PubRank

Kenichi Koike

Author PubWeight™ 70.75‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Spontaneous improvement of hematologic abnormalities in patients having juvenile myelomonocytic leukemia with specific RAS mutations. Blood 2007 2.23
2 Anakinra improves sensory deafness in a Japanese patient with Muckle-Wells syndrome, possibly by inhibiting the cryopyrin inflammasome. Arthritis Rheum 2008 1.72
3 Features and outcome of neonatal leukemia in Japan: experience of the Japan infant leukemia study group. Pediatr Blood Cancer 2006 1.56
4 Association between serum uric acid levels and cardiometabolic risk factors among Japanese junior high school students. Circ J 2010 1.44
5 Serum levels of free light chain before and after chemotherapy in primary systemic AL amyloidosis. Intern Med 2005 1.43
6 Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome. Blood 2003 1.40
7 Right-to-left shunting in the ductus arteriosus is induced readily by intense crying and rapid postural change in neonates with meconium-stained amniotic fluid. Pediatr Crit Care Med 2012 1.38
8 Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions. Blood 2005 1.37
9 Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation. Blood 2010 1.32
10 Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations. Am J Hematol 2007 1.20
11 IL-9 enhances the growth of human mast cell progenitors under stimulation with stem cell factor. J Immunol 2003 1.17
12 ASC, which is composed of a PYD and a CARD, is up-regulated by inflammation and apoptosis in human neutrophils. Biochem Biophys Res Commun 2002 1.16
13 Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. Pediatr Res 2009 1.08
14 Mutations in the ribosomal protein genes in Japanese patients with Diamond-Blackfan anemia. Haematologica 2010 1.07
15 Cytomegalovirus retinitis during maintenance therapy for T-cell acute lymphoblastic leukemia. J Pediatr Hematol Oncol 2013 0.94
16 Neurodevelopmental features in 2q23.1 microdeletion syndrome: report of a new patient with intractable seizures and review of literature. Am J Med Genet A 2012 0.93
17 Allogeneic haematopoietic cell transplantation from alternative donors with a conditioning regimen of low-dose irradiation, fludarabine and cyclophosphamide in Fanconi anaemia. Br J Haematol 2006 0.92
18 Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia. Br J Haematol 2009 0.90
19 CD30+ anaplastic large cell lymphoma complicated by pyoderma gangrenosum with increased levels of serum cytokines. Eur J Haematol 2006 0.90
20 Treatment of neurodegenerative CNS disease in Langerhans cell histiocytosis with a combination of intravenous immunoglobulin and chemotherapy. Pediatr Blood Cancer 2008 0.89
21 Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia. Br J Haematol 2014 0.88
22 Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemia. Br J Haematol 2005 0.88
23 Usefulness of allogeneic hematopoietic stem cell transplantation in first complete remission for pediatric blastic plasmacytoid dendritic cell neoplasm with skin involvement: a case report and review of literature. Pediatr Blood Cancer 2013 0.87
24 Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS). Am J Med Genet A 2015 0.87
25 Effect of parathyroid hormone administration in a patient with severe hypoparathyroidism caused by gain-of-function mutation of calcium-sensing receptor. Endocr J 2006 0.86
26 Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36. Am J Med Genet A 2008 0.86
27 Acquisition of loss of the wild-type NRAS locus with aggressive disease progression in a patient with juvenile myelomonocytic leukemia and a heterozygous NRAS mutation. Haematologica 2007 0.85
28 Serologic analysis of three cases of neonatal alloimmune thrombocytopenia associated with HLA antibodies. Transfusion 2003 0.85
