Area of research
Genetics · Cognitive Neuroscience
Research interest
Research interests include Autism Spectrum Disorder Research, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, and Genetic Associations and Epidemiology.
“I Know It’s Very Spectrum-y”: Autistic Women Reflect on Sensory Aspects of Food and Eating
The contributions of rare inherited and polygenic risk to ASD in multiplex families
The contributions of rare inherited and polygenic risk to ASD in multiplex families.
Prospects for Leveling the Playing Field for Black Children With Autism
A neurogenetic analysis of female autism
Timing of the Diagnosis of Autism in African American Children
Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity
Neural responsivity to social rewards in autistic female youth
A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases
Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
A Quantitative Framework to Evaluate Modeling of Cortical Development by Neural Stem Cells
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15<scp>q</scp>11.2, Specifically Breakpoints 1 to 2
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
Orchestration of Neurodevelopmental Programs by RBFOX1
Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait
Common genetic variants, acting additively, are a major source of risk for autism
Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders
Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts