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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 – 18 of 18 1 Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation. Klusek, Jessica; Fairchild, Amanda; Moser, Carly... In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022) BASE Show details 2 Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation Klusek, Jessica; Fairchild, Amanda; Moser, Carly... In: J Neurodev Disord (2022) BASE Show details 3 Concurrent Associations between Expressive Language Ability and Independence in Adolescents and Adults with Fragile X Syndrome. Abbeduto, Leonard; Klusek, Jessica; Taylor, Julie Lounds... In: Brain sciences, vol 11, iss 9 (2021) BASE Show details 4 Concurrent Associations between Expressive Language Ability and Independence in Adolescents and Adults with Fragile X Syndrome. Abbeduto, Leonard; Klusek, Jessica; Taylor, Julie Lounds... In: Brain sciences, vol 11, iss 9 (2021) BASE Show details 5 Concurrent Associations between Expressive Language Ability and Independence in Adolescents and Adults with Fragile X Syndrome Abbeduto, Leonard; Klusek, Jessica; Taylor, Julie Lounds... In: Brain Sci (2021) BASE Show details 6 Reading in Children With Fragile X Syndrome: Phonological Awareness and Feasibility of Intervention. Adlof, Suzanne M; Klusek, Jessica; Hoffmann, Anne... In: American journal on intellectual and developmental disabilities, vol 123, iss 3 (2018) BASE Show details 7 Curvilinear Association Between Language Disfluency and FMR1 CGG Repeat Size Across the Normal, Intermediate, and Premutation Range. Klusek, Jessica; Porter, Anna; Abbeduto, Leonard... In: Frontiers in genetics, vol 9, iss AUG (2018) BASE Show details 8 Curvilinear Association Between Language Disfluency and FMR1 CGG Repeat Size Across the Normal, Intermediate, and Premutation Range. Klusek, Jessica; Porter, Anna; Abbeduto, Leonard... In: Klusek, Jessica; Porter, Anna; Abbeduto, Leonard; Adayev, Tatyana; Tassone, Flora; Mailick, Marsha R; et al.(2018). Curvilinear Association Between Language Disfluency and FMR1 CGG Repeat Size Across the Normal, Intermediate, and Premutation Range. Frontiers in genetics, 9(AUG), 344. doi:10.3389/fgene.2018.00344. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/0dn6p4z8 (2018) BASE Show details 9 Reading in Children with Fragile X Syndrome: Phonological Awareness and Feasibility of Intervention Adlof, Suzanne M.; Klusek, Jessica; Hoffmann, Anne. - 2018 BASE Show details 10 Pragmatic Language Features of Mothers with the FMR1 Premutation are Associated with the Language Outcomes of Adolescents and Young Adults with Fragile X Syndrome Klusek, Jessica; McGrath, S E; Abbeduto, L... In: Faculty Publications (2016) BASE Show details 11 Reading and Phonological Skills in Boys with Fragile X Syndrome ... Roberts, Jane E.; Hunt, Anna W.; Klusek, Jessica. - : The University of North Carolina at Chapel Hill University Libraries, 2015 BASE Show details 12 Reading and Phonological Skills in Boys with Fragile X Syndrome Klusek, Jessica; Hunt, Anna W.; Mirrett, Penny L.. - 2015 BASE Show details 13 Reading and Phonological Skills in Boys with Fragile X Syndrome Klusek, Jessica; Hunt, Anna W; Mirrett, Penny L... In: Faculty Publications (2015) BASE Show details 14 Cardiac Autonomic Regulation in Autism and Fragile X Syndrome: A Review Klusek, Jessica; Roberts, Jane E.; Losh, Molly. - 2014 BASE Show details 15 Phonological Awareness and Reading in Boys with Fragile X Syndrome Adlof, Suzanne M.; Klusek, Jessica; Shinkareva, Svetlana V.. - 2014 BASE Show details 16 Social Communication and Theory of Mind in Boys with Autism and Fragile X Syndrome Losh, Molly; Martin, Gary E.; Klusek, Jessica; Hogan-Brown, Abigail L.; Sideris, John. - : Frontiers Research Foundation, 2012 Abstract: Impairments in the social use of language, or pragmatics, constitute a core characteristic of autism. Problems with pragmatic language have also been documented in fragile X syndrome (FXS), a monogenic condition that is the most common known genetic cause of autism. Evidence suggests that social cognitive ability, or theory of mind, may also be impaired in both conditions, and in autism, may importantly relate to pragmatic language ability. Given the substantial overlap observed in autism and FXS, this study aimed to better define those social-communicative phenotypes that overlap in these two conditions by comparing pragmatic language ability and theory of mind in children with idiopathic autism and children with FXS, with and without autism, as well as children with Down syndrome and typically developing controls. We further examined correlations between these cognitive-behavioral phenotypes and molecular genetic variation related to the Fragile X Mental Retardation-1 gene (FMR1) in the FXS group. Results indicated that children with idiopathic autism and those with FXS and autism performed comparably on direct-assessment measures of pragmatic language and theory of mind, whereas those with FXS only did not differ from controls. Theory of mind was related to pragmatic language ability in all groups. Pragmatic language and theory of mind also correlated with genetic variation at the FMR1 locus (Cytosine-Guanine-Guanine repeats and percent methylation). These results point toward substantial overlap in the social and language phenotypes in autism and FXS and suggest a molecular genetic basis to these phenotypic profiles. Keyword: Psychology URL: https://doi.org/10.3389/fpsyg.2012.00266 http://www.ncbi.nlm.nih.gov/pubmed/22934085 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422728 BASE Hide details 17 Language characteristics of individuals with Down syndrome Roberts, Joanne E.; Martin, Gary E.; Klusek, Jessica... In: Language, literacy, and genetic syndromes. - Hagerstown, Md. : Lippincott Williams & Wilkins (2009), 112-132 BLLDB OLC Linguistik Show details 18 Language Characteristics of Individuals with Down Syndrome Martin, Gary E.; Klusek, Jessica; Estigarribia, Bruno. - 2009 BASE Show details

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