Area of research
Genetics · Plant Science
Research interest
Research focused on Haploinsufficiency and Genetics, with related work in Inheritance (genetic algorithm), Creatine, Fibroblast growth factor. Notable publications include 'Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome', 'Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway', and 'Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic Autism'.