PubRank

Claire Fieschi

Author PubWeight™ 76.15‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Pyogenic bacterial infections in humans with IRAK-4 deficiency. Science 2003 4.80
2 Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency. Nat Genet 2003 3.95
3 Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. J Exp Med 2008 3.85
4 Common variable immunodeficiency disorders: division into distinct clinical phenotypes. Blood 2008 3.44
5 Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features. Semin Immunol 2006 3.41
6 Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries. Medicine (Baltimore) 2010 2.33
7 X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production. J Exp Med 2006 2.18
8 Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect. Clin Infect Dis 2009 2.00
9 Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations. Nat Genet 2005 1.99
10 Infections in 252 patients with common variable immunodeficiency. Clin Infect Dis 2008 1.93
11 FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function. Blood 2009 1.91
12 Bacillus Calmette Guerin triggers the IL-12/IFN-gamma axis by an IRAK-4- and NEMO-dependent, non-cognate interaction between monocytes, NK, and T lymphocytes. Eur J Immunol 2004 1.83
13 Tuberculosis in children and adults: two distinct genetic diseases. J Exp Med 2005 1.80
14 Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease. Nat Immunol 2011 1.76
15 Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease. PLoS Genet 2006 1.74
16 Interleukin (IL)-12 and IL-23 are key cytokines for immunity against Salmonella in humans. J Infect Dis 2004 1.71
17 Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds. Am J Hum Genet 2001 1.70
18 From idiopathic infectious diseases to novel primary immunodeficiencies. J Allergy Clin Immunol 2005 1.54
19 The human spleen is a major reservoir for long-lived vaccinia virus-specific memory B cells. Blood 2008 1.48
20 Paracoccidioides brasiliensis disseminated disease in a patient with inherited deficiency in the beta1 subunit of the interleukin (IL)-12/IL-23 receptor. Clin Infect Dis 2005 1.46
21 B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease. J Clin Immunol 2010 1.39
22 An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis. Immunity 2013 1.35
23 Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey. Medicine (Baltimore) 2012 1.31
24 Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiency. Clin Infect Dis 2003 1.16
25 A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo. Blood 2008 1.16
26 Interleukin-12 receptor beta 1 chain deficiency in a child with disseminated tuberculosis. Clin Infect Dis 2005 1.14
27 Immunoglobulin dosage and switch from intravenous to subcutaneous immunoglobulin replacement therapy in patients with primary hypogammaglobulinemia: decreasing dosage does not alter serum IgG levels. J Clin Immunol 2010 1.12
28 Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q. Eur J Hum Genet 2006 1.02
29 T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cells. J Immunol 2006 1.01
30 Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections. J Clin Invest 2012 1.00
31 A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease. J Med Genet 2007 0.99
32 Revisiting human primary immunodeficiencies. J Intern Med 2008 0.97
33 Variable outcome of experimental interferon-gamma therapy of disseminated Bacillus Calmette-Guerin infection in two unrelated interleukin-12Rbeta1-deficient Slovakian children. Eur J Pediatr 2005 0.95
34 18F-fluorodeoxyglucose positron emission tomography/computed tomography in AIDS-related Burkitt lymphoma. AIDS Patient Care STDS 2008 0.95
35 Interleukin-12 receptor beta1 deficiency presenting as recurrent Salmonella infection. Clin Infect Dis 2003 0.95
36 Rituximab decreases the risk of lymphoma in patients with HIV-associated multicentric Castleman disease. Blood 2012 0.92
37 High frequency of fatal haemophagocytic lymphohistiocytosis syndrome in enteropathy-associated T cell lymphoma. Dig Liver Dis 2011 0.91
38 Association of IL12RB1 polymorphisms with pulmonary tuberculosis in adults in Morocco. J Infect Dis 2004 0.91
39 Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. J Clin Invest 2017 0.90
40 Oesophageal squamous cell carcinoma in a young adult with IL-12R beta 1 deficiency. J Med Genet 2010 0.90
41 Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency. J Pediatr 2006 0.89
42 Complete deficiency of the IL-12 receptor beta1 chain: three unrelated Turkish children with unusual clinical features. Eur J Pediatr 2006 0.89
43 Granulomatous disease in CVID: retrospective analysis of clinical characteristics and treatment efficacy in a cohort of 59 patients. J Clin Immunol 2012 0.88
44 Dasatinib-induced lupus. Lancet 2008 0.86
45 Intensive chemotherapy regimen (LMB86) for St Jude stage IV AIDS-related Burkitt lymphoma/leukemia: a prospective study. Blood 2007 0.85
46 Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency. J Allergy Clin Immunol 2010 0.81
47 Inherited defects in the interferon-gamma receptor or interleukin-12 signalling pathways are not sufficient to cause allergic disease in children. Eur J Pediatr 2005 0.80
48 Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency. J Clin Immunol 2011 0.77
49 Characteristics of non-Hodgkin lymphoma arising in HIV-infected patients with suppressed HIV replication. AIDS 2009 0.77
50 Retroviral-mediated gene transfer restores IL-12 and IL-23 signaling pathways in T cells from IL-12 receptor beta1-deficient patients. Mol Ther 2004 0.77
51 High risk of infectious disease caused by salmonellae and mycobacteria infections in patients with Crohn disease treated with anti-interleukin-12 antibody. Clin Infect Dis 2005 0.76
52 Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review. Pediatrics 2011 0.76
53 Autoimmune hemolytic anemia and nodular lymphocyte-predominant hodgkin lymphoma: a rare association. Case Rep Hematol 2013 0.75
54 Rectal Lymphogranuloma Venereum in HIV-infected Patients Can Mimic Lymphoma. J Clin Gastroenterol 2016 0.75
55 [Gains of glycosylation mutations]. Med Sci (Paris) 2006 0.75
56 [Rosai-Dorfman disease]. Presse Med 2007 0.75
57 Human herpesvirus 8+ polyclonal IgMλ B-cell lymphocytosis mimicking plasmablastic leukemia/lymphoma in HIV-infected patients. Eur J Haematol 2013 0.75
58 Cutaneous tumor lysis syndrome in a patient with HTLV-1 adult T-cell lymphoma/leukemia. Blood 2009 0.75
59 [Common variable immunodeficiency]. Rev Prat 2007 0.75
60 A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency. J Clin Immunol 2019 0.75