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Onderzoeker
Manon Bouckaert
Profiel
Projecten
Publicaties & datasets
Activiteiten
Prijzen & Erkenningen
Octrooien
14
Resultaten
2025
BioID reveals that NR2E3 mediates transcriptional repression through the AP-1 complex
dr. Edith De Bruycker
Olivier Zwaenepoel
Manon Bouckaert
Georgios Moschonas
Delphine De Sutter
Louis Delhaye
Frauke Coppieters
Sven Eyckerman
Jan Gettemans
Elfride De Baere
C3
Conferentie
2025
Design and evaluation of universal control antisense oligonucleotides across cellular models
Edith De Bruycker
Manon Bouckaert
Emma Delanote
Leander Meuris
Hanne Lenaerts
Lode Denolf
Katrien Remaut
An Staes
Kris Gevaert
Steve Lefever
et al.
C3
Conferentie
2025
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR variant in the RDH12 gene
Manon Bouckaert
Kyana Van Acker
Birthe Hilgen
Maria Georgiou
Filip Van Den Broeck
Edith De Bruycker
Alfredo Dueñas Rey
Emma Delanote
Hanne Lenaerts
Melita Kaltak
et al.
U
Conferentie
2025
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 Bouckaert
Filip Van Den Broeck
M. Ghazvini
Alfredo Dueñas Rey
Hanne Lenaerts
Annelies Dheedene
Kathleen Claes
Elfride De Baere
Bart Leroy
Julie De Zaeytijd
et al.
A1
Artikel in een tijdschrift
in
STEM CELL RESEARCH
2025
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa
Tamar Hayman
Shai Ovadia
Jaya Krishnan
Manon Bouckaert
Daan M. Panneman
Milton English
Johanna Valensi
Frans P.M. Cremers
Tamar Ben Yosef
L. Ingeborgh van den Born
et al.
A1
Artikel in een tijdschrift
in
GENETICS IN MEDICINE
2025
RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)
Mathieu Quinodoz
Elifnaz Celik
Dhryata Kamdar
Francesca Cancellieri
Karolina Kaminska
Mukhtar Ullah
Pilar Barberán-Martínez
Manon Bouckaert
Marta Cortón
Emma Delanote
et al.
A1
Artikel in een tijdschrift
in
AMERICAN JOURNAL OF HUMAN GENETICS
2025
Unravelling the proxisome of photoreceptor-specific nuclear receptor NR2E3 reveals a potential molecular link between transcriptional regulation and splicing in human retina
Edith De Bruycker
Olivier Zwaenepoel
Manon Bouckaert
Georgios Moschonas
Delphine De Sutter
Louis Delhaye
Frauke Coppieters
Sven Eyckerman
Jan Gettemans
Elfride De Baere
C3
Conferentie
2025
2024
Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease
Alfredo Dueñas Rey
Marta del Pozo Valero
Manon Bouckaert
Katherine A. Wood
Filip Van Den Broeck
Malena Daich Varela
Huw B. Thomas
Mattias Van Heetvelde
Marieke De Bruyne
Stijn Van de Sompele
et al.
A1
Artikel in een tijdschrift
in
GENOME MEDICINE
2024
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
Manon Bouckaert
Kyana Van Acker
Maria Georgiou
Filip Van Den Broeck
Margot De Moor
Edith De Bruycker
Alfredo Dueñas Rey
Emma Delanote
Hanne Lenaerts
Melita Kaltak
et al.
C3
Conferentie
2024
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
Manon Bouckaert
Kyana Van Acker
Birthe Hilgen
Maria Georgiou
Filip Van Den Broeck
Margot De Moor
Edith De Bruycker
Alfredo Dueñas Rey
Emma Delanote
Hanne Lenaerts
et al.
C3
Conferentie
2024
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
Manon Bouckaert
Kyana Van Acker
Maria Georgiou
Filip Van Den Broeck
Edith De Bruycker
Alfredo Dueñas Rey
Emma Delanote
Hanne Lenaerts
Melita Kaltak
Elfride De Baere
et al.
C3
Conferentie
2024
Unravelling the interactome of nuclear receptors through proximity dependent biotin labelling
Edith De Bruycker
Olivier Zwaenepoel
Manon Bouckaert
Laure Vandevelde
Delphine De Sutter
Louis Delhaye
Frauke Coppieters
Sven Eyckerman
Elfride De Baere
Jan Gettemans
C3
Conferentie
2024
2023
A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease
Alfredo Dueñas Rey
Manon Bouckaert
Marta del Pozo Valero
Marieke De Bruyne
Mattias Van Heetvelde
Jamie Ellingford
Gavin Arno
Andrew Webster
Carmen Ayuso
Carlo Rivolta
et al.
C3
Conferentie
2023
Identification and characterization of a novel retinaspecific lncRNA upstream ABCA4 with a potential role in ABCA4-associated inherited retinal disease
Alfredo Dueñas Rey
Victor Lopez Soriano
Zelia Corradi
Claire-Marie Dhaenens
Manon Bouckaert
Jasper Verwilt
Avril Watson
Majlinda Lako
Eva D'haene
Karla Alejandra Ruiz Ceja
et al.
C3
Conferentie
2023