Researcher
Bruce Poppe
- Keywords:heritable cancer syndromes, metabolic disorders, medical genetics, clinical genetics, rare diseases
- Disciplines:Nucleic acids, Genetics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 1998 → 30 Sep 2018
Projects
1 - 7 of 7
- Grant in 2018 from the Flemish Community to the Centers for Human GeneticsFrom1 Jan 2018 → 31 Dec 2018Funding: Department Welfare, Public Health and Culture
- ETV6: the AchillesU+2019 heel of early T-cell progenitor T-cell acute lymphoblastic leukemia.From1 Oct 2012 → 30 Sep 2016Funding: FWO fellowships, BOF - Other initiatives
- PHF6: a new tumor suppressor gene in T-cell acute lymphoblastic leukemiaFrom1 Jan 2010 → 31 Dec 2015Funding: FWO research project (including WEAVE projects)
- Deregulated transcriptional networks of regulatory miRNAs and protein coding genes in the pathogenesis of cancerFrom1 Jan 2010 → 31 Oct 2016Funding: BOF - Concerted Research Project from 1994
- The role of PHF6 in normal and malign T-cell development.From1 Oct 2009 → 30 Sep 2013Funding: BOF - Other initiatives, FWO fellowships
- The role of miRNA expression in normal and malignant T-cel developmentFrom1 Jan 2009 → 31 Dec 2014Funding: FWO research project (including WEAVE projects)
- The role of miRNA expression in normal and malignant T-cell developmentFrom1 Jan 2009 → 31 Dec 2010Funding: Foundations, funds and other with scientific goal
Publications
1 - 10 of 113
- A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing(2023)
Authors: Nolwenn Jean-Marçais, Estrella López-Martín, Maria Antonietta Mencarelli, Sébastien Moutton, Rolph Pfundt, Hana Safraou, Christel Thauvin-Robinet, Julien Thevenon, Frédéric Tran Mau-Them, Bert B.A. de Vries, et al.
- Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders(2023)
Authors: Nika Schuermans, Hannah Verdin, Jody Ghijsels, Madeleine Hellemans, Elke Debackere, Elke Bogaert, Sofie Symoens, Leslie Naesens, Elien Lecomte, David Crosiers, et al.
- Twist exome capture allows for lower average sequence coverage in clinical exome sequencing(2023)
Authors: Burcu Yaldiz, Erdi Kucuk, Juliet Hampstead, Tom Hofste, Rolph Pfundt, Jordi Corominas Galbany, Tuula Rinne, Helger G. Yntema, Alexander Hoischen, Marcel Nelen, et al.
- Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3(2022)Volume: 30
Authors: Nika Schuermans, Salima El Chehadeh, Dimitri Hemelsoet, Elke Bogaert, Pascale Hilbert, Nike Van Doninck, Marie-Caroline Taquet, Toon Rosseel, Griet De Clercq, Carole Van Haverbeke, et al.
Pages: 80 - 80 - Prolonged recombinant pregnancy hormone use in BRCA1 and BRCA2 mutation carriers(2021)
Authors: Herman Depypere, Yanrong Su, Nhi Dang, Bruce Poppe, Frank Stanczyk, Jaak Janssens, Jose Russo
Pages: 195 - 203 - Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients(2021)
Authors: Greet Wieme, Jan Kral, Toon Rosseel, Petra Zemankova, Bram Parton, Michal Vocka, Mattias Van Heetvelde, Petra Kleiblova, Bettina Blaumeiser, Jana Soukupova, et al.
Number of pages: 1 - Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients(2021)
Authors: Greet Wieme, Jan Kral, Toon Rosseel, Petra Zemankova, Bram Parton, Michal Vocka, Petra Kleiblova, Bettina Blaumeiser, Jana Soukupova, Jenneke van den Ende, et al.
- A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers(2021)
Authors: Juliette Coignard, Michael Lush, Jonathan Beesley, Tracy A. O'Mara, Joe Dennis, Jonathan P. Tyrer, Daniel R. Barnes, Lesley McGuffog, Goska Leslie, Manjeet K. Bolla, et al.
- Tissue is the issue : when a second biopsy reveals the true diagnosis(2021)
Authors: Anne-Marie Bogaert, Anne Hoorens, Marleen Praet, Jo Van Dorpe, Bruce Poppe, Marie-Angélique De Scheerder
Pages: 429 - 431 - Analysis of patients with a personal and/or family history of pancreatic cancer with a custom designed broad cancer predisposition gene panel(2019)
Authors: Greet Wieme, Toon Rosseel, Bram Parton, Bettina Blaumeiser, Jenneke van den Ende, Sabine Tejpar, Bruce Poppe, Kim De Leeneer, Kathleen Claes
Number of pages: 1