Research Explorer

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Researcher

Marjolein Carron

8 Results

2020

Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos

Thomas NaertDieter TulkensMarjolein CarronAnnekatrien BoelSuzan DemuynckPaul CouckeAndy WillaertKris Vleminckx

A1 Journal Article in SCIENTIFIC REPORTS

RBL1 (p107) functions as tumor suppressor in glioblastoma and small-cell pancreatic neuroendocrine carcinoma in Xenopus tropicalis

Thomas NaertDionysia DimitrakopoulouDieter TulkensSuzan DemuynckMarjolein CarronRivka NoelandersGert Van IsterdaelDieter DeforceChristian VanhoveJo Van DorpeDavid CreytensKris Vleminckx

A1 Journal Article in ONCOGENE

2018

CRISPR/Cas9 mediated knockout of rcbtb1 in Xenopus tropicalis to model RCBTB1-associated retinal disease

Giulia AscariThomas NaertTom Van NieuwenhuysenMarjolein CarronSuzan DemuynckChris GuerinFrauke CoppietersKris VleminckxElfride De Baere

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 SchilSarah NaessensStijn Van de SompeleMarjolein CarronSarah De JaegereFrauke CoppietersBart LeroyElfride De Baere

Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

Kristof Van SchilSarah NaessensStijn Van de SompeleMarjolein CarronCaroline Van CauwenberghMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersKatleen De PreterBart LeroyElfride De Baere

A1 Journal Article in GENETICS IN MEDICINE

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 SchilSarah NaessensStijn Van de SompeleMarjolein CarronSarah De JaegereFrauke CoppietersBart LeroyElfride De Baere

Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

Kristof Van SchilSarah NaessensStijn Van de SompeleMarjolein CarronCaroline Van CauwenberghMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersKatleen De PreterBart LeroyElfride De Baere

Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

Kristof Van SchilSarah NaessensStijn Van de SompeleMarjolein CarronCaroline Van CauwenberghMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersKatleen De PreterBart LeroyElfride De Baere