Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluationOlivier Quenez, Gaël Nicolas, Anne‐Claire Richard et al.|European Journal of Human Genetics|2020Cited by 45
Deciphering dual clinical entities associated with <scp><i>TP53</i></scp> pathogenic variants: Insights from 53,085 <scp>HBOC</scp> panel analyses in French laboratoriesEdwige Kasper, Claude Houdayer, Flavie Boulouard et al.|International Journal of Cancer|2025Cited by 4
Detection of copy number variations from NGS data using read depth information: a diagnostic performance evaluationOlivier Quenez, Gaël Nicolas, Kévin Cassinari et al.|Unknown|2019Cited by 0