Area of research
Genetics · Cognitive Neuroscience
Research interest
Research interests include Autism Spectrum Disorder Research, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, and Genomics and Rare Diseases.
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience
A convergent molecular network underlying autism and congenital heart disease
Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families
Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome
Human 3D cellular model of hypoxic brain injury of prematurity
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Comparative Flavivirus-Host Protein Interaction Mapping Reveals Mechanisms of Dengue and Zika Virus Pathogenesis
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
Whole genome sequencing in psychiatric disorders: the WGSPD consortium
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
Localized JNK signaling regulates organ size during development
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus
No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins
Synaptic, transcriptional and chromatin genes disrupted in autism
The contribution of de novo coding mutations to autism spectrum disorder
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder
Autism spectrum disorders: from genes to neurobiology
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics