PubRank

Eiichi Ishii

Author PubWeight™ 71.45‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Identification of a gene expression signature associated with pediatric AML prognosis. Blood 2003 1.71
2 Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL). Pediatr Blood Cancer 2006 1.56
3 Aurora kinase A-specific T-cell receptor gene transfer redirects T lymphocytes to display effective antileukemia reactivity. Blood 2011 1.54
4 Procalcitonin as a marker of respiratory disorder in neonates. Pediatr Int 2014 1.44
5 FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy. Blood 2003 1.26
6 Frequent co-expression of HoxA9 and Meis1 genes in infant acute lymphoblastic leukaemia with MLL rearrangement. Br J Haematol 2002 1.22
7 Perforin gene mutations in adult-onset hemophagocytic lymphohistiocytosis. Haematologica 2007 1.21
8 Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations. Am J Hematol 2007 1.20
9 Infant acute lymphoblastic leukemia with MLL gene rearrangements: outcome following intensive chemotherapy and hematopoietic stem cell transplantation. Blood 2004 1.18
10 Two distinct gene expression signatures in pediatric acute lymphoblastic leukemia with MLL rearrangements. Cancer Res 2003 1.16
11 Occurrence of haemophagocytic lymphohistiocytosis at less than 1 year of age: analysis of 96 patients. Eur J Pediatr 2005 1.14
12 Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan. Br J Haematol 2003 1.14
13 Hematopoietic stem cell transplantation for familial hemophagocytic lymphohistiocytosis and Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Japan. Pediatr Blood Cancer 2010 1.11
14 Essential roles of perforin in antigen-specific cytotoxicity mediated by human CD4+ T lymphocytes: analysis using the combination of hereditary perforin-deficient effector cells and Fas-deficient target cells. J Immunol 2003 1.05
15 Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis: Results from the Japan Langerhans Cell Histiocytosis Study Group-96 protocol study. Cancer 2006 1.04
16 Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan. Br J Haematol 2002 1.01
17 Clinical and genetic characteristics of XIAP deficiency in Japan. J Clin Immunol 2012 1.00
18 The association of a distinctive allele of NAD(P)H:quinone oxidoreductase with pediatric acute lymphoblastic leukemias with MLL fusion genes in Japan. Haematologica 2005 0.96
19 Characteristics of hemophagocytic lymphohistiocytosis in neonates: a nationwide survey in Japan. J Pediatr 2009 0.95
20 Infants with acute lymphoblastic leukemia and a germline MLL gene are highly curable with use of chemotherapy alone: results from the Japan Infant Leukemia Study Group. Blood 2006 0.91
21 A polymorphism in the promoter of the CD14 gene (CD14/-159) is associated with the development of coronary artery lesions in patients with Kawasaki disease. J Pediatr 2003 0.91
22 Protein-losing gastroenteropathy and retinitis associated with cytomegalovirus infection in an immunocompetent infant: a case report. Eur J Pediatr 2003 0.90
23 An immunologic case study of acute encephalitis with refractory, repetitive partial seizures. Brain Dev 2012 0.90
24 High aromatase activity and overexpression of epidermal growth factor receptor in fibrolamellar hepatocellular carcinoma in a child. J Pediatr Hematol Oncol 2011 0.89
25 Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis. Cancer 2002 0.89
26 Expression of matrix metalloproteinase (MMP) and tissue inhibitor of MMP (TIMP) genes in blasts of infant acute lymphoblastic leukemia with organ involvement. Leuk Res 2007 0.89
27 Risk-directed treatment of infant acute lymphoblastic leukaemia based on early assessment of MLL gene status: results of the Japan Infant Leukaemia Study (MLL96). Br J Haematol 2002 0.89
28 Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. Blood 2011 0.88
29 Expression of the Ikaros gene family in childhood acute lymphoblastic leukaemia. Br J Haematol 2002 0.88
30 Outcome of recurrent or refractory acute lymphoblastic leukemia in infants with MLL gene rearrangements: A report from the Japan Infant Leukemia Study Group. Pediatr Blood Cancer 2009 0.87
31 Early lineage switch in an infant acute lymphoblastic leukemia. Int J Hematol 2009 0.86
32 ACE2 deficiency induced perivascular fibrosis and cardiac hypertrophy during postnatal development in mice. J Am Soc Hypertens 2013 0.86
33 Thromboxane synthesis is increased by upregulation of cytosolic phospholipase A2 and cyclooxygenase-2 in peripheral polymorphonuclear leukocytes during bacterial infection in childhood. Am J Hematol 2003 0.85
