Vivien Béziat

Also affiliated with Université Paris Cité, Hospital for Sick Children Pediatric Center, Assistance Publique – Hôpitaux de Paris, University of the East Ramon Magsaysay Memorial Medical Center, Pediatrics and Genetics, Institut des Maladies Génétiques Imagine, Rockefeller University

Immunology and MicrobiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 54 papers. Top paper: “Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child”.

Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

Nature Medicine(2021)10.1038/s41591-021-01388-5

N/A

2.7DataRank · unranked

113 citations

Rui Yang, Caner Aytekin, David Langlais, Mathieu Bourgey, Taushif Khan +50 more

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

Science(2020)10.1126/science.abd4585

N/A

1.2DataRank · unranked

2821 citations

Lindsey B. Rosen, Qian Zhang, Eleftherios Michailidis, Hans-Heinrich Hoffmann, Yu Zhang +95 more

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

Cell(2024)10.1016/j.cell.2024.04.009

N/A

1.0DataRank · unranked

62 citations

Romain Lévy, Steicy Sobrino, Jingwei Li, Chantal Lagresle‐Peyrou, Hossein Esmaeilzadeh +68 more

Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

Cell(2023)10.1016/j.cell.2022.12.038

N/A

0.724DataRank · unranked

124 citations

Anna‐Lena Neehus, Jérémy Manry, Rui Yang, Jérémie Le Pen, Wassim Daher +80 more

Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2001248118

N/A

0.665DataRank · unranked

83 citations

Bertrand Boisson, Anne Gregor, Vivien Béziat, Stéphanie Boisson-Dupuis, Jacinta Bustamante +11 more

Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

Journal of Clinical Immunology(2022)10.1007/s10875-022-01215-7

N/A

0.657DataRank · unranked

79 citations

Nils Landegren, Paul Bastard, Marie Materna, Mohammadreza Modaresi, Likun Du +19 more

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

The Journal of Experimental Medicine(2022)10.1084/jem.20220028

N/A

0.633DataRank · unranked

67 citations

Kuang‐Chih Hsiao, Qian Zhang, Jérémy Choin, Emma Best, Jie Chen +59 more

Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance

The Journal of Experimental Medicine(2021)10.1084/jem.20202592

N/A

0.619DataRank · unranked

61 citations

Joëlle Khourieh, Peng Zhang, Franck Rapaport, András N. Spaan, Juan Li +31 more

Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling

Immunity(2024)10.1016/j.immuni.2024.10.014

N/A

0.505DataRank · unranked

28 citations

Koji Kitaoka, Kim L. Good‐Jacobson, Darawan Rinchai, Baihao Zhang, Jun Wang +59 more

Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes

Journal of Investigative Dermatology(2021)10.1016/j.jid.2021.10.029

N/A

0.434DataRank · unranked

17 citations

Amir Hossein Saeidian, Leila Youssefian, Zahra Saffarian, Jean-Laurent Casanova, Vivien Béziat +3 more

DOCK2 Deficiency and GATA2 Haploinsufficiency Can Underlie Critical Coronavirus Disease 2019 (COVID-19) Pneumonia

Journal of Clinical Immunology(2025)10.1007/s10875-025-01877-z

N/A

0.269DataRank · unranked

5 citations

Leila Youssefian, Mohammad Amin Tabatabaiefar, Amir Hossein Saeidian, Bahareh Abtahi‐Naeini, Erfan Khorram +21 more

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

The Journal of Experimental Medicine(2021)10.1084/jem.20210566

N/A

0DataRank · unranked

58 citations

Wei‐Te Lei, Peng Zhang, Franck Rapaport, Yoann Seeleuthner, Bingnan Lyu +36 more

Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents

Journal of Clinical Investigation(2021)10.1172/jci150143

N/A

0DataRank · unranked

37 citations

David Langlais, Vivien Béziat, Franck Rapaport, Geetha Rao, Tomi Lazarov +42 more

Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.08.024

N/A

0DataRank · unranked

61 citations

Mathilde Bonnet des Claustres, Matthias Fahrner, Evgeniya Petrova, Lam C. Tsoi, Olivier Gouin +9 more

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Science(2022)10.1126/science.abo3627

N/A

0DataRank · unranked

168 citations

Jérémie Le Pen, Ahmad Yatim, Beihua Dong, Yann Aquino, Masato Ogishi +95 more

Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2102804118

N/A

0DataRank · unranked

85 citations

Anna‐Lena Neehus, Rui Yang, Masato Ogishi, Jérémie Rosain, Fayhan Alroqi +35 more

Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine

The Journal of Experimental Medicine(2021)10.1084/jem.20202486

N/A

0DataRank · unranked

242 citations

Eleftherios Michailidis, Hans-Heinrich Hoffmann, Marwa Chbihi, Tom Le Voyer, Jérémie Rosain +40 more

The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview

International Journal of Molecular Sciences(2022)10.3390/ijms23094547

N/A

0DataRank · unranked

53 citations

Roman Nowicki, F. Herms, Jean-Laurent Casanova, S. Fouéré, Vivien Béziat +1 more

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

The Journal of Experimental Medicine(2022)10.1084/jem.20220484

N/A

0DataRank · unranked

31 citations

Rui Yang, Rémy Rodriguez, Dominic P. Golec, Emmanuel Martin, Quentin Philippot +39 more

Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions

JCI Insight(2022)10.1172/jci.insight.156021

N/A

0DataRank · unranked

18 citations

Leila Youssefian, Charles Huang, Fahimeh Palizban, Mahtab Naji, Zahra Saffarian +21 more

Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency

Journal of Investigative Dermatology(2022)10.1016/j.jid.2022.02.011

N/A

0DataRank · unranked

9 citations

Amir Hossein Saeidian, Ali Reza Tavasoli, Elnaz Kalamati, Karim Naghipoor, Amir Hozhabrpour +12 more

Negative selection on human genes causing severe inborn errors depends on disease outcome and both the mode and mechanism of inheritance

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.07.938894

N/A

0DataRank · unranked

1 citations

Bertrand Boisson, Anne Gregor, Vivien Béziat, Stéphanie Boisson‐Dupuis, Jacinta Bustamante +11 more

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

The Journal of Experimental Medicine(2023)10.1084/jem.20221755

N/A

0DataRank · unranked

114 citations

Daniel Leung, Mana Momenilandi, Lauren C.W. Jones, Lucia Pacillo, Alyssa James +89 more

Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria

Science Immunology(2023)10.1126/sciimmunol.abq5204

N/A

0DataRank · unranked

71 citations

Masato Ogishi, Jonathan Bohlen, Julia Puchan, Andrés A. Arias, Tina Nguyen +53 more

Human inherited CCR2 deficiency underlies progressive polycystic lung disease

Cell(2023)10.1016/j.cell.2023.11.036

N/A

0DataRank · unranked

55 citations

Brenna Carey, Marija Landekic, Patricia Panikulam, Gail Deutsch, Masato Ogishi +69 more

Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

Journal of Clinical Investigation(2023)10.1172/jci168321

N/A

0DataRank · unranked

50 citations

Leen Moens, Masato Ogishi, Darawan Rinchai, Daniela Matuozzo, Mana Momenilandi +31 more

Encephalitis and poor neuronal death–mediated control of herpes simplex virus in human inherited RIPK3 deficiency

Science Immunology(2023)10.1126/sciimmunol.ade2860

N/A

0DataRank · unranked

49 citations

Eduardo J. Garcia Reino, Oliver Harschnitz, Hongyan Guo, Yi‐Hao Chan, Noopur V. Khobrekar +36 more

Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

Cell(2023)10.1016/j.cell.2023.09.024

N/A

0DataRank · unranked

40 citations

Qinhua Zhou, Quentin Philippot, Masato Ogishi, Darawan Rinchai, Tea Nieminen +53 more

Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections

JCI Insight(2023)10.1172/jci.insight.162558

N/A

0DataRank · unranked

18 citations

Leila Youssefian, Mahtab Naji, Hamidreza Mahmoudi, Samantha M. Barnada, Charles Huang +18 more

Inherited human ZNF341 deficiency

Current Opinion in Immunology(2023)10.1016/j.coi.2023.102326

N/A

0DataRank · unranked

15 citations

Claire Fieschi, Mana Momenilandi, Mélanie Migaud, Brahim Belaid, Réda Djidjik +2 more

Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review

Genetics in Medicine(2023)10.1016/j.gim.2023.101028

N/A

0DataRank · unranked

10 citations

Atefeh Sohanforooshan Moghaddam, Mohammad Amin Tabatabaiefar, Roya Sherkat, Leila Youssefian, Amir Hossein Saeidian +9 more

New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome

Journal of Clinical Immunology(2023)10.1007/s10875-023-01517-4

N/A

0DataRank · unranked

13 citations

Marie Materna, Orbicia Riccio, Caroline Schnider, Federica Angelini, Matthieu Perreau +21 more

Impaired thymic AIRE expression underlies autoantibodies against type I IFNs in humans with inborn errors of the alternative NF-kB pathway

HAL (Le Centre pour la Communication Scientifique Directe)(2023)10.22541/au.167330741.18394805/v1

N/A

0DataRank · unranked

2 citations

Adrian Gervais, Jérémie Rosain, Audrey Parent, Axel Cederholm, Darawan Rinchai +95 more

Human inborn errors of immunity to herpes viruses

Current Opinion in Immunology(2020)10.1016/j.coi.2020.01.004

N/A

0DataRank · unranked

95 citations

Vivien Béziat, Trine H. Mogensen, Jean-Laurent Casanova, Stuart G. Tangye, Shen-Ying Zhang +1 more

Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

Trends in Immunology(2024)10.1016/j.it.2023.12.003

N/A

0DataRank · unranked

43 citations

Narissara Suratannon, Daniel Leung, Safa Barış, Ichiro Takeuchi, Simran Samra +17 more

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

Science(2024)10.1126/science.adh4059

N/A

0DataRank · unranked

38 citations

Ottavia M. Delmonte, Marita Bosticardo, Mana Momenilandi, Peyton Conrey, Bénédicte Charmeteau-De Muylder +93 more

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

The Journal of Experimental Medicine(2020)10.1084/jem.20191804

N/A

0DataRank · unranked

113 citations

Simon J. Tavernier, Yin‐Huai Chen, S. Cindy, Marie Materna, Arian Laurence +55 more

Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases

The Journal of Experimental Medicine(2024)10.1084/jem.20231152

N/A

0DataRank · unranked

17 citations

Tom Le Voyer, Xian Liu, Adrian Gervais, Laura Polivka, Axel Cederholm +94 more

A sensitive assay for measuring whole-blood responses to type I IFNs

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2402983121

N/A

0DataRank · unranked

16 citations

Corentin Le Floc’h, Tom Le Voyer, Lucy Bizien, Jonathan Bohlen, Fatih Çelmeli +16 more

The monogenic landscape of human infectious diseases

Journal of Allergy and Clinical Immunology(2024)10.1016/j.jaci.2024.12.1078

N/A

0DataRank · unranked

11 citations

Paul Bastard, Vivien Béziat, Jacinta Bustamante, Aurélie Cobat, Emmanuelle Jouanguy +6 more

Inherited human RelB deficiency impairs innate and adaptive immunity to infection

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2321794121

N/A

0DataRank · unranked

11 citations

Majistor Raj Luxman Maglorius Renkilaraj, Kunihiko Moriya, Malena Pérez Lorenzo, Tina Nguyen, Liwei Gao +24 more

IL-7–dependent and –independent lineages of IL-7R–dependent human T cells

Journal of Clinical Investigation(2024)10.1172/jci180251

N/A

0DataRank · unranked

7 citations

Masato Ogishi, Susanne Unger, Ottavia M. Delmonte, Julio César Orrego, Ahmad Yatim +65 more

