Mutations in Fas Associated with Human Lymphoproliferative Syndrome and AutoimmunityFrédéric Rieux‐Laucat, Jean‐Pierre de Villartay, Françoise Le Deist et al.|Science|1995Cited by 1.3k
Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene TherapySalima Hacein‐Bey‐Abina, Marina Cavazzana, N. M. Wulffraat et al.|New England Journal of Medicine|2002Cited by 1.1k
Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune DeficiencyDespina Moshous, Jean‐Pierre de Villartay, Isabelle Callebaut et al.|Cell|2001Cited by 901
Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with MicrocephalyDietke Buck, Patrick Revy, Laurent Malivert et al.|Cell|2006Cited by 702
Reduced recruitment of 53BP1 during interstrand crosslink repair is associated with genetically inherited attenuation of mitomycin C sensitivity in a family with Fanconi anemiaEmilie Lesport, Jean‐Pierre de Villartay|Oncotarget|2017Cited by 4