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    What is the genetic basis for autism spectrum disorder?

    Do common and rare genetic variations increase the risk of autism?

    Which genes are involved in ASD and schizophrenia?

    What causes autism spectrum disorder (ASD)?

  2. Autism Spectrum Disorder Clinical Exome Sequencing Detects Disease-Causing Glitches References: Synaptic, transcriptional and chromatin genes disrupted in autism.

  3. Abstract. Autism spectrum disorder (ASD) is a highly prevalent and complex genetic disorder. The complex genetic make-up of ASD has been extensively studied and both common and rare genetic variants in up to 1000 genes have been linked to increased ASD risk. While these studies highlight the genetic complexity and begin to provide a window for delineating pathways at risk in ASD, the pathogenicity and specific contribution of many mutations to the disorder are poorly understood.

    • Fatma Ayhan, Genevieve Konopka
    • 2019
  4. Daniel H. Geschwind. Program in Neurogenetics, UCLA Department of Neurology, Center for Autism Research and Treatment, Semel Institute, and Departments of Psychiatry and Human Genetics, David Geffen School of Medicine at UCLA, 695 Charles E Young Drive South, Los Angeles, CA 90095-1761. Find articles by Daniel H. Geschwind.

    • Daniel H. Geschwind
    • 2011
  5. Mar 08, 2019 · For each category, we focus on one gene (CHD8, FOXP1, and RBFOX1) that is significantly linked to ASD and functionally characterized in recent years. Finally, we discuss genetic and transcriptomic overlap between ASD and other neurodevelopmental disorders.

    • Fatma Ayhan, Genevieve Konopka
    • 2019
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