Inborn errors of immunity reveal molecular requirements for generation and maintenance of human CD4+ IL-9–expressing cells

Journal of Allergy and Clinical Immunology(2024)10.1016/j.jaci.2024.11.031

N/A

0DataRank · unranked

5 citations

Corinne D. Mack, Tina Nguyen, Natalie Wong, Kathryn Payne, Lisa Worley +33 more

Whole-Transcriptome Sequencing–Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

JID Innovations(2024)10.1016/j.xjidi.2024.100278

N/A

0DataRank · unranked

3 citations

Amir Hossein Saeidian, Zahra Saffarian, Mona Ariamanesh, Fahimeh Abdollahimajd, Sara Molkara +10 more

Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency

Viruses(2024)10.3390/v16091415

N/A

0DataRank · unranked

2 citations

Hind Ouair, F. Marnissi, Jalila El Bakkouri, Rémi Chevalier, Lazaro Lorenzo +6 more

Case Report of 2 Independent Moroccan Families with Syndromic Epidermodysplasia verruciformis and STK4 Deficiency

Preprints.org(2024)10.20944/preprints202407.1906.v1

N/A

0DataRank · unranked

1 citations

Hind Ouair, F. Marnissi, Jalila El Bakkouri, Rémi Chevalier, Lazaro Lorenzo +6 more

Enhanced TLR7-dependent production of type I interferon by pDCs underlies pandemic chilblains

The Journal of Experimental Medicine(2025)10.1084/jem.20231467

N/A

0DataRank · unranked

8 citations

Danyel Lee, Jérémy Di Domizio, Corentin Le Floc’h, Raphael Jenelten, Jérémie Le Pen +14 more

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

Journal of Clinical Investigation(2020)10.1172/jci139980

N/A

0DataRank · unranked

116 citations

Jérémy Manry, Jie Chen, Jérémie Rosain, Yoann Seeleuthner, Omar AbuZaitun +29 more

Two different forms of inherited human TCRα chain deficiency

Journal of Human Immunity(2025)10.70962/jhi.20250014

N/A

0DataRank · unranked

5 citations

Simin Seyedpour, Tom Le Voyer, Nima Parvaneh, Niloufar Yazdanpanah, Amir Ali Hamidieh +11 more

Inherited IL-18BP deficiency in two Egyptian siblings with fulminant viral hepatitis

Journal of Human Immunity(2025)10.70962/jhi.20250135

N/A

0DataRank · unranked

4 citations

Alperen Baran, Aysima Atılgan Lülecioğlu, Adrian Gervais, Chenglin Zhang, Vivien Béziat +6 more

IRF4 haploinsufficiency in a multiplex family with Whipple’s disease

Journal of Human Immunity(2025)10.70962/jhi.20250009

N/A

0DataRank · unranked

1 citations

Stéphanie Dublanc, Hailun Li, Jean-Philippe Vernhes, Vincent Meynier, Camille Soudée +37 more

Mepolizumab treatment in a child with inherited TYK2 deficiency

Journal of Human Immunity(2025)10.70962/jhi.20250106

N/A

0DataRank · unranked

0 citations

Vivien Béziat, Jean-Laurent Casanova, Audrey Dupond-Athenor, Iris Fagniez, Ji Eun Han +9 more

Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

UNC Libraries(2025)10.17615/zg2n-en48

N/A

0DataRank · unranked

0 citations

Guillaume Vogt, Charles M. Rice, Mathieu Pochon, James P. Di Santo, Qian Zhang +80 more

Inherited human IFN-γ deficiency underlies mycobacterial disease

Journal of Clinical Investigation(2020)10.1172/jci135460

N/A

0DataRank · unranked

139 citations

Jérémie Rosain, Antoine Guérin, Ahmad Al-Khabaz, Carmen Oleaga‐Quintas, Franck Rapaport +25 more