Research Explorer

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Onderzoeker

Manon Bouckaert

Publicaties & datasets

Prijzen & Erkenningen

16 Resultaten

2026

A rare 5’UTR variant in SEC24D reveals translational dysfunction in osteogenesis imperfecta : a roadmap for RNA therapeutic rescue

Osama EssawiTamara JaraysehPiyanoot TapaneeyaphanManon BouckaertSarah NaessensFransiska MalfaitFrauke CoppietersPaul Coucke

A1 Artikel in een tijdschrift in SCIENTIFIC REPORTS

2025

BioID reveals that NR2E3 mediates transcriptional repression through the AP-1 complex

dr. Edith De BruyckerOlivier ZwaenepoelManon BouckaertGeorgios MoschonasDelphine De SutterLouis DelhayeFrauke CoppietersSven EyckermanJan GettemansElfride De Baere

Design and evaluation of universal control antisense oligonucleotides across cellular models

Edith De BruyckerManon BouckaertEmma DelanoteLeander MeurisHanne LenaertsLode DenolfKatrien RemautAn StaesKris GevaertSteve Lefever et al.

Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR variant in the RDH12 gene

Manon BouckaertKyana Van AckerBirthe HilgenMaria GeorgiouFilip Van Den BroeckEdith De BruyckerAlfredo Dueñas ReyEmma DelanoteHanne LenaertsMelita Kaltak et al.

Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A]; [806_810del] variants in the RDH12 gene

Manon BouckaertFilip Van Den BroeckM. GhazviniAlfredo Dueñas ReyHanne LenaertsAnnelies DheedeneKathleen ClaesElfride De BaereBart LeroyJulie De Zaeytijd et al.

A1 Artikel in een tijdschrift in STEM CELL RESEARCH

Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa

Tamar HaymanShai OvadiaJaya KrishnanManon BouckaertDaan M. PannemanMilton EnglishJohanna ValensiFrans P.M. CremersTamar Ben YosefL. Ingeborgh van den Born et al.

A1 Artikel in een tijdschrift in GENETICS IN MEDICINE

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

Mathieu QuinodozElifnaz CelikDhryata KamdarFrancesca CancellieriKarolina KaminskaMukhtar UllahPilar Barberán-MartínezManon BouckaertMarta CortónEmma Delanote et al.

A1 Artikel in een tijdschrift in AMERICAN JOURNAL OF HUMAN GENETICS

Unravelling the proxisome of photoreceptor-specific nuclear receptor NR2E3 reveals a potential molecular link between transcriptional regulation and splicing in human retina

Edith De BruyckerOlivier ZwaenepoelManon BouckaertGeorgios MoschonasDelphine De SutterLouis DelhayeFrauke CoppietersSven EyckermanJan GettemansElfride De Baere

2024

Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease

Alfredo Dueñas ReyMarta del Pozo ValeroManon BouckaertKatherine A. WoodFilip Van Den BroeckMalena Daich VarelaHuw B. ThomasMattias Van HeetveldeMarieke De BruyneStijn Van de Sompele et al.

A1 Artikel in een tijdschrift in GENOME MEDICINE

Comprehensive tissue specificity analysis identifies (novel) retinaspecific, long non-coding RNAs

Emma DelanoteAlfredo Dueñas ReyKarla RuizVictor Lopez SorianoManon BouckaertKelly LemeireJasper VerwiltHanne LenaertsSarah De KeulenaerFilip Van Nieuwerburgh et al.

U Artikel in een tijdschrift in INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene

Manon BouckaertKyana Van AckerMaria GeorgiouFilip Van Den BroeckEdith De BruyckerAlfredo Dueñas ReyEmma DelanoteHanne LenaertsMelita KaltakElfride De Baere et al.

Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene

Manon BouckaertKyana Van AckerMaria GeorgiouFilip Van Den BroeckMargot De MoorEdith De BruyckerAlfredo Dueñas ReyEmma DelanoteHanne LenaertsMelita Kaltak et al.

Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene

Manon BouckaertKyana Van AckerBirthe HilgenMaria GeorgiouFilip Van Den BroeckMargot De MoorEdith De BruyckerAlfredo Dueñas ReyEmma DelanoteHanne Lenaerts et al.

Unravelling the interactome of nuclear receptors through proximity dependent biotin labelling

Edith De BruyckerOlivier ZwaenepoelManon BouckaertLaure VandeveldeDelphine De SutterLouis DelhayeFrauke CoppietersSven EyckermanElfride De BaereJan Gettemans

2023

A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease

Alfredo Dueñas ReyManon BouckaertMarta del Pozo ValeroMarieke De BruyneMattias Van HeetveldeJamie EllingfordGavin ArnoAndrew WebsterCarmen AyusoCarlo Rivolta et al.

Identification and characterization of a novel retinaspecific lncRNA upstream ABCA4 with a potential role in ABCA4-associated inherited retinal disease

Alfredo Dueñas ReyVictor Lopez SorianoZelia CorradiClaire-Marie DhaenensManon BouckaertJasper VerwiltAvril WatsonMajlinda LakoEva D'haeneKarla Alejandra Ruiz Ceja et al.