European Training Network to Diagnose, Understand and Treat Stargardt Disease, a Frequent Inherited Blinding Disorder

Informazioni relative al progetto

StarT

ID dell’accordo di sovvenzione: 813490

DOI

10.3030/813490

Progetto chiuso

Data della firma CE 30 Agosto 2018

Data di avvio 1 Ottobre 2018

Data di completamento 31 Marzo 2023

Finanziato da

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Costo totale

€ 3 776 714,28

Contributo UE

€ 3 768 605,55

Coordinato da

UNIVERSITEIT GENT
Belgium

CORDIS fornisce collegamenti ai risultati finali pubblici e alle pubblicazioni dei progetti ORIZZONTE.

I link ai risultati e alle pubblicazioni dei progetti del 7° PQ, così come i link ad alcuni tipi di risultati specifici come dataset e software, sono recuperati dinamicamente da .OpenAIRE .

Risultati finali

Other (5)

Potential inputs for policy feedback

Consortium should include any relevant information, results, activities who could contribute to any policy development in their domain. This information could then be used for policy feedback purposes.

National fundraising events organised

Aim is to organize 7 national fundraising events

International Conference

In an international conference, we will invite four renowned speakers covering IRD Genomics, Mechanisms of Disease, Models of Disease and Therapeutics areas. The ESR fellows will present their PhD studies and top speakers from the Beneficiaries and POs will be invited. In addition, we will invite representatives of the national patientorganisations to discuss our progress in the fundraising events. Very importantly, one day will be reserved for patients and their family members. ESR fellows and their supervisors will provide oral presentations for this audience on IRD genetics, mechanisms and models of disease and therapeutics.

ESR weblogs, podcasts, vlogs

ESR weblogs, podcasts, vlogs done

Pilot fundraising event organised

Websites, patent fillings, videos etc. (1)

StarT website

StarT website designed

Pubblicazioni

Peer reviewed articles (32)

Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4.

Autori: Nuria Suárez-Herrera, Iris B. Riswick, Irene Vázquez-Domínguez, Lonneke Duijkers, Dyah W. Karjosukarso, Davide Piccolo, Miriam Bauwens, Elfride De Baere, Michael E. Cheetham, Alejandro Garanto, and Rob W.J. Collin.
Pubblicato in: Molecular Therapy, Numero vol. 32, no. 3, 2024, ISSN 1525-0016
Editore: Nature Publishing Group
DOI: 10.1016/j.ymthe.2024.01.019

Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants: Lessons Learned From the ABCA4 Locus

Autori: Benjamin McClinton, Christopher M Watson, Laura A Crinnion, Martin McKibbin, Manir Ali, Chris F Inglehearn, Carmel Toomes
Pubblicato in: Lab Invest, Numero 103(8):100160, 2023, ISSN 0023-6837
Editore: Nature Publishing Group
DOI: 10.1016/j.labinv.2023.100160

Stargardt disease-associated in-frame ABCA4 exon 17 skipping results in significant ABCA4 function

Autori: Melita Kaltak; Rocio Blanco-Garavito; Laurie L. Molday; Claire-Marie Dhaenens; Eric E. Souied; Gerard Platenburg; Jim Swildens; Robert S. Molday; Frans P. M. Cremers
Pubblicato in: Journal of Translational Medicine, Numero 21, 2023, Pagina/e 546, ISSN 1479-5876
Editore: BioMed Central
DOI: 10.1186/s12967-023-04406-x

Effective splicing restoration of a deep-intronic ABCA4 variant in cone photoreceptor precursor cells by CRISPR/SpCas9 approaches

Autori: Pietro De Angeli, Peggy Reuter, Stefan Hauser, Ludger Schöls, Katarina Sting, Bernd Wissinger, Susanne Kohl
Pubblicato in: Molecular Therapy. Nucleic acids, Numero Volume 29, 2022, Pagina/e 511-524, ISSN 2162-2531
Editore: Nature Publishing Group
DOI: 10.1016/j.omtn.2022.07.023

AAV-mediated gene therapy improving mitochondrial function provides benefit in age-related macular degeneration models

