Wouter Steyaert

1.8k citations

27 papers · 651 · h-index 14

Impact in

Aging top 10%
Genetics top 10%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Dermatological and Skeletal Disorders

Papers in

Molecular Biology 17
- CRISPR and Genetic Engineering 5
- Ubiquitin and proteasome pathways 2
- Protein Degradation and Inhibitors 2
- Receptor Mechanisms and Signaling 2
Genetics 16
- Connective tissue disorders research 7
- Genomics and Rare Diseases 5
- Dermatological and Skeletal Disorders 3
- Evolution and Genetic Dynamics 2

Co-authors: Paul Coucke (22 shared papers)Anne De Paepe (10 shared papers)Bert Callewaert (6 shared papers)Andy Willaert (6 shared papers)Annekatrien Boel (4 shared papers)Fransiska Malfait (5 shared papers)Sofie Symoens (6 shared papers)Sanne D’hondt (2 shared papers)
Journals: Scientific Reports (2 papers)Disease Markers (2 papers)Clinica Chimica Acta (1 paper)The FASEB Journal (1 paper)Journal of genetics and genomics (1 paper)
Partner nations: Belgium United States Netherlands

In The Last Decade

Wouter Steyaert

27 papers receiving 645 citations

Peers

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-authors

The 25 scholars most cited alongside Wouter Steyaert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Wouter Steyaert Line = papers co-authored together Wouter Steyaert links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans Orphanet Journal of Rare Diseases ·Sofie Symoens, Fransiska Malfait, Sanne D’hondt, Bert Callewaert, Annelies Dheedene, Wouter Steyaert, Hans Peter Bächinger, Anne De Paepe, Hülya Kayserili, Paul Coucke	2013	99
2	BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment Scientific Reports ·Annekatrien Boel, Wouter Steyaert, Nina De Rocker, Björn Menten, Bert Callewaert, Anne De Paepe, Paul Coucke, Andy Willaert	2016	71
3	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 ·Annekatrien Boel, Hanna De Saffel, Wouter Steyaert, Bert Callewaert, Anne De Paepe, Paul Coucke, Andy Willaert	2018	70
4	CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis Scientific Reports ·Thomas Naert, Robin Colpaert, Tom Van Nieuwenhuysen, Dionysia Dimitrakopoulou, Jannick Leœn, Jurgen Haustraete, Annekatrien Boel, Wouter Steyaert, Trees Lepez, Dieter Deforce, Andy Willaert, David Creytens, Kris Vleminckx	2016	48
5	Novel pathogenic COL11A1/COL11A2 variants in Stickler syndrome detected by targeted NGS and exome sequencing Molecular Genetics and Metabolism ·Frederic Acke, Fransiska Malfait, Olivier Vanakker, Wouter Steyaert, Kim De Leeneer, Geert Mortier, Ingeborg Dhooge, Anne De Paepe, Els De Leenheer, Paul Coucke	2014	43
6	Flexible, Scalable, and Efficient Targeted Resequencing on a Benchtop Sequencer for Variant Detection in Clinical Practice Human Mutation ·Kim De Leeneer, Jan Hellemans, Wouter Steyaert, Steve Lefever, Inge Vereecke, Eveline Debals, Brecht Crombez, Machteld Baetens, Mattias Van Heetvelde, Frauke Coppieters, Jo Vandesompele, Annelies De Jaegher, (unknown), Paul Coucke, Kathleen Claes	2014	43
7	RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder Neurology ·Patrick Santens, Tim Van Damme, Wouter Steyaert, Andy Willaert, Bernard Sablonnière, Anne De Paepe, Paul Coucke, Bart Dermaut	2015	38
8	Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia The American Journal of Human Genetics ·Sofie Symoens, Aileen M. Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Delfien Syx, Sanne D’hondt, Martine Biervliet, Julie De Backer, P. Eckhard Witten, Sergey Leikin, Elena Makareeva, Gabriele Gillessen‐Kaesbach, Ann Huysseune, Kris Vleminckx, Andy Willaert, Anne De Paepe, Joan C. Marini, Paul Coucke	2015	33
9	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 ·Caroline Van Cauwenbergh, Kristof Van Schil, Robrecht Cannoodt, Miriam Bauwens, Thalia Van Laethem, Sarah De Jaegere, Wouter Steyaert, Tom Sante, Björn Menten, Bart P. Leroy, Frauke Coppieters, (unknown)	2016	28
10	Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family Disease Markers ·Delfien Syx, Sofie Symoens, Wouter Steyaert, Anne De Paepe, Paul Coucke, Fransiska Malfait	2015	28
