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Stéphanie Boisson-Dupuis

Stéphanie Boisson-Dupuis

D-Index & Metrics

Immunology

D-Index
77
Citations
24805
World Ranking
1805
National Ranking
67

Medicine

D-Index
77
Citations
24806
World Ranking
18342
National Ranking
607

Overview

Stéphanie Boisson-Dupuis is affiliated with Université Paris Cité in France. Their research spans across multiple intersecting fields including immunology, microbiology, medicine, biochemistry, genetics, and molecular biology. With a focus on immunology, they have contributed extensively to understanding immune function and genetic factors underlying infectious and autoimmune diseases.

The scientist's research topics cover a diverse range of subjects related to immune responses and disorders. These include:

  • Immunodeficiency and Autoimmune Disorders
  • Immune Cell Function and Interaction
  • Tuberculosis Research and Epidemiology
  • Mycobacterium Research and Diagnosis
  • T-cell and B-cell Immunology
  • Blood Disorders and Treatments
  • Interferon and Immune Responses

Notable recent publications by Stéphanie Boisson-Dupuis include:

  • Autoantibodies against type I IFNs in patients with life-threatening COVID-19 (2020, Science)
  • X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19 (2021, Science Immunology)
  • A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection (2020, Cell)
  • Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy (2020, Journal of Clinical Immunology)
  • Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children (2022, Science)

Frequent co-authors reflecting collaborations include:

  • Jean-Laurent Casanova
  • Jacinta Bustamante
  • Laurent Abel
  • Anne Puel
  • Masato Ogishi

Their work has appeared repeatedly in high-impact journals and venues such as:

  • Journal of Clinical Immunology
  • Cell
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Journal of Clinical Investigation
  • The Journal of Experimental Medicine

Boisson-Dupuis's contributions are primarily within immunology, with 97 publications specifically labeled under this subfield, complemented by work in genetics, epidemiology, infectious diseases, and molecular biology. Their investigations often explore the genetic and molecular bases of immune deficiencies and the body's response to infectious agents, including pathogens linked to tuberculosis and SARS-CoV-2.

Best Publications

  • Autoantibodies against type I IFNs in patients with life-threatening COVID-19.

    Paul Bastard;Paul Bastard;Paul Bastard;Lindsey B. Rosen;Qian Zhang;Eleftherios Michailidis

  • Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Qian Zhang;Paul Bastard;Paul Bastard;Zhiyong Liu;Jérémie Le Pen

  • 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

  • Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

    Jacinta Bustamante;Jacinta Bustamante;Jacinta Bustamante;Stéphanie Boisson-Dupuis;Laurent Abel;Jean-Laurent Casanova

  • IRF8 mutations and human dendritic-cell immunodeficiency.

    Sophie Hambleton;Sandra Salem;Jacinta Bustamante;Venetia Bigley

  • Mycobacterial Disease and Impaired IFN-γ Immunity in Humans with Inherited ISG15 Deficiency

    Dusan Bogunovic;Minji Byun;Larissa A. Durfee;Avinash Abhyankar

  • Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

    Xianqin Zhang;Dusan Bogunovic;Béatrice Payelle-Brogard;Véronique Francois-Newton

  • Human genetic and immunological determinants of critical COVID-19 pneumonia

    Unknown

  • 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

  • B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

    Danielle T. Avery;Elissa K. Deenick;Elissa K. Deenick;Cindy S. Ma;Cindy S. Ma;Santi Suryani;Santi Suryani

  • Revisiting Human IL-12Rβ1 Deficiency: A Survey of 141 Patients From 30 Countries

    Ludovic de Beaucoudrey;Arina Samarina;Arina Samarina;Arina Samarina;Jacinta Bustamante;Jacinta Bustamante;Aurélie Cobat;Aurélie Cobat

  • Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations

    Satoshi Okada;Satoshi Okada;Janet G Markle;Elissa K Deenick;Elissa K Deenick;Federico Mele

  • Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense.

    Shen-Ying Zhang;Stéphanie Boisson-Dupuis;Stéphanie Boisson-Dupuis;Ariane Chapgier;Ariane Chapgier;Kun Yang;Kun Yang

  • X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

    Takaki Asano;Bertrand Boisson;Bertrand Boisson;Bertrand Boisson;Fanny Onodi;Daniela Matuozzo;Daniela Matuozzo

  • Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

    Alexandra Y. Kreins;Alexandra Y. Kreins;Michael J. Ciancanelli;Satoshi Okada;Xiao Fei Kong

  • Functional STAT3 deficiency compromises the generation of human T follicular helper cells

    Cindy S. Ma;Cindy S. Ma;Danielle T. Avery;Anna Chan;Marcel Batten;Marcel Batten

  • Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes.

    Stephanie Boisson-Dupuis;Xiao-Fei Kong;Satoshi Okada;Sophie Cypowyj

  • Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

    Jacinta Bustamante;Andres A. Arias;Guillaume Vogt;Capucine Picard

  • Induction of MxA Gene Expression by Influenza A Virus Requires Type I or Type III Interferon Signaling

    Dirk Holzinger;Carl Jorns;Silke Stertz;Stéphanie Boisson-Dupuis

  • The human gene damage index as a gene-level approach to prioritizing exome variants

    Yuval Itan;Lei Shang;Bertrand Boisson;Etienne Patin;Etienne Patin

  • Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

    Guillaume Vogt;Ariane Chapgier;Kun Yang;Kun Yang;Nadia Chuzhanova

Frequent Co-Authors

Laurent Abel
Laurent Abel Université Paris Cité
Jean-Laurent Casanova
Jean-Laurent Casanova The University of Texas Southwestern Medical Center
Jacinta Bustamante
Jacinta Bustamante Rockefeller University
Stuart G. Tangye
Stuart G. Tangye Garvan Institute of Medical Research
Capucine Picard
Capucine Picard Université Paris Cité
Cindy S. Ma
Cindy S. Ma Garvan Institute of Medical Research
Bertrand Boisson
Bertrand Boisson Rockefeller University
Shen-Ying Zhang
Shen-Ying Zhang Rockefeller University
Elissa K. Deenick
Elissa K. Deenick Garvan Institute of Medical Research

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