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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 – 17 of 17 1 Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. Ansar, M.; Riazuddin, S.; Sarwar, M.T.... In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018) BASE Show details 2 Creatine synthesis and exchanges between brain cells: What can be learned from human creatine deficiencies and various experimental models? Hanna-El-Daher, L.; Braissant, O. In: Amino acids, vol. 48, no. 8, pp. 1877-1895 (2016) BASE Show details 3 Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations. Santarelli, Rosamaria; del Castillo, Ignacio; Cama, Elona... In: Hearing research, vol 330, iss Pt B (2015) BASE Show details 4 VoICE: A semi-automated pipeline for standardizing vocal analysis across models. Burkett, Zachary D; Day, Nancy F; Peñagarikano, Olga... In: Scientific reports, vol 5, iss 1 (2015) BASE Show details 5 Phenotype and genotype in 101 males with X-linked creatine transporter deficiency van de Kamp, J.; Bratkovic, D.; Poplawski, N.. - : BMJ Publishing Group, 2014 BASE Show details 6 Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism El-Kordi, Ahmed; Winkler, Daniela; Hammerschmidt, Kurt... In: ISSN: 0166-4328 ; EISSN: 1872-7549 ; Behavioural Brain Research ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01580131 ; Behavioural Brain Research, Elsevier, 2013, 251 (1), pp.41 - 49. ⟨10.1016/j.bbr.2012.11.016⟩ (2013) BASE Show details 7 Genome-wide association study of shared components of reading disability and language impairment. Eicher, JD; Powers, NR; Miller, LL... In: Genes, brain, and behavior, vol 12, iss 8 (2013) BASE Show details 8 Individual common variants exert weak effects on the risk for autism spectrum disorders. Anney, Richard; Klei, Lambertus; Pinto, Dalila... In: Human molecular genetics, vol 21, iss 21 (2012) BASE Show details 9 Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Anney, R; Klei, L; Pinto, D... 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 ; ORA review team (2012) BASE Show details 10 Auditory cortical N100 in pre- and post-synaptic auditory neuropathy to frequency or intensity changes of continuous tones. Dimitrijevic, Andrew; Starr, Arnold; Bhatt, Shrutee... In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, vol 122, iss 3 (2011) BASE Show details 11 Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Newbury, DF; Paracchini, S; Scerri, TS... 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) BASE Show details 12 CNTNAP2 variants affect early language development in the general population. Whitehouse, AJ; Bishop, DV; Fisher, SE... 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 ; ORA review team (2011) BASE Show details 13 Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. Jiang, Yong-Hui; Pan, Yanzhen; Zhu, Li. - : Public Library of Science (PLoS), 2010 BASE Show details 14 Genetic advances in the study of speech and language disorders. Newbury, DF; 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) ; CrossRef (2010) BASE Show details 15 A functional genetic link between distinct developmental language disorders. Vernes, SC; Newbury, DF; Abrahams, BS... 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 (2008) BASE Show details 16 AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review. Braissant, O.; Henry, H. In: Journal of Inherited Metabolic Disease, vol. 31, no. 2, pp. 230-239 (2008) BASE Show details 17 Functional dissection of COP-I subunits in the biogenesis of multivesicular endosomes Gu, F.; Aniento, F.; Parton, R. G.. - : Rockefeller University Press, 1997 BASE Show details

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