Publications
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FOXP1 orchestrates neurogenesis in human cortical basal radial glial cells.
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Normative framework for deriving neural networks with multi-compartmental neurons and non-Hebbian plasticity
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Distinct roles of putative excitatory and inhibitory neurons in the macaque inferior temporal cortex in core object recognition behavior.
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A fast time domain solver for the equilibrium Dyson equation
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Spin-Flip Unitary Coupled Cluster Method: Toward Accurate Description of Strong Electron Correlation on Quantum Computers
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Simple extension of the plane-wave final state in photoemission: Bringing understanding to the photon-energy dependence of two-dimensional materials
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Time-dependent ghost Gutzwiller nonequilibrium dynamics
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Enhancement of charge density wave correlations in a Holstein model with an anharmonic phonon potential
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Low-Scaling Algorithm for the Random Phase Approximation Using Tensor Hypercontraction with k-point Sampling
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Chiral model of twisted bilayer graphene realized in a monolayer
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Pressure-enhanced fractional Chern insulators along a magic line in moiré transition metal dichalcogenides
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Topological superconductivity in doped magnetic moirè semiconductors
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Conformational heterogeneity and probability distributions from single-particle cryo-electron microscopy
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The contributions of rare inherited and polygenic risk to ASD in multiplex families.
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Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.
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Conformational heterogeneity and probability distributions from single-particle cryo-electron microscopy
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The Autism Symptom Dimensions Questionnaire: Development and psychometric evaluation of a new, open-source measure of autism symptomatology.
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On Single Index Models beyond Gaussian Data
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Generative modeling via tensor train sketching
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Large-scale whole genome sequence analysis of 22,000 subjects provides no evidence of FMR1 premutation allele involvement in autism spectrum disorder.
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VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants.
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Mapping disease regulatory circuits at cell-type resolution from single-cell multiomics data
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Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice.
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A Model-Based Method for Minimizing CVaR and Beyond
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SGD with Large Step Sizes Learns Sparse Features
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BridgeStan: Efficient in-memory access to the methods of a Stan model
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Maintaining symmetry during body axis elongation
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Rhesus macaque social functioning is paternally, but not maternally, inherited by sons: Potential implications for autism.
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Unlocking the Potential of Similarity Matching: Scalability, Supervision and Pre-training
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Kernelized Diffusion Maps
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Reprogramming method does not impact the neuronal differentiation potential of 16p11.2 deletion patient iPSCs.
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A note about convected time derivatives for flows of complex fluids
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ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.
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A mixed methods study of autistic adults' mental health therapy experiences.
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Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.
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Many-body delocalization from embedded thermal inclusion
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Nonequilibrium correlation dynamics in the one-dimensional Fermi-Hubbard model: A testbed for the two-particle reduced density matrix theory
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Spin-valley magnetism on the triangular moiré lattice with SU(4) breaking interactions
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A qualitative exploration of autistic mothers' experiences I: Pregnancy experiences.
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Are autistic people disadvantaged by the criminal justice system? A case comparison.
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Phenotypically driven subgroups of ASD display distinct metabolomic profiles.
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Relationship between childhood obesity and autism spectrum disorder varies by child's age and parents' weight status in a sample of sibling dyads.
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Autistic people's perinatal experiences II: A survey of childbirth and postnatal experiences.
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Validity of the SNAP-IV for ADHD assessment in South African children with neurodevelopmental disorders.
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Autism spectrum disorders and brain volume link through a set of mTOR-related genes.
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Multi-omic analysis along the gut-brain axis points to a functional architecture of autism.
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Phenotypic effects of genetic variants associated with autism.
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Developmental molecular controls over arealization of descending cortical motor pathways.