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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 – 15 of 15 1 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants ... Nudel, Ron; Appadurai, Vivek; Buil, Alfonso. - : figshare, 2021 BASE Show details 2 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants ... Nudel, Ron; Appadurai, Vivek; Buil, Alfonso. - : figshare, 2021 BASE Show details 3 Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants Nudel, Ron; Appadurai, Vivek; Buil, Alfonso... In: J Neurodev Disord (2021) BASE Show details 4 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study ... Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : figshare, 2020 BASE Show details 5 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study ... Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : figshare, 2020 BASE Show details 6 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica... In: BMC Neurosci (2020) BASE Show details 7 Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk Nudel, Ron; Christiani, Camilla A. J.; Ohland, Jessica. - : John Wiley & Sons, Inc., 2019 BASE Show details 8 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 9 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry Andrea; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 10 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron. - 2016 BASE Show details 11 Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron. - : BioMed Central Ltd., 2016 BASE Show details 12 <The>> genetics of specific language impairment Nudel, Ron; Ceroni, Fabiola; Simpson, Nuala H.... In: Specific language impairment (Amsterdam, 2015), p. 7-34 MPI für Psycholinguistik Show details 13 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - 2015 BASE Show details 14 Associations of HLA alleles with specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian. - : BioMed Central, 2014 BASE Show details 15 Associations of HLA alleles with specific language impairment Nudel, Ron; Simpson, Nuala H; Baird, Gillian; O'Hare, Anne; Conti-Ramsden, Gina; Bolton, Patrick F.; Hennessy, Elizabeth R; Monaco, Anthony P.; Knight, Julian C; Winney, Bruce; Fisher, Simon E.; Newbury, Dianne F.. - 2014 Abstract: Human leukocyte antigen (HLA) loci have been implicated in several neurodevelopmental disorders in which language is affected. However, to date, no studies have investigated the possible involvement of HLA loci in specific language impairment (SLI), a disorder that is defined primarily upon unexpected language impairment. We report association analyses of single-nucleotide polymorphisms (SNPs) and HLA types in a cohort of individuals affected by language impairment. We perform quantitative association analyses of three linguistic measures and case-control association analyses using both SNP data and imputed HLA types. Quantitative association analyses of imputed HLA types suggested a role for the HLA-A locus in susceptibility to SLI. HLA-A A1 was associated with a measure of short-term memory (P = 0.004) and A3 with expressive language ability (P = 0.006). Parent-of-origin effects were found between HLA-B B8 and HLA-DQA1*0501 and receptive language. These alleles have a negative correlation with receptive language ability when inherited from the mother (P = 0.021, P = 0.034, respectively) but are positively correlated with the same trait when paternally inherited (P = 0.013, P = 0.029, respectively). Finally, case control analyses using imputed HLA types indicated that the DR10 allele of HLA-DRB1 was more frequent in individuals with SLI than population controls (P = 0.004, relative risk = 2.575), as has been reported for individuals with attention deficit hyperactivity disorder (ADHD). These preliminary data provide an intriguing link to those described by previous studies of other neurodevelopmental disorders and suggest a possible role for HLA loci in language disorders. Keyword: Other systems of medicine URL: https://strathprints.strath.ac.uk/47305/1/Nudel_etal_JND_2014_Associations_of_HLA_alleles_with_specific_language_impairment.pdf https://strathprints.strath.ac.uk/47305/ https://doi.org/10.1186/1866-1955-6-1 BASE Hide details

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