Monique Forveille

Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)

Patrick Revy, Taro Muto, Yves Lévy et al. · Cell · 2000 · 1.6K citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +8

Human uracil–DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

Kohsuke Imai, Geir Slupphaug, Wen-I Lee et al. · Nature Immunology · 2003 · 621 citations

Glycoproteomics, Immunogenetics, Genome Instability +10

Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome

Marie‐Olivia Chandesris, Isabelle Melki, Angels Natividad et al. · Medicine · 2012 · 323 citations · Full text

Undetectable CD40 ligand expression on T cells and low B cell responses to CD40 binding agonists in human newborns.

Anne Durandy, Geneviève de Saint Basile, Barbara Lisowska‐Grospierre et al. · The Journal of Immunology · 1995 · 155 citations · Full text

Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination

Kohsuke Imai, Nadia Catalan, Alessandro Plebani et al. · Journal of Clinical Investigation · 2003 · 127 citations · Full text

Histocompatibility, Genetics, Immunodeficiencies +16