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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 – 20 of 20 1 A case of co-occuring synesthesia, autism, prodigious talent and strong structural brain connectivity ... Riedel, Andreas; Maier, Simon; Wenzler, Kerstin. - : figshare, 2020 BASE Show details 2 A case of co-occuring synesthesia, autism, prodigious talent and strong structural brain connectivity ... Riedel, Andreas; Maier, Simon; Wenzler, Kerstin. - : figshare, 2020 BASE Show details 3 A case of co-occuring synesthesia, autism, prodigious talent and strong structural brain connectivity Riedel, Andreas; Maier, Simon; Wenzler, Kerstin... In: BMC psychiatry. - 20, 1 (2020) , 342, ISSN: 1471-244X (2020) BASE Show details 4 The general factor of psychopathology: a comparison with the general factor of intelligence with respect to magnitude and predictive validity Pettersson, Erik; Larsson, Henrik; D'Onofrio, Brian M.... In: World Psychiatry (2020) BASE Show details 5 A case of co-occuring synesthesia, autism, prodigious talent and strong structural brain connectivity Riedel, Andreas; Maier, Simon; Wenzler, Kerstin... In: BMC Psychiatry (2020) BASE Show details 6 Typical vs. atypical: Combining auditory Gestalt perception and acoustic analysis of early vocalisations in Rett syndrome Pokorny, Florian B.; Bartl-Pokorny, Katrin D.; Einspieler, Christa. - 2018 BASE Show details 7 Skills training groups for men with ADHD in compulsory care due to substance use disorder: a feasibility study Bihlar Muld, B.; Jokinen, J.; Bölte, Sven. - 2016 BASE Show details 8 Basic and complex emotion recognition in children with autism: Cross-cultural findings Fridenson-Hayo, S.; Berggren, S.; Lassalle, A.. - 2016 BASE Show details 9 Basic and complex emotion recognition in children with autism: cross-cultural findings Fridenson-Hayo, Shimrit; Berggren, Steve; Lassalle, Amandine. - : BioMed Central, 2016 BASE Show details 10 Neural mechanisms of savant calendar calculating in autism: An MEG-study of few single cases Dubischar-Krivec, Anna Milena; Bölte, Sven; Braun, Christoph... In: Brain and cognition. - San Diego, Calif. [u.a.] : Elsevier Science 90 (2014), 157-164 OLC Linguistik Show details 11 Eye tracking in basic research and clinical practice Bartl-Pokorny, K.; Pokorny, F.; Bölte, Sven. - 2013 BASE Show details 12 Individual common variants exert weak effects on the risk for autism spectrum disorders Anney, R.; Klei, L.; Pinto, D.. - : Oxford University Press, 2012 BASE Show details 13 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 14 Individual common variants exert weak effects on the risk for autism spectrum disorders. Anney, Richard; Klei, Lambertus; Pinto, Dalila; Almeida, Joana; Bacchelli, Elena; Baird, Gillian; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick,; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Casey, Jillian; Conroy, Judith; Correia, Catarina; Corsello, Christina; Crawford, Emily,; De Jonge, Maretha; Delorme, Richard; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget,; Folstein, Susan,; Fombonne, Eric; Gilbert, John; Gillberg, Christopher; Glessner, Joseph,; Green, Andrew; Green, Jonathan; Guter, Stephen,; Heron, Elizabeth,; Holt, Richard; Howe, Jennifer,; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Jacob, Suma; Kenny, Graham,; Kim, Cecilia; Kolevzon, Alexander; Kustanovich, Vlad; Lajonchere, Clara,; Lamb, Janine,; Law-Smith, Miriam; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett,; Liu, Xiao-Qing; Lombard, Frances; Lord, Catherine; Lotspeich, Linda; Lund, Sabata,; Magalhaes, Tiago,; Mantoulan, Carine; Mcdougle, Christopher,; Melhem, Nadine,; Merikangas, Alison; Minshew, Nancy,; Mirza, Ghazala,; Munson, Jeff; Noakes, Carolyn; Nygren, Gudrun; Papanikolaou, Katerina; Pagnamenta, Alistair,; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Posey, David,; Poustka, Fritz; Ragoussis, Jiannis; Regan, Regina; