Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

Cited by (556)

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  19. Rows=Wildlife Corridors: An Urban Resource.
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  26. Genetic Confusion
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  27. References
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  28. Preface
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  29. Social Behavior
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  30. Health, Social Behavior, and Implications
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  31. Faculty Opinions recommendation of Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
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  33. Index
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  36. Notes
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  37. Faculty Opinions recommendation of Inherited and de novo genetic risk for autism impacts shared networks.
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  38. Introduction
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  39. Faculty Opinions recommendation of Inherited and de novo genetic risk for autism impacts shared networks.
    R. Frank Kooy · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
  40. Afterword
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  41. Transtorno do Espectro do Autismo: Um estudo epidemiológico no Norte de Minas Gerais
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  50. Genes and their Involvement in the Pathogenesis of Autism Spectrum Disorder: Insights from Earlier Genetic Studies
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  51. Dedication
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  52. Copyright Page
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  57. Additional file 3 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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  58. Additional file 4 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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  59. Additional file 1 of Pharmacotherapy of restricted/repetitive behavior in autism spectrum disorder:a systematic review and meta-analysis
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  60. Additional file 2 of Pharmacotherapy of restricted/repetitive behavior in autism spectrum disorder:a systematic review and meta-analysis
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  61. Additional file 2 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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  63. Additional file 1 of Maternal age, autistic-like traits and mentalizing as predictors of child autistic-like traits in a population-based cohort
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  64. Additional file 1 of Association between rare, genetic variants linked to autism and ultrasonography fetal anomalies in children with autism spectrum disorder
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  77. CYFIP1 overexpression amplifies IL-6/STAT3 and IFN-γ/STAT1 signaling: potential implications for neuroinflammation and autism spectrum disorder
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