Karin W. Littink

1.1k citations

13 papers · 711 indexed · h-index 12

Molecular Biology
Ophthalmology top 2%
Cellular and Molecular Neuroscience top 10%
Genetics
Cell Biology top 10%

Co-authors: Frans P.M. Cremers Rob W.J. Collin Anneke I. den Hollander L. Ingeborgh van den Born Carel B. Hoyng Marijke N. Zonneveld B. Jeroen Klevering Robert K. Koenekoop
Topics: Retinal Development and Disorders (12 papers)Retinal Diseases and Treatments (8 papers)Ocular Disorders and Treatments (3 papers)
Cited by: Ophthalmology Molecular Biology Cellular and Molecular Neuroscience
Journals: Ophthalmology The American Journal of Human Genetics Investigative Ophthalmology & Visual Science
Partner nations: Netherlands Germany Canada

In The Last Decade

Karin W. Littink

13 papers receiving 706 citations

Peers

Countries citing papers authored by Karin W. Littink

Since Specialization

Citations

This map shows the geographic impact of Karin W. Littink'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 Karin W. Littink with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin W. Littink more than expected).

Fields of papers citing papers by Karin W. Littink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karin W. Littink. 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 Karin W. Littink. The network helps show where Karin W. Littink may publish in the future.

Co-authorship network of co-authors of Karin W. Littink

This figure shows the co-authorship network connecting the top 25 collaborators of Karin W. Littink. A scholar is included among the top collaborators of Karin W. Littink based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karin W. Littink. Karin W. Littink is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome 2018 ·Genes ·Karin W. Littink,(unknown),Frans C. C. Riemslag,(unknown),Maria van Genderen,Frans P.M. Cremers,Rob W.J. Collin,(unknown)	30
2	A homogenous frameshift mutation in LRAT causes retinitis punctata albescens. 2012 ·Data Archiving and Networked Services (DANS) ·Karin W. Littink,Maria M. van Genderen,Mary J. van Schooneveld,Linda Visser,Frans C. C. Riemslag,Jan E.E. Keunen,Björn Bakker,Marijke N. Zonneveld,Anneke I. den Hollander,Frans P.M. Cremers,L. Ingeborgh van den Born	34
3	A Homozygous Frameshift Mutation in LRAT Causes Retinitis Punctata Albescens 2012 ·Ophthalmology ·Karin W. Littink,Maria M. van Genderen,Mary van Schooneveld,Linda Visser,Frans C. C. Riemslag,Jan E.E. Keunen,(unknown),(unknown),Anneke Den Hollander,Frans P.M. Cremers,(unknown)	2
4	The Power of Homozygosity Mapping: Discovery of New Genetic Defects in Patients with Retinal Dystrophy 2011 ·Advances in experimental medicine and biology ·Karin W. Littink,Anneke I. den Hollander,Frans P.M. Cremers,Rob W.J. Collin	12
5	High-Resolution Homozygosity Mapping Is a Powerful Tool to Detect Novel Mutations Causative of Autosomal Recessive RP in the Dutch Population 2011 ·Investigative Ophthalmology & Visual Science ·Rob W.J. Collin,L. Ingeborgh van den Born,B. Jeroen Klevering,Marta de Castro‐Miró,Karin W. Littink,(unknown),Maleeha Azam,(unknown),Marijke N. Zonneveld,(unknown),Anna M. Siemiatkowska,Tim M. Strom,Jayne Y. Hehir‐Kwa,Hester Y. Kroes,(unknown),Mary J. van Schooneveld,John R. Heckenlively,Carel B. Hoyng,Anneke I. den Hollander,Frans P.M. Cremers	54
6	Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa 2010 ·The American Journal of Human Genetics ·Rob W.J. Collin,(unknown),Karin W. Littink,Stavit A. Shalev,Hanna J. Garzozi,(unknown),(unknown),Frans P.M. Cremers,Anneke I. den Hollander,B. Jeroen Klevering,Tamar Ben‐Yosef	68
