Frauke Coppieters

3.4k total citations · 1 hit paper
46 papers, 1.7k citations indexed

About

Frauke Coppieters is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Frauke Coppieters has authored 46 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 14 papers in Ophthalmology and 13 papers in Genetics. Recurrent topics in Frauke Coppieters's work include Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (12 papers) and RNA regulation and disease (7 papers). Frauke Coppieters is often cited by papers focused on Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (12 papers) and RNA regulation and disease (7 papers). Frauke Coppieters collaborates with scholars based in Belgium, United States and Netherlands. Frauke Coppieters's co-authors include Elfride De Baere, Steve Lefever, Bart P. Leroy, Françoise Meire, Claus Bachert, Tatiana A. Mishchenko, Victoria D. Turubanova, Olga Krysko, Iuliia Efimova and Maria V. Vedunova and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Frauke Coppieters

43 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Vaccination with early ferroptotic cancer cells induces efficient antitumor immunity

2020 367 citations Iuliia Efimova, Elena Catanzaro et al. Journal for ImmunoTherapy of Cancer profile →

Peers

Frauke Coppieters

GENET

OPHTH

PRM

Yumei Li United States

Heinrich Schrewe Germany

Christel Kockx Netherlands

Joseph C. Giacalone United States

Josephine C. Dorsman Netherlands

Xianjun Zhu China

Charlotte Andrieu‐Soler France

Emil Bogenmann United States

R.L. Eddy United States

Rahat Perveen United Kingdom

Yumei Li United States

Frauke Coppieters

1.9k ×1.5

439 ×0.9

GENET

503 ×1.2

OPHTH

157 ×0.5

PRM

80 ×0.4

Citations per year, relative to Frauke Coppieters Frauke Coppieters (= 1×) peers Yumei Li

Countries citing papers authored by Frauke Coppieters

Since Specialization

Citations

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

Fields of papers citing papers by Frauke Coppieters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frauke Coppieters

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

All Works

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20 of 20 papers shown

Mukherjee, Rajarshi, Chris F. Inglehearn, Frauke Coppieters, et al.. (2024). Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci. Nature Communications. 15(1). 1600–1600. 9 indexed citations

Krysko, Olga, Andrea Teufelberger, Natalie De Ruyck, et al.. (2023). Differential protease content of mast cells and the processing of IL-33 in Alternaria alternata induced allergic airway inflammation in mice. Frontiers in Immunology. 14. 1040493–1040493. 3 indexed citations

Helsmoortel, Céline, Pieter‐Jan Volders, Jo Vandesompele, et al.. (2022). Performance Evaluation of Three DNA Sample Tracking Tools in a Whole Exome Sequencing Workflow. Molecular Diagnosis & Therapy. 26(4). 411–419. 2 indexed citations

Vedunova, Maria V., Victoria D. Turubanova, Iuliia Efimova, et al.. (2022). DC vaccines loaded with glioma cells killed by photodynamic therapy induce Th17 anti-tumor immunity and provide a four-gene signature for glioma prognosis. Cell Death and Disease. 13(12). 1062–1062. 30 indexed citations

Afoakwa, Emmanuel Ohene, Frauke Coppieters, S.T. Lowor, et al.. (2021). Selection and validation of reference genes for accurate RT-qPCR gene expression normalization in cacao beans during fermentation. Tree Genetics & Genomes. 17(1). 2 indexed citations

Naert, Thomas, Toon Rosseel, Dario Priem, et al.. (2020). Functional characterization of a Xenopus tropicalis knockout and a human cellular model of RCBTB1-associated inherited retinal disease shows involvement of RCBTB1 in the cellular response to oxidative stress. Investigative Ophthalmology & Visual Science. 61(7). 1125–1125. 1 indexed citations

Efimova, Iuliia, Elena Catanzaro, Louis Van der Meeren, et al.. (2020). Vaccination with early ferroptotic cancer cells induces efficient antitumor immunity. Journal for ImmunoTherapy of Cancer. 8(2). e001369–e001369. 367 indexed citations breakdown →

Schil, Kristof Van, Caroline Van Cauwenbergh, Toon Rosseel, et al.. (2019). Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes. Ghent University Academic Bibliography (Ghent University). 1 indexed citations

Naessens, Sarah, Julie De Zaeytijd, Delfien Syx, et al.. (2019). The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond. Human Mutation. 40(5). 539–551. 10 indexed citations

10.

Coppieters, Frauke, et al.. (2019). The development of a novel SNP genotyping assay to differentiate cacao clones. Scientific Reports. 9(1). 9512–9512. 15 indexed citations

11.

Bogaert, Debby, Mélissa Dullaers, Hye Sun Kuehn, et al.. (2017). Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes. Scientific Reports. 7(1). 3702–3702. 22 indexed citations

12.

Stoop, Hans, Frank Peelman, Anne‐Laure Todeschini, et al.. (2016). NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development. Genetics in Medicine. 19(4). 367–376. 90 indexed citations

13.

Bauwens, Miriam, Sophie Walraedt, Patricia Delbeke, et al.. (2015). Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus. Investigative Ophthalmology & Visual Science. 56(3). 1701–1710. 23 indexed citations

14.

Schil, Kristof Van, Marcus Karlstetter, Françoise Meire, et al.. (2014). Homozygous deletion of glutamate receptor gene GRID2 causes new human hotfoot mutant phenotype, characterized by early-onset cerebellar ataxia and retinal dystrophy. European Journal of Human Genetics. 22. 83–84. 2 indexed citations

15.

Brecelj, Jelka, Maja Šuštar, Frauke Coppieters, et al.. (2012). Enhanced S-cone syndrome with preserved macular structure and severely depressed retinal function. Documenta Ophthalmologica. 125(2). 161–168. 8 indexed citations

16.

Kohl, Susanne, Frauke Coppieters, Françoise Meire, et al.. (2012). A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia. The American Journal of Human Genetics. 91(3). 527–532. 134 indexed citations

17.

Zaeytijd, Julie De, Frauke Coppieters, Linda Visser, et al.. (2011). Phenotype of RDH12-related Early-Onset Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 52(14). 2380–2380. 1 indexed citations

18.

Coppieters, Frauke, Steve Lefever, Bart P. Leroy, & Elfride De Baere. (2010). CEP290, a gene with many faces: mutation overview and presentation of CEP290base. Human Mutation. 31(10). 1097–1108. 210 indexed citations

19.

Coppieters, Frauke, Ingele Casteels, Françoise Meire, et al.. (2010). Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes. Human Mutation. 31(10). E1709–E1766. 110 indexed citations

20.

Coppieters, Frauke, Elise Héon, Igor Cima, et al.. (2009). Exploring the Role of Genes of the Retinal Transcription Network in Retinal Degeneration. Investigative Ophthalmology & Visual Science. 50(13). 3745–3745. 1 indexed citations

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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