PubRank

Dirk Roos

Author PubWeight™ 95.54‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Chronic granulomatous disease: the European experience. PLoS One 2009 3.04
2 Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease. Nat Med 2007 2.63
3 LAD-1/variant syndrome is caused by mutations in FERMT3. Blood 2008 2.22
4 Retracted CXCR2 mediates NADPH oxidase-independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation. Nat Med 2010 2.17
5 Single-cell Raman and fluorescence microscopy reveal the association of lipid bodies with phagosomes in leukocytes. Proc Natl Acad Sci U S A 2005 2.02
6 Natural history and early diagnosis of LAD-1/variant syndrome. Blood 2006 1.85
7 Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis. Blood 2004 1.65
8 Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B. Hum Mutat 2009 1.62
9 Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura. Blood 2007 1.60
10 Human NLRP3 inflammasome activation is Nox1-4 independent. Blood 2010 1.59
11 Infiltrated neutrophils acquire novel chemokine receptor expression and chemokine responsiveness in chronic inflammatory lung diseases. J Immunol 2008 1.56
12 Evidence consistent with human L1 retrotransposition in maternal meiosis I. Am J Hum Genet 2002 1.56
13 Repression of rac2 mRNA expression by Anaplasma phagocytophila is essential to the inhibition of superoxide production and bacterial proliferation. J Immunol 2002 1.52
14 Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency. Blood 2013 1.51
15 Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD). Hum Mutat 2010 1.49
16 Current concepts of hyperinflammation in chronic granulomatous disease. Clin Dev Immunol 2011 1.36
17 Mitochondrial membrane potential in human neutrophils is maintained by complex III activity in the absence of supercomplex organisation. PLoS One 2008 1.28
18 Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. J Allergy Clin Immunol 2013 1.25
19 Complement receptor 3, not Dectin-1, is the major receptor on human neutrophils for beta-glucan-bearing particles. Mol Immunol 2009 1.22
20 Intracellular expression of reactive oxygen species-generating NADPH oxidase NOX4 in normal and cancer thyroid tissues. Endocr Relat Cancer 2010 1.20
21 Mannose-binding lectin (MBL) facilitates opsonophagocytosis of yeasts but not of bacteria despite MBL binding. J Immunol 2008 1.19
22 Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization. Transfusion 2005 1.18
23 Granulocyte colony-stimulating factor inhibits the mitochondria-dependent activation of caspase-3 in neutrophils. Blood 2002 1.15
24 Unusual late presentation of X-linked chronic granulomatous disease in an adult female with a somatic mosaic for a novel mutation in CYBB. Blood 2004 1.15
25 Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship. Blood 2005 1.15
26 Refractive index sensing of green fluorescent proteins in living cells using fluorescence lifetime imaging microscopy. Biophys J 2008 1.14
27 Continuous translocation of Rac2 and the NADPH oxidase component p67(phox) during phagocytosis. J Biol Chem 2003 1.12
28 Tumor necrosis factor alpha induces a caspase-independent death pathway in human neutrophils. Blood 2002 1.08
29 Immunology. Lethal weapons. Science 2002 1.06
30 Apoptotic neutrophils in the circulation of patients with glycogen storage disease type 1b (GSD1b). Blood 2003 1.06
31 Expression of myeloperoxidase (MPO) by neutrophils is necessary for their activation by anti-neutrophil cytoplasm autoantibodies (ANCA) against MPO. J Leukoc Biol 2003 1.06
32 Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients. Clin Immunol 2008 1.05
33 Hematologically important mutations: leukocyte adhesion deficiency (first update). Blood Cells Mol Dis 2011 1.04
34 Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections. Blood 2006 1.01
35 Bid truncation, bid/bax targeting to the mitochondria, and caspase activation associated with neutrophil apoptosis are inhibited by granulocyte colony-stimulating factor. J Immunol 2004 0.96
36 The Rh complex exports ammonium from human red blood cells. Br J Haematol 2003 0.95
37 Functional epitope on human neutrophil flavocytochrome b558. J Immunol 2003 0.95
38 TLR expression on neutrophils at the pulmonary site of infection: TLR1/TLR2-mediated up-regulation of TLR5 expression in cystic fibrosis lung disease. J Immunol 2008 0.94
39 Activation of AP-1 through reactive oxygen species by angiotensin II in rat cardiomyocytes. Free Radic Biol Med 2005 0.93
40 Mannan-binding lectin (MBL)-mediated opsonization is enhanced by the alternative pathway amplification loop. Mol Immunol 2006 0.93
41 Pathogenesis of diseases associated with antineutrophil cytoplasm autoantibodies. Hum Immunol 2004 0.92
42 Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution melting. J Mol Diagn 2010 0.92
43 Dysregulation of innate immune receptors on neutrophils in chronic granulomatous disease. J Allergy Clin Immunol 2007 0.91
44 Neutrophil responsiveness to IgG, as determined by fixed ratios of mRNA levels for activating and inhibitory FcgammaRII (CD32), is stable over time and unaffected by cytokines. Blood 2006 0.90
45 Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease. J Allergy Clin Immunol 2010 0.90
46 Mannose-binding lectin (MBL) substitution: recovery of opsonic function in vivo lags behind MBL serum levels. J Immunol 2009 0.89
47 Deconjugation kinetics of glucuronidated phase II flavonoid metabolites by beta-glucuronidase from neutrophils. Drug Metab Pharmacokinet 2010 0.89
48 Delayed but functional neutrophil extracellular trap formation in neonates. Blood 2009 0.88