Autori: Sophia Millington-Ward, Naomi Chadderton, Laura K Finnegan, Iris J M Post, Matthew Carrigan, Tom Gardiner, Elisa Peixoto, Daniel Maloney, Marian M Humphries, Alan Stitt, Thierry Léveillard, Pete Humphries, Paul F Kenna, Arpad Palfi, G Jane Farrar
Pubblicato in: Clinical and Translational Medicine, Numero 12:e952, 2022, Pagina/e 1-7, ISSN 2001-1326
Editore: Wiley
DOI: 10.1002/ctm2.952

Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategies

Autori: Benjamin McClinton, Laura A. Crinnion, Martin McKibbin, Rajarshi Mukherjee, James A. Poulter, Claire E. L. Smith, Manir Ali, Christopher M. Watson, Chris F. Inglehearn, Carmel Toomes
Pubblicato in: Molecular Genetics & Genomic Medicine, Numero e2164, 2023, ISSN 2324-9269
Editore: John Wiley & Sons
DOI: 10.1002/mgg3.2164

Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A

Autori: Nuria Suárez-Herrera; Nico Leijsten; Silvia Albert; Nathalie M. Bax; Carel B. Hoyng; Frans P.M. Cremers; Alejandro Garanto; Rob W.J. Collin
Pubblicato in: Stem Cell Research, Numero 73 (2023) 103252, 2023, ISSN 1873-5061
Editore: Elsevier
DOI: 10.1016/j.scr.2023.103252

Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease

Autori: Mubeen Khan, Gavin Arno, Ana Fakin, David A. Parfitt, Patty P.A. Dhooge, Silvia Albert, Nathalie M. Bax, Lonneke Duijkers, Michael Niblock, Kwan L. Hau, Edward Bloch, Elena R. Schiff, Davide Piccolo, Michael C. Hogden, Carel B. Hoyng, Andrew R. Webster, Frans P.M. Cremers, Michael E. Cheetham, Alejandro Garanto, Rob W.J. Collin
Pubblicato in: Molecular Therapy - Nucleic Acids, Numero 21, 2020, Pagina/e 412-427, ISSN 2162-2531
Editore: Nature Publishing Group
DOI: 10.1016/j.omtn.2020.06.007

Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK

Autori: Benjamin Mc Clinton, Zelia Corradi, Martin McKibbin, Daan M. Panneman, Susanne Roosing, Erica G. M. Boonen, Manir Ali, Christopher M. Watson, David H. Steel, Frans P. M. Cremers, Chris F. Inglehearn, Rebekkah J. Hitti-Malin and Carmel Toomes
Pubblicato in: Genes, Numero 14(1), 191, 2023, Pagina/e 1-14, ISSN 2073-4425
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/genes14010191

AAV-PHP.eB transduces both the inner and outer retina with high efficacy in mice

Autori: Arpad Palfi, Naomi Chadderton, Sophia Millington-Ward, Iris Post, Pete Humphries, Paul F. Kenna, G. Jane Farrar
Pubblicato in: Molecular Therapy. Methods & Clinical Development, Numero Volume 25, 2022, Pagina/e 236-249, ISSN 2329-0501
Editore: Cell Press
DOI: 10.1016/j.omtm.2022.03.016

ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease

Autori: Zelia Corradi; Manar Salameh; Mubeen Khan; Elise Héon; Ketan Mishra; Rebekkah J. Hitti-Malin; Yahya AlSwaiti; Alice Aslanian; Eyal Banin; Brian P. Brooks; Wadih M. Zein; Robert B. Hufnagel; Susanne Roosing; Claire‐Marie Dhaenens; Dror Sharon; Frans P. M. Cremers; Alaa AlTalbishi
Pubblicato in: Investigative ophthalmology and visual science, Numero vol.63, 20, 2022, ISSN 0146-0404
Editore: Association for Research in Vision and Ophthalmology
DOI: 10.1167/iovs.63.4.20

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

Autori: 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, Miriam Bauwens, Hanne Lenaerts, Quinten Mahieu, Dragana Josifova; Genomics England Research Consortium; Carlo Rivolta, Raymond T O'Keefe, Jamie Ellingford, Andrew R Webster, Gavin Arno, Carmen Ayuso,
Pubblicato in: Genome Medicine, Numero 16:7, 2024, ISSN 1756-994X
Editore: BioMed Central
DOI: 10.1186/s13073-023-01277-1

Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data

Autori: Karla Alejandra Ruiz-Ceja; Dalila Capasso; Michele Pinelli; Eugenio Del Prete; Diego Carrella; Diego di Bernardo; Sandro Banfi
Pubblicato in: BMC genomics, Numero 24(1):206, 2023, ISSN 1471-2164
Editore: BioMed Central
DOI: 10.1186/s12864-023-09300-w

Retinal organoids provide unique insights into molecular signatures of inherited retinal disease throughout retinogenesis

Autori: Avril Watson; Majlinda Lako
Pubblicato in: Journal of Anatomy, Numero 2022 Sep 29, 2022, Pagina/e 1-18, ISSN 0021-8782
Editore: Blackwell Publishing Inc.
DOI: 10.1111/joa.13768

Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4

Autori: Tomasz Z. Tomkiewicz,Nuria Suárez-Herrera,Frans P. M. Cremers, Rob W. J. Collin and Alejandro Garanto
Pubblicato in: International Journal of Molecular Sciences, Numero 22(9):4621, 2021, Pagina/e 1-17, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms22094621

Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severity

Autori: Stéphanie S. Cornelis, Esmee H. Runhart, Miriam Bauwens, Zelia Corradi, Elfride De Baere, Susanne Roosing, Lonneke Haer-Wigman, Claire-Marie Dhaenens, Anneke T. Vulto-van Silfhout, Frans P.M. Cremers
Pubblicato in: American Journal of Human Genetics, Numero Volume 109, issue 3, 2022, Pagina/e 498-507, ISSN 0002-9297
Editore: University of Chicago Press
DOI: 10.1016/j.ajhg.2022.01.008

Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci

Autori: Victor Lopez Soriano, Alfredo Dueñas Rey, Rajarshi Mukherjee; Genomics England Research Consortium; Frauke Coppieters, Miriam Bauwens, Andy Willaert, Elfride De Baere
Pubblicato in: Nature Communications, Numero 15(1):1600, 2024, ISSN 2041-1723
Editore: Nature Publishing Group
DOI: 10.1038/s41467-024-45381-1

Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patients

Autori: Laura Whelan, Adrian Dockery, Kirk A J Stephenson, Julia Zhu, Ella Kopčić, Iris J M Post, Mubeen Khan, Zelia Corradi, Niamh Wynne, James J O' Byrne, Emma Duignan, Giuliana Silvestri, Susanne Roosing, Frans P M Cremers, David J Keegan, Paul F Kenna, G Jane Farrar
Pubblicato in: Scientific Reports, Numero 13(1):9380, 2023, ISSN 2045-2322
Editore: Nature Publishing Group
DOI: 10.1038/s41598-023-35889-9

ABCA4 Variant c.5714+5G>A in Trans With Null Alleles Results in Primary RPE Damage.

Autori: Jana Sajovic, Andrej Meglic, Zelia Corradi, Mubeen Khan, Aleš Maver, Martina Jarc Vidmar, Marko Hawlina, Frans P. M. Cremers, and Ana Fakin
Pubblicato in: Investigative Ophthalmology & Visual Science, Numero vol. 64 | no. 12 | article 33, 2023, ISSN 0146-0404
Editore: Association for Research in Vision and Ophthalmology
DOI: 10.1167/iovs.64.12.33

Splicing defects and CRISPR-Cas9 correction in isogenic homozygous photoreceptor precursors harboring clustered deep-intronic ABCA4 variants

Autori: Pietro De Angeli, Arturo Flores-Tufiño, Katarina Stingl, Laura Kühlewein, Eleonora Roschi, Bernd Wissinger, Susanne Kohl
Pubblicato in: Molecular Therapy Nucleic Acids, Numero 35(1)102113, 2023, ISSN 2162-2531
Editore: Nature Publishing Group
DOI: 10.1016/j.omtn.2023.102113

RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models

Autori: Sophia Millington-Ward, Naomi Chadderton, Laura K. Finnegan, Iris J. M. Post, Matthew Carrigan, Rachel Nixon, Marian M. Humphries, Pete Humphries, Paul F. Kenna, Arpad Palfi and G. Jane Farrar
Pubblicato in: International Journal of Molecular Sciences, Numero 24, 3847, 2023, Pagina/e 1-14, ISSN 1422-0067
Editore: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms24043847

