Made available in DSpace on 2022-05-02T18:42:56Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-05-14; A measurement of the Higgs boson mass is presented based on the combined data samples of the ATLAS and CMS experiments at the CERN LHC in the H→γγ and H→ZZ→4 decay channels. The results are obtained from a simultaneous fit to the reconstructed invariant mass peaks in the two channels and for the two exp...
Made available in DSpace on 2022-05-03T17:58:33Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-05-14; A measurement of the Higgs boson mass is presented based on the combined data samples of the ATLAS and CMS experiments at the CERN LHC in the H→γγ and H→ZZ→4 decay channels. The results are obtained from a simultaneous fit to the reconstructed invariant mass peaks in the two channels and for the two exp...
Made available in DSpace on 2021-06-25T10:51:09Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-01-01; Natural Sciences and Engineering Research Council of Canada; Fakulta Elektrotechniky a Informatiky, Vysoká Škola Bánská - Technická Univerzita Ostrava; Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica; Corporación de Fomento de la Producción; Seventh Framework Programme; ...
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Made available in DSpace on 2018-11-26T22:16:26Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-05-14; ANPCyT (Argentina); YerPhI (Armenia); ARC (Australia); BMWFW (Austria); FWF (Austria); ANAS (Azerbaijan); SSTC (Belarus); FNRS (Belgium); FWO (Belgium); Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES); Fundação de ...
An increase in HIV diagnoses in men who have sex with men (MSM) in high-income countries was identified from 2000-2005. We sought to investigate recent trends through 2014 to better inform treatment and prevention strategies.
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 (Stage...
Autism spectrum disorder (ASD) is a highly heritable disorder of complex and heterogeneous aetiology. It is primarily characterized by altered cognitive ability including impaired language and communication skills and fundamental deficits in social reciprocity. Despite some notable successes in neuropsychiatric genetics, overall, the high heritability of ASD (~90%) remains poorly explained by common genetic ris...
Recent genome-wide association studies (GWAS) have implicated a range of genes from discrete biological pathways in the aetiology of autism. However, despite the strong influence of genetic factors, association studies have yet to identify statistically robust, replicated major effect genes or SNPs. We apply the principle of the SNP ratio test methodology described by O'Dushlaine et al to over 2100 families fro...
The autism spectrum disorders (ASDs) are a group of conditions characterized by impairments in reciprocal social interaction and communication, and the presence of restricted and repetitive behaviours. Individuals with an ASD vary greatly in cognitive development, which can range from above average to intellectual disability. Although ASDs are known to be highly heritable ( approximately 90%), the underlying ge...