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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 The influence of contextual constraint on verbal selection mechanisms and its neural correlates in Parkinson’s disease Isaacs, Megan L.; McMahon, Katie L.; Angwin, Anthony J.. - : Springer New York LLC, 2020 BASE Show details 2 A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence Hill, W. D.; Marioni, R. E.; Maghzian, O.. - : Nature Publishing Group, 2018 BASE Show details 3 Describing placebo phenomena in medicine: a linguistic approach Sussex, Roland. - : Academic Press Inc., 2018 BASE Show details 4 Remedial interventions for developmental dyslexia: How neuropsychological evidence can inspire and support a rehabilitation training Cancer, Alice (orcid:0000-0003-3545-8540); Antonietti, Alessandro (orcid:0000-0002-7212-8076). - : Edizioni Universitarie di Lettere Economia Diritto, 2017 BASE Show details 5 Decreased integrity of the fronto-temporal fibers of the left inferior occipito-frontal fasciculus associated with auditory verbal hallucinations in schizophrenia Oestreich, Lena K. L.; McCarthy-Jones, Simon; Whitford, Thomas J.. - : Springer New York LLC, 2016 BASE Show details 6 Polygenic risk of spasmodic dysphonia is associated with vulnerable sensorimotor connectivity Putzel, Gregory Garbès; Battistella, Giovanni; Rumbach, Anna F.. - : Oxford University Press, 2016 BASE Show details 7 Healing Our Race-Linked Wounds Ferguson, Carroy U In: Carroy U "Cuf" Ferguson, Ph.D. (2015) BASE Show details 8 Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins Hill, W. D.; Davies, G.; Van De Lagemaat, L. N.. - : Nature Publishing Group, 2014 BASE Show details 9 Childhood intelligence is heritable, highly polygenic and associated with FNBP1L Benyamin, B.; St Pourcain, B.; Davis, O. S.. - : Nature Publishing, 2014 BASE Show details 10 Autonomic responsivity and semantic associative competences in disturb of consciousness M. Balconi; R. Stoppelli; M.E. Vanutelli. - : Edizioni Universitarie di Lettere Economia Diritto, 2014 BASE Show details 11 Language changes coincide with motor and fMRI changes following upper extremity motor therapy for hemiparesis: a brief report Harnish, Stacy; Meinzer, Marcus; Trinastic, Jonathan. - : Springer, 2014 BASE Show details 12 Distinct neural substrates for semantic knowledge and naming in the temporoparietal network Gesierich, Benno; Jovicich, Jorge; Riello, Marianna. - : Oxford University Press (OUP), 2012 BASE Show details 13 Neural mechanisms underlying the facilitation of naming in aphasia using a semantic task: an fMRI study Heath, Shiree; McMahon, Katie L.; Nickels, Lyndsey. - : BioMed Central, 2012 BASE Show details 14 Genome-wide association studies establish that human intelligence is highly heritable and polygenic Davies, G.; Tenesa, A.; Payton, A.. - : Nature Publishing Group, 2011 BASE Show details 15 Perceptual and semantic contributions to repetition priming of environmental sounds DE Lucia, Marzia; Cocchi, Luca; Martuzzi, Roberto. - : Oxford University Press, 2010 BASE Show details 16 Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation Bates, T. C.; Lind, P.A.; Luciano, M.; Montgomery, G. W.; Martin, N. G.; Wright, M. J.. - : Nature Publishing Group, 2010 Abstract: The status of DYX1C1 (C15q21.3) as a susceptibility gene for dyslexia is unclear. We report the association of this gene with reading and spelling ability in a sample of adolescent twins and their siblings. Family-based association analyses were carried out on 13 single-nucleotide polymorphisms (SNPs) in DYX1C1, typed in 790 families with up to 5 offspring and tested on 6 validated measures of lexical processing (irregular word) and grapheme-phoneme decoding (pseudo-word) reading-and spelling-based measures of dyslexia, as well as a short-term memory measure. Significant association was observed at the misssense mutation rs17819126 for all reading measures and for spelling of lexical processing words, and at rs3743204 for both irregular and nonword reading. Verbal short-term memory was associated with rs685935. Support for association was not found at rs3743205 and rs61761345 as previously reported by Taipale et al., but these SNPs had very low (0.002 for rs3743205) minor allele frequencies in this sample. These results suggest that DYX1C1 influences reading and spelling ability with additional effects on short-term information storage or rehearsal. Missense mutation rs17819126 is a potential functional basis for the association of DYX1C1 with dyslexia. Molecular Psychiatry (2010) 15, 1190-1196; doi:10.1038/mp.2009.120; published online 10 November 2009 Keyword: 1312 Molecular Biology; 2738 Psychiatry and Mental health; 2804 Cellular and Molecular Neuroscience; Dyslexia; Reading ability; Spelling ability URL: https://espace.library.uq.edu.au/view/UQ:239425 BASE Hide details 17 The contribution of the parietal lobes to speaking and writing Brownsett, Sonia L. E.; Wise, Richard J. S.. - 2010 BASE Show details 18 Language control and lexical competition in bilinguals: An event-related fMRI study Abutalebi, Jubin; Annoni, Jean-Marie; Zimine, Ivan. - : OXFORD UNIV PRESS INC, 2008 BASE Show details

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