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Medicine

D-Index
76
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20156
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18820
National Ranking
629

Overview

Lionel Galicier is affiliated with the Université Paris Cité in France, contributing extensively to the field of Medicine with a focus on hematology and related disciplines. Their body of work spans over 200 publications, emphasizing several subfields including Hematology, Immunology, Oncology, Genetics, and Epidemiology.

The scientist's research topics include:

  • Platelet Disorders and Treatments
  • Viral-associated cancers and disorders
  • Complement system in diseases
  • Cytomegalovirus and herpesvirus research
  • Blood groups and transfusion
  • Immunodeficiency and Autoimmune Disorders
  • Parvovirus B19 Infection Studies

Among Lionel Galicier's notable recent papers are:

  • "Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter study" (2022) published in Blood
  • "A regimen with caplacizumab, immunosuppression, and plasma exchange prevents unfavorable outcomes in immune-mediated TTP" (2020) published in Blood
  • "Clinical characteristics, management and outcome of COVID-19-associated immune thrombocytopenia: a French multicentre series" (2020) published in British Journal of Haematology
  • "Complement C5 inhibition in patients with COVID-19 - a promising target?" (2020) published in Haematologica
  • "Management of HIV-infected patients in the intensive care unit" (2020) published in Intensive Care Medicine

Frequent coauthors collaborating with Lionel Galicier include:

  • David Boutboul
  • Éric Oksenhendler
  • Marion Malphettes
  • Paul Coppo
  • Élie Azoulay

The scientist has published prominently in several journals and venues, notably:

  • Blood (13 publications)
  • La Revue de Médecine Interne (13 publications)
  • British Journal of Haematology (7 publications)
  • Blood Advances (6 publications)
  • American Journal of Hematology (5 publications)

Lionel Galicier's accumulated work largely concentrates on clinical and translational research at the intersection of immune regulation, blood disorders, and infectious complications. They have contributed to understanding therapeutic strategies in complex hematological conditions including thrombocytopenia, immune-mediated thrombotic microangiopathies, and the role of complement inhibition in disease processes.

Best Publications

  • Development and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndrome.

    Laurence Fardet;Lionel Galicier;Olivier Lambotte;Christophe Marzac

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

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

  • Infections in 252 patients with common variable immunodeficiency.

    Eric Oksenhendler;Laurence Gérard;Claire Fieschi;Marion Malphettes

  • High incidence of Kaposi sarcoma-associated herpesvirus-related non-Hodgkin lymphoma in patients with HIV infection and multicentric Castleman disease.

    Eric Oksenhendler;Emmanuelle Boulanger;Lionel Galicier;Ming-Qing Du

  • Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects.

    B. Piqueras;C. Lavenu-Bombled;L. Galicier;F.Bergeron-Van Der Cruyssen

  • 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

  • Predictive Features of Severe Acquired ADAMTS13 Deficiency in Idiopathic Thrombotic Microangiopathies: The French TMA Reference Center Experience

    Paul Coppo;Michael Schwarzinger;Marc Buffet;Alain Wynckel

  • Reactive Hemophagocytic Syndrome in Adults: A Retrospective Analysis of 162 Patients

    Sébastien Rivière;Lionel Galicier;Paul Coppo;Christophe Marzac

  • Rituximab efficacy and safety in adult splenectomy candidates with chronic immune thrombocytopenic purpura: results of a prospective multicenter phase 2 study

    Bertrand Godeau;Raphael Porcher;Olivier Fain;François Lefrère

  • Efficacy and safety of first-line rituximab in severe, acquired thrombotic thrombocytopenic purpura with a suboptimal response to plasma exchange. Experience of the French Thrombotic Microangiopathies Reference Center

    Antoine Froissart;Marc Buffet;Agnès Veyradier;Pascale Poullin

  • Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy

    Eric Mariotte;Elie Azoulay;Lionel Galicier;Eric Rondeau

  • Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study

    Elodie Elkaim;Elodie Elkaim;Benedicte Neven;Benedicte Neven;Benedicte Neven;Julie Bruneau;Julie Bruneau;Kanako Mitsui-Sekinaka

  • Microbial ecology perturbation in human IgA deficiency

    Jehane Fadlallah;Hela El Kafsi;Delphine Sterlin;Catherine Juste

  • Prospective study of rituximab in chemotherapy-dependent human immunodeficiency virus associated multicentric Castleman's disease: ANRS 117 CastlemaB Trial.

    Laurence Gérard;Alice Bérezné;Lionel Galicier;Véronique Meignin

  • Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura.

    Marie Moatti-Cohen;Céline Garrec;Martine Wolf;Pierre Boisseau

  • Effect of anakinra versus usual care in adults in hospital with COVID-19 and mild-to-moderate pneumonia (CORIMUNO-ANA-1): a randomised controlled trial

    Pierre-Louis Tharaux;Gilles Pialoux;Arthur Pavot;Xavier Mariette

  • Severe ADAMTS13 Deficiency in Adult Idiopathic Thrombotic Microangiopathies Defines a Subset of Patients Characterized by Various Autoimmune Manifestations, Lower Platelet Count, and Mild Renal Involvement

    Paul Coppo;Djaouida Bengoufa;Agnès Veyradier;Martine Wolf

  • Autoimmune thrombocytopenic purpura and common variable immunodeficiency: analysis of 21 cases and review of the literature.

    Marc Michel;Valérie Chanet;Lionel Galicier;Marc Ruivard

  • Understanding organ dysfunction in hemophagocytic lymphohistiocytosis.

    Caroline Créput;Lionel Galicier;Sophie Buyse;Elie Azoulay

  • Intensive care in patients with newly diagnosed malignancies and a need for cancer chemotherapy.

    Michael Darmon;Guillaume Thiery;Magali Ciroldi;Sandra de Miranda

Frequent Co-Authors

Eric Oksenhendler
Eric Oksenhendler Université Paris Cité
Elie Azoulay
Elie Azoulay Université Paris Cité
Claire Fieschi
Claire Fieschi Université Paris Cité
Olivier Fain
Olivier Fain Université Paris Cité
Olivier Lambotte
Olivier Lambotte University of Paris-Saclay
Michael Darmon
Michael Darmon Université Paris Cité
Olivier Hermine
Olivier Hermine Necker-Enfants Malades Hospital
Capucine Picard
Capucine Picard Université Paris Cité
Alain Fischer
Alain Fischer Collège de France
Zahir Amoura
Zahir Amoura Université Paris Cité

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