Bertrand Boisson
Bertrand Boisson
Senior Research Associate
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Cited by
Cited by
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Q Zhang, P Bastard, Z Liu, J Le Pen, M Moncada-Velez, J Chen, M Ogishi, ...
Science 370 (6515), eabd4570, 2020
Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants
A Belkadi, A Bolze, Y Itan, A Cobat, QB Vincent, A Antipenko, L Shang, ...
Proceedings of the National Academy of Sciences 112 (17), 5473-5478, 2015
Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency
D Bogunovic, M Byun, LA Durfee, A Abhyankar, O Sanal, D Mansouri, ...
Science 337 (6102), 1684-1688, 2012
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation
X Zhang, D Bogunovic, B Payelle-Brogard, V Francois-Newton, SD Speer, ...
Nature 517 (7532), 89-93, 2015
Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency
MJ Ciancanelli, SXL Huang, P Luthra, H Garner, Y Itan, S Volpi, ...
Science 348 (6233), 448-453, 2015
TNF and IL-1 exhibit distinct ubiquitin requirements for inducing NEMO–IKK supramolecular structures
N Tarantino, JY Tinevez, EF Crowell, B Boisson, R Henriques, M Mhlanga, ...
Journal of Cell Biology 204 (2), 231-245, 2014
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency
B Boisson, E Laplantine, C Prando, S Giliani, E Israelsson, Z Xu, ...
Nature immunology 13 (12), 1178-1186, 2012
Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations
S Okada, JG Markle, EK Deenick, F Mele, D Averbuch, M Lagos, ...
Science 349 (6248), 606-613, 2015
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
Host cell traversal is important for progression of the malaria parasite through the dermis to the liver
R Amino, D Giovannini, S Thiberge, P Gueirard, B Boisson, JF Dubremetz, ...
Cell host & microbe 3 (2), 88-96, 2008
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ...
Nature genetics 48 (9), 1071-1076, 2016
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
AY Kreins, MJ Ciancanelli, S Okada, XF Kong, N Ramírez-Alejo, SS Kilic, ...
Journal of Experimental Medicine 212 (10), 1641-1662, 2015
Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma
M Byun, A Abhyankar, V Lelarge, S Plancoulaine, A Palanduz, L Telhan, ...
Journal of Experimental Medicine 207 (11), 2307-2312, 2010
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis
B Boisson, C Wang, V Pedergnana, L Wu, S Cypowyj, M Rybojad, ...
Immunity 39 (4), 676-686, 2013
The mutation significance cutoff: gene-level thresholds for variant predictions
Y Itan, L Shang, B Boisson, MJ Ciancanelli, JG Markle, ...
Nature methods 13 (2), 109-110, 2016
Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms
C Giglione, A Serero, M Pierre, B Boisson, T Meinnel
The EMBO journal 19 (21), 5916-5929, 2000
Genetic diagnosis using whole exome sequencing in common variable immunodeficiency
P Maffucci, CA Filion, B Boisson, Y Itan, L Shang, JL Casanova, ...
Frontiers in immunology 7, 220, 2016
The human gene damage index as a gene-level approach to prioritizing exome variants
Y Itan, L Shang, B Boisson, E Patin, A Bolze, M Moncada-Vélez, E Scott, ...
Proceedings of the National Academy of Sciences 112 (44), 13615-13620, 2015
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
B Boisson, E Laplantine, K Dobbs, A Cobat, N Tarantino, M Hazen, ...
Journal of Experimental Medicine 212 (6), 939-951, 2015
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