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      Big data approaches to decomposing heterogeneity across the autism spectrum

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      1 , 2 , 2 , 3 , 4 ,   2 , 5
      Molecular psychiatry

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          Abstract

          Autism is a diagnostic label based on behavior. While the diagnostic criteria attempt to maximize clinical consensus, it also masks a wide degree of heterogeneity between and within individuals at multiple levels of analysis. Understanding this multi-level heterogeneity is of high clinical and translational importance. Here we present organizing principles to frame research examining multi-level heterogeneity in autism. Theoretical concepts such as ‘spectrum’ or ‘autisms’ reflect non-mutually exclusive explanations regarding continuous/dimensional or categorical/qualitative variation between and within individuals. However, common practices of small sample size studies and case-control models are suboptimal for tackling heterogeneity. Big data is an important ingredient for furthering our understanding heterogeneity in autism. In addition to being ‘feature-rich’, big data should be both ‘broad’ (i.e. large sample size) and ‘deep’ (i.e. multiple levels of data collected on the same individuals). These characteristics increase the likelihood that the study results are more generalizable and facilitate evaluation of the utility of different models of heterogeneity. A model’s utility can be measured by its ability to explain clinically or mechanistically important phenomena, and also by explaining how variability manifests across different levels of analysis. The directionality for explaining variability across levels can be bottom-up or top-down, and should include the importance of development for characterizing changes within individuals. While progress can be made with ‘supervised’ models built upon a priori or theoretically predicted distinctions or dimensions of importance, it will become increasingly important to complement such work with unsupervised data-driven discoveries that leverage unknown and multivariate distinctions within big data. A better understanding of how to model heterogeneity between autistic people will facilitate progress towards precision medicine for symptoms that cause suffering, and person-centered support.

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          Autism spectrum disorders: developmental disconnection syndromes.

          Autism is a common and heterogeneous childhood neurodevelopmental disorder. Analogous to broad syndromes such as mental retardation, autism has many etiologies and should be considered not as a single disorder but, rather, as 'the autisms'. However, recent genetic findings, coupled with emerging anatomical and functional imaging studies, suggest a potential unifying model in which higher-order association areas of the brain that normally connect to the frontal lobe are partially disconnected during development. This concept of developmental disconnection can accommodate the specific neurobehavioral features that are observed in autism, their emergence during development, and the heterogeneity of autism etiology, behaviors and cognition.
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            Evaluating the replicability of social science experiments in Nature and Science between 2010 and 2015

            Being able to replicate scientific findings is crucial for scientific progress1-15. We replicate 21 systematically selected experimental studies in the social sciences published in Nature and Science between 2010 and 201516-36. The replications follow analysis plans reviewed by the original authors and pre-registered prior to the replications. The replications are high powered, with sample sizes on average about five times higher than in the original studies. We find a significant effect in the same direction as the original study for 13 (62%) studies, and the effect size of the replications is on average about 50% of the original effect size. Replicability varies between 12 (57%) and 14 (67%) studies for complementary replicability indicators. Consistent with these results, the estimated true-positive rate is 67% in a Bayesian analysis. The relative effect size of true positives is estimated to be 71%, suggesting that both false positives and inflated effect sizes of true positives contribute to imperfect reproducibility. Furthermore, we find that peer beliefs of replicability are strongly related to replicability, suggesting that the research community could predict which results would replicate and that failures to replicate were not the result of chance alone.
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              Die „Autistischen Psychopathen” im Kindesalter

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                Author and article information

                Journal
                9607835
                Mol Psychiatry
                Mol. Psychiatry
                Molecular psychiatry
                1359-4184
                1476-5578
                21 November 2018
                07 January 2019
                October 2019
                21 September 2019
                : 24
                : 10
                : 1435-1450
                Affiliations
                [1 ]Department of Psychology, University of Cyprus, Nicosia, Cyprus
                [2 ]Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom
                [3 ]Centre for Addiction and Mental Health and The Hospital for Sick Children, Department of Psychiatry, University of Toronto, Toronto, Canada
                [4 ]Department of Psychiatry, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan
                [5 ]Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, United Kingdom
                Author notes
                Corresponding Author: Michael V. Lombardo, Department of Psychology, University of Cyprus, 1 Panepistimiou Avenue, 2109 Aglantzia, Nicosia, Cyprus, Telephone: +357 22 892243, mvlombardo@ 123456gmail.com .
                Article
                EMS80490
                10.1038/s41380-018-0321-0
                6754748
                30617272
                09a61c6d-a45e-4840-bad6-e312af2eab35

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                Molecular medicine
                Molecular medicine

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