Françoise Le Deist - Concepedia

Author

Françoise Le Deist

Also Known As

F Le Deist, F. L. Deist, F. Le Deist, FRANCOISE LE DEIST, FRANÇOISE LE DEIST, Francoise Le Deist, Francoise le Deist, Françoise Le Deist, Françoise le Deist, Françoise Deist

284

Publications

34.7K

Citations

H-Index

161

Concepts

All Affiliations

Inserm Hôpital Necker-Enfants Malades Institut Necker Enfants Malades Centre Hospitalier Universitaire Sainte-Justine Université de Montréal

About

Françoise Le Deist is an author at Inserm specializing in medicine, immunology, and autoimmunity.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	80	19.4K
2	Allergy	7	7	753
3	Public Health	4	4	282
4	Natural Sciences	3	3	254
5	Health Sciences	1	1	15

Françoise Le Deist

174

Publications

30.6K

Citations

H-Index

Page 1

	Year	Citations
<i>LMO2</i> -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1 S. Hacein-Bey-Abina, Christof von Kalle, Manfred Schmidt, Science Primary ImmunodeficiencyHuman RetrovirusT-regulatory CellImmunologyPathology	2003	3.5K
Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease Marina Cavazzana, Salima Hacein‐Bey, Geneviève de Saint Basile, Science Adaptive Immune SystemImmunodeficienciesImmunologyImmune RegulationPathology	2000	2.6K
Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity Frédéric Rieux‐Laucat, Françoise Le Deist, Claire Hivroz, Science GeneticsApoptosisImmunologyPathologyCell Death	1995	1.3K
Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis Susan E. Stepp, Rémi Dufourcq-Lagelouse, Françoise Le Deist, Science	1999	1.2K
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome Gaël Ménasché, Élodie Pastural, Jérôme Feldmann, Nature Genetics Mendelian DisorderAutoimmune DiseaseDisease MechanismGenetic DisorderGenetics	2000	940
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, Cell Is MutatedLymphoid NeoplasiaHematological MalignancyGranulocyteMedicine	2003	916
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, Cell Primary ImmunodeficiencyIs MutatedGenome InstabilityImmunogeneticsAutoimmune Disease	2001	893
Impairment of Mycobacterial Immunity in Human Interleukin-12 Receptor Deficiency Frédéric Altare, Anne Durandy, David A. Lammas, Science InflammationInterferon GammaAutoimmune DiseaseMycobacterial ImmunityImmunodeficiencies	1998	840
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling Rainer Döffinger, Asma Smahi, Christine Bessia, Nature Genetics Primary ImmunodeficiencyPathogenesisImmunologyPathologyImpaired Nf-κb Signaling	2001	817
Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly Dietke Buck, Laurent Malivert, Régina de Chasseval, Cell Primary ImmunodeficiencyIs MutatedMedicineImmunodeficienciesImmunology	2006	697

Page 1