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Researcher
Marjolein Carron
Profile
Projects
Publications
Activities
8
Results
2020
Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos
Thomas Naert
Dieter Tulkens
Marjolein Carron
Annekatrien Boel
Suzan Demuynck
Paul Coucke
Andy Willaert
Kris Vleminckx
A1
Journal Article
in
SCIENTIFIC REPORTS
2020
RBL1 (p107) functions as tumor suppressor in glioblastoma and small-cell pancreatic neuroendocrine carcinoma in Xenopus tropicalis
Thomas Naert
Dionysia Dimitrakopoulou
Dieter Tulkens
Suzan Demuynck
Marjolein Carron
Rivka Noelanders
Gert Van Isterdael
Dieter Deforce
Christian Vanhove
Jo Van Dorpe
David Creytens
Kris Vleminckx
A1
Journal Article
in
ONCOGENE
2020
2018
CRISPR/Cas9 mediated knockout of rcbtb1 in Xenopus tropicalis to model RCBTB1-associated retinal disease
Giulia Ascari
Thomas Naert
Tom Van Nieuwenhuysen
Marjolein Carron
Suzan Demuynck
Chris Guerin
Frauke Coppieters
Kris Vleminckx
Elfride De Baere
C3
Conference
2018
Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes
Kristof Van Schil
Sarah Naessens
Stijn Van de Sompele
Marjolein Carron
Sarah De Jaegere
Frauke Coppieters
Bart Leroy
Elfride De Baere
C3
Conference
2018
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
Kristof Van Schil
Sarah Naessens
Stijn Van de Sompele
Marjolein Carron
Caroline Van Cauwenbergh
Mattias Van Heetvelde
Miriam Bauwens
Hannah Verdin
Frauke Coppieters
Katleen De Preter
Bart Leroy
Elfride De Baere
A1
Journal Article
in
GENETICS IN MEDICINE
2018
2017
Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes
Kristof Van Schil
Sarah Naessens
Stijn Van de Sompele
Marjolein Carron
Sarah De Jaegere
Frauke Coppieters
Bart Leroy
Elfride De Baere
C3
Conference
2017
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
Kristof Van Schil
Sarah Naessens
Stijn Van de Sompele
Marjolein Carron
Caroline Van Cauwenbergh
Mattias Van Heetvelde
Miriam Bauwens
Hannah Verdin
Frauke Coppieters
Katleen De Preter
Bart Leroy
Elfride De Baere
C3
Conference
2017
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
Kristof Van Schil
Sarah Naessens
Stijn Van de Sompele
Marjolein Carron
Caroline Van Cauwenbergh
Mattias Van Heetvelde
Miriam Bauwens
Hannah Verdin
Frauke Coppieters
Katleen De Preter
Bart Leroy
Elfride De Baere
C3
Conference
2017