Area of research
Genetics · Molecular Biology
Research interest
Research interests include Congenital heart defects research, Neurotransmitter Receptor Influence on Behavior, Genomic variations and chromosomal abnormalities, and Autism Spectrum Disorder Research.
Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
A normative chart for cognitive development in a genetically selected population
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Fragile X Syndrome
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome
Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study
Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome
PEMapper and PECaller provide a simplified approach to whole-genome sequencing
An epigenetic clock for gestational age at birth based on blood methylation data
Cross-Disorder Comparison of Four Neuropsychiatric CNV Loci
The Gut Microbiome: A New Frontier in Autism Research
Alcohol and alcohol-related harm in China: policy changes needed
Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms
Randomized clinical trial of disulfiram for cocaine dependence or abuse during buprenorphine treatment
Predictors of remission in depression to individual and combined treatments (PReDICT): study protocol for a randomized controlled trial
DNA methylation in neonates born to women receiving psychiatric care
Depression and anxiety symptoms among women who carry the <i>FMR1</i> premutation: Impact of raising a child with fragile X syndrome is moderated by <i>CRHR1</i> polymorphisms
Pharmacogenetic Association of the Galanin Receptor (GALR1) SNP rs2717162 with Smoking Cessation