Literature DB >> 14729831

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

C Marino, R Giorda, L Vanzin, M Nobile, M L Lorusso, C Baschirotto, L Riva, M Molteni, M Battaglia.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2004        PMID： 14729831      PMCID： PMC1757239          DOI： 10.1136/jmg.2003.010603

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


× No keyword cloud information.
  12 in total

1.  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

2.  DCDC2 genetic variants and susceptibility to developmental dyslexia.

Authors:  Cecilia Marino; Haiying Meng; Sara Mascheretti; Marianna Rusconi; Natalie Cope; Roberto Giorda; Massimo Molteni; Jeffrey R Gruen
Journal:  Psychiatr Genet       Date:  2012-02       Impact factor: 2.458

3.  KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.

Authors:  Sara Mascheretti; Valentina Riva; Roberto Giorda; Silvana Beri; Lara Francesca Emilia Lanzoni; Maria Rosaria Cellino; Cecilia Marino
Journal:  J Hum Genet       Date:  2014-01-16       Impact factor: 3.172

4.  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

5.  No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.

Authors:  Giulia Bellini; Carmela Bravaccio; Filippo Calamoneri; Maria Donatella Cocuzza; Pasquale Fiorillo; Antonella Gagliano; Domenico Mazzone; Emanuele Miraglia del Giudice; Geoffredo Scuccimarra; Roberto Militerni; Antonio Pascotto
Journal:  J Mol Neurosci       Date:  2005       Impact factor: 3.444

Review 6.  Genetics of dyslexia: the evolving landscape.

Authors:  Johannes Schumacher; Per Hoffmann; Christine Schmäl; Gerd Schulte-Körne; Markus M Nöthen
Journal:  J Med Genet       Date:  2007-02-16       Impact factor: 6.318

7.  An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.

Authors:  S Mascheretti; A Bureau; V Trezzi; R Giorda; C Marino
Journal:  Hum Genet       Date:  2015-04-28       Impact factor: 4.132

8.  Linkage analyses of chromosomal region 18p11-q12 in dyslexia.

Authors:  J Schumacher; I R König; E Plume; P Propping; A Warnke; M Manthey; M Duell; A Kleensang; D Repsilber; M Preis; H Remschmidt; A Ziegler; M M Nöthen; G Schulte-Körne
Journal:  J Neural Transm (Vienna)       Date:  2005-08-03       Impact factor: 3.575

9.  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

Review 10.  Genetics of developmental dyslexia.

Authors:  Thomas S Scerri; Gerd Schulte-Körne
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-11-29       Impact factor: 4.785
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.