34 Missense mutation and defective function of ATM in a childhood acute leukemia patient with MLL gene rearrangement. Blood 2003 0.85
35 Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes. PLoS One 2010 0.85
36 Prognostic factors of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children: report of the Japan Histiocytosis Study Group. Pediatr Blood Cancer 2014 0.85
37 Activation of central adenosine A(2A) receptors lowers the seizure threshold of hyperthermia-induced seizure in childhood rats. Seizure 2010 0.84
38 Beta-hydroxybutyrate alters GABA-transaminase activity in cultured astrocytes. Brain Res 2009 0.84
39 Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people. J Hum Genet 2005 0.84
40 Long-term outcome of coil occlusion in patients with patent ductus arteriosus. Circ J 2010 0.84
41 Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukaemia. Br J Haematol 2006 0.83
42 Reduced-intensity conditioning in unrelated donor cord blood transplantation for familial hemophagocytic lymphohistiocytosis. Am J Hematol 2012 0.83
43 Expression of CD180, a toll-like receptor homologue, is up-regulated in children with Kawasaki disease. J Mol Med (Berl) 2005 0.83
44 Neonatal iliopsoas abscess. Pediatr Int 2012 0.82
45 Successful bone marrow transplantation in a patient with c-mpl-mutated congenital amegakaryocytic thrombocytopenia from a carrier donor. Pediatr Transplant 2005 0.82
46 A nationwide survey of newly diagnosed childhood idiopathic thrombocytopenic purpura in Japan. J Pediatr Hematol Oncol 2009 0.81
47 Leukotriene synthesis is increased by transcriptional up-regulation of 5-lipoxygenase, leukotriene A4 hydrolase, and leukotriene C4 synthase in asthmatic children. J Asthma 2003 0.81
48 Detection of T-cell receptor gene rearrangement in children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis using the BIOMED-2 multiplex polymerase chain reaction combined with GeneScan analysis. Clin Chim Acta 2011 0.81
49 Novel dominant-negative mutant of GATA3 in HDR syndrome. J Mol Med (Berl) 2010 0.81
50 Hemophagocytic lymphohistiocytosis after hematopoietic stem cell transplantation in children: a nationwide survey in Japan. Pediatr Blood Cancer 2011 0.81
51 Life-threatening acute renal failure due to imperforate hymen in an infant. Pediatr Int 2012 0.80
52 Interleukin-18 primes human basophilic KU812 cells for higher leukotriene synthesis. Prostaglandins Leukot Essent Fatty Acids 2005 0.80
53 Anticonvulsive effect of paeoniflorin on experimental febrile seizures in immature rats: possible application for febrile seizures in children. PLoS One 2012 0.80
54 Association of transforming growth factor-beta1 gene polymorphism in the development of Epstein-Barr virus-related hematologic diseases. Haematologica 2007 0.79
55 ETV6-ARNT fusion in a patient with childhood T lymphoblastic leukemia. Cancer Genet Cytogenet 2010 0.79
56 Treatment of a child with myeloid/NK cell precursor acute leukemia with L-asparaginase and unrelated cord blood transplantation. Int J Hematol 2002 0.79
57 Clinical features and outcome of MLL gene rearranged acute lymphoblastic leukemia in infants with additional chromosomal abnormalities other than 11q23 translocation. Leuk Res 2008 0.79
58 Renal inflammatory changes in acute hepatic failure-associated acute kidney injury. Am J Nephrol 2013 0.79
59 Carbamazepine-induced drug-induced hypersensitivity syndrome in a 14-year-old Japanese boy. Epilepsia 2008 0.78
60 CLTC-ALK fusion as a primary event in congenital blastic plasmacytoid dendritic cell neoplasm. Genes Chromosomes Cancer 2013 0.78
61 CBL mutations in infant acute lymphoblastic leukaemia. Br J Haematol 2011 0.78
62 Clinical characteristics and outcomes of chédiak-Higashi syndrome: a nationwide survey of Japan. Pediatr Blood Cancer 2013 0.78
63 Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis. Pediatr Allergy Immunol 2012 0.78
64 Nationwide survey of single-system single site Langerhans cell histiocytosis in Japan. Pediatr Blood Cancer 2010 0.78
65 L-arginine is effective in stroke-like episodes of MELAS associated with the G13513A mutation. Brain Dev 2010 0.77
66 Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis. Br J Haematol 2008 0.77
67 Consensus guideline for diagnosis and treatment of childhood idiopathic thrombocytopenic purpura. Int J Hematol 2006 0.77
