Fabio Candotti
Fabio Candotti
Full Professor of Medicine, Lausanne University Hospital and University of Lausanne
Verified email at
Cited by
Cited by
Activated STING in a vascular and pulmonary syndrome
Y Liu, AA Jesus, B Marrero, D Yang, SE Ramsey, ...
New England Journal of Medicine 371 (6), 507-518, 2014
Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
P Macchi, A Villa, S Giliani, MG Sacco, A Frattini, F Porta, AG Ugazio, ...
Nature 377 (6544), 65-68, 1995
Actionable diagnosis of neuroleptospirosis by next-generation sequencing
MR Wilson, SN Naccache, E Samayoa, M Biagtan, H Bashir, G Yu, ...
New England Journal of Medicine 370 (25), 2408-2417, 2014
Early-onset stroke and vasculopathy associated with mutations in ADA2
Q Zhou, D Yang, AK Ombrello, AV Zavialov, C Toro, AV Zavialov, ...
New England Journal of Medicine 370 (10), 911-920, 2014
Engraftment potential of human amnion and chorion cells derived from term placenta
M Bailo, M Soncini, E Vertua, PB Signoroni, S Sanzone, G Lombardi, ...
Transplantation 78 (10), 1439-1448, 2004
Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans
F Candotti, KL Shaw, L Muul, D Carbonaro, R Sokolic, C Choi, ...
Blood, The Journal of the American Society of Hematology 120 (18), 3635-3646, 2012
The altered landscape of the human skin microbiome in patients with primary immunodeficiencies
J Oh, AF Freeman, M Park, R Sokolic, F Candotti, SM Holland, JA Segre, ...
Genome research 23 (12), 2103-2114, 2013
Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: long-term results of the first clinical gene therapy trial
LM Muul, LM Tuschong, SL Soenen, GJ Jagadeesh, WJ Ramsey, Z Long, ...
Blood, The Journal of the American Society of Hematology 101 (7), 2563-2569, 2003
How I treat ADA deficiency
HB Gaspar, A Aiuti, F Porta, F Candotti, MS Hershfield, LD Notarangelo
Blood, The Journal of the American Society of Hematology 114 (17), 3524-3532, 2009
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness
C Lagresle-Peyrou, EM Six, C Picard, F Rieux-Laucat, V Michel, A Ditadi, ...
Nature genetics 41 (1), 106-111, 2009
Structural and functional basis for JAK3-deficient severe combined immunodeficiency
F Candotti, SA Oakes, JA Johnston, S Giliani, RF Schumacher, P Mella, ...
Blood, The Journal of the American Society of Hematology 90 (10), 3996-4003, 1997
Immune response to fetal calf serum by two adenosine deaminase-deficient patients after T cell gene therapy
L Tuschong, SL Soenen, RM Blaese, F Candotti, LM Muul
Human gene therapy 13 (13), 1605-1610, 2002
Clinical manifestations and pathophysiological mechanisms of the Wiskott-Aldrich syndrome
F Candotti
Journal of clinical immunology 38 (1), 13-27, 2018
X-SCID transgene leukaemogenicity
AJ Thrasher, HB Gaspar, C Baum, U Modlich, A Schambach, F Candotti, ...
Nature 443 (7109), E5-E6, 2006
Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs
M Pesu, F Candotti, M Husa, SR Hofmann, LD Notarangelo, JJ O'Shea
Immunological reviews 203 (1), 127-142, 2005
Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency
JM Puck, AE Pepper, PS Henthorn, F Candotti, J Isakov, T Whitwam, ...
Blood, The Journal of the American Society of Hematology 89 (6), 1968-1977, 1997
Unexpected effects of FERM domain mutations on catalytic activity of Jak3: structural implication for Janus kinases
YJ Zhou, M Chen, NA Cusack, LH Kimmel, KS Magnuson, JG Boyd, W Lin, ...
Molecular cell 8 (5), 959-969, 2001
Transfer of the hsv-tk gene into donor peripheral blood lymphocytes for in vivo modulation of donor anti-tumor immunity after allogeneic bone marrow transplantation. the san …
C Bordignon, C Bonini, S Verzeletti, N Nobili, D Maggioni, C Traversari, ...
Human gene therapy 6 (6), 813-819, 1995
Complex effects of naturally occurring mutations in the JAK3 pseudokinase domain: evidence for interactions between the kinase and pseudokinase domains
M Chen, A Cheng, F Candotti, YJ Zhou, A Hymel, A Fasth, ...
Molecular and Cellular Biology 20 (3), 947-956, 2000
Somatic mosaicism in Wiskott–Aldrich syndrome suggests in vivo reversion by a DNA slippage mechanism
T Wada, SH Schurman, M Otsu, EK Garabedian, HD Ochs, DL Nelson, ...
Proceedings of the National Academy of Sciences 98 (15), 8697-8702, 2001
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