Research: Funded Publications
Explore publications and preprints from SFARI-funded investigators and researchers using SFARI-supported data and resources.
Results
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Concise review: Induced pluripotent stem cell models for neuropsychiatric diseases.
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The central amygdala controls learning in the lateral amygdala.
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Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
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Recurrent de novo mutations in neurodevelopmental disorders: Properties and clinical implications.
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Cellular phenotypes in human iPSC-derived neurons from a genetic model of autism spectrum disorder.
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De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability and autism.
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Incorporating social media into your support tool box: Points to consider from genetics-based communities.
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Associations between familial rates of psychiatric disorders and de novo genetic mutations in autism.
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Foxp1 in forebrain pyramidal neurons controls gene expression required for spatial learning and synaptic plasticity.
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Temporal control of mammalian cortical neurogenesis by m6A methylation.
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Decreased parvalbumin mRNA levels in cerebellar Purkinje cells in autism.
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Subcortical brain and behavior phenotypes differentiate infants with autism versus language delay.
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Cell biology of astrocyte-synapse interactions.
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
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Associations between family member BMI and obesity status of children with autism spectrum disorder.
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Indexcov: fast coverage quality control for whole-genome sequencing.
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Gene disrupting mutations associated with regression in autism spectrum disorder.
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Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of autism spectrum disorder
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Critical region within 22q11.2 linked to higher rate of autism spectrum disorder.
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Brainwide mapping of endogenous serotonergic transmission via chemogenetic-fMRI.
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Genomic patterns of de novo mutation in simplex autism.
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Foxp1 regulation of neonatal vocalizations via cortical development.
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Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome.
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Native KCC2 interactome reveals PACSIN1 as a critical regulator of synaptic inhibition.
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Preference for novel faces in male infant monkeys predicts cerebrospinal fluid oxytocin concentrations later in life.
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Beyond excitation/inhibition imbalance in multidimensional models of neural circuit changes in brain disorders.
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The immune signaling adaptor LAT contributes to the neuroanatomical phenotype of 16p11.2 BP2-BP3 CNVs.
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Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.
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Autism spectrum disorder: Neuropathology and animal models.
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The knockout of Synapsin II in mice impairs social behavior and functional connectivity generating an ASD-like phenotype.
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Differences in neural correlates of speech perception in 3-month-olds at high and low risk for autism spectrum disorder.
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A profile of auditory-responsive neurons in the larval zebrafish brain.
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Gating of social reward by oxytocin in the ventral tegmental area.
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Maternal gut bacteria promote neurodevelopmental abnormalities in mouse offspring.
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Reversing behavioural abnormalities in mice exposed to maternal inflammation.
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EEG power at three months in infants at high familial risk for autism.
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Microglia emerge as central players in brain disease.
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Exonic mosaic mutations contribute risk for autism spectrum disorder.
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Feasibility of conducting autism biomarker research in the clinical setting.
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Neural correlates of sensory hyporesponsiveness in toddlers at high risk for autism spectrum disorder.
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NKCC1 chloride importer antagonists attenuate many neurological and psychiatric disorders.
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Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.
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Placebo-like response in absence of treatment in children with autism.
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The spatiotemporal organization of the striatum encodes action space.
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Functional significance of rare neuroligin 1 variants found in autism.
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High resolution measurement of DUF1220 domain copy number from whole genome sequence data.
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Modulation of prefrontal cortex excitation/inhibition balance rescues social behavior in CNTNAP2-deficient mice.
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Increased extra-axial cerebrospinal fluid in high-risk infants who later develop autism.