Area of research
Pediatrics, Perinatology and Child Health · Genetics
Research interest
Research interests include Fetal and Pediatric Neurological Disorders, Genomic variations and chromosomal abnormalities, Functional Brain Connectivity Studies, and Advanced Neuroimaging Techniques and Applications.
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study
The Contribution of the Corpus Callosum to Language Lateralization
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications
White Matter Changes of Neurite Density and Fiber Orientation Dispersion during Human Brain Maturation
Aberrant White Matter Microstructure in Children with 16p11.2 Deletions
Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria
Deletion 16p13.11 uncovers <i>NDE1</i> mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption
Test–Retest Reliability of Computational Network Measurements Derived from the Structural Connectome of the Human Brain
Resting-State Networks and the Functional Connectome of the Human Brain in Agenesis of the Corpus Callosum
The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing
Dual-Mode Modulation of Smad Signaling by Smad-Interacting Protein Sip1 Is Required for Myelination in the Central Nervous System
Autism Traits in Individuals with Agenesis of the Corpus Callosum