Sarah Naessens

460 total citations
2 papers, 29 citations indexed

About

Sarah Naessens is a scholar working on Molecular Biology, Neurology and Ophthalmology. According to data from OpenAlex, Sarah Naessens has authored 2 papers receiving a total of 29 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 1 paper in Neurology and 1 paper in Ophthalmology. Recurrent topics in Sarah Naessens's work include Vascular Malformations Diagnosis and Treatment (1 paper), Connexins and lens biology (1 paper) and Retinal Diseases and Treatments (1 paper). Sarah Naessens is often cited by papers focused on Vascular Malformations Diagnosis and Treatment (1 paper), Connexins and lens biology (1 paper) and Retinal Diseases and Treatments (1 paper). Sarah Naessens collaborates with scholars based in Belgium and United States. Sarah Naessens's co-authors include Frauke Coppieters, Elfride De Baere, Steve Lefever, Frank Peelman, Julie De Zaeytijd, Roosmarijn E. Vandenbroucke, Delfien Syx, Bart P. Leroy and Caroline Van Cauwenbergh and has published in prestigious journals such as Human Mutation and Genes.

In The Last Decade

Sarah Naessens

2 papers receiving 29 citations

Peers

Countries citing papers authored by Sarah Naessens

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Naessens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Naessens

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

All Works

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2 of 2 papers shown

#	Work	Indexed citations
1	The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond 2019 ·Human Mutation ·Sarah Naessens, Julie De Zaeytijd, Delfien Syx, Roosmarijn E. Vandenbroucke, (unknown), Caroline Van Cauwenbergh, Bart P. Leroy, Frank Peelman, Frauke Coppieters	10
2	Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing NR2E3-Associated Autosomal Dominant Retinitis Pigmentosa 2019 ·Genes ·Sarah Naessens, (unknown), Steve Lefever, Frauke Coppieters, Elfride De Baere	19

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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