Aziz Bousfiha

Mother Hospital — India

Immunology and Microbiology · Life Sciences

39h-index11.0kcitations57works4.32yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(43), Immune Cell Function and Interaction(17), T-cell and B-cell Immunology(12), Blood disorders and treatments(10), Immune Response and Inflammation(6)

Publications57 total

CHARGE Syndrome in a Six-Month-Old Male Infant: A Case Report
Cureus·2025Open Access
SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency
The Journal of Experimental Medicine·2024· 17 citedOpen Access
[Cystic fibrosis in Morroco : what do words mean without action ?]
PubMed·2024
Bare Lymphocyte Syndrome Case Report: A Rare Ibd Mimicking Entity
SSRN Electronic Journal·2024Open Access
Human <i>RELA</i> dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
The Journal of Experimental Medicine·2023· 28 citedOpen Access
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
Journal of Clinical Investigation·2023· 44 citedOpen Access
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
The Journal of Experimental Medicine·2023· 53 citedOpen Access
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
The Journal of Experimental Medicine·2022· 35 citedOpen Access
African Society for Immunodeficiency (Asid) Guidelines for Diagnosis and Management of Inborn Errors of Immunity in Africa: Core Concept, Development and Initial Results
2022· 1 citedOpen Access
The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
The Journal of Allergy and Clinical Immunology In Practice·2022· 58 citedOpen Access
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity
Journal of Clinical Immunology·2022· 465 citedOpen Access
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
The Journal of Experimental Medicine·2022· 61 citedOpen Access
Human T-bet governs the generation of a distinct subset of CD11c <sup>high</sup> CD21 <sup>low</sup> B cells
Science Immunology·2022· 76 citedOpen Access
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
Journal of Clinical Immunology·2022· 1.1k citedOpen Access
A partial form of inherited human USP18 deficiency underlies infection and inflammation
The Journal of Experimental Medicine·2022· 66 citedOpen Access
The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies
2022· 24 citedOpen Access
Orientations diagnostiques et classification des déficits immunitaires primitifs
Elsevier eBooks·2022
High Th2 cytokine levels and upper airway inflammation in human inherited T-bet deficiency
The Journal of Experimental Medicine·2021· 35 citedOpen Access
Human <i>STAT3</i> variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
The Journal of Experimental Medicine·2021· 59 citedOpen Access
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity
Journal of Clinical Immunology·2021· 70 citedOpen Access
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Frequent Co-authors

Jean‐Laurent Casanova(39), Jacinta Bustamante(25), Capucine Pïcard(24), Stuart G. Tangye(22), Anne Puel(21), Fatima Ailal(18), Laurent Abel(18), Stéphanie Boisson‐Dupuis(18), José Luis Franco(17), Steven M. Holland(16), Waleed Al–Herz(13), Jamila El Baghdadi(13), Christoph Klein(12), Jennifer M. Puck(12), Kathleen E. Sullivan(12), Charlotte Cunningham‐Rundles(11), Tomohiro Morio(11), Jérémie Rosain(11), Talal A. Chatila(10), Amos Etzioni(10)