Stefano Volpi
Stefano Volpi
Istituto Gaslini, Genova, Italy
Verified email at
TitleCited byYear
Bone marrow‐derived mesenchymal stem cells induce both polyclonal expansion and differentiation of B cells isolated from healthy donors and systemic lupus erythematosus patients
E Traggiai, S Volpi, F Schena, M Gattorno, F Ferlito, L Moretta, A Martini
Stem cells 26 (2), 562-569, 2008
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, 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
A three-dimensional model of human lung development and disease from pluripotent stem cells
YW Chen, SX Huang, ALRT De Carvalho, SH Ho, MN Islam, S Volpi, ...
Nature cell biology 19 (5), 542, 2017
B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice
M Recher, SO Burns, A Miguel, S Volpi, C Dahlberg, JE Walter, K Moffitt, ...
Blood 119 (12), 2819-2828, 2012
Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling
I Melki, Y Rose, C Uggenti, L Van Eyck, ML Frémond, N Kitabayashi, ...
Journal of Allergy and Clinical Immunology 140 (2), 543-552. e5, 2017
Dependence of immunoglobulin class switch recombination in B cells on vesicular release of ATP and CD73 ectonucleotidase activity
F Schena, S Volpi, CE Faliti, F Penco, S Santi, M Proietti, U Schenk, ...
Cell reports 3 (6), 1824-1831, 2013
Type I interferon-mediated autoinflammation due to DNase II deficiency
MP Rodero, A Tesser, E Bartok, GI Rice, E Della Mina, M Depp, B Beitz, ...
Nature communications 8 (1), 2176, 2017
Type I interferonopathies in pediatric rheumatology
S Volpi, P Picco, R Caorsi, F Candotti, M Gattorno
Pediatric Rheumatology 14 (1), 35, 2016
Powering the immune system: mitochondria in immune function and deficiency
MA Walker, S Volpi, KB Sims, JE Walter, E Traggiai
Journal of immunology research 2014, 2014
Novel genome-editing tools to model and correct primary immunodeficiencies
LM Ott de Bruin, S Volpi, K Musunuru
Frontiers in immunology 6, 250, 2015
Allele-specific regulation of primary cilia function by the von Hippel–Lindau tumor suppressor
MP Lolkema, DA Mans, LH Ulfman, S Volpi, EE Voest, RH Giles
European Journal of Human Genetics 16 (1), 73, 2008
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with Wiskott–Aldrich syndrome
AE O’Connell, S Volpi, K Dobbs, C Fiorini, E Tsitsikov, H de Boer, ...
Frontiers in immunology 5, 340, 2014
Type I interferon pathway activation in COPA syndrome
S Volpi, J Tsui, M Mariani, C Pastorino, R Caorsi, O Sacco, A Ravelli, ...
Clinical Immunology 187, 33-36, 2018
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay
S Volpi, Y Yamazaki, PM Brauer, E van Rooijen, A Hayashida, ...
Journal of Experimental Medicine 214 (3), 623-637, 2017
Next‐generation sequencing reveals restriction and clonotypic expansion of Treg cells in juvenile idiopathic arthritis
LA Henderson, S Volpi, F Frugoni, E Janssen, S Kim, RP Sundel, ...
Arthritis & Rheumatology 68 (7), 1758-1768, 2016
Enhancement of muscle T regulatory cells and improvement of muscular dystrophic process in mdx mice by blockade of extracellular ATP/P2X axis
E Gazzerro, S Baldassari, S Assereto, F Fruscione, A Pistorio, C Panicucci, ...
The American journal of pathology 185 (12), 3349-3360, 2015
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
E Crestani, S Volpi, F Candotti, S Giliani, LD Notarangelo, J Chu, ...
Journal of Allergy and Clinical Immunology 136 (5), 1401-1404. e3, 2015
Predisposition to infection and SIRS in mitochondrial disorders: 8 years' experience in an academic center
MA Walker, N Slate, A Alejos, S Volpi, RS Iyengar, D Sweetser, KB Sims, ...
The Journal of Allergy and Clinical Immunology: In Practice 2 (4), 465-468. e1, 2014
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
I Brigida, M Zoccolillo, MP Cicalese, L Pfajfer, F Barzaghi, S Scala, ...
Blood 132 (22), 2362-2374, 2018
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