Vincent Pedergnana
Vincent Pedergnana
Genome Institute of Singapore, A*STAR
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Cited by
Cited by
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
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
Exome and genome sequencing for inborn errors of immunity
I Meyts, B Bosch, A Bolze, B Boisson, Y Itan, A Belkadi, V Pedergnana, ...
Journal of Allergy and Clinical Immunology 138 (4), 957-969, 2016
Inherited DOCK2 deficiency in patients with early-onset invasive infections
K Dobbs, C Domínguez Conde, SY Zhang, S Parolini, M Audry, J Chou, ...
New England Journal of Medicine 372 (25), 2409-2422, 2015
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both
F Lanternier, SA Mahdaviani, E Barbati, H Chaussade, Y Koumar, R Levy, ...
Journal of Allergy and Clinical Immunology 135 (6), 1558-1568. e2, 2015
Genome sequencing analysis identifies Epstein–Barr virus subtypes associated with high risk of nasopharyngeal carcinoma
M Xu, Y Yao, H Chen, S Zhang, SM Cao, Z Zhang, B Luo, Z Liu, Z Li, ...
Nature genetics, 1, 2019
Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections
A Crequer, A Troeger, E Patin, CS Ma, C Picard, V Pedergnana, C Fieschi, ...
The Journal of clinical investigation 122 (9), 3239-3247, 2012
Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood
M Byun, CS Ma, A Akçay, V Pedergnana, U Palendira, J Myoung, ...
Journal of Experimental Medicine 210 (9), 1743-1759, 2013
Inherited CARD9 Deficiency in 2 Unrelated Patients With Invasive Exophiala Infection
F Lanternier, E Barbati, U Meinzer, L Liu, V Pedergnana, M Migaud, ...
The Journal of infectious diseases 211 (8), 1241-1250, 2014
Genome-to-genome analysis highlights the effect of the human innate and adaptive immune systems on the hepatitis C virus
MA Ansari, V Pedergnana, CLC Ip, A Magri, A Von Delft, D Bonsall, ...
Nature genetics 49 (5), 666, 2017
Merkel cell polyomavirus infection occurs during early childhood and is transmitted between siblings
C Martel-Jantin, V Pedergnana, JTJ Nicol, V Leblond, DA Trégouët, ...
Journal of Clinical Virology 58 (1), 288-291, 2013
Human adaptive immunity rescues an inborn error of innate immunity
L Israel, Y Wang, K Bulek, E Della Mina, Z Zhang, V Pedergnana, ...
Cell 168 (5), 789-800. e10, 2017
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
A Belkadi, V Pedergnana, A Cobat, Y Itan, QB Vincent, A Abhyankar, ...
Proceedings of the National Academy of Sciences 113 (24), 6713-6718, 2016
Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus
V Pedergnana, M Abdel-Hamid, J Guergnon, A Mohsen, L Le Fouler, ...
PloS one 7 (6), e38578, 2012
EVER2 deficiency is associated with mild T-cell abnormalities
A Crequer, C Picard, V Pedergnana, A Lim, SY Zhang, L Abel, S Majewski, ...
Journal of clinical immunology 33 (1), 14-21, 2013
Modifier locus of the skeletal muscle involvement in Emery–Dreifuss muscular dystrophy
B Granger, L Gueneau, V Drouin-Garraud, V Pedergnana, F Gagnon, ...
Human genetics 129 (2), 149-159, 2011
Interferon lambda 4 impacts the genetic diversity of hepatitis C virus
MA Ansari, E Aranday-Cortes, CLC Ip, A Da Silva Filipe, LS Hin, ...
eLife, 2019
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review
S Leroy, D Moshous, O Cassar, Y Reguerre, M Byun, V Pedergnana, ...
Pediatrics 129 (1), e199-e203, 2012
Host genetic factors associated with hepatocellular carcinoma in patients with hepatitis C virus infection: a systematic review
AJ Walker, CJ Peacock, V Pedergnana, STOP‐HCV Consortium, ...
Journal of viral hepatitis 25 (5), 442-456, 2018
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency
R Martínez-Barricarte, O Megged, P Stepensky, P Casimir, ...
Journal of clinical immunology 34 (8), 904-909, 2014
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