Rob Collin

10.2k citations

160 papers · 7.8k · 2 hit papers · h-index 51

Impact in

Ophthalmology top 0.2%
- Retinal Diseases and Treatments
Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Molecular Biology 131
- Retinal Development and Disorders 104
- CRISPR and Genetic Engineering 25
- RNA regulation and disease 14
- Advanced biosensing and bioanalysis techniques 12
Ophthalmology 28
- Retinal Diseases and Treatments 24

Co-authors: Frans P.M. Cremers (60 shared papers)Anneke I. den Hollander (32 shared papers)Carel B. Hoyng (33 shared papers)Alejandro Garanto (38 shared papers)B. Jeroen Klevering (14 shared papers)Caroline C. W. Klaver (10 shared papers)L. Ingeborgh van den Born (27 shared papers)Ronald Roepman (9 shared papers)
Journals: Investigative Ophthalmology & Visual Science (17 papers)The American Journal of Human Genetics (12 papers)Human Mutation (8 papers)Ophthalmology (8 papers)Molecular Therapy — Nucleic Acids (6 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Rob Collin

156 papers receiving 7.7k citations

Rob Collin's Hit Papers

align trajectories log scale

Delivery of oligonucleotide‐based therapeutics: challenges and opportunities 2021 · 293 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2021 EMBO Molecular Medicine
2018 Progress in Retinal and Eye Research

Peers

Countries citing papers authored by Rob Collin

Since Specialization

Citations

This map shows the geographic impact of Rob Collin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rob Collin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rob Collin more than expected).

Fields of papers citing papers by Rob Collin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rob Collin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rob Collin. The network helps show where Rob Collin may publish in the future.