68 Postnatal interleukin-1β enhances adulthood seizure susceptibility and neuronal cell death after prolonged experimental febrile seizures in infantile rats. Acta Neurol Belg 2013 0.77
69 Pediatric subcutaneous panniculitis-like T-cell lymphoma with favorable result by immunosuppressive therapy: a report of two cases. Pediatr Hematol Oncol 2014 0.77
70 Autoimmune neutropenia of infancy with multiple brain abscesses during the course of human herpesvirus-6 infection. Int J Hematol 2006 0.77
71 Feasibility of reduced-intensity conditioning followed by unrelated cord blood transplantation for primary hemophagocytic lymphohistiocytosis: a nationwide retrospective analysis in Japan. Int J Hematol 2013 0.77
72 Interleukin-1beta enhances susceptibility to hyperthermia-induced seizures in developing rats. Seizure 2008 0.77
73 Gene-modified human α/β-T cells expressing a chimeric CD16-CD3ζ receptor as adoptively transferable effector cells for anticancer monoclonal antibody therapy. Cancer Immunol Res 2014 0.77
74 A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosis. Int J Hematol 2006 0.76
75 Postnatal interleukin-1β administration after experimental prolonged febrile seizures enhances epileptogenesis in adulthood. Metab Brain Dis 2015 0.76
76 Adenosine A1 receptor blockage mediates theophylline-associated seizures. Epilepsia 2009 0.76
77 Engraftment and dissemination of T lymphocytes from primary haemophagocytic lymphohistiocytosis in scid mice. Br J Haematol 2003 0.76
78 Clinical characteristics and outcome of Wilms tumors with a favorable histology in Japan: a report from the Study Group for Pediatric Solid Malignant Tumors in the Kyushu Area, Japan. J Pediatr Surg 2006 0.76
79 Long-term follow-up of children with refractory immune thrombocytopenia treated with rituximab. Int J Hematol 2014 0.76
80 Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children. J Clin Immunol 2011 0.76
81 Macrolide antibiotics inhibit prostaglandin E2 synthesis and mRNA expression of prostaglandin synthetic enzymes in human leukocytes. Prostaglandins Leukot Essent Fatty Acids 2003 0.75
82 Over-activation of adenosine A(2A) receptors and sudden unexpected death in epilepsy. Epilepsy Behav 2012 0.75
83 Evaluation of swallowing function in Duchenne muscular dystrophy. Dev Med Child Neurol 2008 0.75
84 Differences in automated analyzers for assessing the use of imprecise serum chloride concentrations as indirect predictors of serum bromide concentrations. Epilepsy Res 2011 0.75
85 [Recent progress in leukemic stem cell research for childhood leukemia]. Rinsho Ketsueki 2015 0.75
86 [Outcome and pathogenesis of infant leukemia]. Rinsho Ketsueki 2004 0.75
87 [Defect of secretory granules and hematologic disorders]. Rinsho Ketsueki 2008 0.75
88 Disodium cromoglycate suppresses the induction of cysteinyl leukotriene synthesis during granulocytic differentiation in HL-60 cells. Respir Med 2004 0.75
89 Tsukamurella inchonensis infection in a child with Hodgkin's lymphoma. Pediatr Int 2015 0.75
90 Idiopathic childhood occipital epilepsy of Gastaut: report of 12 patients. Pediatr Neurol 2011 0.75
91 Lineage-dependent skewing of loss of heterozygosity (LOH) of KRAS gene in a case of juvenile myelomonocytic leukemia. Eur J Haematol 2014 0.75
92 Identification of simultaneous mutation of fibrinogen alpha chain and protein C genes in a Japanese kindred. Br J Haematol 2003 0.75
93 Partial tandem duplication of MLL gene in acute myeloid leukemia with translocation (11;17)(q23;q12-21). Am J Hematol 2005 0.75
94 A four-year-old girl with cough, haemoptysis and anaemia. Acta Paediatr 2006 0.75
95 Use of a hand-made balloon-expandable covered stent for native coarctation of the aorta in an adult patient: a report of a first case in Japan. J Cardiol 2010 0.75
96 Familial hemophagocytic lymphohistiocytosis with the MUNC13-4 mutation: a case report. Eur J Pediatr 2006 0.75
97 Atypical childhood absence epilepsy with preceding or simultaneous generalized tonic clonic seizures. Brain Dev 2010 0.75
98 [Treatment outcome of non-Hodgkin lymphoma in childhood: KYCCSG NHL-89, 96]. Rinsho Ketsueki 2012 0.75
99 [Genetic defects and pathogenesis of hemophagocytic syndrome]. Rinsho Ketsueki 2006 0.75
100 Successful outcome of mismatched hematopoietic stem cell transplantation from a related donor in an infant with acute lymphoblastic leukemia and 9;11 translocation: case report and review of the literature. Int J Hematol 2005 0.75
101 [Progress in the molecular analysis of infant leukemias]. Rinsho Ketsueki 2009 0.75