Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)Patrick Revy, Anne Durandy, Masamichi Muramatsu et al.|Cell|2000Cited by 1.6k
The EUROclass trial: defining subgroups in common variable immunodeficiencyClaudia Wehr, Klaus Warnatz, Teemu Kivioja et al.|Blood|2007Cited by 860
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
ICOS Deficiency Is Associated with a Severe Reduction of CXCR5+CD4 Germinal Center Th CellsLukas Bossaller, Klaus Warnatz, Jan A. Burger et al.|The Journal of Immunology|2006Cited by 376
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsÀngela Deyà‐Martínez, Manfred Fliegauf, Nils Klammer et al.|Journal of Allergy and Clinical Immunology|2020Cited by 127