Jean‐Louis Stephan

Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly

Dietke Buck, Laurent Malivert, Régina de Chasseval et al. · Cell · 2006 · 697 citations · Full text

Primary Immunodeficiency, Is Mutated, Medicine +10

Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease

Françoise Bernaudin, Gèrard Socié, Mathieu Kuentz et al. · Blood · 2007 · 494 citations · Full text

Mutations in <i>STAT3</i> and <i>IL12RB1</i> impair the development of human IL-17–producing T cells

Ludovic de Beaucoudrey, Anne Puel, Orchidée Filipe‐Santos et al. · The Journal of Experimental Medicine · 2008 · 428 citations · Full text

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous et al. · Blood · 2010 · 364 citations · Full text

Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome

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