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael,; Schlitt, Sabine; Shah, Naisha; Sheffield, Val,; Soorya, Latha; Sousa, Inês; Stoppioni, Vera; Sykes, Nuala; Tancredi, Raffaella; Thompson, Ann,; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John,; Volkmar, Fred; Vorstman, Jacob; Wallace, Simon; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Bailey, Anthony,; Battaglia, Agatino; Cantor, Rita,; Coon, Hilary; Cuccaro, Michael,; Dawson, Geraldine; Ennis, Sean; Freitag, Christine,; Geschwind, Daniel,; Haines, Jonathan,; Klauck, Sabine,; Mcmahon, William,; Maestrini, Elena; Miller, Judith; Monaco, Anthony,; Nelson, Stanley,; Nurnberger, John,; Oliveira, Guiomar; Parr, Jeremy,; Pericak-Vance, Margaret,; Piven, Joseph; Schellenberg, Gerard,; Scherer, Stephen,; Vicente, Astrid,; Wassink, Thomas,; Wijsman, Ellen,; Betancur, Catalina; Buxbaum, Joseph,; Cook, Edwin,; Gallagher, Louise; Gill, Michael; Hallmayer, Joachim; Paterson, Andrew,; Sutcliffe, James,; Szatmari, Peter; Vieland, Veronica,; Hakonarson, Hakon; Devlin, Bernie In: ISSN: 0964-6906 ; EISSN: 1460-2083 ; Human Molecular Genetics ; https://www.hal.inserm.fr/inserm-00723650 ; Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (21), pp.4781-92. &#x27E8;10.1093/hmg/dds301&#x27E9; (2012) Abstract: International audience ; While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To produce a more comprehensive picture, we report Stage 2 of the Autism Genome Project genome-wide association study, adding 1301 ASD families and bringing the total to 2705 families analysed (Stages 1 and 2). In addition to evaluating the association of individual single nucleotide polymorphisms (SNPs), we also sought evidence that common variants, en masse, might affect the risk. Despite genotyping over a million SNPs covering the genome, no single SNP shows significant association with ASD or selected phenotypes at a genome-wide level. The SNP that achieves the smallest P-value from secondary analyses is rs1718101. It falls in CNTNAP2, a gene previously implicated in susceptibility for ASD. This SNP also shows modest association with age of word/phrase acquisition in ASD subjects, of interest because features of language development are also associated with other variation in CNTNAP2. In contrast, allele scores derived from the transmission of common alleles to Stage 1 cases significantly predict case status in the independent Stage 2 sample. Despite being significant, the variance explained by these allele scores was small (Vm< 1%). Based on results from individual SNPs and their en masse effect on risk, as inferred from the allele score results, it is reasonable to conclude that common variants affect the risk for ASD but their individual effects are modest. Keyword: [SDV.GEN]Life Sciences [q-bio]/Genetics URL: https://doi.org/10.1093/hmg/dds301 https://www.hal.inserm.fr/inserm-00723650/document https://www.hal.inserm.fr/inserm-00723650/file/Anney_GWAS_AGP_Hum_Mol_Genet_2012.pdf https://www.hal.inserm.fr/inserm-00723650 BASE Hide details 15 Individual common variants exert weak effects on the risk for autism spectrum disorders ... Folstein, Susan E.; Crawford, Emily L.; Glessner, Joseph T.. - : The University of North Carolina at Chapel Hill University Libraries, 2012 BASE Show details 16 Individual common variants exert weak effects on the risk for autism spectrum disorders Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 17 Individual common variants exert weak effects on risk for Autism Spectrum Disorders Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 18 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 19 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details 20 Individual common variants exert weak effects on the risk for autism spectrum disorderspi Anney, Richard; Klei, Lambertus; Pinto, Dalila. - : Oxford University Press, 2012 BASE Show details

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