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Onderzoeker
Sylvia De Brakeleer
- Trefwoorden:Geneeskunde
- Disciplines:Moleculaire diagnostiek, Genetica, Kankerbiologie, Genetische predispositie, Analyse van next-generation sequence data
Affiliaties
- Observerende Klinische wetenschappen (Departement)
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Vanaf8 apr 2019 → 28 jun 2019 - Faculteit van de Geneeskunde en Farmacie (Faculteit)
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Vanaf14 aug 2015 → 28 jun 2016 - Observerende Klinische wetenschappen (Departement)
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Vanaf1 jan 2014 → 28 jun 2019 - Laboratorium Moleculaire Oncologie (Onderzoeksgroep)
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Vanaf1 jan 2010 → 22 mrt 2021 - Embryologie en Menselijke Genetica (Departement)
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Vanaf1 mrt 2003 → 31 dec 2013
Publicaties
11 - 14 van 14
- Systematic Detection of Pathogenic Alu Element Insertions in NGS-Based Diagnostic Screens: The BRCA1/BRCA2 Example(2013)
Auteurs: Sylvia De Brakeleer, Erik Teugels
Pagina's: 785-791 - Correlation of EGFR, IDH1 and PTEN status with the outcome of patients with recurrent glioblastoma treated in a phase II clinical trial with the EGFR-blocking monoclonal antibody cetuximab(2012)
Auteurs: Shasha Lv, Erik Teugels, Jan Sadones, Sylvia De Brakeleer, Johnny Duerinck, Stephanie Du Four, Alex Michotte, Jacques De Grève, Bart Neyns
Pagina's: 1029-1035 - Cancer predisposing missense and protein truncating BARD1 mutations in non BRCA1 or BRCA2 breast cancer families(2010)
Auteurs: Sylvia De Brakeleer, Jacques De Grève, Remy Loris, Nicolas Janin, Willy Lissens, Erika Sermijn, Erik Teugels
Pagina's: 1175-1185 - Hereditary breast cancer: from bench to bedside.(2008)
Auteurs: Sylvia De Brakeleer, Erik Teugels, Erika Sermijn, Zhuo Ren
Pagina's: 605-613
Gelinkte datasets
1 - 7 van 7
- Additional file 9: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 1: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 6: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 4: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 11: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 5: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)
- Additional file 3: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families (Creator)