Understanding and Rescuing the Splicing Defect Caused by the Frequent ABCA4 Variant c.4253+43G>A Underlying Stargardt Disease

Autori: Nuria Suárez-Herrera, Alejandro Garanto, Rob W J Collin
Pubblicato in: Nucleic Acid Therapeutics, Numero vol. 34, No. 2, 2024, ISSN 2159-3337
Editore: Mary Ann Liebert Inc.
DOI: 10.1089/nat.2023.0076

Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability

Autori: Zelia Corradi, Mubeen Khan, Rebekkah Hitti-Malin, Ketan Mishra, Laura Whelan, Stephanie S. Cornelis, ABCA4-Study Group, Carel B. Hoyng, Kati Kampjarvi, Caroline C.W. Klaver, Petra Liskova, Heidi Stohr, Bernhard H.F. Weber, Sandro Banfi, G. Jane Farrar, Dror Sharon, Jana Zernant, Rando Allikmets, Claire-Marie Dhaenens, and Frans P.M. Cremers
Pubblicato in: HGG advances, Numero 4, 100237, 2023, ISSN 2666-2477
Editore: Elsevier Inc
DOI: 10.1016/j.xhgg.2023.100237

Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>C

Autori: Melita Kaltak, Petra de Bruijn, Davide Piccolo, Sang-Eun Lee, Kalyan Dulla, Thomas Hoogenboezem, Wouter Beumer, Andrew R. Webster, Rob W.J. Collin, Michael E. Cheetham, Gerard Platenburg, Jim Swildens
Pubblicato in: Molecular Therapy Nucleic Acids, Numero 31, 2023, Pagina/e 674-688, ISSN 2162-2531
Editore: Nature Publishing Group
DOI: 10.1016/j.omtn.2023.02.020

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement

Autori: Sabrina Mechaussier, Basamat Almoallem, Christina Zeitz, Kristof Van Schil, Laila Jeddawi, Jo Van Dorpe, Alfredo Dueñas Rey, Christel Condroyer, Olivier Pelle, Michel Polak, Nathalie Boddaert, Nadia Bahi-Buisson, Mara Cavallin, Jean-Louis Bacquet, Alexandra Mouallem-Bézière, Olivia Zambrowski, José Alain Sahel, Isabelle Audo, Josseline Kaplan, Jean-Michel Rozet, Elfride De Baere, Isabelle Perr
Pubblicato in: The American Journal of Human Genetics, Numero 106/6, 2020, Pagina/e 859-871, ISSN 0002-9297
Editore: University of Chicago Press
DOI: 10.1016/j.ajhg.2020.04.018

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

Autori: Mubeen Khan, Stéphanie S. Cornelis, Marta Del Pozo-Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTalbishi, Elfride De Baere, Sandro Banfi, Eyal Banin, Miriam Bauwens, Tamar Ben-Yosef, Camiel J. F. Boon, L. Ingeborgh van den Born, Sabine Defoort, Aurore Devos, Adrian Dockery, Lubica Dudakova, Ana Fakin, G. Jane Farrar, Juliana Maria Ferraz Sallum, Kaoru
Pubblicato in: Genetics in Medicine, 2020, ISSN 1098-3600
Editore: Lippincott Williams & Wilkins Ltd.
DOI: 10.1038/s41436-020-0787-4

QR-1011 restores defective ABCA4 splicing caused by multiple severe ABCA4 variants underlying Stargardt disease

Autori: Kaltak, M.; de Bruijn, Petra; van Leeuwen, Willemijn; Platenburg, G.; Cremers, F.P.M.; Collin, R.W.J.; Swildens, J.
Pubblicato in: Scientific Reports, Numero 14:684, 2024, ISSN 2045-2322
Editore: Nature Publishing Group
DOI: 10.1038/s41598-024-51203-7

Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss

Autori: Giulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, Julie De Zaeytijd, Michel Van Lint, Miriam Bauwens, Mattias Van Heetvelde, Gavin Arno, Julie Jacob, David Creytens, Jo Van Dorpe, Thalia Van Laethem, Toon Rosseel, Tim De Pooter, Peter De Rijk, Wouter De Coster, Björn Menten, Alfredo Dueñas Rey, Mojca Strazisar, Mette Bertelsen, Lisbeth Tranebjaerg, Elfride De Baere
Pubblicato in: Front Cell Dev Biol, Numero Volume 9, 2021, Pagina/e 664317, ISSN 2296-634X
Editore: Frontiers Media
DOI: 10.3389/fcell.2021.664317

Stargardt disease-associated missense and synonymous ABCA4 variants result in aberrant splicing.

