Research Explorer

Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.

Project

Design of a novel antisense oligonucleotide therapy for inherited blindness

Outputs & Impact

Publications & research data ( 5 )

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 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

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 Journal Article 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 Journal Article in GENETICS IN MEDICINE

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.

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 Journal Article in GENOME MEDICINE

Activities ( 0 )

Results

Impact narratives ( 0 )

Patents ( 0 )