thuy Truong; Andrew Kenneth Adams; Steven Paniagua; Jan C Frijters; Richard Boada; Dina E Hill; Maureen W Lovett; E Mark Mahone; Erik G Willcutt; Maryanne Wolf; John C Defries; Alessandro Gialluisi; Clyde Francks; Simon E Fisher; Richard K Olson; Bruce F Pennington; Shelley D Smith; Joan Bosson-Heenan; Jeffrey R Gruen
Journal:  J Med Genet       Date:  2019-04-17       Impact factor: 6.318

Review 4.  The new genetics of intelligence.

Authors:  Robert Plomin; Sophie von Stumm
Journal:  Nat Rev Genet       Date:  2018-01-08       Impact factor: 53.242

Review 5.  The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder.

Authors:  Marianthi Georgitsi; Iasonas Dermitzakis; Evgenia Soumelidou; Eleni Bonti
Journal:  Brain Sci       Date:  2021-05-14

6.  Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.

Authors:  Amaia Carrion-Castillo; Sara B Estruch; Ben Maassen; Barbara Franke; Clyde Francks; Simon E Fisher
Journal:  Hum Genet       Date:  2021-06-02       Impact factor: 4.132

7.  Association between genes regulating neural pathways for quantitative traits of speech and language disorders.

Authors:  Penelope Benchek; Robert P Igo; Heather Voss-Hoynes; Barbara Lewis; Catherine M Stein; Sudha K Iyengar; Yvonne Wren; Gabrielle Miller; Barbara Truitt; Wen Zhang; Michael Osterman; Lisa Freebairn; Jessica Tag; H Gerry Taylor; E Ricky Chan; Panos Roussos
Journal:  NPJ Genom Med       Date:  2021-07-27       Impact factor: 8.617

  7 in total

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