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V. Béziat · SciRah

Researcher profile · Semantic Scholar

V. Béziat

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V. Béziat — researcher profile on SciRah

h-index: 53
Works: 161
Citations: 14K

Most-cited papers

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19
P. Bastard, Lindsey B. Rosen, Qian Zhang, E. Michailidis +95 more
2020Science2,497 citations Open access
Semantic Scholar
Autoantibodies neutralizing type I IFNs are present in ~ 4% of uninfected individuals over 70 years and account for ~ 20% of COVID-19 deaths
P. Bastard, A. Gervais, T. Le Voyer, J. Rosain +177 more
2021Science immunology555 citations Open access
Semantic Scholar
X-linked recessive TLR7 deficiency in 1% of men under 60 years with life-threatening COVID-19
Takaki Asano, B. Boisson, Fanny Onodi, Daniela Matuozzo +103 more
2021Science immunology359 citations Open access
Semantic Scholar
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine
P. Bastard, E. Michailidis, H. Hoffmann, Marwa Chbihi +41 more
2021Journal of Experimental Medicine211 citations Open access
Semantic Scholar
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies
J. Manry, P. Bastard, A. Gervais, T. Le Voyer +175 more
2022Proceedings of the National Academy of Sciences of the United States of America138 citations Open access
Semantic Scholar
Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children
Danyel Lee, J. Le Pen, A. Yatim, Bei-Hua Dong +99 more
2022Science134 citations Open access
Semantic Scholar
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
V. Béziat, S. Tavernier, Yin-Huai Chen, Cindy S. Ma +55 more
2020Journal of Experimental Medicine119 citations Open access
Semantic Scholar
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria
J. Rosain, Anna-Lena Neehus, J. Manry, Rui Yang +81 more
2023Cell98 citations Open access
Semantic Scholar
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency.
P. Bastard, J. Manry, Jie Chen, J. Rosain +30 more
2020Journal of Clinical Investigation98 citations Open access
Semantic Scholar
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Masato Ogishi, Rui Yang, C. Aytekin, D. Langlais +51 more
2021Nature Medicine96 citations Open access
Semantic Scholar
Inherited human IFNγ deficiency underlies mycobacterial disease.
Gaspard Kerner, J. Rosain, A. Guérin, Ahmad Alkhabaz +26 more
2020Journal of Clinical Investigation96 citations Open access
Semantic Scholar
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
T. Le Voyer, Audrey V. Parent, Xian Liu, Axel Cederholm +137 more
2023Nature90 citations Open access
Semantic Scholar
Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy
V. Béziat, Franck Rapaport, Jiafen Hu, M. Titeux +70 more
2021Cell80 citations Open access
Semantic Scholar
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Mehul Sharma, D. Leung, M. Momenilandi, L. Jones +90 more
2023Journal of Experimental Medicine71 citations Open access
Semantic Scholar
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease
T. Le Voyer, Anna-Lena Neehus, Rui Yang, Masato Ogishi +36 more
2021Proceedings of the National Academy of Sciences of the United States of America69 citations Open access
Semantic Scholar
Human inborn errors of immunity to herpes viruses
E. Jouanguy, V. Béziat, T. Mogensen, J. Casanova +2 more
2020Current Opinion in Immunology67 citations Open access
Semantic Scholar
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes
P. Bastard, Kuang-Chih Hsiao, Qian Zhang, J. Choin +60 more
2022Journal of Experimental Medicine65 citations Open access
Semantic Scholar
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance
Franck Rapaport, B. Boisson, A. Gregor, V. Béziat +12 more
2021Proceedings of the National Academy of Sciences of the United States of America62 citations Open access
Semantic Scholar
The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies
J. Manry, P. Bastard, A. Gervais, Tom Le Voyer +176 more
2022Research Square61 citations Open access
Semantic Scholar
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome
Hassan Abolhassani, N. Landegren, P. Bastard, M. Materna +20 more
2022Journal of Clinical Immunology60 citations Open access
Semantic Scholar
Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses.
C. Barbieux, Mathilde Bonnet Des Claustres, M. Fahrner, E. Petrova +10 more
2021Journal of Allergy and Clinical Immunology60 citations Open access
Semantic Scholar
Distinct antibody repertoires against endemic human coronaviruses in children and adults
Taushif Khan, Mahbuba Rahman, Fatima Al Ali, Susie S. Y. Huang +21 more
2020bioRxiv60 citations Open access
Semantic Scholar
Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria
Quentin Philippot, Masato Ogishi, J. Bohlen, Julia Puchan +54 more
2023Science immunology55 citations Open access
Semantic Scholar
The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview
D. Purzycka-Bohdan, R. Nowicki, F. Herms, J. Casanova +2 more
2022International Journal of Molecular Sciences55 citations Open access
Semantic Scholar
Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus
Clémence David, C. Arango-Franco, M. Badonyi, Julien Fouchet +28 more
