Rob W J Collin

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 28

Top Topics

Optical Coherence Tomography

Top Venues

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, Dyah W Karjosukarso, Zelia Corradi, Femke Bukkems, Lonneke Duijkers, Frans P M Cremers, Carel B Hoyng, Alejandro Garanto, Rob W J Collin
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells 13 (7) (2024)
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, Dyah W Karjosukarso, Zelia Corradi, Femke Bukkems, Lonneke Duijkers, Frans P M Cremers, Carel B Hoyng, Alejandro Garanto, Rob W J Collin
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells 13 (7) (2024)
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, Dyah W Karjosukarso, Zelia Corradi, Femke Bukkems, Lonneke Duijkers, Frans P M Cremers, Carel B Hoyng, Alejandro Garanto, Rob W J Collin
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells 13 (7) (2024)
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, Dyah W Karjosukarso, Zelia Corradi, Femke Bukkems, Lonneke Duijkers, Frans P M Cremers, Carel B Hoyng, Alejandro Garanto, Rob W J Collin
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells 13 (7) (2024)
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, Dyah W Karjosukarso, Zelia Corradi, Femke Bukkems, Lonneke Duijkers, Frans P M Cremers, Carel B Hoyng, Alejandro Garanto, Rob W J Collin
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells 13 (7) (2024)
Irene Vázquez-Domínguez, Alejandro Allo Anido, Lonneke Duijkers, Tamara Hoppenbrouwers, Anita D M Hoogendoorn, Céline Koster, Rob W J Collin, Alejandro Garanto
Efficacy, biodistribution and safety comparison of chemically modified antisense oligonucleotides in the retina. Nucleic acids research (2024)
Siebren Faber, Stef J F Letteboer, Katrin Junger, Rossano Butcher, Trinadh V Satish Tammana, Sylvia E C van Beersum, Marius Ueffing, Rob W J Collin, Qin Liu, Karsten Boldt, Ronald Roepman
PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia. Cells 12 (2) (2023)
Siebren Faber, Stef J F Letteboer, Katrin Junger, Rossano Butcher, Trinadh V Satish Tammana, Sylvia E C van Beersum, Marius Ueffing, Rob W J Collin, Qin Liu, Karsten Boldt, Ronald Roepman
PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia. Cells 12 (2) (2023)
Siebren Faber, Stef J F Letteboer, Katrin Junger, Rossano Butcher, Trinadh V Satish Tammana, Sylvia E C van Beersum, Marius Ueffing, Rob W J Collin, Qin Liu, Karsten Boldt, Ronald Roepman
PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia. Cells 12 (2) (2023)
Siebren Faber, Stef J F Letteboer, Katrin Junger, Rossano Butcher, Trinadh V Satish Tammana, Sylvia E C van Beersum, Marius Ueffing, Rob W J Collin, Qin Liu, Karsten Boldt, Ronald Roepman
PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia. Cells 12 (2) (2023)
Tomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, Alejandro Garanto, Rob W J Collin
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease. Cells 11 (24) (2022)
Tomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, Alejandro Garanto, Rob W J Collin
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease. Cells 11 (24) (2022)
Tess A V Afanasyeva, Yan-Ting Schnellbach, Toby J Gibson, Ronald Roepman, Rob W J Collin
PCARE requires coiled coil, RP62 kinase-binding and EVH1 domain-binding motifs for ciliary expansion. Human molecular genetics 31 (15) (2022)
Irene Vázquez-Domínguez, Lonneke Duijkers, Zeinab Fadaie, Eef C W Alaerds, Merel A Post, Edwin M van Oosten, Luke O'Gorman, Michael Kwint, Louet Koolen, Anita D M Hoogendoorn, Hester Y Kroes, Christian Gilissen, Frans P M Cremers, Rob W J Collin, Susanne Roosing, Alejandro Garanto
