Cecilia Mancini is an experienced researcher with a background in molecular biology and more than 10 years of experience in medical genetics and functional genomics. She received her academic training at the University of Turin, where she earned a PhD in Human Genetics, developing expertise in the molecular mechanisms underlying neurogenetic disorders. Her current research focuses on genomic and gene expression analysis in rare diseases. She has extensive experience with next-generation sequencing and high-throughput approaches, enabling comprehensive characterization of genetic variation.