Literature DB >> 15520411

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.

T S Scerri, S E Fisher, C Francks, I L MacPhie, S Paracchini, A J Richardson, J F Stein, A P Monaco.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2004        PMID： 15520411      PMCID： PMC1735619          DOI： 10.1136/jmg.2004.018341

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  39 in total

1.  Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

Authors:  C E Szalkowski; J R Hinman; S W Threlkeld; Y Wang; A LePack; G D Rosen; J J Chrobak; J J LoTurco; R H Fitch
Journal:  Genes Brain Behav       Date:  2010-11-25       Impact factor: 3.449

2.  Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.

Authors:  Caitlin E Szalkowski; Christopher G Fiondella; Albert M Galaburda; Glenn D Rosen; Joseph J Loturco; R Holly Fitch
Journal:  Int J Dev Neurosci       Date:  2012-02-03       Impact factor: 2.457

3.  Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Authors:  Jessica Becker; Darina Czamara; Tom S Scerri; Franck Ramus; Valéria Csépe; Joel B Talcott; John Stein; Andrew Morris; Kerstin U Ludwig; Per Hoffmann; Ferenc Honbolygó; Dénes Tóth; Fabien Fauchereau; Caroline Bogliotti; Stéphanie Iannuzzi; Yves Chaix; Sylviane Valdois; Catherine Billard; Florence George; Isabelle Soares-Boucaud; Christophe-Loïc Gérard; Sanne van der Mark; Enrico Schulz; Anniek Vaessen; Urs Maurer; Kaisa Lohvansuu; Heikki Lyytinen; Marco Zucchelli; Daniel Brandeis; Leo Blomert; Paavo H T Leppänen; Jennifer Bruder; Anthony P Monaco; Bertram Müller-Myhsok; Juha Kere; Karin Landerl; Markus M Nöthen; Gerd Schulte-Körne; Silvia Paracchini; Myriam Peyrard-Janvid; Johannes Schumacher
Journal:  Eur J Hum Genet       Date:  2013-09-11       Impact factor: 4.246

4.  TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

Authors:  Haiying Meng; Karl Hager; Matthew Held; Grier P Page; Richard K Olson; Bruce F Pennington; John C DeFries; Shelley D Smith; Jeffrey R Gruen
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

5.  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

Review 6.  From human genetics and genomics to pharmacogenetics and pharmacogenomics: past lessons, future directions.

Authors:  Daniel W Nebert; Ge Zhang; Elliot S Vesell
Journal:  Drug Metab Rev       Date:  2008       Impact factor: 4.518

7.  The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.

Authors:  Isabel Tapia-Páez; Kristiina Tammimies; Satu Massinen; Ananda L Roy; Juha Kere
Journal:  FASEB J       Date:  2008-04-29       Impact factor: 5.191

8.  The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.

Authors:  Kristiina Tammimies; Isabel Tapia-Páez; Joëlle Rüegg; Gustaf Rosin; Juha Kere; Jan-Åke Gustafsson; Ivan Nalvarte
Journal:  Mol Endocrinol       Date:  2012-03-01

9.  Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.

Authors:  K G Wigg; Y Feng; J Crosbie; R Tannock; J L Kennedy; A Ickowicz; M Malone; R Schachar; C L Barr
Journal:  Genes Brain Behav       Date:  2008-11       Impact factor: 3.449

10.  Allelic variants of DYX1C1 are not associated with dyslexia in India.

Authors:  Pushpa Saviour; Satish Kumar; U Kiran; Rajasekhara Reddy Ravuri; V R Rao; Nallur Basappa Ramachandra
Journal:  Indian J Hum Genet       Date:  2008-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.