Associated Papers
Gene dosage of independent dynein arm motor preassembly factors influences cilia assembly in Chlamydomonas reinhardtii.
Penny GM et al.
Plos Genetics, 2024
Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms.
Mascheretti S et al.
Translational Psychiatry, 2017
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK et al.
Psychiatric Genetics, 2014
Molecular genetics of dyslexia: an overview.
Carrion-Castillo A et al.
Dyslexia (chichester, England), 2013
Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.
Jamadar S et al.
Brain Imaging and Behavior, 2013
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.
Tran C et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.
Zou L et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2012
The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.
Tammimies K et al.
Molecular Endocrinology (baltimore, Md.), 2012
Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population.
Zhang Y et al.
Plos One, 2012
Approach to epigenetic analysis in language disorders.
Smith SD
Journal of Neurodevelopmental Disorders, 2011
Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.
Jamadar S et al.
Schizophrenia Research, 2011
Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.
Lim CK et al.
Behavioral and Brain Functions : Bbf, 2011
Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
Paracchini S et al.
Genes, Brain, and Behavior, 2011
Genetics of developmental dyslexia.
Scerri TS et al.
European Child & Adolescent Psychiatry, 2010
Allelic variants of DYX1C1 are not associated with dyslexia in India.
Saviour P et al.
Indian Journal of Human Genetics, 2008
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
Tapia-Páez I et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2008
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.
Marino C et al.
European Journal of Human Genetics : Ejhg, 2005
Family-based association study of DYX1C1 variants in autism.
Ylisaukko-Oja T et al.
European Journal of Human Genetics : Ejhg, 2005
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.
Bellini G et al.
Journal of Molecular Neuroscience : Mn, 2005
Support for EKN1 as the susceptibility locus for dyslexia on 15q21.
Wigg KG et al.
Molecular Psychiatry, 2004