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Marie Ouachée-Chardin

Observed names: M Chardin-Ouachée, M Houachée-Chardin, M Ouachee, M Ouachée, M Ouachée-Chardin, M. Ouache-Chardin, M. Ouachee-Chardin, M. Ouachée, M. Ouachée-Chardin, M. Ouachée‐Chardin, Marie Ouachee, Marie Ouachee Chardin, Marie Ouachee-Chardin, Marie Ouachee‐Chardin, Marie Ouachée, Marie Ouachée-Chardin, Marie Ouachée, Marie Ouachée Chardin, Marie Ouachée-chardin, Marie Ouachée‐Chardin, Marie Ouchée‐Chardin, Marie ouachée-Chardin, O Marie, OUACHEE-CHARDIN, Marie, Ouachee-Chardin Marie, Ouachée-Chardin, Marie
Observed institutions: Lyon 1 Université, Hôpital Necker-Enfants Malades, Université Paris Cité, Institut Necker Enfants Malades, Hôpital Armand-Trousseau, Institut d’Hématologie et d’Oncologie Pédiatrique, Sorbonne Paris Cité, Assistance Publique – Hôpitaux de Paris, Centre Hospitalier Régional et Universitaire de Nancy, Hospices Civils de Lyon, Centre Léon Bérard, Association Robert Debré, Dana-Farber Cancer Institute, Centre Hospitalier Universitaire de Limoges, Hôpital Robert-Debré, Centre Hospitalier d'Arras, Wilhelmina Children's Hospital, Université Paris Diderot, Université Paris Descartes, Laboratoire d'hématologie
ORCID: 0000-0002-6773-8363
Observed ORCID: 0000-0002-6773-8363
OpenAlex ID: A5026579222
Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
2003 · Jérôme Feldmann, Isabelle Callebaut, et al. · Cell · 951
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Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
2010 · Anne Puel, Rainer Döffinger, et al. · The Journal of Experimental Medicine · 749
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Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
2016 · Julie Toubiana, Satoshi Okada, et al. · Blood · 610
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Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
2010 · Jana Pachlopnik Schmid, Danielle Canioni, et al. · Blood · 371
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Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies
2017 · Alain Fischer, Johan Provot, et al. · Journal of Allergy and Clinical Immunology · 335
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
2017 · Federica Barzaghi, Laura Cristina Amaya Hernandez, et al. · Journal of Allergy and Clinical Immunology · 327
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Hematopoietic Stem Cell Transplantation in Hemophagocytic Lymphohistiocytosis: A Single-Center Report of 48 Patients
2006 · Marie Ouachée-Chardin, Caroline Elie, et al. · PEDIATRICS · 278
Immunotherapy of Familial Hemophagocytic Lymphohistiocytosis With Antithymocyte Globulins: A Single-Center Retrospective Report of 38 Patients
2007 · Nizar Mahlaoui, Marie Ouachée-Chardin, et al. · PEDIATRICS · 254
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia
2012 · Marlène Pasquet, Christine Bellanné-Chantelot, et al. · Blood · 228
Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients
2018 · Jean Donadieu, Marie Lamant, et al. · Haematologica · 199
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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
2020 · Vivien Béziat, Simon J. Tavernier, et al. · The Journal of Experimental Medicine · 140
Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis
2002 · Jérôme Feldmann, Françoise Le Deist, et al. · British Journal of Haematology · 140
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Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome
2018 · Christine Bellanné-Chantelot, Barbara Schmaltz-Panneau, et al. · Blood · 136
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Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders
2017 · James Slack, Michael H. Albert, et al. · Journal of Allergy and Clinical Immunology · 114
Monitoring Cytomegalovirus Infection in Adult and Pediatric Bone Marrow Transplant Recipients by a Real-Time PCR Assay Performed with Blood Plasma
2003 · Marianne Leruez-Ville, Marie Ouachée, et al. · Journal of Clinical Microbiology · 114
Improved outcome of treatment-resistant high-risk Langerhans cell histiocytosis after allogeneic stem cell transplantation with reduced-intensity conditioning
2005 · M Steiner, S Matthes-Martin, et al. · Bone Marrow Transplantation · 105
Identification of human herpesvirus 6 variants A and B by primer-specific real-time PCR may help to revisit their respective role in pathology
2005 · David Boutolleau, Caroline Duros, et al. · Journal of Clinical Virology · 100
Hematopoietic stem cell transplantation in severe congenital neutropenia: experience of the French SCN register
2004 · C Ferry, M Ouachée, et al. · Bone Marrow Transplantation · 76
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PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects
2018 · Aurélie Berland, Jérémie Rosain, et al. · Journal of Allergy and Clinical Immunology · 74
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Adenovirus infection and disease in paediatric haematopoietic stem cell transplant patients: clues for antiviral pre-emptive treatment
2015 · L. Feghoul, S. Chevret, et al. · Clinical Microbiology and Infection · 73
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Inborn errors of immunity: Manifestation, treatment, and outcome—an ESID registry 1994–2024 report on 30,628 patients
2025 · Gerhard Kindle, Mickaël Alligon, et al. · Journal of Human Immunity · 57
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Strains Responsible for Invasive Meningococcal Disease in Patients With Terminal Complement Pathway Deficiencies
2017 · Jérémie Rosain, Eva Hong, et al. · The Journal of Infectious Diseases · 57
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Description of an adenovirus A31 outbreak in a paediatric haematology unit
2006 · M Leruez-Ville, M Chardin-Ouachée, et al. · Bone Marrow Transplantation · 56
Severe cardiac involvement in children with systemic sclerosis and myositis.
2002 · Pierre Quartier, Damien Bonnet, et al. · PubMed · 52
Human leucocyte antigen‐identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft‐versus‐host disease and pre‐existing viral infections
2006 · Raffaele Renella, Capucine Picard, et al. · British Journal of Haematology · 49
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Works count: 106
Citation count: 6,270
H-index: 30
I10-index: 46
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