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 TulkensNicole A. EdwardsMarjolein CarronNikko-Ideen ShaidaniMarcin WlizlaAnnekatrien BoelSuzan DemuynckMarko E. HorbPaul CouckeAndy WillaertAaron M. ZornKris 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 NoelandersLiza EeckhoutGert 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 SompeleNuria Gruartmoner RouraMarjolein CarronKatharina DannhausenSarah De JaegereMaxim VanpanteghemFrauke CoppietersMarcus KarlstetterBryan TsouThomas LangmannFrançoise MeireReza MaroofianAndrew H CrosbyIrina BalikovaMichel Van LintAndrew WebsterMichel MichaelidesBart 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 CarronAlexander AslanidisCaroline Van CauwenberghAnja Kathrin MayerMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersMichael E GreenbergMarty G YangMarcus KarlstetterThomas LangmannKatleen De PreterSusanne KohlTimothy J CherryBart 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 SompeleNuria Gruartmoner RouraMarjolein CarronKatharina DannhausenSarah De JaegereMaxim VanpanteghemFrauke CoppietersMarcus KarlstetterBryan TsouThomas LangmannFrançoise MeireReza MaroofianAndrew H CrosbyIrina BalikovaMichel Van LintAndrew WebsterMichel MichaelidesBart 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 CarronAlexander AslanidisCaroline Van CauwenberghAnja Kathrin MayerMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersMichael E GreenbergMarty G YangMarcus KarlstetterThomas LangmannKatleen De PreterSusanne KohlTimothy CherryBart 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 CarronAlexander AslanidisCaroline Van CauwenberghAnne Kathrin MayerMattias Van HeetveldeMiriam BauwensHannah VerdinFrauke CoppietersMichael E GreenbergMarty G YangMarcus KarlstetterThomas LangmannKatleen De PreterSusanne KohlTimothy J CherryBart LeroyElfride De Baere