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Françoise Le Deist

Françoise Le Deist

D-Index & Metrics

Immunology

D-Index
73
Citations
30482
World Ranking
2085
National Ranking
43

Overview

Françoise Le Deist is affiliated with the University of Montreal in Canada. They have contributed to academic research within their field, although specific details on recent papers, co-authors, publication venues, and book publications are not available.

The scope of their scholarly activities is characterized by the absence of specified main fields of study, subfields, and principal topics of work in the provided data. This limits the ability to pinpoint particular areas of specialization or research themes.

Their scholarly output does not list any recent papers with titles, years, or publication venues, which suggests that such data might not be publicly documented or submitted at this time. Similarly, no information is provided regarding frequent collaborators or co-authors.

There is no record of awards or honors associated with Françoise Le Deist in the shared information, and the scientist is currently living.

Best Publications

  • Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

    Marina Cavazzana-Calvo;Salima Hacein-Bey;Geneviève De Saint Basile;Fabian Gross

  • A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency

    Salima Hacein-Bey-Abina;Christof Von Kalle;Manfred Schmidt;Françoise Le Deist

  • Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

    Susan E. Stepp;Rémi Dufourcq-Lagelouse;Françoise Le Deist;Françoise Le Deist;Sadhna Bhawan

  • Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

    Salima Hacein-Bey-Abina;Françoise Le Deist;Frédérique Carlier;Cécile Bouneaud

  • Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

    Jérôme Feldmann;Isabelle Callebaut;Graça Raposo;Stéphanie Certain

  • Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency

    Despina Moshous;Isabelle Callebaut;Régina de Chasseval;Barbara Corneo

  • Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency

    Frédéric Altare;Anne Durandy;David Lammas;Jean-François Emile

  • X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.

    Rainer Döffinger;Asma Smahi;Christine Bessia;Frédéric Geissmann

  • Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly.

    Dietke Buck;Laurent Malivert;Régina de Chasseval;Anne Barraud

  • XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

    Stéphanie Rigaud;Marie-Claude Fondanèche;Nathalie Lambert;Nathalie Lambert;Benoit Pasquier

  • CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humans

    Sandra Weller;Ahmad Faili;Corinne Garcia;Moritz C. Braun

  • Eculizumab in severe Shiga-toxin-associated HUS.

    Anne-Laure Lapeyraque;Michal Malina;Véronique Fremeaux-Bacchi;Tobias Boppel

  • Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells.

    Marjorie Côte;Mickaël M. Ménager;Agathe Burgess;Nizar Mahlaoui

  • A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

    Gilles Courtois;Asma Smahi;Janine Reichenbach;Rainer Döffinger

  • Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients.

    Sophie Dupuis-Girod;Jacques Medioni;Elie Haddad;Pierre Quartier

  • 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;Jana Pachlopnik Schmid;Danielle Canioni;Despina Moshous;Despina Moshous;Fabien Touzot

  • Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patients.

    Pierre Quartier;Marianne Debré;Jacques De Blic;Rodolphe de Sauverzac

  • Autoimmune Lymphoproliferative Syndrome with Somatic Fas Mutations

    Eliska Holzelova;Cédric Vonarbourg;Marie Claude Stolzenberg;Peter D. Arkwright

  • WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.

    Karl Balabanian;Bernard Lagane;José Luis Pablos;Lysiane Laurent

  • Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency Medical and Immunological Implications

    Claire Fieschi;Stéphanie Dupuis;Emilie Catherinot;Jacqueline Feinberg

Frequent Co-Authors

Alain Fischer
Alain Fischer Collège de France
Marina Cavazzana-Calvo
Marina Cavazzana-Calvo Necker-Enfants Malades Hospital
Geneviève de Saint Basile
Geneviève de Saint Basile Necker-Enfants Malades Hospital
Jean-Laurent Casanova
Jean-Laurent Casanova The University of Texas Southwestern Medical Center
Stéphane Blanche
Stéphane Blanche Université Paris Cité
Jean-Pierre de Villartay
Jean-Pierre de Villartay Université Paris Cité
Claude Griscelli
Claude Griscelli Necker-Enfants Malades Hospital
Frédéric Rieux-Laucat
Frédéric Rieux-Laucat Université Paris Cité
Elie Haddad
Elie Haddad University of Montreal
Capucine Picard
Capucine Picard Université Paris Cité

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