29 Long-term haematological improvement after non-intensive or no chemotherapy in juvenile myelomonocytic leukaemia and poor correlation with adult myelodysplasia spliceosome-related mutations. Br J Haematol 2012 0.84
30 Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia. Blood 2012 0.83
31 Food allergy after cord blood transplantation in children. Br J Haematol 2012 0.83
32 Transcriptional profiling in hepatoblastomas using high-density oligonucleotide DNA array. Cancer Genet Cytogenet 2003 0.82
33 Long-term survival after nonintensive chemotherapy in some juvenile myelomonocytic leukemia patients with CBL mutations, and the possible presence of healthy persons with the mutations. Blood 2010 0.82
34 Regulation of mast cell development. Chem Immunol Allergy 2005 0.82
35 Neurodegenerative central nervous system disease as late sequelae of Langerhans cell histiocytosis. Report from the Japan LCH Study Group. Haematologica 2008 0.81
36 Cerebellar ataxia in pediatric patients with Langerhans cell histiocytosis. J Pediatr Hematol Oncol 2004 0.81
37 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
38 IL-6 enhances IgE-dependent histamine release from human peripheral blood-derived cultured mast cells. Cytokine 2002 0.81
39 Synergism between stem cell factor and granulocyte-macrophage colony-stimulating factor on cell proliferation by induction of cyclins. Cytokine 2002 0.81
40 Analysis of histone modification around the CpG island region of the p15 gene in acute myeloblastic leukemia. Leuk Res 2006 0.81
41 Low toxicity of a conditioning with 8-Gy total body irradiation, fludarabine and cyclophosphamide as preparative regimen for allogeneic hematopoietic stem cell transplantation in pediatric hematological malignancies. Pediatr Transplant 2008 0.81
42 Superoxide dismutase (SOD) as a potential inhibitory mediator of inflammation via neutrophil apoptosis. Free Radic Res 2005 0.81
43 Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing. Am J Med Genet A 2012 0.80
44 Long-term follow-up of plasma cells in bone marrow and serum free light chains in primary systemic AL amyloidosis. Intern Med 2008 0.80
45 Analysis of class I and II aberrations in Iraqi childhood acute myeloid leukemia using filter paper cards. Ann Hematol 2014 0.80
46 High-dose melphalan followed by autologous stem cell support in primary systemic AL amyloidosis with multiple organ involvement. Intern Med 2005 0.79
47 Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction. Gene 2013 0.79
48 STI571 inhibits growth and adhesion of human mast cells in culture. J Leukoc Biol 2003 0.79
49 Specific autoantibodies to platelet glycoproteins in Epstein-Barr virus-associated immune thrombocytopenia. Int J Hematol 2003 0.78
50 Increased pretransplant QT dispersion as a risk factor for the development of cardiac complications during and after preparative conditioning for pediatric allogeneic hematopoietic stem cell transplantation. Pediatr Transplant 2010 0.78
51 Novel compound heterozygous mutation of the MC2R gene in a patient with familial glucocorticoid deficiency. J Pediatr Endocrinol Metab 2006 0.78
52 A possible role for the production of multiple HLA antibodies in fatal platelet transfusion refractoriness after peripheral blood progenitor cell transplantation from the mother in a patient with relapsed leukemia. Transfusion 2007 0.78
53 Effect of the mutant microphthalmia-associated transcription factor found in Tietz syndrome on the in vitro development of mast cells. J Pediatr Hematol Oncol 2010 0.78
54 Development of two cytogenetically abnormal clones from multipotential hematopoietic stem cells in a patient with juvenile myelomonocytic leukemia. Leuk Res 2005 0.78
55 A case of Behcet's disease associated with myelodysplastic syndrome involving trisomy 8 and a gain-of-function mutation in SHP-2. Rheumatology (Oxford) 2011 0.78