Autori: Melita Kaltak, Zelia Corradi, Rob W J Collin, Jim Swildens, Frans P M Cremers
Pubblicato in: Human Molecular Genetics, Numero 32 (21), 2023, Pagina/e 3078-3089, ISSN 0964-6906
Editore: Oxford University Press
DOI: 10.1093/hmg/ddad129

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis.

Autori: Nuzhat N, Van Schil K, Liakopoulos S, Bauwens M, Dueñas Rey A, Käseberg S, Jäger M, Willer JR, Winter J, Truong HM, Gruartmoner N, Van Heetvelde M, Wolf JC, Merget R, Grasshoff-Derr S, Van Dorpe J, Hoorens A, Stöhr H, Mansard L, Roux AF, Langmann T, Dannhausen K, Rosenkranz D, Wissing KM, Van Lint M, Rossmann H, Häuser F, Nürnberg P, Thiele H, Zechner U, Pearring JN, De Baere E, Bolz HJ
Pubblicato in: The Journal of Clinical Investigation, Numero e161156, 2023, ISSN 0021-9738
Editore: American Society for Clinical Investigation
DOI: 10.1172/jci161156

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

Autori: Stijn Van de Sompele, Kent W Small, Munevver Burcu Cicekdal, Víctor López Soriano, Eva D'haene, Fadi S Shaya, Steven Agemy, Thijs Van der Snickt, Alfredo Dueñas Rey, Toon Rosseel, Mattias Van Heetvelde, Sarah Vergult, Irina Balikova, Arthur A Bergen, Camiel J F Boon, Julie De Zaeytijd, Chris F Inglehearn, Bohdan Kousal, Bart P Leroy, Carlo Rivolta, Veronika Vaclavik, Jenneke van den Ende, Mary
Pubblicato in: American Journal of Human Genetics, Numero Volume 109, issue 11, 2022, Pagina/e 2029-2048, ISSN 0002-9297
Editore: University of Chicago Press
DOI: 10.1016/j.ajhg.2022.09.013

Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform

Autori: Marta Del Pozo-Valero, Basamat Almoallem, Alfredo Dueñas Rey, Quinten Mahieu, Mattias Van Heetvelde, Laila Jeddawi, Miriam Bauwens, Elfride De Baere
Pubblicato in: Clinical Genetics, Numero 2024 Mar 11, 2024, ISSN 0009-9163
Editore: Blackwell Publishing Inc.
DOI: 10.1111/cge.14517

Other (1)

Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci

Autori: Eva D’haene, Victor López Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Bastos Neto, José Luis Gómez-Skarmeta, Juan R. Martínez-Morales, Miriam Bauwens, Juan J. Tena, Elfride De Baere
Pubblicato in: bioRxiv, 2023
Editore: cold spring harbor laboratory
DOI: 10.1101/2023.06.20.543842

Book chapters (1)

Development and Use of Cellular Systems to Assess and Correct Splicing Defects

Autori: Nuria Suárez-Herrera, Tomasz Z Tomkiewicz, Alejandro Garanto, Rob W J Collin
Pubblicato in: Methods in Molecular Biology, Numero MIMB, volume 2434, 2022, Pagina/e 145-165, ISBN 978-1-0716-2010-6
Editore: Humana Press
DOI: 10.1007/978-1-0716-2010-6_9

Diritti di proprietà intellettuale

Other (1)

System and method for editing genomic DNA to modulate splicing

Numero candidatura/pubblicazione: PCT/ EP2023/052609
Data: 2023-02-08
Candidato/i: EBERHARD KARLS UNIVERSITAET TUEBINGEN

Patent (1)

ANTISENSE OLIGONUCLEOTIDES FOR THE TREATMENT OF STARGARDT DISEASE

Numero candidatura/pubblicazione: 20 21079723
Data: 2021-10-26
Candidato/i: PROQR THERAPEUTICS NV