The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner. Cells 11 (22) (2022)
Tomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, Alejandro Garanto, Rob W J Collin
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease Cells 11 (24) (2022)
Tomasz Z Tomkiewicz, Sara E Nieuwenhuis, Frans P M Cremers, Alejandro Garanto, Rob W J Collin
Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease. Cells 11 (24) (2022)
Tomasz Z Tomkiewicz, Nuria Suárez-Herrera, Frans P M Cremers, Rob W J Collin, Alejandro Garanto
Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4. International journal of molecular sciences 22 (9) (2021)
Suzan M Hammond, Annemieke M Aartsma-Rus, Sandra Alves, Sven Even F Borgos, Ronald A M Buijsen, Rob W J Collin, Giuseppina Covello, Michela Alessandra Denti, Lourdes Ruiz Desviat, Lucía Echevarría, Camilla Foged, Gisela Gaina, Alejandro Garanto, Aurelie T Goyenvalle, Magdalena Guzowska, Irina Kholodnyuk, David R Jones, Sabine Krause, Taavi Lehto, Marisol Montolio, Willeke M C van Roon-Mom, Virginia Arechavala-Gomeza
Delivery of oligonucleotide-based therapeutics: challenges and opportunities. EMBO molecular medicine 13 (4) (2021)
Manon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, Timo Mulders, Lonneke Haer-Wigman, Camiel J F Boon, Caroline C W Klaver, L Ingeborgh van den Born, Carel B Hoyng, Frans P M Cremers, Anneke I den Hollander, Claire-Marie Dhaenens, Rob W J Collin
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease. Human mutation 42 (12) (2021)
Renske Schellens, Erik de Vrieze, Pam Graave, Sanne Broekman, Kerstin Nagel-Wolfrum, Theo Peters, Hannie Kremer, Rob W J Collin, Erwin van Wijk
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for EYS-Associated Retinitis Pigmentosa. International journal of molecular sciences 22 (17) (2021)
Mubeen Khan, Stéphanie S Cornelis, Riccardo Sangermano, Iris J M Post, Amber Janssen Groesbeek, Jan Amsu, Christian Gilissen, Alejandro Garanto, Rob W J Collin, Frans P M Cremers
In or Out? New Insights on Exon Recognition through Splice-Site Interdependency. International journal of molecular sciences 21 (7) (2020)
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W J Collin
Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges. Genes 10 (9) (2019)
Alejandro Garanto, Lonneke Duijkers, Tomasz Z Tomkiewicz, Rob W J Collin
Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic ABCA4 Variant c.4539+2001G>A in Stargardt Disease. Genes 10 (6) (2019)
Karin W Littink, Patricia T Y Stappers, Frans C C Riemslag, Herman E Talsma, Maria M van Genderen, Frans P M Cremers, Rob W J Collin, L Ingeborgh van den Born
Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68. Genes 9 (3) (2018)
Lonneke Duijkers, L Ingeborgh van den Born, John Neidhardt, Nathalie M Bax, Laurence H M Pierrache, B Jeroen Klevering, Rob W J Collin, Alejandro Garanto
Antisense Oligonucleotide-Based Splicing Correction in Individuals with Leber Congenital Amaurosis due to Compound Heterozygosity for the c.2991+1655A>G Mutation in CEP290. International journal of molecular sciences 19 (3) (2018)
Karin W Littink, Patricia T Y Stappers, Frans C C Riemslag, Herman E Talsma, Maria M van Genderen, Frans P M Cremers, Rob W J Collin, L Ingeborgh van den Born
Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 9 (2) (2018)
Muriël Messchaert, Margo Dona, Sanne Broekman, Theo A Peters, Julio C Corral-Serrano, Ralph W N Slijkerman, Erwin van Wijk, Rob W J Collin
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish. PloS one 13 (7) (2018)
Muriël Messchaert, Lonneke Haer-Wigman, Muhammad I Khan, Frans P M Cremers, Rob W J Collin
EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa. Human mutation 39 (2) (2017)