49 An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3' haplotypes could modify circulating levels of mannose-binding lectin. Hum Genet 2005 0.88
50 Complement receptor 3 and Toll-like receptor 4 act sequentially in uptake and intracellular killing of unopsonized Salmonella enterica serovar Typhimurium by human neutrophils. Infect Immun 2007 0.88
51 Acute lymphoblastic leukemia in a patient with chronic granulomatous disease and a novel mutation in CYBB: first report. Am J Hematol 2005 0.86
52 Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case study. PLoS One 2009 0.85
53 Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections. Blood 2002 0.85
54 Growth factors G-CSF and GM-CSF differentially preserve chemotaxis of neutrophils aging in vitro. Exp Hematol 2007 0.85
55 H9c2 cardiomyoblasts produce thyroid hormone. Am J Physiol Cell Physiol 2008 0.85
56 Lessons learned from phagocytic function studies in a large cohort of patients with recurrent infections. J Clin Immunol 2011 0.85
57 Functional analysis of two-amino acid substitutions in gp91 phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells. Hum Genet 2004 0.85
58 Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1. Prenat Diagn 2002 0.84
59 SIRPα controls the activity of the phagocyte NADPH oxidase by restricting the expression of gp91(phox). Cell Rep 2012 0.84
60 Homocysteine affects cardiomyocyte viability: concentration-dependent effects on reversible flip-flop, apoptosis and necrosis. Apoptosis 2007 0.84
61 Celiac disease and pulmonary hemosiderosis in a patient with chronic granulomatous disease. Pediatr Pulmonol 2004 0.84
62 Single-cell optical imaging of the phagocyte NADPH oxidase. Antioxid Redox Signal 2006 0.84
63 Primary immunodeficiency caused by an exonized retroposed gene copy inserted in the CYBB gene. Hum Mutat 2014 0.84
64 Molecular basis of glutathione reductase deficiency in human blood cells. Blood 2006 0.83
65 Application of a human multidrug transporter (ABCG2) variant as selectable marker in gene transfer to progenitor cells. Hum Gene Ther 2003 0.83
66 Parenteral lipids modulate leukocyte phenotypes in whole blood, depending on their fatty acid composition. Clin Nutr 2005 0.83
67 Diurnal fluctuation of leukocyte G6PD activity. A possible explanation for the normal neutrophil bactericidal activity and the low incidence of pyogenic infections in patients with severe G6PD deficiency in Israel. Pediatr Res 2004 0.82
68 Granulocyte concentrates: prolonged functional capacity during storage in the presence of phenotypic changes. Haematologica 2008 0.82
69 A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation. J Hum Genet 2009 0.82
70 Homocysteine-induced apoptosis in endothelial cells coincides with nuclear NOX2 and peri-nuclear NOX4 activity. Cell Biochem Biophys 2013 0.82
71 Resonance Raman imaging of the NADPH oxidase subunit cytochrome b558 in single neutrophilic granulocytes. J Am Chem Soc 2003 0.82
72 A novel splice variant of FcγRIIa: a risk factor for anaphylaxis in patients with hypogammaglobulinemia. J Allergy Clin Immunol 2013 0.81
73 beta-Globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays. Eur J Hum Genet 2004 0.81
74 Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humans. PLoS One 2013 0.80
75 Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous disease. Eur J Hum Genet 2013 0.79
76 Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous disease. Biochim Biophys Acta 2013 0.79
77 A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous disease. Blood Cells Mol Dis 2005 0.78
78 Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease. Pediatr Infect Dis J 2011 0.78
79 The search for a genetic defect in Polish patients with chronic granulomatous disease. Arch Immunol Ther Exp (Warsz) 2004 0.78
80 Two X-linked chronic granulomatous disease patients with unusual NADPH oxidase properties. J Clin Immunol 2011 0.78
81 Plasma levels of mannan-binding lectin in relation to periodontitis and smoking. J Periodontol 2005 0.78
82 Priming by tumor necrosis factor-alpha of human neutrophil NADPH-oxidase activity induced by anti-proteinase-3 or anti-myeloperoxidase antibodies. J Leukoc Biol 2006 0.78
83 Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different families. J Clin Immunol 2012 0.77
84 Molecular basis of autosomal recessive chronic granulomatous disease in iran. J Clin Immunol 2010 0.77
85 Lipid effects on neutrophil calcium signaling induced by opsonized particles: platelet activating factor is only part of the story. Clin Nutr 2004 0.77
86 Lymphadenopathy after BCG vaccination in a child with chronic granulomatous disease. Pediatr Dermatol 2004 0.77
87 Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiency. Ann Hematol 2012 0.76
88 A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II. Am J Med Genet A 2005 0.76
89 Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece. J Clin Immunol 2013 0.76
90 Pro-myeloperoxidase, a target antigen for antineutrophil cytoplasm autoantibodies: comment on the article by Russell et al. Arthritis Rheum 2002 0.75
91 Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1. Am J Hematol 2012 0.75
92 Recurrent pyoderma gangrenosum and cystic acne associated with leucocyte adhesion deficiency due to novel mutations in ITGB2: successful treatment with infliximab and adalimumab. Acta Derm Venereol 2015 0.75
93 Decreased redox state in red blood cells from patients with sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 2002 0.75
94 Prenatal diagnosis of chronic granulomatous disease in a male fetus. Iran J Allergy Asthma Immunol 2009 0.75