Publications
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Using focal cooling to link neural dynamics and behavior
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Anterior thalamic dysfunction underlies cognitive deficits in a subset of neuropsychiatric disease models
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Preterm birth alters the development of cortical microstructure and morphology at term-equivalent age.
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An Improved and Physically Motivated Scheme for Matching Galaxies with Dark Matter Halos
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Dissecting autism and schizophrenia through neuroimaging genomics.
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Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies.
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Cardiovascular brain impulses in Alzheimer's disease
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Joint encoding of facial identity, orientation, gaze, and expression in the middle dorsal face area
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A Solar System formation analogue in the Ophiuchus star-forming complex
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Phase Retrieval with Holography and Untrained Priors: Tackling the Challenges of Low-Photon Nanoscale Imaging
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A characteristic optical variability time scale in astrophysical accretion disks
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Lévy Walks and Path Chaos in the Dispersal of Elongated Structures Moving across Cellular Vortical Flows
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Locally ordered representation of 3D space in the entorhinal cortex
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Motor training improves coordination and anxiety in symptomatic MECP2-null mice despite impaired functional connectivity within the motor circuit.
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A Deep-learning Approach for Live Anomaly Detection of Extragalactic Transients
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Charging up the periphery: Glial ionic regulation in sensory perception.
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Loss of Tsc1 from striatal direct pathway neurons impairs endocannabinoid-LTD and enhances motor routine learning.
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Improving the measurement of alexithymia in autistic adults: A psychometric investigation of the 20-item Toronto Alexithymia Scale and generation of a general alexithymia factor score using item response theory.
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Population calcium responses of Purkinje cells in the oculomotor cerebellum driven by non-visual input
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Targeted long-read sequencing identifies missing disease-causing variation.
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Active microphase separation in mixtures of microtubules and tip-accumulating molecular motors
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Autism spectrum disorder/intellectual disability-associated mutations in trio disrupt neuroligin 1-mediated synaptogenesis.
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"Guilt by association" is not competitive with genetic association for identifying autism risk genes.
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The role of the Cer1 transposon in horizontal transfer of transgenerational memory
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Application of ensemble pharmacophore-based virtual screening to the discovery of novel antimitotic tubulin inhibitors
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A multiscale biophysical model gives quantized metachronal waves in a lattice of cilia
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Age-dating Red Giant Stars Associated with Galactic Disk and Halo Substructures
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Age-dating Red Giant Stars Associated with Galactic Disk and Halo Substructures
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Multi-omic profiling of primary mouse neutrophils predicts a pattern of sex and age-related functional regulation
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Predictive encoding of motion begins in the primate retina
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A database and deep learning toolbox for noise-optimized, generalized spike inference from calcium imaging
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Decoding disease: from genomes to networks to phenotypes
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Paradoxical hyperexcitability from NAV1.2 sodium channel loss in neocortical pyramidal cells.
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Scn2a severe hypomorphic mutation decreases excitatory synaptic input and causes autism-associated behaviors
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Improving MP2 bandgaps with low-scaling approximations to EOM-CCSD
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Interplay between breathing-mode distortions and magnetic order in rare-earth nickelates from ab initio magnetic models
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Hartree-Fock study of the moiré Hubbard model for twisted bilayer transition metal dichalcogenides
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Machine learning band gaps from the electron density
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COP-E-CAT: Cleaning and Organization Pipeline for EHR Computational and Analytic Tasks
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Neurodevelopmental phenotypes in individuals with pathogenic variants in CHAMP1.
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Availability of services and caregiver burden: Supporting individuals with neurogenetic conditions during the COVID-19 pandemic.
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Computational methods to measure patterns of gaze in toddlers with autism spectrum disorder.
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Associations between social camouflaging and internalizing symptoms in autistic and non-autistic adolescents.
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Differential effects by sex with Kmt5b loss.
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Towards a data driven approach to screen for autism risk at 12 months of age.
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Sensory coding and the causal impact of mouse cortex in a visual decision
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Dynamic and reversible remapping of network representations in an unchanging environment
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Recent ultra-rare inherited variants implicate new autism candidate risk genes.