Bertrand Boisson

Also affiliated with Université Paris Cité, Pediatrics and Genetics, Human Genetic of Infectious Diseases, Institut des Maladies Génétiques Imagine, Université Paris Dauphine-PSL, Rockefeller University

Immunology and MicrobiologyBiochemistry, Genetics and Molecular Biology

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 58 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

Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

The Journal of Experimental Medicine(2022)10.1084/jem.20220258

N/A

1.3DataRank · unranked

47 citations

Paul Bastard, Pascal Chappert, Giovanna Barba–Spaeth, Slim Fourati, Alexis Vanderberghe +47 more

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

Science Immunology(2021)10.1126/sciimmunol.abl4348

N/A

0.907DataRank · unranked

422 citations

Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada‐Vélez, Majistor Raj Luxman Maglorius Renkilaraj +95 more

Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions

Cell Reports(2020)10.1016/j.celrep.2020.107633

N/A

0.683DataRank · unranked

94 citations

María Bravo García‐Morato, Conor Gruber, Sara Murias Loza, Muhammad Nasir Hayat Malik, Fahad Alsohime +31 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

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

Is Your Kid Actin Out? A Series of Six Patients With Inherited Actin-Related Protein 2/3 Complex Subunit 1B Deficiency and Review of the Literature

The Journal of Allergy and Clinical Immunology In Practice(2023)10.1016/j.jaip.2022.12.045

N/A

0.425DataRank · unranked

16 citations

Marco Antonio Yamazaki‐Nakashimada, Edna Venegas‐Montoya, Selma Scheffler‐Mendoza, Lina María Castaño‐Jaramillo, Edgar Alejandro Medina-Torres +21 more

Role of clonal inflammatory microglia in histiocytosis-associated neurodegeneration

Neuron(2025)10.1016/j.neuron.2025.02.007

N/A

0.375DataRank · unranked

10 citations

Stamatina Fragkogianni, Maria Pokrovskii, Carina Meyer, Estibaliz Lopez-Rodrigo, Yang Hu +32 more

Multi-batch cytometry data integration for optimal immunophenotyping

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.14.202432

N/A

0.367DataRank · unranked

4 citations

Rui Yang, Conor Gruber, Simon J. Pelham, András N. Spaan, Jérémie Rosain +10 more

A microglia clonal inflammatory disorder in Alzheimer’s disease

eLife(2024)10.7554/elife.96519

N/A

0.363DataRank · unranked

7 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y. Hayashi +21 more

A microglia clonal inflammatory disorder in Alzheimer’s Disease

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.25.577216

N/A

0.334DataRank · unranked

5 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y. Hayashi +21 more

Common variable immunodeficiency: autoimmune cytopenias and advances in molecular diagnosis

Hematology(2024)10.1182/hematology.2024000538

N/A

0.312DataRank · unranked

7 citations

Jean-Laurent Casanova, Bertrand Boisson, Charlotte Cunningham-Rundles

DOCK8 and STAT3 cooperate to restrain IgE-inducing T follicular helper cells

The Journal of Experimental Medicine(2025)10.1084/jem.20241707

N/A

0.269DataRank · unranked

5 citations

Courtney Fisher, Meng-Ping Lu, Jessica Grassmann, Corinne D. Mack, Roukaya Yaakoubi +20 more

Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiency

Journal of Human Immunity(2025)10.70962/jhi.20250018

N/A

0.208DataRank · unranked

3 citations

Rob J.W. Arts, Catherine M. Biggs, Laleh Habibi, Laura Batlle-Masó, Arjan van Laarhoven +28 more

ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

eLife(2024)10.7554/elife.96085

N/A

0.104DataRank · unranked

1 citations

Tomi Lazarov, Natasha Jordan, Bertrand Boisson, María Tello‐Lafoz, Barbara P. Craddock +20 more

A microglia clonal inflammatory disorder in Alzheimer’s Disease

eLife(2024)10.7554/elife.96519.1

N/A

0.104DataRank · unranked

1 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y. Hayashi +21 more

Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin

Science(2022)10.1126/science.abm6380

N/A

0DataRank · unranked

69 citations

Anna‐Lena Neehus, Emmanuel Laplantine, Frederik Staels, Masato Ogishi, Yoann Seeleuthner +57 more

DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling

Science Immunology(2022)10.1126/sciimmunol.abi4611

N/A

0DataRank · unranked

51 citations

Kim S. Robinson, Kenneth Lay, Jasmine C. Wong, Ricardo Moreno Traspas, Nasrin Nabavizadeh +24 more

Genome-wide detection of human variants that disrupt intronic branchpoints

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2211194119

N/A

0DataRank · unranked

47 citations

Quentin Philippot, Weicheng Ren, Wei‐Te Lei, Juan Li, Peter D. Stenson +11 more

Genome-wide detection of human variants that disrupt intronic branchpoints

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.18.488668

N/A

0DataRank · unranked

7 citations

Quentin Philippot, Weicheng Ren, Wei‐Te Lei, Juan Li, Peter D. Stenson +11 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 RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity

The Journal of Experimental Medicine(2023)10.1084/jem.20212276

N/A

0DataRank · unranked

40 citations

Tomohiro Nakano, Yoshitaka Honda, Miyuki Tsumura, Masato Ogishi, Motoshi Sonoda +23 more

Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling

Nature Communications(2023)10.1038/s41467-023-39272-0

N/A

0DataRank · unranked

20 citations

Hye Sun Kuehn, Brigette Boast, SuJin Hwang, Douglas B. Kuhns, Jennifer Stoddard +23 more

Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2314225120

N/A

0DataRank · unranked

19 citations

Matthieu Chaldebas, Masato Ogishi, Fahd Al Qureshah, Khoren Ponsin, Yi Feng +15 more

Novel NF-kappa B Inhibitor Alpha Gain-of-Function Variant in an Infant with Lymphocytosis and Recurrent Serratia Bacteremia

Journal of Clinical Immunology(2023)10.1007/s10875-023-01481-z

N/A

0DataRank · unranked

3 citations

Takaki Asano, Jean-Laurent Casanova, Bertrand Boisson, Amer Khojah, Lauren Gunderman

Genetics and clinical phenotypes in common variable immunodeficiency

Frontiers in Genetics(2024)10.3389/fgene.2023.1272912

N/A

0DataRank · unranked

38 citations

Jean-Laurent Casanova, Bertrand Boisson, Charlotte Cunningham‐Rundles

Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency

Nature Immunology(2024)10.1038/s41590-024-01817-w

N/A

0DataRank · unranked

34 citations

Kalpana Manthiram, Pallavi Pimpale Chavan, Eva Rieser, Önay Veli, Öykü Kaya +57 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

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

A microglia clonal inflammatory disorder in Alzheimer’s Disease

eLife(2024)10.7554/elife.96519.2

N/A

0DataRank · unranked

2 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y. Hayashi +21 more

ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

medRxiv(2024)10.1101/2024.02.15.24302255

N/A

0DataRank · unranked

0 citations

Tomi Lazarov, Natasha Jordan, Bertrand Boisson, María Tello‐Lafoz, Barbara P. Craddock +20 more

ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis

eLife(2024)10.7554/elife.96085.1

N/A

0DataRank · unranked

0 citations

Tomi Lazarov, Natasha Jordan, Bertrand Boisson, María Tello‐Lafoz, Barbara P. Craddock +20 more

Reviewer #1 (Public review): A microglia clonal inflammatory disorder in Alzheimer’s Disease

(2024)10.7554/elife.96519.2.sa2

N/A

0DataRank · unranked

0 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y Hayashi +21 more

A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

Cell(2020)10.1016/j.cell.2020.05.016

N/A

0DataRank · unranked

235 citations

Helen C. Su, Laurent Abel, Alessandro Aiuti, Saleh Al‐Muhsen, Andrés A. Arias +59 more

Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency

Journal of Human Immunity(2025)10.70962/jhi.20250016

N/A

0DataRank · unranked

6 citations

Andrés Caballero-Oteyza, Mingyu Yang, Michele Proietti, Samaneh Delavari, Patrick Maffucci +9 more

