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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 68 1 Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula Pimenta, J; Lopes, AM; Carracedo, A. - : Nature Publishing Group, 2019 BASE Show details 2 Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder. Berg, Elizabeth L; Copping, Nycole A; Rivera, Josef K... In: Autism research : official journal of the International Society for Autism Research, vol 11, iss 4 (2018) BASE Show details 3 Non-invasive measurement of mRNA decay reveals translation initiation as the major determinant of mRNA stability Chan, Leon Y; Mugler, Christopher F; Heinrich, Stephanie. - : eLife Sciences Publications, Ltd, 2018 BASE Show details 4 Paraplangia sinespeculo, a new genus and species of bush-cricket, with notes on its biology and a key to the genera of Phaneropterinae (Orthoptera: Tettigonioidea) from Madagascar Heller, K.; Hemp, C.; Massa, B.. - : Orthopterists' Society, 2018. : country:US, 2018 BASE Show details 5 Y chromosomal evidence on the origin of northern Thai people. Brunelli, Andrea; Kampuansai, Jatupol; Seielstad, Mark... In: PloS one, vol 12, iss 7 (2017) BASE Show details 6 7p22.1 microduplication syndrome: Refinement of the critical region. Ronzoni, L; Grassi, FS; Pezzani, L. - 2017 BASE Show details 7 Coevolution of genes and languages and high levels of population structure among the highland populations of Daghestan. Karafet, Tatiana M; Bulayeva, Kazima B; Nichols, Johanna... In: Journal of human genetics, vol 61, iss 3 (2016) BASE Show details 8 A human neurodevelopmental model for Williams syndrome. Chailangkarn, Thanathom; Trujillo, Cleber A; Freitas, Beatriz C... In: Nature, vol 536, iss 7616 (2016) BASE Show details 9 A human neurodevelopmental model for Williams syndrome. Chailangkarn, Thanathom; Trujillo, Cleber A; Freitas, Beatriz C... In: Nature, vol 536, iss 7616 (2016) BASE Show details 10 Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. Leppa, Virpi M; Kravitz, Stephanie N; Martin, Christa Lese... In: American journal of human genetics, vol 99, iss 3 (2016) BASE Show details 11 Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. D'Angelo, D.; Lebon, S.; Chen, Q.... In: Jama Psychiatry, vol. 73, no. 1, pp. 20-30 (2016) BASE Show details 12 The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition. Hippolyte, L.; Maillard, A.M.; Rodriguez-Herreros, B.... In: Biological psychiatry, vol. 80, no. 2, pp. 129-139 (2016) BASE Show details 13 Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal data Kushniarevich, A.; Utevska, O.; Chuhryaeva, M.. - : Public Library of Science, 2015 BASE Show details 14 A novel multi-alignment pipeline for high-throughput sequencing data. Huang, Shunping; Holt, James; Kao, Chia-Yu... In: Database : the journal of biological databases and curation, vol 2014, iss 0 (2014) BASE Show details 15 Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Simpson, NH; Addis, L; Brandler, WM... 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 (2014) BASE Show details 16 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Nudel, R; Simpson, NH; Baird, G... 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 (2014) BASE Show details 17 Las leyes de la lingüística en los sistemas de comunicación Hernández-Fernández, Antoni. - : Universitat de Barcelona, 2014 In: TDX (Tesis Doctorals en Xarxa) (2014) BASE Show details 18 Las leyes de la lingüística en los sistemas de comunicación Hernández-Fernández, Antoni. - : Universitat de Barcelona, 2014 BASE Show details 19 The XY gene hypothesis of psychosis: origins and current status. Crow, TJ In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013) BASE Show details 20 TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Wiszniewski, W; Hunter, JV; Hanchard, NA... 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 (2013) BASE Show details Page: 1 2 3 4

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