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Bertrand Boisson
Affiliation : Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Human Genetic of Infectious Diseases · Institut des Maladies Génétiques Imagine · Rockefeller University
- 14Publications (affiliation in the United States)
- 212Total publications
- 25218Citations
- 68h-index
Research profile
Bertrand Boisson has 14 indexed publications (2015–2026). Their work appears mainly in “The Journal of Experimental Medicine”, “Science Immunology” and “Proceedings of the National Academy of Sciences”. Their most cited article, “Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome” (2015), has been cited 364 times. 3 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France, Austria, Iran, United Kingdom.
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Create my free profile Add my publicationsResearch areas
- Immunodeficiency and Autoimmune Disorders
- T-cell and B-cell Immunology
- Blood disorders and treatments
- Genomics and Rare Diseases
- interferon and immune responses
Publications (14)
- Human LFA-1 governs T cell immune surveillance of the skin
- Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis
- Phenotypes of 126 Moroccan HIES patients according to NIH Score
- Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
- Hyperimmunoglobulinémie E et Déficits Immunitaires Héréditaires
- Human T-bet governs the generation of a distinct subset of CD11c high CD21 low B cells
- Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
- Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents
- F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects
- A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
- T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
- Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons
- Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
- Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
Publication venues
- The Journal of Experimental Medicine × 4
- Science Immunology × 3
- Proceedings of the National Academy of Sciences × 2
- La Tunisie Médicale × 1
- PubMed Central × 1
- Journal of Clinical Investigation × 1
Publications per year
- 20262
- 20241
- 20232
- 20221
- 20212
- 20191
- 20183
- 20161
- 20151
Collaborations
Partner institutions : Université Paris Descartes · Assistance Publique – Hôpitaux de Paris · Howard Hughes Medical Institute · National Institutes of Health · National Institute of Allergy and Infectious Diseases
Co-authors’ countries : France · Austria · Iran · United Kingdom
Co-authors
- Jean‐Laurent Casanova
- Laurent Abel
- Anne Puel
- Stéphanie Boisson‐Dupuis
- Vivien Béziat
- Masato Ogishi
- Jacinta C. Bustamante
- Peng Zhang
- Shen‐Ying Zhang
- Jessica N. Peel
- Rui Yang
- Juan Li
Bibliographic data from OpenAlex (open database).
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