Lisette Hetterschijt

1.4k total citations
12 papers, 381 citations indexed

About

Lisette Hetterschijt is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Lisette Hetterschijt has authored 12 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Lisette Hetterschijt's work include Retinal Development and Disorders (6 papers), Genetic and Kidney Cyst Diseases (4 papers) and Cellular transport and secretion (4 papers). Lisette Hetterschijt is often cited by papers focused on Retinal Development and Disorders (6 papers), Genetic and Kidney Cyst Diseases (4 papers) and Cellular transport and secretion (4 papers). Lisette Hetterschijt collaborates with scholars based in Netherlands, Germany and United States. Lisette Hetterschijt's co-authors include Erwin van Wijk, Theo Peters, Hannie Kremer, Margo Dona, Ronald Roepman, Erik de Vrieze, Helma van den Hurk, Lilian Vreede, J.J.M. van Groningen and Ad Geurts van Kessel and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Lisette Hetterschijt

12 papers receiving 376 citations

Peers

Countries citing papers authored by Lisette Hetterschijt

Since Specialization

Citations

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

Fields of papers citing papers by Lisette Hetterschijt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisette Hetterschijt. 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 Lisette Hetterschijt. The network helps show where Lisette Hetterschijt may publish in the future.

Co-authorship network of co-authors of Lisette Hetterschijt

This figure shows the co-authorship network connecting the top 25 collaborators of Lisette Hetterschijt. A scholar is included among the top collaborators of Lisette Hetterschijt 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 Lisette Hetterschijt. Lisette Hetterschijt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina 2022 ·Journal of Proteomics ·(unknown), Ralph Slijkerman, Lisette Hetterschijt, Theo Peters, Sanne Broekman, Aurélie Clément, Monte Westerfield, Jennifer B. Phillips, Karsten Boldt, Hannie Kremer, Erik de Vrieze, Erwin van Wijk	2
2	Usherin defects lead to early-onset retinal dysfunction in zebrafish 2018 ·Experimental Eye Research ·Margo Dona, Ralph Slijkerman, (unknown), Sanne Broekman, Jeremy Wegner, (unknown), Theo Peters, Lisette Hetterschijt, (unknown), Erik de Vrieze, Nasrin Sorusch, Uwe Wolfrum, Hannie Kremer, Stephan C. F. Neuhauss, Jingjing Zang, Maarten Kamermans, Monte Westerfield, Jennifer B. Phillips, Erwin van Wijk	51
3	Poor Splice-Site Recognition in a Humanized Zebrafish Knockin Model for the Recurrent Deep-Intronic c.7595-2144A>G Mutation in USH2A 2018 ·Zebrafish ·Ralph Slijkerman, (unknown), Sanne Broekman, Erik de Vrieze, Lisette Hetterschijt, Theo Peters, (unknown), Hannie Kremer, Erwin van Wijk	20
4	Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa 2017 ·Journal of Medical Genetics ·Thanh-Minh T. Nguyen, Sarah Hull, Ronald Roepman, L. Ingeborgh van den Born, Machteld M. Oud, Erik de Vrieze, Lisette Hetterschijt, Stef J.F. Letteboer, Sylvia E. C. van Beersum, Ellen A.W. Blokland, Helger G. Yntema, Frans P.M. Cremers, Paul A. van der Zwaag, Gavin Arno, Erwin van Wijk, Andrew R. Webster, Lonneke Haer‐Wigman	18
5	Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation 2016 ·Molecular Therapy — Nucleic Acids ·(unknown), Christel Vaché, Margo Dona, Gema García‐García, Mireille Claustres, Lisette Hetterschijt, Theo Peters, Bas P. Hartel, Ronald J. E. Pennings, (unknown), Elena Aller, Alejandro Garanto, Rob W.J. Collin, Hannie Kremer, Anne‐Françoise Roux, Erwin van Wijk	104
6	The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking 2015 ·PLoS Genetics ·Ruxandra Bachmann‐Gagescu, Margo Dona, Lisette Hetterschijt, E.L.G.M. Tonnaer, Theo Peters, Erik de Vrieze, Dorus A. Mans, Sylvia E. C. van Beersum, Ian G. Phelps, Heleen H. Arts, Jan E.E. Keunen, Marius Ueffing, Ronald Roepman, Karsten Boldt, Dan Doherty, Cecilia B. Moens, Stephan C. F. Neuhauss, Hannie Kremer, Erwin van Wijk	59
7	The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically 2012 ·PubMed ·Ferry F.J. Kersten, Erwin van Wijk, Lisette Hetterschijt, (unknown), Theo Peters, Mariam G. Aslanyan, Bert van der Zwaag, Uwe Wolfrum, Jan E.E. Keunen, Ronald Roepman, Hannie Kremer	14
8	FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies 2012 ·Human Molecular Genetics ·Silvio Alessandro Di Gioia, Stef J.F. Letteboer, Corinne Kostic, Dikla Bandah‐Rozenfeld, Lisette Hetterschijt, Dror Sharon, Yvan Arsenijévic, Ronald Roepman, Carlo Rivolta	44
9	The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia 2012 ·SHILAP Revista de lepidopterología ·(unknown), Karlien L. M. Coene, Karsten Boldt, (unknown), Jeroen van Reeuwijk, (unknown), Emine Bolat, Lude Franke, Lisette Hetterschijt, (unknown), (unknown), Heymut Omran, (unknown), Marius Ueffing, Ronald Roepman	1
10	The Mitotic Arrest Deficient Protein MAD2B Interacts with the Clathrin Light Chain A during Mitosis 2010 ·PLoS ONE ·(unknown), Lilian Vreede, J.J.M. van Groningen, Lisette Hetterschijt, (unknown), Patrick A.M. Jansen, Helma van den Hurk, Diederik R.H. de Bruijn, Ad Geurts van Kessel	27
11	The Mitotic Arrest Deficient Protein MAD2B Interacts with the Small GTPase RAN throughout the Cell Cycle 2009 ·PLoS ONE ·(unknown), J.J.M. van Groningen, Lilian Vreede, Lisette Hetterschijt, Helma van den Hurk, Diederik R.H. de Bruijn, (unknown), Ad Geurts van Kessel	24
12	The renal cell carcinoma-associated oncogenic fusion protein PRCCTFE3 provokes p21WAF1/CIP1-mediated cell cycle delay 2009 ·Experimental Cell Research ·(unknown), J.J.M. van Groningen, Lilian Vreede, Lisette Hetterschijt, (unknown), Helma van den Hurk, Ad Geurts van Kessel	17

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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