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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 Page: 1 2 Hits 1 – 20 of 25 1 Family-based genetic investigation of SLI (Andres et al., 2020) ... Andres, Erin M.; Earnest, Kathleen Kelsey; Smith, Shelley D.. - : ASHA journals, 2020 BASE Show details 2 Family-based genetic investigation of SLI (Andres et al., 2020) ... Andres, Erin M.; Earnest, Kathleen Kelsey; Smith, Shelley D.. - : ASHA journals, 2020 BASE Show details 3 Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment Andres, Erin M.; Earnest, Kathleen Kelsey; Smith, Shelley D.... In: J Speech Lang Hear Res (2020) BASE Show details 4 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia ... Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin. - : ETH Zurich, 2019 BASE Show details 5 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin... In: Translational Psychiatry, 9 (1) (2019) BASE Show details 6 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-schreiber, Nazanin. - 2019 BASE Show details 7 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-schreiber, Nazanin. - 2019 BASE Show details 8 Genome-wide screening for DNA variants associated with reading and language traits Gialluisi, Alessandro; Newbury, Dianne F; Wilcutt, Erik G; Olson, Richard K; DeFries, John C; Brandler, William M; Pennington, Bruce F; Smith, Shelley D; Scerri, Thomas S; Simpson, Nuala H; The SLI Consortium; Luciano, Michelle; Evans, David M; Bates, Timothy C; Stein, John F; Talcott, Joel B; Monaco, Anthony P; Paracchini, Silvia; Francks, Clyde; Fisher, Simon E. - 2015 Abstract: This research was funded by: Max Planck Society, the University of St Andrews - Grant Number: 018696, US National Institutes of Health - Grant Number: P50 HD027802, Wellcome Trust - Grant Number: 090532/Z/09/Z, and Medical Research Council Hub Grant Grant Number: G0900747 91070 ; Reading and language abilities are heritable traits that are likely to share some genetic influences with each other. To identify pleiotropic genetic variants affecting these traits, we first performed a genome‐wide association scan (GWAS) meta‐analysis using three richly characterized datasets comprising individuals with histories of reading or language problems, and their siblings. GWAS was performed in a total of 1862 participants using the first principal component computed from several quantitative measures of reading‐ and language‐related abilities, both before and after adjustment for performance IQ. We identified novel suggestive associations at the SNPs rs59197085 and rs5995177 (uncorrected P ≈ 10–7 for each SNP), located respectively at the CCDC136/FLNC and RBFOX2 genes. Each of these SNPs then showed evidence for effects across multiple reading and language traits in univariate association testing against the individual traits. FLNC encodes a structural protein involved in cytoskeleton remodelling, while RBFOX2 is an important regulator of alternative splicing in neurons. The CCDC136/FLNC locus showed association with a comparable reading/language measure in an independent sample of 6434 participants from the general population, although involving distinct alleles of the associated SNP. Our datasets will form an important part of on‐going international efforts to identify genes contributing to reading and language skills. ; Publisher PDF ; Peer reviewed Keyword: BDC; BF; BF Psychology; CLDRC; Developmental dyslexia; GWAS; Language; Meta-analysis; Pleiotropic variants; QH426; QH426 Genetics; Reading; Reading disability; SLIC; Specific language impairment URL: http://hdl.handle.net/10023/6497 https://onlinelibrary.wiley.com/doi/full/10.1111/gbb.12158#support-information-section https://doi.org/10.1111/gbb.12158 BASE Hide details 9 Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ Eicher, John D.; Powers, Natalie R.; Miller, Laura L.. - : Springer Berlin Heidelberg, 2014 BASE Show details 10 The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language Anthoni, Heidi; Sucheston, Lara E.; Lewis, Barbara A.. - : Springer US, 2012 BASE Show details 11 Genetics of dyslexia : cognitive analysis, candidate genes, comorbidities, and etiologic interactions Pennington, Bruce F.; McGrath, Lauren M.; Smith, Shelley D. In: The genetics of cognitive neuroscience (Cambridge, MA, 2009), p. 177-194 MPI für Psycholinguistik Show details 12 Gene X Environment interactions in reading disability and attention-deficit/hyperactivity disorder Pennington, Bruce F.; McGrath, Lauren; Rosenberg, Jenni... In: Developmental psychology. - Richmond, Va. [u.a.] : American Psychological Association 45 (2009) 1, 77-89 BLLDB Show details 13 Planning studies of etiology Smith, Shelley D.; Morris, Colleen A. In: Applied psycholinguistics. - Cambridge [u.a.] : Cambridge Univ. Press 26 (2005) 1, 97-110 BLLDB Show details 14 Localization and identification of genes affecting language and learning Smith, Shelley D. In: Developmental language disorders (Mahwah, 2004), p. 329-354 MPI für Psycholinguistik Show details 15 Localization and identification of genes affecting language and learning Smith, Shelley D. In: Developmental language disorders. - Mahwah, NJ [u.a.] : Lawrence Erlbaum (2004), 329-354 BLLDB Show details 16 A twin and family study of the association between immune system dysfunction and dyslexia using blood serum immunoassay and survey data Gilger, Jeffrey W.; Pennington, Bruce F.; Harbeck, Ronald J.... In: Brain and cognition. - San Diego, Calif. [u.a.] : Elsevier Science 36 (1998) 3, 310-333 BLLDB Show details 17 CLINICS ISSUE - GENETICS AND HEARING - Medical Genetic Evaluation for the Etiology of Hearing Loss in Children Smith, Shelley D.; Bradley Schaefer, G.; Horton, Mark B.... In: Journal of communication disorders. - New York, NY : Elsevier 31 (1998) 5, 371-390 OLC Linguistik Show details 18 CLINICS ISSUE - GENETICS AND HEARING - Single Gene Influences on Radiologically-Detectable Malformations of the Inner Ear Smith, Shelley D.; Harker, Lee A. In: Journal of communication disorders. - New York, NY : Elsevier 31 (1998) 5, 391-410 OLC Linguistik Show details 19 Developmental dyslexia : neural, cognitive, and genetic mechanisms Tallal, Paula (Mitarb.); Galaburda, Albert M. (Mitarb.); Goldinger, Stephen D. (Mitarb.). - Baltimore, Md. : York Press, 1996 BLLDB UB Frankfurt Linguistik Show details 20 Genetics Brzustowicz, Linda M. (Mitarb.); Smith, Shelley D. (Mitarb.); Pennington, Bruce F. (Mitarb.)... In: Toward a genetics of language. - Mahwah, N.J. : Erlbaum (1996), 1-110 BLLDB Show details Page: 1 2

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