Area of research
Genetics · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Biology, Genetics, Autism, Autism spectrum disorder, Copy-number variation, and Gene.
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes
Phenotypic spectrum associated with <i><scp>PTCHD1</scp></i> deletions and truncating mutations includes intellectual disability and autism spectrum disorder
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes