• Refine your search:
  • 
    Keyword:
    
    • Female (8)
    • Humans (8)
    • Male (8)
    • Risk Assessment (8)
    • Child (6)
    • Language Development Disorders (4)
    • Preschool (4)
    • Follow-Up Studies (3)
    • 80 and over (2)
    • Adolescent (2)
    •   more
  • 
    Creator / Publisher:
    
    • Adams, C (2)
    • Bishop, DV (2)
    • Laws, G (2)
    • Norbury, CF (2)
    • Addis, L (1)
    • Banks, E. (1)
    • Beale, T (1)
    • Beharry, A. (1)
    • Belsky, Jay (1)
    • Bradley, J (1)
    •   more
  • 
    Year:
    
    • 2020 (2)
    • 2019 (1)
    • 2015 (1)
    • 2011 (1)
    • 2010 (1)
    • 2006 (2)
  • 
    Medium
  • 
    Type:
    
    • Article (8)
  • 
    BLLDB-Access:
    • free (8)
    • subject to license (0)

Search in the Catalogues and Directories

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 – 8 of 8 1 Role of maternal age at birth in child development among Indigenous and non-Indigenous Australian children in their first school year: a population-based cohort study Hanly, M.; Falster, K.; Banks, E.. - : Elsevier, 2020 BASE Show details 2 Prospective cohort study on the predictors of fall risk in 119 patients with bilateral vestibulopathy Dobbels, Bieke; Lucieer, Florence; Mertens, Griet... In: ISSN: 1932-6203 ; PLOS ONE, Vol. 15, No 3 (2020) P. e0228768 (2020) BASE Show details 3 Predictive Factors of Swallowing Disorders and Bronchopneumonia in Acute Ischemic Stroke. Beharry, A.; Michel, P.; Faouzi, M.... In: Journal of stroke and cerebrovascular diseases, vol. 28, no. 8, pp. 2148-2154 (2019) BASE Show details 4 Child effects and child care: Implications for risk and adjustment. Snell, Emily K; Hindman, Annemarie H; Belsky, Jay In: Development and psychopathology, vol 27, iss 4 Pt 1 (2015) BASE Show details 5 Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Newbury, DF; Paracchini, S; Scerri, TS; Winchester, L; Addis, L; Richardson, AJ; Walter, J; Stein, JF; Talcott, JB; 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 (2011) Abstract: Dyslexia (or reading disability) and specific language impairment (or SLI) are common childhood disorders that show considerable co-morbidity and diagnostic overlaps and have been suggested to share some genetic aetiology. Recently, genetic risk variants have been identified for SLI and dyslexia enabling the direct evaluation of possible shared genetic influences between these disorders. In this study we investigate the role of variants in these genes (namely MRPL19/C20RF3, ROBO1, DCDC2, KIAA0319, DYX1C1, CNTNAP2, ATP2C2 and CMIP) in the aetiology of SLI and dyslexia. We perform case-control and quantitative association analyses using measures of oral and written language skills in samples of SLI and dyslexic families and cases. We replicate association between KIAA0319 and DCDC2 and dyslexia and provide evidence to support a role for KIAA0319 in oral language ability. In addition, we find association between reading-related measures and variants in CNTNAP2 and CMIP in the SLI families. Keyword: 5' Untranslated Regions; Alleles; Carrier Proteins; Case-Control Studies; Child; Cohort Studies; Dyslexia; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Language Development Disorders; Male; Membrane Proteins; Microtubule-Associated Proteins; Nerve Tissue Proteins; Polymorphism; Risk Assessment; Single Nucleotide URL: https://doi.org/10.1007/s10519-010-9424-3 BASE Hide details 6 Congenital profound hearing loss: management of hypoplastic and aplastic vestibulocochlear nerves. Seymour, FK; Cruise, A; Lavy, JA... In: Cochlear Implants Int , 11 Sup pp. 213-216. (2010) (2010) BASE Show details 7 High heritability of speech and language impairments in 6-year-old twins demonstrated using parent and teacher report. Bishop, DV; Laws, G; Adams, C... 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 (2006) BASE Show details 8 High heritability of speech and language impairments in 6-year-old twins demonstrated using parent and teacher report. Bishop, DV; Laws, G; Adams, C... In: Behav Genet , 36 (2) pp. 173-184. (2006) (2006) BASE Show details

Mobile view All Catalogues UB Frankfurt Linguistik 0 IDS Mannheim 0 OLC Linguistik 0 UB Frankfurt Retrokatalog 0 DNB Subject Category Language 0 Institut für Empirische Sprachwissenschaft 0 Leibniz-Centre General Linguistics (ZAS) 0 Bibliographies BLLDB 0 BDSL 0 IDS Bibliografie zur deutschen Grammatik 0 IDS Bibliografie zur Gesprächsforschung 0 IDS Konnektoren im Deutschen 0 IDS Präpositionen im Deutschen 0 IDS OBELEX meta 0 MPI-SHH Linguistics Collection 0 MPI for Psycholinguistics 0 Linked Open Data catalogues Annohub 0 Online resources Link directory 0 Journal directory 0 Database directory 0 Dictionary directory 0 Open access documents BASE 8 Linguistik-Repository 0 IDS Publikationsserver 0 Online dissertations 0 Language Description Heritage 0