56 Prophylactic treatment for hypertension and seizure in a case of allogeneic hematopoietic stem cell transplantation after posterior reversible encephalopathy syndrome. Pediatr Transplant 2010 0.78
57 Risk factors for diabetes mellitus and impaired glucose tolerance following allogeneic hematopoietic stem cell transplantation in pediatric patients with hematological malignancies. Int J Hematol 2014 0.78
58 Granulocyte-macrophage colony-stimulating factor induces de novo methylation of the p15 CpG island in hematopoietic cells. Cytokine 2005 0.78
59 Cardiovascular Remodeling and Dysfunction Across a Range of Growth Restriction Severity in Small for Gestational Age Infants　- Implications for Fetal Programming. Circ J 2016 0.78
60 Ela2 mutations and clinical manifestations in familial congenital neutropenia. J Pediatr Hematol Oncol 2009 0.78
61 Identification of a high incidence region for retroviral vector integration near exon 1 of the LMO2 locus. Retrovirology 2009 0.78
62 VAD with or without subsequent high-dose melphalan followed by autologous stem cell support in AL amyloidosis: Japanese experience and criteria for patient selection. Amyloid 2004 0.78
63 Successful cord blood transplantation after repeated transfusions of unmobilized neutrophils in addition to antifungal treatment in an infant with chronic granulomatous disease complicated by invasive pulmonary aspergillosis. Transfusion 2013 0.77
64 Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan. Genes Chromosomes Cancer 2014 0.77
65 ARF tumor suppressor induces mitochondria-dependent apoptosis by modulation of mitochondrial Bcl-2 family proteins. J Biol Chem 2003 0.77
66 Serial monitoring of Mucorales DNA load in serum samples of a patient with disseminated mucormycosis after allogeneic bone marrow transplantation. Int J Hematol 2014 0.77
67 Nephrotic syndrome due to primary AL amyloidosis, successfully treated with VAD and subsequent high-dose melphalan followed by autologous peripheral blood stem cell transplantation. Intern Med 2003 0.77
68 Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants. Eur J Pediatr 2014 0.77
69 Factor H gene variants in Japanese: its relation to atypical hemolytic uremic syndrome. Mol Immunol 2011 0.76
70 Monitoring serum IL-18 levels is useful for treatment of a patient with systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome. Pediatr Rheumatol Online J 2011 0.76
71 A complex karyotype, including a three-way translocation generating a NUP98-HOXD13 transcript, in an infant with acute myeloid leukemia. Cancer Genet Cytogenet 2007 0.76
72 Successful treatment of fulminant Wilson's disease without liver transplantation. Pediatr Int 2014 0.76
73 Successful unrelated cord blood transplantation using a reduced-intensity conditioning regimen in a 6-month-old infant with congenital neutropenia complicated by severe pneumonia. Int J Hematol 2004 0.76
74 Polymyxin-direct hemoperfusion for sepsis-induced multiple organ failure. Pediatr Blood Cancer 2010 0.76
75 Genetic analysis of TP53 in childhood myelodysplastic syndrome and juvenile myelomonocytic leukemia. Leuk Res 2011 0.76
76 HLA-identical sibling peripheral blood stem cell transplantation in children and adolescents. Biol Blood Marrow Transplant 2002 0.76
77 Viral infections in juvenile myelomonocytic leukemia: prevalence and clinical implications. J Pediatr Hematol Oncol 2004 0.76
78 Extremely low flow tracheal gas insufflation of helium-oxygen mixture improves gas exchange in a rabbit model of piston-type high-frequency oscillatory ventilation. Biomed Eng Online 2013 0.75
79 Frequent coexistence of RAS mutations in RUNX1-mutated acute myeloid leukemia in Arab Asian children. Pediatr Blood Cancer 2014 0.75
80 HDM2 impairs Noxa transcription and affects apoptotic cell death in a p53/p73-dependent manner in neuroblastoma. Eur J Cancer 2010 0.75
