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      Autism spectrum disorder and schizophrenia: An updated conceptual review

      1 , 2 , 3 , 1 , 2 , 4
      Autism Research
      Wiley

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          Most cited references189

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          Diagnostic and Statistical Manual of Mental Disorders

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            Executive Functions

            Executive functions (EFs) make possible mentally playing with ideas; taking the time to think before acting; meeting novel, unanticipated challenges; resisting temptations; and staying focused. Core EFs are inhibition [response inhibition (self-control—resisting temptations and resisting acting impulsively) and interference control (selective attention and cognitive inhibition)], working memory, and cognitive flexibility (including creatively thinking “outside the box,” seeing anything from different perspectives, and quickly and flexibly adapting to changed circumstances). The developmental progression and representative measures of each are discussed. Controversies are addressed (e.g., the relation between EFs and fluid intelligence, self-regulation, executive attention, and effortful control, and the relation between working memory and inhibition and attention). The importance of social, emotional, and physical health for cognitive health is discussed because stress, lack of sleep, loneliness, or lack of exercise each impair EFs. That EFs are trainable and can be improved with practice is addressed, including diverse methods tried thus far.
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              Biological Insights From 108 Schizophrenia-Associated Genetic Loci

              Summary Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be detected by genome-wide association studies. Here, we report a multi-stage schizophrenia genome-wide association study of up to 36,989 cases and 113,075 controls. We identify 128 independent associations spanning 108 conservatively defined loci that meet genome-wide significance, 83 of which have not been previously reported. Associations were enriched among genes expressed in brain providing biological plausibility for the findings. Many findings have the potential to provide entirely novel insights into aetiology, but associations at DRD2 and multiple genes involved in glutamatergic neurotransmission highlight molecules of known and potential therapeutic relevance to schizophrenia, and are consistent with leading pathophysiological hypotheses. Independent of genes expressed in brain, associations were enriched among genes expressed in tissues that play important roles in immunity, providing support for the hypothesized link between the immune system and schizophrenia.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Autism Research
                Autism Research
                Wiley
                1939-3792
                1939-3806
                March 2022
                December 29 2021
                March 2022
                : 15
                : 3
                : 384-412
                Affiliations
                [1 ]Department of Psychiatry, Division of Child and Adolescent Psychiatry Columbia University Vagelos College of Physicians and Surgeons New York New York USA
                [2 ]Department of Psychiatry, Division of Child and Adolescent Psychiatry New York State Psychiatric Institute New York New York USA
                [3 ]Seaver Autism Center for Research and Treatment Icahn School of Medicine at Mount Sinai, Department of Psychiatry New York New York USA
                [4 ]Center for Autism and the Developing Brain New York‐Presbyterian Westchester Behavioral Health Center White Plains New York USA
                Article
                10.1002/aur.2659
                34967130
                2e66281c-53fc-4eac-bb96-2f132a57280e
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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