Harmonization of whole genome sequencing data for gene-environment interaction ana...
Identification of copy number variations (CNVs) in a cohort of children and adoles...
Characterization of INDELs and small CNVs in patients with autism spectrum disorder
Impact of genetic variants on genomic stability and their effects on the phenotype
Systematic approach and diagnosis of 46, XY differences of sex development: molecu...
CNVs/InDels analysis based on exome data in the etiology of ASD