Author

V. Beziat

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1

Frequent Co-Authors

J.-L. Casanova· 3 shared L. Abel· 3 shared A. Cobat· 2 shared J. Bustamante· 2 shared N. Marr· 2 shared A. Guerin· 1 shared A. Karimi· 1 shared A. Sayeed· 1 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersImmunology

J.-L. Casanova

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3 papers

Recent·Most cited

A novel patient with inherited TNF deficiency and tuberculosis

N. Keating, M. Mesdaghi, Z. Chavoshzadeh, A. Karimi, M. Saberi, S. Unal, V. Meynier, C. Soudee, C. Laine, A. Solgi, S. Sharafian, A.-S. LHonneur, M. Migaud, Y. Seeleuthner, A. Cobat, , Stephanie Boisson-Dupuis

The paper reports three patients with inherited TNF deficiency who developed tuberculosis, showing TNF's essential role in immunity against M. tuberculosis.

medRxiv · Nov 9, 2026 · PreprintGenetic & Genomic Medicine

Distinct antibody repertoires against endemic human coronaviruses in children and adults

T. Khan, M. Rahman, F. Al Ali, S. S. Huang, M. Ata, Q. Zhang, P. Bastard, Z. Liu, E. Jouanguy, V. Beziat, A. Cobat, G. K. Nasrallah, H. Yassine, M. Smatti, A. Sayeed, , N. Marr

The paper analyzes antibody repertoires against endemic human coronaviruses in children and adults, finding distinct epitope targets and cross-reactivity patterns.

bioRxiv · Jun 21, 2020Immunology

IRF4 haploinsufficiency in a family with Whipples disease

A. Guerin, G. Kerner, N. Marr, J. G. Markle, F. Fenollar, N. Wong, S. Boughorbel, D. T. Avery, C. Ma, S. Bougarn, M. Bouaziz, V. Beziat, E. Della Mina, T. Lazarovt, L. Worley, , J.-L. Casanova

This study identifies IRF4 haploinsufficiency as the genetic cause of Whipples disease in a family, showing age-dependent incomplete penetrance and chronic Tw carriage preceding disease onset.

bioRxiv · Oct 3, 2017Immunology