Published in Br J Haematol on April 01, 2003
High risk of subsequent neoplasms continues with extended follow-up of childhood Hodgkin's disease: report from the Late Effects Study Group. J Clin Oncol (2003) 3.14
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor. Nat Genet (2008) 2.24
Aberrant DNA hypermethylation signature in acute myeloid leukemia directed by EVI1. Blood (2010) 2.15
Inactivation of HOXA genes by hypermethylation in myeloid and lymphoid malignancy is frequent and associated with poor prognosis. Clin Cancer Res (2007) 2.08
Identification of a vacuolar sucrose transporter in barley and Arabidopsis mesophyll cells by a tonoplast proteomic approach. Plant Physiol (2006) 2.02
Effectiveness and safety of procalcitonin-guided antibiotic therapy in lower respiratory tract infections in "real life": an international, multicenter poststudy survey (ProREAL). Arch Intern Med (2012) 2.01
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. Blood (2002) 1.83
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus. Nat Genet (2012) 1.82
Second primary tumors in neurofibromatosis 1 patients treated for optic glioma: substantial risks after radiotherapy. J Clin Oncol (2006) 1.63
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3. Blood (2009) 1.62
Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia. Br J Haematol (2005) 1.53
The impact of monitoring Epstein-Barr virus PCR in paediatric bone marrow transplant patients: can it successfully predict outcome and guide intervention? Pediatr Blood Cancer (2006) 1.49
Interventions for preventing oral mucositis for patients with cancer receiving treatment. Cochrane Database Syst Rev (2011) 1.49
The Arabidopsis vacuolar malate channel is a member of the ALMT family. Plant J (2007) 1.40
Classification schemes for tumors diagnosed in adolescents and young adults. Cancer (2006) 1.35
Molecular identification and physiological characterization of a novel monosaccharide transporter from Arabidopsis involved in vacuolar sugar transport. Plant Cell (2006) 1.31
PmSUC3: characterization of a SUT2/SUC3-type sucrose transporter from Plantago major. Plant Cell (2003) 1.30
Excellent outcome of matched unrelated donor transplantation in paediatric aplastic anaemia following failure with immunosuppressive therapy: a United Kingdom multicentre retrospective experience. Br J Haematol (2012) 1.29
HLA-A alleles and infectious mononucleosis suggest a critical role for cytotoxic T-cell response in EBV-related Hodgkin lymphoma. Proc Natl Acad Sci U S A (2010) 1.27
Interventions for treating oral mucositis for patients with cancer receiving treatment. Cochrane Database Syst Rev (2010) 1.25
Vacuolar transporters in their physiological context. Annu Rev Plant Biol (2012) 1.18
Genetic variation in the folate metabolic pathway and risk of childhood leukemia. Blood (2010) 1.14
Comparative incidence patterns and trends of gonadal and extragonadal germ cell tumors in England, 1979 to 2003. Cancer (2012) 1.10
AtALMT9 is a malate-activated vacuolar chloride channel required for stomatal opening in Arabidopsis. Nat Commun (2013) 1.10
Age-incidence patterns of primary CNS tumors in children, adolescents, and adults in England. Neuro Oncol (2008) 1.08
The human leukocyte antigen class I region is associated with EBV-positive Hodgkin's lymphoma: HLA-A and HLA complex group 9 are putative candidate genes. Cancer Epidemiol Biomarkers Prev (2006) 1.07
Changes in cancer incidence in teenagers and young adults (ages 13 to 24 years) in England 1979-2003. Cancer (2008) 1.06
Malignant peripheral nerve sheath tumours in inherited disease. Clin Sarcoma Res (2012) 1.03
Genetic susceptibility to childhood common acute lymphoblastic leukaemia is associated with polymorphic peptide-binding pocket profiles in HLA-DPB1*0201. Hum Mol Genet (2002) 1.02
Germline mutations and polymorphisms in the NFKBIA gene in Hodgkin lymphoma. Int J Cancer (2005) 0.97
Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry-based blood group genotyping--the alternative approach. Transfus Med Rev (2013) 0.95
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations. Genes Chromosomes Cancer (2005) 0.93
Registration and classification of adolescent and young adult cancer cases. Pediatr Blood Cancer (2008) 0.93
Cancer at ages 15-29 years: the contrasting incidence in India and England. Pediatr Blood Cancer (2010) 0.92
An epidemiologic study of index and family infectious mononucleosis and adult Hodgkin's disease (HD): evidence for a specific association with EBV+ve HD in young adults. Int J Cancer (2003) 0.91
Further clues concerning the aetiology of childhood central nervous system tumours. Eur J Cancer (2004) 0.90
The contrasting age-incidence patterns of bone tumours in teenagers and young adults: Implications for aetiology. Int J Cancer (2012) 0.89
