Onderzoeker
Mattias Van Heetvelde
- Trefwoorden:niet-coderende RNA, medische genetica, erfelijke kankersyndromen
- Disciplines:Genetica, Computationele transcriptomics en epigenomics, Kankerbiologie
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf19 nov 2018 → Heden - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 jan 2014 → 31 jan 2018 - Vakgroep Medische Basiswetenschappen (Departement)
Lid
Vanaf1 okt 2013 → 31 dec 2013
Projecten
1 - 1 of 1 results
- miRNAs als alternatieve second hits en potentiële therapeutische targets in erfelijke borst- en ovariumkankerVanaf1 jan 2014 → 31 dec 2017Financiering: IWT persoonsgebonden financ. - specialisatiebeurzen
Publicaties
1 - 10 of 12 results
- Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing(2020)
Auteurs: Giulia Ascari, Nanna D. Rendtorff, Julie Jacob, Julie De Zaeytijd, Valerie Baumont, Marieke De Bruyne, Toon Rosseel, Mattias Van Heetvelde, Tim De Pooter, Wouter De Coster, et al.
Aantal pagina's: 1 - miRNA expression profiles in BRCA1-associated breast cancers reveal upregulation of specific miRNAs in tumors lacking a clear second hit in a large proportion of the tumour(2019)Volume: 30
Auteurs: Mattias Van Heetvelde, Mieke R Van Bockstal, Jo Van Dorpe, Kim De Leeneer, Anne Vral, Kathleen Claes
Aantal pagina's: 1 - Second hits in BRCA1- and BRCA2-associated breast and ovarian cancer : connecting coding to non-coding mechanisms of inactivation(2019)
Auteurs: Mattias Van Heetvelde
Pagina's: 234 p. - Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations(2018)
Auteurs: Timothy R Rebbeck, Tara M Friebel, Eitan Friedman, Ute Hamann, Dezheng Huo, Ava Kwong, Edith Olah, Olufunmilayo I. Olopade, Angela R Solano, Soo-Hwang Teo, et al.
Pagina's: 593 - 620 - Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations(2018)
Auteurs: Kristof Van Schil, Sarah Naessens, Stijn Van De Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja Kathrin Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, et al.
Pagina's: 202 - 213 - Accurate detection and quantification of epigenetic and genetic second hits in BRCA1 and BRCA2-associated hereditary breast and ovarian cancer reveals multiple co-acting second hits(2018)
Auteurs: Mattias Van Heetvelde, Mieke Van Bockstal, Bruce Poppe, Kathleen Lambein, Toon Rosseel, Lilit Atanesyan, Dieter Deforce, Ivo Van Den Berghe, Kim De Leeneer, Jo Van Dorpe, et al.
Pagina's: 125 - 133 - Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations(2017)
Auteurs: Kristof Van Schil, Sarah Naessens, Stijn Van De Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja Kathrin Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, et al.
Aantal pagina's: 1 - Evaluation of relative quantification of alternatively spliced transcripts using droplet digital PCR(2017)
Auteurs: Mattias Van Heetvelde, Wouter Van Loocke, Wim Trypsteen, Annelot Baert, Katrien Vanderheyden, Brecht Crombez, Joke Vandesompele, Kim De Leeneer, Kathleen Claes
Pagina's: 40 - 48 - Second hit landscape in BRCA-associated breast cancer(2017)
Auteurs: Mattias Van Heetvelde, Mieke Van Bockstal, Trees Lepez, Steve Lefever, Leen Pieters, Kathleen Lambein, Marleen Praet, Ivo Van Den Berghe, Frauke Coppieters, Nadine Van Roy, et al.
Aantal pagina's: 1 - Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores(2017)
Auteurs: Julie Lecarpentier, Valentina Silvestri, Karoline B Kuchenbaecker, Daniel Barrowdale, Joe Dennis, Lesley McGuffog, Penny Soucy, Goska Leslie, Piera Rizzolo, Anna Sara Navazio, et al.
Pagina's: 2240 - 2250