Gaël Mouillot

Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect.

É. Oksenhendler, B. Bonnotte, J. Viallard, 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency.

J. Casanova, É. Oksenhendler, M. Conley, 2011, The Journal of allergy and clinical immunology.

Modulation of HLA-G Expression in Human Neural Cells after Neurotropic Viral Infections

N. Rouas-Freiss, P. Moreau, E. Carosella, 2005, Journal of Virology.

B-Cell and T-Cell Phenotypes in CVID Patients Correlate with the Clinical Phenotype of the Disease

É. Oksenhendler, P. Debré, M. Morisset, 2010, Journal of Clinical Immunology.

Autoimmunity in common variable immunodeficiency: correlation with lymphocyte phenotype in the French DEFI study.

É. Oksenhendler, A. Korganow, M. Carmagnat, 2011, Journal of autoimmunity.

HLA-G gene repression is reversed by demethylation

J. Dausset, P. Moreau, E. Carosella, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency

É. Oksenhendler, I. Durieu, F. T. P. Group, 2011, Journal of Clinical Immunology.