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Best Female Scientists
2025
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Immunology
France
2026

D-Index & Metrics

Best Female Scientists

D-Index
124
Citations
52508
World Ranking
462
National Ranking
21

Immunology

D-Index
127
Citations
56180
World Ranking
263
National Ranking
6

Medicine

D-Index
127
Citations
56209
World Ranking
2841
National Ranking
72

Research.com Recognitions

  • 2026 - Research.com Immunology in France Leader Award
  • 2025 - Research.com Best Female Scientists Award
  • 2025 - Research.com Immunology in France Leader Award
  • 2023 - Research.com Immunology in France Leader Award
  • 2023 - Research.com Medicine in France Leader Award
  • 2022 - Research.com Immunology in France Leader Award

Overview

Capucine Picard is affiliated with Université Paris Cité in France and has contributed extensively to the fields of Medicine, Immunology and Microbiology, and Biochemistry, Genetics and Molecular Biology. Their research predominantly focuses on Immunology, Genetics, Epidemiology, Molecular Biology, and Oncology.

Their work covers several key topics including Immunodeficiency and Autoimmune Disorders, Blood disorders and treatments, Immune Cell Function and Interaction, T-cell and B-cell Immunology, Cytomegalovirus and herpesvirus research, Chronic Lymphocytic Leukemia Research, and Viral-associated cancers and disorders.

Capucine Picard's recent publications include the following papers:

  • Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee, 2020, Journal of Clinical Immunology
  • Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee, 2022, Journal of Clinical Immunology
  • Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification, 2020, Journal of Clinical Immunology
  • The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity, 2022, Journal of Clinical Immunology
  • The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee, 2021, Journal of Clinical Immunology

Their frequent co-authors include Bénédicte Neven, Alain Fischer, Frédéric Rieux-Laucat, Despina Moshous, and Jean-Laurent Casanova.

Publication venues where Capucine Picard has frequently published are:

  • Journal of Clinical Immunology
  • Blood
  • The Journal of Experimental Medicine
  • Journal of Allergy and Clinical Immunology
  • Journal of Human Immunity

Capucine Picard's research contributions span crucial aspects of human immunology, focusing on the classification and phenotypic updates of inborn errors of immunity. Their publications have been disseminated mainly through journals specializing in clinical immunology and hematology, reflecting an emphasis on immune system functioning and disorders.

Best Publications

  • Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors.

    Jérôme Cros;Nicolas Cagnard;Kevin Woollard;Natacha Patey

  • TLR3 deficiency in patients with herpes simplex encephalitis.

    Shen Ying Zhang;Shen Ying Zhang;Emmanuelle Jouanguy;Emmanuelle Jouanguy;Sophie Ugolini;Asma Smahi

  • Pyogenic Bacterial Infections in Humans with MyD88 Deficiency

    Horst Von Bernuth;Capucine Picard;Capucine Picard;Zhongbo Jin;Rungnapa Pankla;Rungnapa Pankla

  • Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

    Stuart G. Tangye;Waleed Al-Herz;Aziz Bousfiha;Talal Chatila

  • Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity

    Anne Puel;Sophie Cypowyj;Jacinta Bustamante;Jill Wright

  • Herpes simplex virus encephalitis in human UNC-93B deficiency.

    Armanda Casrouge;Shen Ying Zhang;Shen Ying Zhang;Céline Eidenschenk;Emmanuelle Jouanguy;Emmanuelle Jouanguy

  • International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

    Capucine Picard;H. Bobby Gaspar;Waleed Al-Herz;Aziz Bousfiha

  • Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

    Luyan Liu;Satoshi Okada;Xiao Fei Kong;Alexandra Y. Kreins

  • Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

    Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova

  • Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency

    Salima Hacein-Bey-Abina;Julia Hauer;Annick Lim;Capucine Picard

  • Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

    Ivan Angulo;Oscar Vadas;Fabien Garçon;Edward Banham-Hall

  • Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I

    Anne Puel;Anne Puel;Rainer Döffinger;Angels Natividad;Angels Natividad;Maya Chrabieh;Maya Chrabieh

  • Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.

    Aziz Bousfiha;Leila Jeddane;Capucine Picard;Waleed Al-Herz

  • The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

    Markus G. Seidel;Gerhard Kindle;Benjamin Gathmann;Isabella Quinti

  • Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features.

    Orchidée Filipe-Santos;Jacinta Bustamante;Ariane Chapgier;Guillaume Vogt

  • The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.

    Aziz Bousfiha;Leïla Jeddane;Capucine Picard;Fatima Ailal

  • Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations

    Nadia Jeremiah;Bénédicte Neven;Matteo Gentili;Isabelle Callebaut

  • STIM1 Mutation Associated with a Syndrome of Immunodeficiency and Autoimmunity

    Capucine Picard;Christie Ann McCarl;Alexander Papolos;Sara Khalil

  • Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.

    Julie Toubiana;Satoshi Okada;Satoshi Okada;Julia Hiller;Matias Oleastro

  • Clinical features of dominant and recessive interferon γ receptor 1 deficiencies

    Susan E. Dorman;Capucine Picard;Capucine Picard;David Lammas;Klaus Heyne

  • Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells

    Ludovic de Beaucoudrey;Ludovic de Beaucoudrey;Anne Puel;Anne Puel;Orchidée Filipe-Santos;Orchidée Filipe-Santos;Aurélie Cobat;Aurélie Cobat

Frequent Co-Authors

Jean-Laurent Casanova
Jean-Laurent Casanova The University of Texas Southwestern Medical Center
Alain Fischer
Alain Fischer Collège de France
Laurent Abel
Laurent Abel Université Paris Cité
Bénédicte Neven
Bénédicte Neven Université Paris Cité
Jacinta Bustamante
Jacinta Bustamante Rockefeller University
Despina Moshous
Despina Moshous Necker-Enfants Malades Hospital
Stéphane Blanche
Stéphane Blanche Université Paris Cité
Frédéric Rieux-Laucat
Frédéric Rieux-Laucat Université Paris Cité
Stéphanie Boisson-Dupuis
Stéphanie Boisson-Dupuis Université Paris Cité

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Related Online Degrees & Career Pathways

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Exploring these educational pathways can provide a solid platform for a rewarding immunology career in the USA.

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