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Frank Speleman

Researcher Next ID · RN-039543

Researcher · Biochemistry, Genetics and Molecular Biology

Ghent University

Ghent, Belgium

Accepting doctoral researchersFunding unknown
Works count
812
Citation count
26,337
H-index
83
i10-index
276

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Neuroblastoma Research and Treatments
Cancer, Hypoxia, and Metabolism
Protein Degradation and Inhibitors
Genomic variations and chromosomal abnormalities
Acute Myeloid Leukemia Research

Publications

  • A mechanistic classification of clinical phenotypes in neuroblastoma

    Science · 2018 · https://doi.org/10.1126/science.aat6768

  • Mutational dynamics between primary and relapse neuroblastomas

    Nature Genetics · 2015 · 10.1038/ng.3349

  • Therapeutic targeting of the MYC signal by inhibition of histone chaperone FACT in neuroblastoma

    Science Translational Medicine · 2015 · https://doi.org/10.1126/scitranslmed.aab1803

  • Mutational dynamics between primary and relapse neuroblastomas

    Nature Genetics · 2015 · 10.1038/ng.3349

  • Emergence of New ALK Mutations at Relapse of Neuroblastoma

    Journal of Clinical Oncology · 2014 · https://doi.org/10.1200/jco.2013.54.0674

  • RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer

    Nature · 2014 · 10.1038/nature13485

  • RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer

    Nature · 2014 · 10.1038/nature13485

  • Comprehensive Analysis of Transcriptome Variation Uncovers Known and Novel Driver Events in T-Cell Acute Lymphoblastic Leukemia

    PLoS Genetics · 2013 · https://doi.org/10.1371/journal.pgen.1003997

  • LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression

    Nature Genetics · 2012 · 10.1038/ng.2436

  • LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression

    Nature Genetics · 2012 · 10.1038/ng.2436

  • A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL)

    Nature Genetics · 2011 · https://doi.org/10.1038/ng.858

  • Meta-analysis of Neuroblastomas Reveals a Skewed ALK Mutation Spectrum in Tumors with MYCN Amplification

    Clinical Cancer Research · 2010 · https://doi.org/10.1158/1078-0432.ccr-09-2660

  • PHF6 mutations in adult acute myeloid leukemia

    Leukemia · 2010 · https://doi.org/10.1038/leu.2010.247

  • miR-9, a MYC/MYCN-activated microRNA, regulates E-cadherin and cancer metastasis

    Nature Cell Biology · 2010 · 10.1038/ncb2024

  • PHF6 mutations in T-cell acute lymphoblastic leukemia

    Nature Genetics · 2010 · 10.1038/ng.542

  • The miR-17-92 MicroRNA Cluster Regulates Multiple Components of the TGF-β Pathway in Neuroblastoma

    Molecular Cell · 2010 · 10.1016/j.molcel.2010.11.038

  • miR-9, a MYC/MYCN-activated microRNA, regulates E-cadherin and cancer metastasis

    Nature Cell Biology · 2010 · 10.1038/ncb2024

  • PHF6 mutations in T-cell acute lymphoblastic leukemia

    Nature Genetics · 2010 · 10.1038/ng.542

  • The miR-17-92 MicroRNA Cluster Regulates Multiple Components of the TGF-β Pathway in Neuroblastoma

    Molecular Cell · 2010 · 10.1016/j.molcel.2010.11.038

  • Overall Genomic Pattern Is a Predictor of Outcome in Neuroblastoma

    Journal of Clinical Oncology · 2009 · https://doi.org/10.1200/jco.2008.16.0630

  • A novel and universal method for microRNA RT-qPCR data normalization

    Genome biology · 2009 · 10.1186/gb-2009-10-6-r64

  • International consensus for neuroblastoma molecular diagnostics: report from the International Neuroblastoma Risk Group (INRG) Biology Committee

    British Journal of Cancer · 2009 · https://doi.org/10.1038/sj.bjc.6605014

  • Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study

    The Lancet Oncology · 2009 · https://doi.org/10.1016/s1470-2045(09)70154-8

  • Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

    Journal of Medical Genetics · 2009 · https://doi.org/10.1136/jmg.2008.063412

  • A novel and universal method for microRNA RT-qPCR data normalization

    Genome biology · 2009 · 10.1186/gb-2009-10-6-r64

  • Identification of ALK as a major familial neuroblastoma predisposition gene

    Nature · 2008 · 10.1038/nature07261

  • High-throughput stem-loop RT-qPCR miRNA expression profiling using minute amounts of input RNA

    Nucleic Acids Research · 2008 · 10.1093/nar/gkn725

  • Identification of ALK as a major familial neuroblastoma predisposition gene

    Nature · 2008 · 10.1038/nature07261

  • High-throughput stem-loop RT-qPCR miRNA expression profiling using minute amounts of input RNA

    Nucleic Acids Research · 2008 · 10.1093/nar/gkn725

  • Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

    New England Journal of Medicine · 2008 · https://doi.org/10.1056/nejmoa0805384

  • qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data

    Genome biology · 2007 · 10.1186/gb-2007-8-2-r19

  • Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

    Nature Genetics · 2007 · https://doi.org/10.1038/ng2025

  • qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data

    Genome biology · 2007 · 10.1186/gb-2007-8-2-r19

  • Unequivocal Delineation of Clinicogenetic Subgroups and Development of a New Model for Improved Outcome Prediction in Neuroblastoma

    Journal of Clinical Oncology · 2005 · https://doi.org/10.1200/jco.2005.06.104

  • Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

    Nature Genetics · 2004 · https://doi.org/10.1038/ng1453

  • Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    Nature Genetics · 2003 · 10.1038/ng1122

  • Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    Nature Genetics · 2003 · 10.1038/ng1122

  • ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma

    Blood · 2003 · https://doi.org/10.1182/blood-2003-04-1050

  • Elimination of Primer–Dimer Artifacts and Genomic Coamplification Using a Two-Step SYBR Green I Real-Time RT-PCR

    Analytical Biochemistry · 2002 · 10.1006/abio.2001.5564

  • Elimination of Primer–Dimer Artifacts and Genomic Coamplification Using a Two-Step SYBR Green I Real-Time RT-PCR

    Analytical Biochemistry · 2002 · 10.1006/abio.2001.5564

  • Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein–methyltransferase superfamily

    Genes & Development · 2001 · 10.1101/gad.870101

  • Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein–methyltransferase superfamily

    Genes & Development · 2001 · 10.1101/gad.870101

  • Exhaustive mutation analysis of theNF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects

    Human Mutation · 2000 · https://doi.org/10.1002/1098-1004(200006)15:6<541::aid-humu6>3.0.co;2-n

  • EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts

    Nature Genetics · 1993 · 10.1038/ng0893-341

  • EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts

    Nature Genetics · 1993 · 10.1038/ng0893-341

Current projects

    No projects listed.