Publications by authors named "I Rabkina"

Article Synopsis
  • Genetic changes affecting a protein called HNRNPU are found in several brain disorders in kids.
  • HNRNPU is important for the brain's growth, especially in the part called the cerebellum, but we don’t know how it affects this area yet.
  • Researchers found that when HNRNPU is missing, it changes how brain cells develop, which might connect to issues like epilepsy, autism, and learning challenges.
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We argue that pretense can be viewed as analogical projection: a structural comparison between the pretend scenario and its real-world counterpart that leads to inferences about the pretend scenario. For example, in pretending to make a phone call with a banana, a number pad might be projected on the banana's surface. We model two empirical studies of early childhood pretense, and show how successful pretense requires making and accepting such inferences, while failed pretense can be traced to failure of such projection.

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Goal or intent recognition, where one agent recognizes the goals or intentions of another, can be a powerful tool for effective teamwork and improving interaction between agents. Such reasoning can be challenging to perform, however, because observations of an agent can be unreliable and, often, an agent does not have access to the reasoning processes and mental models of the other agent. Despite this difficulty, recent work has made great strides in addressing these challenges.

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CASK-related disorders are genetically defined neurodevelopmental syndromes. There is limited information about the effects of CASK mutations in human neurons. Therefore, we sought to delineate CASK-mutation consequences and neuronal effects using induced pluripotent stem cell-derived neurons from two mutation carriers.

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Challenges in social communication and interaction are core features of autism spectrum disorder (ASD) for which social skills group training (SSGT) is a commonly used intervention. SSGT has shown modest and heterogeneous effects. One of the major genetic risk factors in ASD is rare copy number variation (CNV).

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