Wouter Steyaert

1.7k total citations
27 papers, 639 citations indexed

About

Wouter Steyaert is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Wouter Steyaert has authored 27 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Genetics and 4 papers in Surgery. Recurrent topics in Wouter Steyaert's work include Connective tissue disorders research (7 papers), Genomics and Rare Diseases (6 papers) and CRISPR and Genetic Engineering (6 papers). Wouter Steyaert is often cited by papers focused on Connective tissue disorders research (7 papers), Genomics and Rare Diseases (6 papers) and CRISPR and Genetic Engineering (6 papers). Wouter Steyaert collaborates with scholars based in Belgium, United States and Netherlands. Wouter Steyaert's co-authors include Paul Coucke, Anne De Paepe, Bert Callewaert, Andy Willaert, Annekatrien Boel, Fransiska Malfait, Sofie Symoens, Björn Menten, Annelies Dheedene and Hans Peter Bächinger and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Wouter Steyaert

27 papers receiving 632 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Wouter Steyaert Belgium 14 392 318 86 59 54 27 639
Muneera Alshammari Saudi Arabia 14 473 1.2× 406 1.3× 72 0.8× 85 1.4× 51 0.9× 18 749
Véronique Geoffroy France 12 559 1.4× 510 1.6× 58 0.7× 64 1.1× 70 1.3× 17 775
Jiangxia Li China 18 478 1.2× 119 0.4× 85 1.0× 64 1.1× 123 2.3× 40 755
Lucie Dupuis Canada 13 243 0.6× 335 1.1× 88 1.0× 92 1.6× 51 0.9× 28 554
Jennifer E. Posey United States 16 481 1.2× 394 1.2× 41 0.5× 54 0.9× 83 1.5× 61 813
Javad Nadaf Canada 13 419 1.1× 293 0.9× 59 0.7× 44 0.7× 174 3.2× 31 859
Fulya Taylan Sweden 16 346 0.9× 267 0.8× 89 1.0× 57 1.0× 82 1.5× 43 618
Pamela Magini Italy 16 347 0.9× 349 1.1× 42 0.5× 27 0.5× 119 2.2× 38 717
Bérengère de Martinville United States 17 616 1.6× 389 1.2× 51 0.6× 50 0.8× 69 1.3× 27 980

Countries citing papers authored by Wouter Steyaert

Since Specialization
Citations

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

Fields of papers citing papers by Wouter Steyaert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wouter Steyaert

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

All Works

20 of 20 papers shown
1.
Verdin, Hannah, et al.. (2024). Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples. Journal of Genetic Counseling. 34(1). e1899–e1899. 1 indexed citations
2.
Steyaert, Wouter, Lonneke Haer‐Wigman, Rolph Pfundt, et al.. (2023). Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation. Nature Communications. 14(1). 6845–6845. 5 indexed citations
3.
Šablauskas, Karolis, Wouter Steyaert, Michael Kwint, et al.. (2022). DeNovoCNN: a deep learning approach to de novo variant calling in next generation sequencing data. Nucleic Acids Research. 50(17). e97–e97. 11 indexed citations
4.
Steyaert, Wouter, Paul Coucke, Joris Delanghe, et al.. (2022). G protein–coupled receptor kinase 6 (GRK6) regulates insulin processing and secretion via effects on proinsulin conversion to insulin. Journal of Biological Chemistry. 298(10). 102421–102421. 5 indexed citations
5.
Steyaert, Wouter, Thierry Bové, Thomas Martens, et al.. (2022). Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA. Genes. 13(7). 1214–1214. 8 indexed citations
6.
Steyaert, Wouter, Jeffrey Benovic, John W.M. Creemers, et al.. (2022). Hypergastrinemia, a clue leading to the identification of an atypical form of diabetes mellitus type 2. Clinica Chimica Acta. 532. 79–83. 3 indexed citations
7.
Steyaert, Wouter, et al.. (2021). Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a model. Journal of genetics and genomics. 48(4). 289–299. 3 indexed citations
8.
Boel, Annekatrien, Wouter Steyaert, Bert Callewaert, et al.. (2018). CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragments. Disease Models & Mechanisms. 11(10). 68 indexed citations
9.
Steyaert, Wouter, Annekatrien Boel, Paul Coucke, & Andy Willaert. (2018). BATCH-GE: Analysis of NGS Data for Genome Editing Assessment. Methods in molecular biology. 1865. 83–90. 2 indexed citations
10.
Mosquera, Laura Muiño, Anne De Paepe, Wouter Steyaert, et al.. (2018). Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome. Circulation Genomic and Precision Medicine. 11(6). e002039–e002039. 17 indexed citations
11.
Symoens, Sofie, Wouter Steyaert, Anne De Paepe, et al.. (2017). Tissue‐specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome. American Journal of Medical Genetics Part A. 173(4). 1047–1050. 11 indexed citations
12.
Shah, Khadim, Raja Hussain Ali, Muhammad Ansar, et al.. (2016). Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP. BMC Medical Genetics. 17(1). 13–13. 4 indexed citations
13.
Cauwenbergh, Caroline Van, Kristof Van Schil, Robrecht Cannoodt, et al.. (2016). arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs. Genetics in Medicine. 19(4). 457–466. 28 indexed citations
14.
Naert, Thomas, Jurgen Haustraete, Annekatrien Boel, et al.. (2016). CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis. Scientific Reports. 6(1). 35264–35264. 48 indexed citations
15.
Boel, Annekatrien, Wouter Steyaert, Nina De Rocker, et al.. (2016). BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment. Scientific Reports. 6(1). 30330–30330. 70 indexed citations
16.
Symoens, Sofie, Aileen M. Barnes, Charlotte Gistelinck, et al.. (2015). Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia. The American Journal of Human Genetics. 97(4). 521–534. 32 indexed citations
17.
Leeneer, Kim De, Wouter Steyaert, Karen De Pauw, et al.. (2015). Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population. Disease Markers. 2015. 1–6. 8 indexed citations
18.
Hosen, Mohammad Jakir, Filip Van Nieuwerburgh, Wouter Steyaert, et al.. (2014). Efficiency of Exome Sequencing for the Molecular Diagnosis of Pseudoxanthoma Elasticum. Journal of Investigative Dermatology. 135(4). 992–998. 23 indexed citations
19.
Acke, Frederic, Fransiska Malfait, Olivier Vanakker, et al.. (2014). Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing. Molecular Genetics and Metabolism. 113(3). 230–235. 41 indexed citations
20.
Symoens, Sofie, Fransiska Malfait, Bert Callewaert, et al.. (2013). Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans. Orphanet Journal of Rare Diseases. 8(1). 154–154. 98 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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