81 Cryptic insertion into 11q23 of MLLT10 not involved in t(1;15;11;10)(p36;q11;q23;q24) in infant acute biphenotypic leukemia. Cancer Genet Cytogenet 2009 0.75
82 Skin infiltration of juvenile myelomonocytic leukemia. J Dermatol 2004 0.75
83 Disappearance of minimal residual disease after the early withdrawal of immunosuppressants in a patient with juvenile myelomonocytic leukemia. Pediatr Blood Cancer 2010 0.75
84 Retrospective analysis of risk factors for development of liver dysfunction in transient leukemia of Down syndrome. Leuk Lymphoma 2011 0.75
85 [Diagnosis of H. pylori infection in children]. Nihon Rinsho 2009 0.75
86 High incidence of meropenem resistance among alpha-hemolytic streptococci in children with cancer. Pediatr Int 2009 0.75
87 Gastroduodenal lesions in primary AL amyloidosis. Gastrointest Endosc 2002 0.75
88 Increasing Risk of Disturbed Root Development in Permanent Teeth in Childhood Cancer Survivors Undergoing Cancer Treatment at Older Age. J Pediatr Hematol Oncol 2017 0.75
89 Reflex seizures induced by micturition and defecation, successfully treated with clobazam and phenytoin. Epileptic Disord 2011 0.75
90 Viral Infections in Juvenile Myelomonocytic Leukemia: Prevalence and Clinical Implications. J Pediatr Hematol Oncol 2004 0.75
91 Generalised acanthosis nigricans in childhood with short stature associated with poor response to growth hormone provocation. Acta Derm Venereol 2014 0.75
92 Genetic evaluation of childhood acute lymphoblastic leukemia in Iraq using FTA cards. Pediatr Blood Cancer 2012 0.75
93 Urinary excretion of ganciclovir contributes to improvement of adenovirus-associated hemorrhagic cystitis after allogeneic bone marrow transplantation. Pediatr Transplant 2008 0.75
94 Prognostic Significance of QT Interval Dispersion in the Response to Intravenous Immunoglobulin Therapy in Kawasaki Disease. Circ J 2017 0.75
95 IgM AL amyloidosis due to B cell lymphoproliferative disorder: efficacy of high-dose melphalan followed by autologous stem cell transplantation. Amyloid 2004 0.75
96 Evaluation of intensive chemotherapy in AL amyloidosis: usefulness of flow cytometric analysis of plasma cells in bone marrow. Amyloid 2003 0.75
97 [Molecular mechanism and progress in treatment of juvenile myelomonocytic leukemia (JMML)]. Rinsho Ketsueki 2013 0.75
98 Effective combination therapy using interferon-gamma and interleukin-2 for disseminated Mycobacterium avium complex infection in a pediatric patient with AIDS. Clin Infect Dis 2005 0.75
99 Telecommunication system for children undergoing stem cell transplantation. Pediatr Int 2011 0.75
100 Bilineage acute leukemia of T-lymphoid and myeloid lineages. Haematologica 2004 0.75
101 Distinct response in maintenance of human naive and memory B cells via IL-21 receptor and TCL1/Akt pathways. Cell Immunol 2009 0.75
102 Replaced platelet concentrates containing a new additive solution, M-sol: safety and efficacy for pediatric patients. Transfusion 2012 0.75
103 Dramatic Reduction in Tumor Size During 5 Months of Pazopanib Therapy in Combination With Ifosfamide, Carboplatin, and Etoposide in an Early Infant With Progressive Soft Tissue Sarcoma. J Pediatr Hematol Oncol 2017 0.75
104 Long-term epidemiologic longitudinal study on the effect of vaccines on public inoculation. Turk J Pediatr 2013 0.75
105 Critical illness polyneuropathy and myopathy caused by Bacillus cereus sepsis in acute lymphoblastic leukemia. J Pediatr Hematol Oncol 2012 0.75
106 Impact of Decreased Serum Insulin-Like Growth Factor-1 Levels on Central Aortic Compliance in Small-for-Gestational-Age Infants. Neonatology 2016 0.75
107 [Fanconi's pancytopenia syndrome]. Nihon Rinsho 2006 0.75
108 The clinical characteristics of vitamin D deficiency in childhood: a systematic literature review of Japanese patients. J Pediatr Endocrinol Metab 2010 0.75