| 38049555 | Characterisation of FLT3 alterations in childhood acute lymphoblastic leukaemia. | Br J Cancer | 2024 |
| 37777587 | Repurposing disulfiram, an alcohol-abuse drug, in neuroblastoma causes KAT2A downregulation and in vivo activity with a water/oil emulsion. | Sci Rep | 2023 |
| 35198911 | Identification of new ETV6 modulators through a high-throughput functional screening. | iScience | 2022 |
| 35703228 | Distinct transcriptomic profile of small arteries of hypertensive patients with chronic kidney disease identified miR-338-3p targeting GPX3 and PTPRS. | J Hypertens | 2022 |
| 33161775 | Chromosome 2 Fragment Substitutions in Dahl Salt-Sensitive Rats and RNA Sequencing Identified <i>Enpep</i> and <i>Hs2st1</i> as Vascular Inflammatory Modulators. | Hypertension | 2021 |
| 33654212 | Publisher Correction: Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity. | Sci Rep | 2021 |
| 34331108 | Repurposing proscillaridin A in combination with decitabine against embryonal rhabdomyosarcoma RD cells. | Cancer Chemother Pharmacol | 2021 |
| 32415257 | Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity. | Sci Rep | 2020 |
| 33245684 | Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia. | Epigenomics | 2020 |
| 32115655 | Circulating let-7g-5p and miR-191-5p Are Independent Predictors of Chronic Kidney Disease in Hypertensive Patients. | Am J Hypertens | 2020 |
| 30575814 | Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma. | Oncogene | 2019 |
| 31196146 | Heart failure drug proscillaridin A targets MYC overexpressing leukemia through global loss of lysine acetylation. | J Exp Clin Cancer Res | 2019 |
| 30929512 | miR-431-5p Knockdown Protects Against Angiotensin II-Induced Hypertension and Vascular Injury. | Hypertension | 2019 |
| 29365312 | Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy. | Blood Adv | 2018 |
| 30341373 | Genome wide mapping of ETV6 binding sites in pre-B leukemic cells. | Sci Rep | 2018 |
| 30440012 | Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes. | PLoS One | 2018 |
| 28069604 | KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemia. | Blood | 2017 |
| 28346506 | Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia. | PLoS One | 2017 |
| 29113332 | LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response. | Oncotarget | 2017 |
| 27980230 | A childhood acute lymphoblastic leukemia-specific lncRNA implicated in prednisolone resistance, cell proliferation, and migration. | Oncotarget | 2017 |
| 27540136 | CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia. | Haematologica | 2016 |
| 27842494 | SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing. | BMC Genomics | 2016 |
| 27602765 | Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations. | Oncotarget | 2016 |
| 26201965 | Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes. | BMC Cancer | 2015 |
| 26345285 | A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells. | BMC Cancer | 2015 |
| 24038028 | Impact of promoter polymorphisms in key regulators of the intrinsic apoptosis pathway on the outcome of childhood acute lymphoblastic leukemia. | Haematologica | 2014 |
| 23722552 | Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia. | Cancer Res | 2013 |
| 21573116 | ALG: automated genotype calling of Luminex assays. | PLoS One | 2011 |
| 20617153 | Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia. | J Biomed Biotechnol | 2010 |
| 20460642 | Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. | Haematologica | 2010 |
| 11774269 | Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. | Int J Cancer | 2002 |
| 11943609 | Analyses of bulky DNA adduct levels in human breast tissue and genetic polymorphisms of cytochromes P450 (CYPs), myeloperoxidase (MPO), quinone oxidoreductase (NQO1), and glutathione S-transferases (GSTs). | Mutat Res | 2002 |
| 11291049 | Genetic susceptibility to breast cancer in French-Canadians: role of carcinogen-metabolizing enzymes and gene-environment interactions. | Int J Cancer | 2001 |
| 10868688 | Genetic polymorphisms of N-acetyltransferases 1 and 2 and gene-gene interaction in the susceptibility to childhood acute lymphoblastic leukemia. | Cancer Epidemiol Biomarkers Prev | 2000 |
| 10542112 | Rapid detection of CYP1A1, CYP2D6, and NAT variants by multiplex polymerase chain reaction and allele-specific oligonucleotide assay. | Anal Biochem | 1999 |
| 10082612 | Phylogenetic affinities of tarsier in the context of primate Alu repeats. | Mol Phylogenet Evol | 1999 |
| 10029576 | Susceptibility to childhood acute lymphoblastic leukemia: influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 genetic polymorphisms. | Blood | 1999 |
| 9691987 | Chromosomal assignment of loci susceptible to replication errors by radiation hybrid mapping. | Mutat Res | 1998 |
| 9591122 | Isolation of stable bacterial artificial chromosome DNA using a modified alkaline lysis method. | Biotechniques | 1998 |
| 9792139 | Genomic loci susceptible to replication errors in cancer cells. | Br J Cancer | 1998 |
| 9694666 | Monophyletic origin of Alu elements in primates. | J Mol Evol | 1998 |
| 8665504 | Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction. | Cancer Res | 1996 |
| 7838713 | A young Alu subfamily amplified independently in human and African great apes lineages. | Nucleic Acids Res | 1994 |
| 1507221 | Alu RNA transcripts in human embryonal carcinoma cells. Model of post-transcriptional selection of master sequences. | J Mol Biol | 1992 |
| 1618495 | Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. | Hum Genet | 1992 |
| 1709156 | Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units. | J Biol Chem | 1991 |
| 1710278 | Evolution of mouse B1 repeats: 7SL RNA folding pattern conserved. | J Mol Evol | 1991 |