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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 Hits 1 – 20 of 53 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 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 3 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 4 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 5 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 6 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 7 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 8 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 9 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 10 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 11 Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion Mei, Cristina; Fedorenko, Evelina; Amor, David J.. - : Springer International Publishing, 2018 BASE Show details 12 Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex Guadalupe, Tulio; Mathias, Samuel R.; vanErp, Theo G. M.... In: ISSN: 1931-7557 ; EISSN: 1931-7565 ; Brain imaging and behavior (Brain Imaging Behav) ; https://hal.archives-ouvertes.fr/hal-01382787 ; Brain imaging and behavior (Brain Imaging Behav), Secaucus, NJ : Springer, 2017, 11 (5), pp.1497-1514. ⟨10.1007/s11682-016-9629-z⟩ (2017) BASE Show details 13 Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia Morgan, Angela T.; Haaften, Leenke van; van Hulst, Karen. - : Nature Publishing Group UK, 2017 BASE Show details 14 Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment Chen, Xiaowei Sylvia; Reader, Rose H.; Hoischen, Alexander. - : Nature Publishing Group, 2017 BASE Show details 15 Common polygenic risk for ASD and ADHD is associated with childhood linguistic traits within the general population, but with opposite effects St Pourcain, Beate; Verhoef, Ellen; Fisher, Simon E.. - : Elsevier, 2017 BASE Show details 16 Genes, brain, and language: a brief introduction to the special issue Zubicaray, Greig de; Fisher, Simon E.. - : Academic Press, 2017 BASE Show details 17 Building Bridges between Genes, Brains, and Language Fisher, Simon E. In: Birdsong, speech, and language : exploring the evolution of mind and brain (2016), S. 425-454 Leibniz-Zentrum Allgemeine Sprachwissenschaft Show details 18 BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription Dias, Cristina; Estruch, Sara B.; Graham, Sarah A.... In: ISSN: 0002-9297 ; EISSN: 1537-6605 ; American Journal of Human Genetics ; https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01680178 ; American Journal of Human Genetics, Elsevier (Cell Press), 2016, 99 (2), pp.253 - 274. ⟨10.1016/j.ajhg.2016.05.030⟩ (2016) BASE Show details 19 A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 Fedorenko, Evelina; Morgan, Angela; Murray, Elizabeth. - : Nature Publishing Group, 2016 BASE Show details 20 A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice. Chabout, Jonathan; Sarkar, Abhra; Patel, Sheel R. - : Frontiers Media SA, 2016 BASE Show details Page: 1 2 3

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