11	Efficiency of Exome Sequencing for the Molecular Diagnosis of Pseudoxanthoma Elasticum Journal of Investigative Dermatology ·Mohammad Jakir Hosen, Filip Van Nieuwerburgh, Wouter Steyaert, Dieter Deforce, Ludovic Martin, Georges Lefthériotis, Anne De Paepe, Paul Coucke, Olivier Vanakker	2014	23
12	Exome sequencing revealed a novel biallelic deletion in theDCAF17gene underlying Woodhouse Sakati syndrome Clinical Genetics ·Raja Hussain Ali, Khadim Shah, Abdul Nasır, Wouter Steyaert, Paul Coucke, Wasim Ahmad	2015	20
13	Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum American Journal of Medical Genetics Part A ·Ilse Meerschaut, Aude Beyens, Wouter Steyaert, Riet De Rycke, Katrien Bonte, Tine De Backer, Sandra Janssens, Joseph Panzer, Frank Plasschaert, Daniël De Wolf, Bert Callewaert	2019	17
14	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 ·Laura Muiño Mosquera, Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Anne De Paepe, Wouter Steyaert, Sofie Symoens, Paul Coucke, Bert Callewaert, Marjolijn Renard, Julie De Backer	2018	17
15	DeNovoCNN: a deep learning approach to de novo variant calling in next generation sequencing data Nucleic Acids Research ·Gelana Khazeeva, Karolis Šablauskas, Bart van der Sanden, Wouter Steyaert, Michael Kwint, Dmitrijs Rots, Max Hinne, Marcel van Gerven, Helger G. Yntema, Lisenka E.L.M. Vissers, Christian Gilissen	2022	12
16	Tissue‐specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome American Journal of Medical Genetics Part A ·Sofie Symoens, Wouter Steyaert, Lynn Demuynck, Anne De Paepe, Karin E. M. Diderich, Fransiska Malfait, Paul Coucke	2017	11
17	Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population Disease Markers ·Osama Essawi, Mohammad Farraj, Kim De Leeneer, Wouter Steyaert, Karen De Pauw, Anne De Paepe, Kathleen Claes, Tamer Essawi, Paul Coucke	2015	8
18	Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA Genes ·Ilse Meerschaut, Wouter Steyaert, Thierry Bové, Katrien François, Thomas Martens, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, Lara Moons, Petra Vermassen, Sofie Symoens, Paul Coucke, Daniël De Wolf, Bert Callewaert	2022	8
19	Future perspectives of genome-scale sequencing Acta Clinica Belgica ·Wouter Steyaert, Steven Callens, Paul Coucke, Bart Dermaut, Dimitri Hemelsoet, Wim Terryn, Bruce Poppe	2018	8
20	G protein–coupled receptor kinase 6 (GRK6) regulates insulin processing and secretion via effects on proinsulin conversion to insulin Journal of Biological Chemistry ·Matthew J. Varney, Wouter Steyaert, Paul Coucke, Joris Delanghe, David Uehling, Babu Joseph, Richard Marcellus, Rima Al‐awar, Jeffrey Benovic	2022	6

About Wouter Steyaert

Wouter Steyaert is a scholar working on Molecular Biology, Genetics, Surgery, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine, having authored 27 papers that have together received 651 indexed citations. Recurring topics across this work include Connective tissue disorders research (7 papers), Genomics and Rare Diseases (5 papers), CRISPR and Genetic Engineering (5 papers), Dermatological and Skeletal Disorders (3 papers), Ubiquitin and proteasome pathways (2 papers), Protein Degradation and Inhibitors (2 papers), Evolution and Genetic Dynamics (2 papers) and Receptor Mechanisms and Signaling (2 papers). The work is most often cited by research in Aging (22 citations), Genetics (308 citations), Molecular Biology (361 citations), Rheumatology (67 citations) and Business and International Management (7 citations). Wouter Steyaert has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Paul Coucke, Anne De Paepe, Bert Callewaert, Andy Willaert, Annekatrien Boel, Fransiska Malfait, Sofie Symoens, Sanne D’hondt, Björn Menten and Hans Peter Bächinger. Their work appears in journals such as Scientific Reports, Disease Markers, Clinica Chimica Acta, The FASEB Journal and Journal of genetics and genomics.

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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Wouter Steyaert

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Wouter Steyaert

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About Wouter Steyaert

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