Interventions for preventing oral mucositis for patients with cancer receiving treatment. Cochrane Database Syst Rev (2010) 0.88
Quantitative detection of changes in the leaf-mesophyll tonoplast proteome in dependency of a cadmium exposure of barley (Hordeum vulgare L.) plants. Proteomics (2009) 0.88
Novel Sinorhizobium meliloti quorum sensing positive and negative regulatory feedback mechanisms respond to phosphate availability. Mol Microbiol (2009) 0.88
Are reported increases in incidence of primary CNS tumours real? An analysis of longitudinal trends in England, 1979-2003. Eur J Cancer (2010) 0.88
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay. Blood (2011) 0.88
Geographical and ecological analyses of childhood acute leukaemias and lymphomas in north-west England. Br J Haematol (2003) 0.87
Cancer incidence and mortality among the parents of a population-based series of 2604 children with cancer. Cancer Epidemiol Biomarkers Prev (2003) 0.87
Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site. Cancer Genet Cytogenet (2004) 0.87
Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling. J Med Genet (2013) 0.86
Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FA. Blood (2011) 0.86
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes Chromosomes Cancer (2007) 0.86
Ribosomal RNA gene sequences confirm that protistan endoparasite of larval cod Gadus morhua is Ichthyodinium sp. Dis Aquat Organ (2010) 0.84
Interventions for treating oral candidiasis for patients with cancer receiving treatment. Cochrane Database Syst Rev (2010) 0.84
Network analysis identifies protein clusters of functional importance in juvenile idiopathic arthritis. Arthritis Res Ther (2014) 0.83
Temporal expression program of quorum sensing-based transcription regulation in Sinorhizobium meliloti. J Bacteriol (2013) 0.83
Space-time clustering patterns in childhood solid tumours other than central nervous system tumours. Int J Cancer (2003) 0.82
Is there a common aetiology for certain childhood malignancies? Results of cross-space-time clustering analyses. Eur J Cancer (2005) 0.82
Epigenetic inactivation of TWIST2 in acute lymphoblastic leukemia modulates proliferation, cell survival and chemosensitivity. Haematologica (2011) 0.81
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma. Fam Cancer (2012) 0.81
Fanconi and Glanzmann: the men and their works. Br J Haematol (2002) 0.80
Relationship between height at diagnosis and bone tumours in young people: a meta-analysis. Cancer Causes Control (2011) 0.80
Geographical and ecological analyses of childhood Wilms' tumours and soft-tissue sarcomas in North West England. Eur J Cancer (2003) 0.80
Correspondence re: R. Varon et al., Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res., 61: 3570-3572, 2001. Cancer Res (2003) 0.80
Bone mineral density in childhood survivors of acute lymphoblastic leukemia treated without cranial irradiation. J Clin Endocrinol Metab (2004) 0.80
Cancer risks among relatives of children with Hodgkin and non-Hodgkin lymphoma. Int J Cancer (2008) 0.79
Pediatric perspective on pharmacogenomics. Pharmacogenomics (2013) 0.79
Boerhaave syndrome following chemotherapy in a child with acute lymphoblastic leukemia. Pediatr Blood Cancer (2004) 0.79
Pollicization of the index finger in Fanconi anaemia: appearances and functionality 40 years after the intervention. Br J Haematol (2014) 0.78
Identification of a rare polymorphism in the human TP53 promoter. Cancer Genet Cytogenet (2002) 0.77
Pseudoautosomal linkage of familial Hodgkin's lymphoma: molecular analysis of a unique family with Leri-Weill dyschondrosteosis and Hodgkins lymphoma. Br J Haematol (2003) 0.77
Physical exercise induces specific adaptations resulting in reduced organ injury and mortality during severe polymicrobial sepsis. Crit Care Med (2013) 0.76
Phosphorylation of the leukemic oncoprotein EVI1 on serine 196 modulates DNA binding, transcriptional repression and transforming ability. PLoS One (2013) 0.76
Identification of MAIN, a factor involved in genome stability in the meristems of Arabidopsis thaliana. Plant J (2013) 0.76
Cultured autografting for juvenile myelomonocytic leukaemia. Br J Haematol (2002) 0.76
Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia. Br J Haematol (2006) 0.76
UK case control study of brain tumours in children, teenagers and young adults: a pilot study. BMC Res Notes (2014) 0.75
A molecular, genetic, and diagnostic spotlight on fanconi anemia. Anemia (2012) 0.75
Median percent change: a robust alternative for assessing temporal trends. Cancer Epidemiol (2013) 0.75
Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome. Blood Cells Mol Dis (2003) 0.75
Acquired chemosensitivity after insect bite in a boy with leukaemia. Br J Haematol (2006) 0.75