7	Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa 2010 ·Human Mutation ·Isabel Barragán,Salud Borrego,(unknown),María González‐del Pozo,Javier Santoyo‐López,Carmen Ayuso,Montserrat Baiget,José M. Millán,Marcela Mena,(unknown),Isabelle Audo,Christina Zeitz,Karin W. Littink,Joaquı́n Dopazo,(unknown),Guillermo Antiñolo	71
8	Mutations in the EYS Gene Account for Approximately 5% of Autosomal Recessive Retinitis Pigmentosa and Cause a Fairly Homogeneous Phenotype 2010 ·Ophthalmology ·Karin W. Littink,L. Ingeborgh van den Born,Robert K. Koenekoop,Rob W.J. Collin,Marijke N. Zonneveld,Ellen A.W. Blokland,(unknown),Thomas Theelen,Carel B. Hoyng,Frans P.M. Cremers,Anneke I. den Hollander,B. Jeroen Klevering	65
9	A Novel Nonsense Mutation inCEP290Induces Exon Skipping and Leads to a Relatively Mild Retinal Phenotype 2010 ·Investigative Ophthalmology & Visual Science ·Karin W. Littink,Jan-Willem R. Pott,Rob W.J. Collin,Hester Y. Kroes,Joanne Verheij,Ellen A.W. Blokland,Marta de Castro‐Miró,Carel B. Hoyng,Caroline C. W. Klaver,Robert K. Koenekoop,Klaus Rohrschneider,Frans P.M. Cremers,L. Ingeborgh van den Born,Anneke I. den Hollander	56
10	Novel Null Mutations in theEYSGene Are a Frequent Cause of Autosomal Recessive Retinitis Pigmentosa in the Israeli Population 2010 ·Investigative Ophthalmology & Visual Science ·Dikla Bandah‐Rozenfeld,Karin W. Littink,Tamar Ben‐Yosef,Tim M. Strom,Itay Chowers,Rob W.J. Collin,Anneke I. den Hollander,L. Ingeborgh van den Born,Marijke N. Zonneveld,Saul Merin,Eyal Banin,Frans P.M. Cremers,Dror Sharon	53
11	Homozygosity Mapping in Patients with Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations 2010 ·Investigative Ophthalmology & Visual Science ·Karin W. Littink,Robert K. Koenekoop,L. Ingeborgh van den Born,Rob W.J. Collin,Luminita Moruz,Joris A. Veltman,Susanne Roosing,Marijke N. Zonneveld,Amer Omar,Mahshad Darvish-Zargar,Irma López,Hester Y. Kroes,Maria M. van Genderen,Carel B. Hoyng,Klaus Rohrschneider,Mary J. van Schooneveld,Frans P.M. Cremers,Anneke I. den Hollander	81
12	A Novel Homozygous Nonsense Mutation inCABP4Causes Congenital Cone–Rod Synaptic Disorder 2009 ·Investigative Ophthalmology & Visual Science ·Karin W. Littink,Maria M. van Genderen,Rob W.J. Collin,Susanne Roosing,Arjan P.M. de Brouwer,Frans C. C. Riemslag,Hanka Venselaar,Alberta A. H. J. Thiadens,Carel B. Hoyng,Klaus Rohrschneider,Anneke I. den Hollander,Frans P.M. Cremers,L. Ingeborgh van den Born	59
13	Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa 2008 ·The American Journal of Human Genetics ·Rob W.J. Collin,Karin W. Littink,B. Jeroen Klevering,L. Ingeborgh van den Born,Robert K. Koenekoop,Marijke N. Zonneveld,Ellen A.W. Blokland,Tim M. Strom,Carel B. Hoyng,Anneke I. den Hollander,Frans P.M. Cremers	126

About Karin W. Littink

Karin W. Littink is a scholar working on Ophthalmology, Cell Biology and Molecular Biology, having authored 13 papers that have together received 711 indexed citations. Recurring topics across this work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Ocular Disorders and Treatments (3 papers). The work is most often cited by research in Ophthalmology (328 citations), Molecular Biology (669 citations) and Cellular and Molecular Neuroscience (146 citations). Karin W. Littink has collaborated with scholars based in Netherlands, Germany and Canada. Frequent co-authors include Frans P.M. Cremers, Rob W.J. Collin, Anneke I. den Hollander, L. Ingeborgh van den Born, Carel B. Hoyng, Marijke N. Zonneveld, B. Jeroen Klevering, Robert K. Koenekoop, Ellen A.W. Blokland and Tim M. Strom. Their work appears in journals such as Ophthalmology, The American Journal of Human Genetics and Investigative Ophthalmology & Visual Science.

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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