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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 3 Hits 1 – 20 of 41 1 Study of central exclusive [Image: see text] production in proton-proton collisions at [Formula: see text] and 13TeV Sirunyan, A. M.; Tumasyan, A.; Adam, W.... In: Eur Phys J C Part Fields (2020) BASE Show details 2 Aspectos pragmáticos y discursivos de los usos eufemísticos en la comunicación pública Fernández-Smith, G. (Gérard). - : Servicio de Publicaciones de la Universidad de Navarra, 2018 BASE Show details 3 Search for dark matter produced in association with heavy-flavor quark pairs in proton-proton collisions at [Formula: see text] Sirunyan, A. M.; Tumasyan, A.; Adam, W.. - : Springer Berlin Heidelberg, 2017 BASE Show details 4 A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence Spain, S L; Pedroso, I; Kadeva, N. - : Nature Publishing Group, 2016 BASE Show details 5 Marco legal y planificación lingüística en las comunidades bilingües de España Fernández-Smith, G. (Gérard); Escoriza-Morera, L. (Luis). - : Servicio de Publicaciones de la Universidad de Navarra, 2015 BASE Show details 6 Common variation near ROBO2 is associated with expressive vocabulary in infancy O’Reilly, P.F.; Ang, Q.W.; Miller, L.. - : Nature Publishing Group, 2014 BASE Show details 7 Childhood intelligence is heritable, highly polygenic and associated with FNBP1L Benyamin, B.; St. Pourcain, B.; Davis, O.S.P.. - : Nature Publishing Group, 2014 BASE Show details 8 Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Benyamin, B; Pourcain, B; Davis, OS... In: Mol Psychiatry , 19 (2) 253 - 258. (2014) (2014) BASE Show details 9 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 10 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 11 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 12 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Nudel, R; Simpson, N H; Baird, G; O'Hare, A; Conti-Ramsden, G; Bolton, P F; Hennessy, E R; Ring, S M; Smith, G D; Francks, C; Paracchini, S; Monaco, A P; Fisher, S E; Newbury, D F. - 2014 Abstract: Specific language impairment (SLI) is a neurodevelopmental disorder that affects linguistic abilities when development is otherwise normal. We report the results of a genome-wide association study of SLI which included parent-of-origin effects and child genotype effects and used 278 families of language-impaired children. The child genotype effects analysis did not identify significant associations. We found genome-wide significant paternal parent-of-origin effects on chromosome 14q12 (P = 3.74 × 10(-8) ) and suggestive maternal parent-of-origin effects on chromosome 5p13 (P = 1.16 × 10(-7) ). A subsequent targeted association of six single-nucleotide-polymorphisms (SNPs) on chromosome 5 in 313 language-impaired individuals and their mothers from the ALSPAC cohort replicated the maternal effects, albeit in the opposite direction (P = 0.001); as fathers' genotypes were not available in the ALSPAC study, the replication analysis did not include paternal parent-of-origin effects. The paternally-associated SNP on chromosome 14 yields a non-synonymous coding change within the NOP9 gene. This gene encodes an RNA-binding protein that has been reported to be significantly dysregulated in individuals with schizophrenia. The region of maternal association on chromosome 5 falls between the PTGER4 and DAB2 genes, in a region previously implicated in autism and ADHD. The top SNP in this association locus is a potential expression QTL of ARHGEF19 (also called WGEF) on chromosome 1. Members of this protein family have been implicated in intellectual disability. In summary, this study implicates parent-of-origin effects in language impairment, and adds an interesting new dimension to the emerging picture of shared genetic etiology across various neurodevelopmental disorders. Keyword: Other systems of medicine URL: https://doi.org/10.1111/gbb.12127 https://strathprints.strath.ac.uk/47290/1/Nudel_etal_GBB_2014_Genome_wide_association_analyses_of_child_genotype_effects.pdf https://strathprints.strath.ac.uk/47290/ BASE Hide details 13 Benessere e paesaggio. Appunti su un diritto e su una osmosi. Margarito M.. - : Edizioni Trauben, 2014. : country:ITA, 2014. : place:Torino, 2014 BASE Show details 14 Precisiones terminológicas y conceptuales en el ámbito de la lingüística textual y discursiva Fernández-Smith, G. (Gérard). - : Servicio de Publicaciones de la Universidad de Navarra, 2014 BASE Show details 15 Genome-wide association study of shared components of reading disability and language impairment. Eicher, JD; Powers, NR; Miller, LL... In: Genes, brain, and behavior, vol 12, iss 8 (2013) BASE Show details 16 Childhood intelligence is heritable, highly polygenic and associated with FNBP1L Benyamin, B; Pourcain, BSt; Davis, OS. - 2013 BASE Show details 17 The Extent of the Lordship of Chirk, 1332 Rex Smith, G In: Cambrian medieval Celtic studies. - Aberystwyth : CMCS (2012) 63, 91-100 OLC Linguistik Show details 18 Collaborative working: Speech and Language Therapy and the Stroke Association. Scantlebury, K.; Bixley, Morag; Smith, G.. - 2012 BASE Show details 19 The Manor of Aberffraw, 1284-1339 Rex Smith, G In: Cambrian medieval Celtic studies. - Aberystwyth : CMCS (2010) 60, 81-92 OLC Linguistik Show details 20 The Penmachno Letter Patent and the Welsh Uprising of 1294-95 Smith, G Rex In: Cambrian medieval Celtic studies. - Aberystwyth : CMCS (2009) 58, 49-68 OLC Linguistik Show details Page: 1 2 3

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