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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 3 4 Hits 1 – 20 of 70 1 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans Sønderby, Ida E.; van der Meer, Dennis; Moreau, Clara. - : Springer Nature, 2021 BASE Show details 2 Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction den Hoed, Joery; de Boer, Elke; Voisin, Norine... In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://hal-univ-rennes1.archives-ouvertes.fr/hal-03268683 ; American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (2), pp.346-356. ⟨10.1016/j.ajhg.2021.01.007⟩ (2021) BASE Show details 3 Lessons From the First Decade of the Native American Summer Research Internship at the University of Utah Holsti, Maija; Clark, Ed; Fisher, Simon... In: Acad Med (2021) BASE Show details 4 Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults Guadalupe, Tulio; Kong, Xiang-Zhen; Akkermans, Sophie E. A.... In: Brain Struct Funct (2021) BASE Show details 5 Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies Shapland, Chin Yang; Verhoef, Ellen; Davey Smith, George... In: NPJ Sci Learn (2021) BASE Show details 6 Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia Gialluisi, Alessandro; Andlauer, Till,; Mirza-Schreiber, Nazanin... In: ISSN: 1359-4184 ; EISSN: 1476-5578 ; Molecular Psychiatry ; https://hal.archives-ouvertes.fr/hal-02976104 ; Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-00898-x⟩ (2020) BASE Show details 7 Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations Connaughton, Dervla,; Dai, Rufeng; Owen, Danielle,... In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://www.hal.inserm.fr/inserm-02964365 ; American Journal of Human Genetics, Elsevier (Cell Press), 2020, 107 (4), pp.727-742. ⟨10.1016/j.ajhg.2020.08.013⟩ (2020) BASE Show details 8 Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila Castells-Nobau, Anna; Eidhof, Ilse; Fenckova, Michaela... In: ISSN: 1932-6203 ; EISSN: 1932-6203 ; PLoS ONE ; https://hal.sorbonne-universite.fr/hal-02045748 ; PLoS ONE, Public Library of Science, 2019, 14 (2), pp.e0211652. ⟨10.1371/journal.pone.0211652⟩ (2019) BASE Show details 9 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till,; Mirza-Schreiber, Nazanin... In: ISSN: 2158-3188 ; EISSN: 2158-3188 ; Translational Psychiatry ; https://hal.archives-ouvertes.fr/hal-02158502 ; Translational Psychiatry, Nature Pub. Group, 2019, 9, pp.77. ⟨10.1038/s41398-019-0402-0⟩ (2019) BASE Show details 10 Genome sequencing for rightward hemispheric language dominance Carrion‐Castillo, Amaia; Van der Haegen, Lise; Tzourio‐Mazoyer, Nathalie... In: ISSN: 1601-1848 ; EISSN: 1601-183X ; Genes, Brain and Behavior ; https://hal.archives-ouvertes.fr/hal-02093544 ; Genes, Brain and Behavior, Wiley, 2019, pp.e12572. ⟨10.1111/gbb.12572⟩ (2019) BASE Show details 11 Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets Postema, Merel; Van Rooij, Daan,; Anagnostou, Evdokia... In: ISSN: 2041-1723 ; EISSN: 2041-1723 ; Nature Communications ; https://hal.archives-ouvertes.fr/hal-02365089 ; Nature Communications, Nature Publishing Group, 2019, 10 (1), ⟨10.1038/s41467-019-13005-8⟩ (2019) BASE Show details 12 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia ... Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin. - : ETH Zurich, 2019 BASE Show details 13 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin... In: Translational Psychiatry, 9 (1) (2019) BASE Show details 14 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-schreiber, Nazanin. - 2019 BASE Show details 15 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-schreiber, Nazanin. - 2019 BASE Show details 16 Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language Verhoef, Ellen; Demontis, Ditte; Burgess, Stephen. - : Springer Nature, 2019 BASE Show details 17 Defining the biological bases of individual differences in musicality Gingras, Bruno; Honing, Henkjan; Peretz, Isabelle... In: The origins of musicality (Cambridge, 2018), p. 221-250 MPI für Psycholinguistik Show details 18 Molecular genetic methods Kovel, Carolien G. F. de; Fisher, Simon E. In: Research methods in psycholinguistics and the neurobiology of language (Hoboken, NJ, 2018), p. 330-353 MPI für Psycholinguistik 19 A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development Eising, Else; Carrion-Castillo, Amaia; Vino, Arianna... In: ISSN: 1359-4184 ; EISSN: 1476-5578 ; Molecular Psychiatry ; https://hal.archives-ouvertes.fr/hal-01726218 ; Molecular Psychiatry, Nature Publishing Group, In press (2018) BASE Show details 20 CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna... In: ISSN: 2041-1723 ; EISSN: 2041-1723 ; Nature Communications ; https://hal.sorbonne-universite.fr/hal-01922858 ; Nature Communications, Nature Publishing Group, 2018, 9 (1), pp.4619. ⟨10.1038/s41467-018-06014-6⟩ (2018) BASE Show details Page: 1 2 3 4

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