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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 29 1 CATALISE: A multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children Bishop, D.V.M.; Snowling, M.J.; Thompson, P.A.. - : Public Library of Science, 2016 BASE Show details 2 CATALISE: A multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children Bishop, DVM; Snowling, MJ; Thompson, PA... In: PLoS ONE , 11 (7) , Article e0158753. (2016) (2016) BASE Show details 3 The impact of nonverbal ability on prevalence and clinical presentation of language disorder: evidence from a population study Norbury, CF; Gooch, D; Wray, C... In: Journal of Child Psychology and Psychiatry (2016) (In press). (2016) BASE Show details 4 CATALISE: A multinational and multidisciplinary Delphi consensus study. Identifying language impairments in children Baird, G; Carter, G; Westerveld, M. - : Public Library of Science, 2016 BASE Show details 5 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 6 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 7 Associations of HLA alleles with 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) (2014) BASE Show details 8 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 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 ; 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 10 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 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. - 2014 BASE Show details 12 Individual common variants exert weak effects on the risk for autism spectrum disorders Anney, R.; Klei, L.; Pinto, D.. - : Oxford University Press, 2012 BASE Show details 13 Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Anney, R; Klei, L; Pinto, D... 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 ; ORA review team (2012) BASE Show details 14 Non-word repetition in adolescents with Specific Language Impairment and Autism plus Language Impairments: a qualitative analysis Riches, N.G.; Loucas, Tom; Baird, G.. - : Elsevier, 2011 BASE Show details 15 Non-word repetition in adolescents with Specific Language Impairment and Autism plus Language Impairments: A qualitative analysis Riches NG; Loucas T; Baird G... In: Journal of Communication Disorders, 08-07-2010 (2010) BASE Show details 16 Speech perception and phonological short-term memory capacity in language impairment: preliminary evidence from adolescents with specific language impairment (SLI) and autism spectrum disorders (ASD) Chandler S; Simonoff E; Riches NG... In: International Journal of Language and Communication Disorders, May-June 2010 (2010) BASE Show details 17 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 18 Loss of language in early development of autism and specific language impairment Pickles, A; Simonoff, E; Conti-Ramsden, G... In: JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY , 50 (7) 843 - 852. (2009) (2009) BASE Show details 19 CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment Ragoussis, Jiannis; Everitt, Andrea; Addis, L.. - 2009 BASE Show details 20 Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment Falcaro, M.; Pickles, A.; Newbury, D. F.; Addis, L.; Banfield, E.; Fisher, S. E.; Monaco, A. P.; Simkin, Z.; Conti-Ramsden, G.; Cleak, J. D.; Cardon, L. R.; Merriden, M. J.; Goodyer, I. M.; Simonoff, E.; Bolton, P. F.; Slonims, V.; Baird, G.; Everitt, Andrea; Hennessy, E.; Shaw, D.; Helms, P. J.; Kindley, A. D.; Clark, Ann; Watson, Jocelynne; O'Hare, Anne; Seckl, J.; Cowie, H.; Cohen, W.; Nasir, J.; Bishop, DVM. - 2008 Abstract: Deficits in phonological short-term memory and aspects of verb grammar morphology have been proposed as phenotypic markers of specific language impairment (SLI) with the suggestion that these traits are likely to be under different genetic influences. This investigation in 300 first-degree relatives of 93 probands with SLI examined familial aggregation and genetic linkage of two measures thought to index these two traits, non-word repetition and tense marking. In particular, the involvement of chromosomes 16q and 19q was examined as previous studies found these two regions to be related to SLI. Results showed a strong association between relatives' and probands' scores on non-word repetition. In contrast, no association was found for tense marking when examined as a continuous measure. However, significant familial aggregation was found when tense marking was treated as a binary measure with a cut-off point of -1.5 SD, suggestive of the possibility that qualitative distinctions in the trait may be familial while quantitative variability may be more a consequence of non-familial factors. Linkage analyses supported previous findings of the SLI Consortium of linkage to chromosome 16q for phonological short-term memory and to chromosome 19q for expressive language. In addition, we report new findings that relate to the past tense phenotype. For the continuous measure, linkage was found on both chromosomes, but evidence was stronger on chromosome 19. For the binary measure, linkage was observed on chromosome 19 but not on chromosome 16. 2007 The Authors. ; casl ; 7 ; pub ; 559 ; pub ; 4 Keyword: Familial aggregation; Grammatical morphology; Linkage analysis; Phonological short-term memory; Selected sample; Specific language impairment URL: https://hdl.handle.net/20.500.12289/559 https://doi.org/10.1111/j.1601-183X.2007.00364.x https://eresearch.qmu.ac.uk/handle/20.500.12289/559 BASE Hide details Page: 1 2

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