2024Journal of Experimental Medicine54 citations Open access
Semantic Scholar
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice
M. Momenilandi, R. Lévy, Steicy Sobrino, Jingwei J. Li +69 more
2024Cell51 citations Open access
Semantic Scholar
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency
Juan Li, Wei-Te Lei, Peng Zhang, Franck Rapaport +37 more
2021Journal of Experimental Medicine51 citations Open access
Semantic Scholar
Effectiveness and safety of ruxolitinib for the treatment of refractory systemic idiopathic juvenile arthritis like associated with interstitial lung disease : a case report
B. Bader-Meunier, A. Hadchouel, L. Berteloot, L. Polivka +3 more
2020Annals of the Rheumatic Diseases49 citations Open access
Semantic Scholar
Human inherited CCR2 deficiency underlies progressive polycystic lung disease
Anna-Lena Neehus, B. Carey, Marija Landekic, Patricia Panikulam +70 more
2024Cell46 citations
Semantic Scholar
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
Takaki Asano, J. Khourieh, Peng Zhang, Franck Rapaport +32 more
2021Journal of Experimental Medicine46 citations Open access
Semantic Scholar
Human genetic dissection of papillomavirus-driven diseases: New insight into their pathogenesis
V. Béziat
2020Human Genetics46 citations Open access
Semantic Scholar
Fatal Cytomegalovirus Infection in an Adult with Inherited NOS2 Deficiency
S. Drutman, D. Mansouri, S. Mahdaviani, Anna-Lena Neehus +22 more
2020New England Journal of Medicine42 citations Open access
Semantic Scholar
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria
J. Bohlen, Qin-Hua Zhou, Quentin Philippot, Masato Ogishi +54 more
2023Cell40 citations Open access
Semantic Scholar
Encephalitis and poor neuronal death-mediated control of herpes simplex virus in human inherited RIPK3 deficiency
Zhiyong Liu, Eduardo J. Garcia Reino, O. Harschnitz, Hong-Yan Guo +37 more
2023Science immunology40 citations Open access
Semantic Scholar
Efficacy of dupilumab for controlling severe atopic dermatitis in a patient with hyper-IgE syndrome
R. Lévy, V. Béziat, C. Barbieux, A. Puel +3 more
2020Journal of Clinical Immunology39 citations Open access
Semantic Scholar
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children
P. Bastard, A. Gervais, Maki Taniguchi, Liisa Saare +83 more
2024Journal of Experimental Medicine37 citations Open access
Semantic Scholar
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling
Masato Ogishi, Koji Kitaoka, K. Good-Jacobson, Darawan Rinchai +60 more
2024Immunity34 citations Open access
Semantic Scholar
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
G. Bucciol, Leen Moens, Masato Ogishi, Darawan Rinchai +32 more
2023Journal of Clinical Investigation32 citations Open access
Semantic Scholar
Human genetic and immunological dissection of papillomavirus-driven diseases: New insights into their pathogenesis
V. Béziat, J. Casanova, E. Jouanguy
2021Current Opinion in Virology31 citations Open access
Semantic Scholar
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
R. Lévy, F. Gothe, M. Momenilandi, T. Magg +78 more
2022Journal of Experimental Medicine30 citations Open access
Semantic Scholar
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
Masato Ogishi, Rui Yang, Rémy Rodriguez, Dominic P. Golec +40 more
2022Journal of Experimental Medicine29 citations Open access
Semantic Scholar
Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.
R. Lévy, D. Langlais, V. Béziat, Franck Rapaport +43 more
2021Journal of Clinical Investigation27 citations Open access
Semantic Scholar
The immunopathological landscape of human pre-TCRα deficiency: from rare to common variants
M. Materna, O. Delmonte, M. Bosticardo, M. Momenilandi +94 more
2024Science24 citations Open access
Semantic Scholar
Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing.
M. Fusaro, J. Rosain, Virginie Grandin, N. Lambert +41 more
2020Journal of Allergy and Clinical Immunology24 citations Open access
Semantic Scholar
Human inborn errors of immunity to oncogenic viruses
V. Béziat, E. Jouanguy
2021Current Opinion in Immunology20 citations Open access
Semantic Scholar
Human inherited CCR2 deficiency underlies progressive polycystic lung disease
Anna-Lena Neehus, B. Carey, Marija Landekic, Patricia Panikulam +68 more
2023Cell18 citations Open access
Semantic Scholar
Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections
A. Saeidian, L. Youssefian, M. Naji, H. Mahmoudi +19 more
2023JCI Insight18 citations Open access
Semantic Scholar
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases
J. Rosain, T. Le Voyer, Xian Liu, A. Gervais +95 more
2024Journal of Experimental Medicine17 citations Open access
Semantic Scholar
Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions
A. Saeidian, L. Youssefian, Charles Y. Huang, Fahimeh Palizban +22 more
2022JCI Insight17 citations Open access
Semantic Scholar
A sensitive assay for measuring whole-blood responses to type I IFNs
A. Gervais, Corentin Le Floc'h, T. Le Voyer, Lucy Bizien +17 more
2024Proceedings of the National Academy of Sciences of the United States of America15 citations Open access
Semantic Scholar

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