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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 20 of 20 1 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, A; Andlauer, TFM; Mirza-Schreiber, N. - 2019 BASE Show details 2 The neuronal migration hypothesis of dyslexia: a critical evaluation 30 years on Guidi, LG; Velayos-Baeza, A; Martinez-Garay, I. - 2018 BASE Show details 3 The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on Guidi, LG; Velayos-Baeza, A; Martinez-Garay, I. - 2018 BASE Show details 4 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, K; Frinton, E; Nudel, R... In: Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes (2016) BASE Show details 5 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Newbury, D; Pettigrew, KA; Frinton, E... In: Symplectic Elements at Oxford ; Added by author ; ORA review team (2016) BASE Show details 6 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. Pettigrew, KA; Frinton, E; Nudel, R. - 2016 BASE Show details 7 Genome-wide screening for DNA variants associated with reading and language traits Gialluisi, A; Newbury, D F; Wilcutt, E G. - : Blackwell Publishing Ltd, 2014 BASE Show details 8 Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Simpson, NH; Addis, L; Brandler, WM... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014) BASE Show details 9 Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia Simpson, NH; Addis, L; Brandler, WM... In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014) BASE Show details 10 Genome-wide screening for DNA variants associated with reading and language traits. Gialluisi, A; Newbury, DF; Wilcutt, EG... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014) BASE Show details 11 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, J; Czamara, D; Scerri, TS... In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014) BASE Show details 12 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Becker, J; Czamara, D; Scerri, TS... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014) BASE Show details 13 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Nudel, R; Simpson, NH; Baird, G... In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014) BASE Show details 14 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Nudel, R; Simpson, NH; Baird, G... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014) BASE Show details 15 Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment Nudel, R.; Simpson, N. H.; Baird, G.. - : Blackwell Publishing Ltd, 2014 BASE Show details 16 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Nudel, R; Simpson, N H; Baird, G. - 2014 BASE Show details 17 DCDC2, KIAA0319 and CMIP are associated with reading-related traits Scerri, TS; Morris, AP; Buckingham, L-L... In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2011) BASE Show details 18 DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Scerri, TS; Morris, AP; Buckingham, LL... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011) BASE Show details 19 Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Newbury, DF; Paracchini, S; Scerri, TS; Winchester, L; Addis, L; Richardson, AJ; Walter, J; Stein, JF; Talcott, JB; Monaco, AP In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011) Abstract: Dyslexia (or reading disability) and specific language impairment (or SLI) are common childhood disorders that show considerable co-morbidity and diagnostic overlaps and have been suggested to share some genetic aetiology. Recently, genetic risk variants have been identified for SLI and dyslexia enabling the direct evaluation of possible shared genetic influences between these disorders. In this study we investigate the role of variants in these genes (namely MRPL19/C20RF3, ROBO1, DCDC2, KIAA0319, DYX1C1, CNTNAP2, ATP2C2 and CMIP) in the aetiology of SLI and dyslexia. We perform case-control and quantitative association analyses using measures of oral and written language skills in samples of SLI and dyslexic families and cases. We replicate association between KIAA0319 and DCDC2 and dyslexia and provide evidence to support a role for KIAA0319 in oral language ability. In addition, we find association between reading-related measures and variants in CNTNAP2 and CMIP in the SLI families. Keyword: 5' Untranslated Regions; Alleles; Carrier Proteins; Case-Control Studies; Child; Cohort Studies; Dyslexia; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Language Development Disorders; Male; Membrane Proteins; Microtubule-Associated Proteins; Nerve Tissue Proteins; Polymorphism; Risk Assessment; Single Nucleotide URL: https://doi.org/10.1007/s10519-010-9424-3 BASE Hide details 20 CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Clark, A; Bishop, DV; Monaco, AP... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009) BASE Show details

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