Primary disorders of polyubiquitination: Dual roles in autoinflammation and immunodeficiency

The Journal of Experimental Medicine(2025)10.1084/jem.20241047

N/A

0DataRank · unranked

4 citations

Bertrand Boisson, Seth L. Masters, András N. Spaan

Expanding the utility of variant effect predictions with phenotype-specific models

Nature Communications(2025)10.1038/s41467-025-66607-w

N/A

0DataRank · unranked

3 citations

Meltem Ece Kars, Baptiste Milisavljevic, Matthew Mort, Peter D. Stenson, Jean-Laurent Casanova +6 more

A novel CARD11 heterozygous missense variant in a CADINS patient

Journal of Allergy and Clinical Immunology Global(2025)10.1016/j.jacig.2025.100461

N/A

0DataRank · unranked

1 citations

Mehdi Adeli, Dinesh Velayutham, Salim Bougarn, Manar Ata, Fatima Alali +9 more

A microglia clonal inflammatory disorder in Alzheimer’s disease

eLife(2025)10.7554/elife.96519.3

N/A

0DataRank · unranked

10 citations

Stamatina Fragkogianni, Leslie Weber, Tomi Lazarov, Yang Hu, Samantha Y. Hayashi +21 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

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

PAX1 is essential for development and function of the human thymus

Science Immunology(2020)10.1126/sciimmunol.aax1036

N/A

0DataRank · unranked

98 citations

Raúl Urrutia, Luis M. Franco, Silvia Giliani, Kejian Zhang, Anas M. Alazami +23 more

The genetic basis of pneumococcal and staphylococcal infections: inborn errors of human TLR and IL-1R immunity

Human Genetics(2020)10.1007/s00439-020-02111-z

N/A

0DataRank · unranked

21 citations

Bertrand Boisson

Multibatch Cytometry Data Integration for Optimal Immunophenotyping

The Journal of Immunology(2020)10.4049/jimmunol.2000854

N/A

0DataRank · unranked

38 citations

Rui Yang, Conor Gruber, Peng Zhang, Simon J. Pelham, András N. Spaan +11 more

Detection of homozygous and hemizygous partial exon deletions by whole-exome sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.23.217976

N/A

0DataRank · unranked

2 citations

Yoann Seeleuthner, Gaspard Kerner, Mélanie Migaud, Jérémie Rosain, Bertrand Boisson +7 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

A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

Nature Immunology(2021)10.1038/s41590-021-01030-z

N/A

0DataRank · unranked

72 citations

Laurent Abel, Donald C. Vinh, Elżbieta Kaja, Beth A. Drolet, Qian Zhang +51 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

Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.003

N/A

0DataRank · unranked

23 citations

Sze Hwee Seet, Michael Maier, Ayşe Gürel, Ricardo Moreno Traspas, Cheryl Lee +67 more

Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing

NAR Genomics and Bioinformatics(2021)10.1093/nargab/lqab037

N/A

0DataRank · unranked

13 citations

Yoann Seeleuthner, Gaspard Kerner, Mélanie Migaud, Jérémie Rosain, Bertrand Boisson +7 more

Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish

medRxiv(2021)10.1101/2021.03.31.21253863

N/A

0DataRank · unranked

0 citations

Sze Hwee Seet, Michael Maier, Ricardo Moreno Traspas, Cheryl Lee, Zhang Shan +42 more

Human genetic and immunological determinants of critical COVID-19 pneumonia

Nature(2022)10.1038/s41586-022-04447-0

N/A

0DataRank · unranked

393 citations

Paul Bastard, COVID Human Genetic Effort, Adem Karbuz, Adrian Gervais, Ahmad Abou Tayoun +95 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

Human T-bet governs the generation of a distinct subset of CD11c high CD21 low B cells

Science Immunology(2022)10.1126/sciimmunol.abq3277

N/A

0DataRank · unranked

86 citations

Danielle T. Avery, Katherine Jackson, Masato Ogishi, Ibtihal Benhsaien, Likun Du +31 more