Co-authors

The 25 scholars most cited alongside Rob Collin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rob Collin Line = papers co-authored together Rob Collin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 160 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Non-syndromic retinitis pigmentosa Progress in Retinal and Eye Research ·Sanne K. Verbakel, Ramon A. C. van Huet, Camiel Boon, Anneke I. den Hollander, Rob Collin, Caroline C. W. Klaver, Carel B. Hoyng, Ronald Roepman Hit paper breakdown →	2018	712
2	Delivery of oligonucleotide‐based therapeutics: challenges and opportunities EMBO Molecular Medicine ·Suzan M. Hammond, Annemieke M Aartsma-Rus, Sandra Alves, Sven Even Borgos, Ronald A.M. Buijsen, Rob Collin, Giuseppina Covello, Michela Alessandra Denti Hit paper breakdown →	2021	293
3	Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy Nature Genetics ·Edgar A. Otto, Toby W. Hurd, Rannar Airik, Moumita Chaki, Weibin Zhou, Corinne Stoetzel, Suresh B. Patil, Shawn Levy	2010	276
4	Next‐generation genetic testing for retinitis pigmentosa Human Mutation ·Kornelia Neveling, Rob Collin, Christian Gilissen, Ramon A. C. van Huet, Linda Visser, Michael P. Kwint, Sabine J. Gijsen, Marijke N. Zonneveld	2012	251
5	Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations Progress in Retinal and Eye Research ·Frans P.M. Cremers, Winston Lee, Rob Collin, Rando L. Allikmets	2020	226
6	Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy The American Journal of Human Genetics ·Konstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, C. Erik Van Nouhuys, F. Nienke Boonstra, Ellen A.W. Blokland, Peer Arts, Nienke Wieskamp	2010	182
7	Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders The American Journal of Human Genetics ·Alberta A. H. J. Thiadens, Anneke I. den Hollander, Susanne Roosing, Sander B. Nabuurs, Renate C. Zekveld-Vroon, Rob Collin, Robert K. Koenekoop, Mary J. van Schooneveld	2009	175
8	Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides Genetics in Medicine ·Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, Esmee H. Runhart, Miriam Bauwens, Nathalie M. Bax, L. Ingeborgh van den Born, Muhammad Imran Khan	2019	159
9	ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature Proceedings of the National Academy of Sciences ·Rob Collin, Konstantinos Nikopoulos, Margo Dona, Christian Gilissen, Alexander Hoischen, F. Nienke Boonstra, James A. Poulter, Hiroyuki Kondo	2013	143
10	Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa The American Journal of Human Genetics ·Rob Collin, Karin W. Littink, B. Jeroen Klevering, L. Ingeborgh van den Born, Robert K. Koenekoop, Marijke N. Zonneveld, Ellen A.W. Blokland, Tim Matthias Strom	2008	140
11	Splice-Modulating Oligonucleotide QR-110 Restores CEP290 mRNA and Function in Human c.2991+1655A>G LCA10 Models Molecular Therapy — Nucleic Acids ·Kalyan Dulla, Mònica Aguilà, Amelia Lane, Katarina Jovanović, David A. Parfitt, Iris A. E. Schulkens, Hee Lam Chan, Iris Schmidt	2018	137
12	Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP Human Mutation ·Konstantinos Nikopoulos, Hanka Venselaar, Rob Collin, Rosa Riveiro-Álvarez, F. Nienke Boonstra, Johanna M. M. Hooymans, Arijit Mukhopadhyay, Deborah J. Shears	2010	130
13	Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome Human Molecular Genetics ·Kinga M. Bujakowska, Qi Zhang, Anna M. Siemiatkowska, Qin Liu, Emily Place, Marni J. Falk, Mark B. Consugar, Marie‐Elise Lancelot	2014	130
14	ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants Genetics in Medicine ·Alejandro Garanto, Riccardo Sangermano, Sarah Naessens, Nicole Weisschuh, Julie De Zaeytijd, Mubeen Khan, Françoise Sadler, Irina Balikova	2019	120
15	Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation Molecular Therapy — Nucleic Acids ·Radulfus WN Slijkerman, Christel Vaché, Margo Dona, Gema García‐García, Mireille Claustres, Lisette Hetterschijt, Theo A. Peters, Bas P. Hartel	2016	116
16	Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications Scientific Reports ·Irene Perea‐Romero, Gema Gordo, Ionut-Florin Iancu, Marta Del Pozo‐Valero, Berta Almoguera, Fiona Blanco‐Kelly, Ester Carreño, Belén Jimenez‐Rolando	2021	116
17	Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290 Molecular Therapy — Nucleic Acids ·Rob Collin, Anneke I. den Hollander, Saskia D. van der Velde-Visser, Jeannette L. Bennicelli, Jean Bennett, Frans P.M. Cremers	2012	115
18	Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease The American Journal of Human Genetics ·Sílvia Albert, Alejandro Garanto, Riccardo Sangermano, Mubeen Khan, Nathalie M. Bax, Carel B. Hoyng, Jana Zernant, Winston Lee	2018	112
19	Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease Ophthalmology ·Riccardo Sangermano, Nathalie M. Bax, Miriam Bauwens, L. Ingeborgh van den Born, Alejandro Garanto, Rob Collin, Angelique Goercharn-Ramlal, Anke H.A. den Engelsman-van Dijk	2016	106
20	BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome Archives of Ophthalmology ·Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Audrey Sénéćhal, Thomy J.L. de Ravel, Sandro Banfi, Susanne Kohl, Carmen Ayuso, Dror Sharon	2012	104

About Rob Collin

Rob Collin is a scholar working on Molecular Biology, Ophthalmology, Sensory Systems, Cell Biology and Genetics, having authored 160 papers that have together received 7.8k indexed citations. Recurring topics across this work include Retinal Development and Disorders (104 papers), CRISPR and Genetic Engineering (25 papers), Retinal Diseases and Treatments (24 papers), Hearing, Cochlea, Tinnitus, Genetics (18 papers), Cellular transport and secretion (17 papers), RNA regulation and disease (14 papers), Advanced biosensing and bioanalysis techniques (12 papers) and Photoreceptor and optogenetics research (11 papers). The work is most often cited by research in Ophthalmology (1.6k citations), Sensory Systems (520 citations), Molecular Biology (6.1k citations), Genetics (1.5k citations) and Cellular and Molecular Neuroscience (787 citations). Rob Collin has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Frans P.M. Cremers, Anneke I. den Hollander, Carel B. Hoyng, Alejandro Garanto, B. Jeroen Klevering, Caroline C. W. Klaver, L. Ingeborgh van den Born, Ronald Roepman, Ramon A. C. van Huet and Camiel Boon. Their work appears in journals such as Investigative Ophthalmology & Visual Science, The American Journal of Human Genetics, Human Mutation, Ophthalmology and Molecular Therapy — Nucleic Acids.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Rob Collin

Rob Collin's Hit Papers

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About Rob Collin

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