Research: Funded Publications
Explore publications and preprints from SFARI-funded investigators and researchers using SFARI-supported data and resources.
Results
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FGF acts as a co-transmitter through adenosine A(2A) receptor to regulate synaptic plasticity.
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A translational profiling approach for the molecular characterization of CNS cell types.
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Application of a translational profiling approach for the comparative analysis of CNS cell types.
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Understanding synapses: past, present, and future.
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Autism and brain development.
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Neuroligins and neurexins link synaptic function to cognitive disease.
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Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.
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Deletion of MeCP2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.
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Cell type-specific regulation of DARPP-32 phosphorylation by psychostimulant and antipsychotic drugs.
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Distinct face-processing strategies in parents of autistic children.
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Identifying autism loci and genes by tracing recent shared ancestry.
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Gene expression patterns in visual cortex during the critical period: Synaptic stabilization and reversal by visual deprivation.
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Tuned responses of astrocytes and their influence on hemodynamic signals in the visual cortex.
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MeCP2, a key contributor to neurological disease, activates and represses transcription.
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Unusually rapid evolution of neuroligin-4 in mice.
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CASK functions as a Mg2+-independent neurexin kinase.
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Role for metabotropic glutamate receptor 5 ( mGluR5 ) in the pathogenesis of fragile X syndrome.
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Association between microdeletion and microduplication at 16p11.2 and autism.
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Evidence for a role of the 5-HT1B receptor and its adaptor protein, p11, in L -DOPA treatment of an animal model of Parkinsonism.
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Fragile X: translation in action.
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Correction of fragile X syndrome in mice.
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Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions.
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A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
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Ten_m3 regulates eye-specific patterning in the mammalian visual pathway and is required for binocular vision.
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A unified genetic theory for sporadic and inherited autism.
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Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice.
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Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III.
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Strong association of de novo copy number mutations with autism.
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Phosphodiesterase 1B differentially modulates the effects of methamphetamine on locomotor activity and spatial learning through DARPP32-dependent pathways: evidence from PDE1B-DARPP32 double-knockout mice.
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Brain evolution and uniqueness in the human genome.
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Cocaine-induced dendritic spine formation in D1 and D2 dopamine receptor-containing medium spiny neurons in nucleus accumbens.