Associated Papers
rs67047829 genotypes of ERV3-1/ZNF117 are associated with lower body mass index in the Polish population.
Clark JSC et al.
Scientific Reports, 2023
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.
Emdin CA et al.
Nature Communications, 2018
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
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.
Pohler E et al.
Nature Genetics, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.
Thompson ER et al.
Plos Genetics, 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
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
Newbury DF et al.
Behavior Genetics, 2011
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Dahdouh F et al.
Psychiatric Genetics, 2009
Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.
Wigg KG et al.
Genes, Brain, and Behavior, 2008
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
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
Brkanac Z et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2007
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
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Taipale M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2003