Paul Coucke

19.2k total citations
261 papers, 8.0k citations indexed

About

Paul Coucke is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Paul Coucke has authored 261 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Genetics, 117 papers in Molecular Biology and 53 papers in Cell Biology. Recurrent topics in Paul Coucke's work include Connective tissue disorders research (90 papers), Dermatological and Skeletal Disorders (44 papers) and Hearing, Cochlea, Tinnitus, Genetics (29 papers). Paul Coucke is often cited by papers focused on Connective tissue disorders research (90 papers), Dermatological and Skeletal Disorders (44 papers) and Hearing, Cochlea, Tinnitus, Genetics (29 papers). Paul Coucke collaborates with scholars based in Belgium, United States and Netherlands. Paul Coucke's co-authors include Anne De Paepe, Guy Van Camp, Patrick J. Willems, Bart Loeys, Sofie Symoens, Fransiska Malfait, Bert Callewaert, Andy Willaert, Julie De Backer and Olivier Vanakker and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Paul Coucke

253 papers receiving 7.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paul Coucke Belgium	49	3.7k	3.3k	1.4k	1.1k	973	261	8.0k
Susan H. Blanton United States	43	2.3k 0.6×	2.8k 0.8×	828 0.6×	542 0.5×	676 0.7×	189	6.2k
William Reardon United Kingdom	53	5.2k 1.4×	6.5k 2.0×	1.8k 1.3×	598 0.5×	648 0.7×	195	11.9k
Sally A. Camper United States	64	3.6k 1.0×	7.0k 2.1×	873 0.6×	734 0.7×	311 0.3×	217	13.0k
Lies H. Hoefsloot Netherlands	45	1.7k 0.5×	3.7k 1.1×	909 0.7×	292 0.3×	324 0.3×	136	6.6k
Mireille Claustres France	46	1.8k 0.5×	4.3k 1.3×	841 0.6×	367 0.3×	189 0.2×	221	8.2k
Thomas Gridley United States	68	2.6k 0.7×	12.8k 3.9×	1.0k 0.7×	1.9k 1.7×	559 0.6×	146	17.7k
Dominique Weil France	53	1.4k 0.4×	6.7k 2.0×	2.6k 1.9×	854 0.8×	307 0.3×	184	9.8k
Kathryn S.E. Cheah Hong Kong	50	2.3k 0.6×	5.3k 1.6×	736 0.5×	964 0.9×	2.4k 2.5×	153	10.6k
Niklas Dahl Sweden	50	2.9k 0.8×	5.9k 1.8×	231 0.2×	1.3k 1.2×	569 0.6×	245	9.8k
Lin Gan United States	52	1.1k 0.3×	6.7k 2.0×	907 0.7×	1.0k 0.9×	191 0.2×	187	9.6k

Countries citing papers authored by Paul Coucke

Since Specialization

Citations

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

Fields of papers citing papers by Paul Coucke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Coucke

This figure shows the co-authorship network connecting the top 25 collaborators of Paul Coucke. A scholar is included among the top collaborators of Paul Coucke 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 Paul Coucke. Paul Coucke 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

Boel, Annekatrien, Mina Popovic, Petra De Sutter, et al.. (2023). Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos. Molecular Therapy. 31(8). 2326–2341. 3 indexed citations

Boel, Annekatrien, Björn Menten, Petra De Sutter, et al.. (2022). TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo. Human Reproduction. 37(8). 1760–1773. 23 indexed citations

Acke, Frederic, Wim Wuyts, Kristof Van Schil, et al.. (2022). Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?. Genes. 14(1). 105–105. 3 indexed citations

Fischer, Suzanne, Laurence Campens, Andreas Pasch, et al.. (2022). Serum Calcification Propensity T50 Associates with Disease Severity in Patients with Pseudoxanthoma Elasticum. Journal of Clinical Medicine. 11(13). 3727–3727. 7 indexed citations

Naert, Thomas, Matt van de Rijn, Benjamin A. Alman, et al.. (2021). CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping. Proceedings of the National Academy of Sciences. 118(47). 9 indexed citations

Vergult, Sarah, Annelies Dheedene, Björn Menten, et al.. (2021). A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome. Genes. 12(7). 1048–1048. 7 indexed citations

Hanisch, Franz‐Georg, Geert Goeminne, Andreja Rajković, et al.. (2021). Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures. PLoS Genetics. 17(6). e1009603–e1009603. 6 indexed citations

Boel, Annekatrien, Aude Beyens, Marjolijn Renard, et al.. (2020). Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects. Human Molecular Genetics. 29(9). 1476–1488. 4 indexed citations

Bek, Jan Willem, Chen Shochat, Adelbert De Clercq, et al.. (2020). Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR-Based Functional Screening of Osteoporosis Candidate Genes. Journal of Bone and Mineral Research. 36(9). 1749–1764. 18 indexed citations

10.

Hosen, Mohammad Jakir, Ludovic Martin, Julie De Zaeytijd, et al.. (2020). VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum. Clinical Genetics. 98(1). 74–79. 9 indexed citations

11.

Gistelinck, Charlotte, Ronald Y. Kwon, Fransiska Malfait, et al.. (2018). Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies. Proceedings of the National Academy of Sciences. 115(34). E8037–E8046. 69 indexed citations

12.

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

13.

Gistelinck, Charlotte, Jane Lee, Sarah K. McMenamin, et al.. (2017). MicroCT-Based Phenomics in the Zebrafish Skeleton Reveals Virtues of Deep Phenotyping in a Distributed Organ System. Zebrafish. 15(1). 77–78. 7 indexed citations

14.

Symoens, Sofie, Andy Willaert, Tamer Essawi, et al.. (2017). Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected families. Molecular Genetics & Genomic Medicine. 6(1). 15–26. 25 indexed citations

15.

Willaert, Andy, Kris Vleminckx, Petra Vermassen, et al.. (2016). Studying the functionality of the homologous repair pathway in zebrafish embryos : heading for an in vivo functional test to evaluate the pathogenicity of BRCA2 variants. Ghent University Academic Bibliography (Ghent University). 1 indexed citations

16.

Delbeke, Patricia, Patrick Van Bogaert, Georges Rodesch, et al.. (2014). Congenital Fixed Dilated Pupils Due to ACTA2– Multisystemic Smooth Muscle Dysfunction Syndrome. Journal of Neuro-Ophthalmology. 34(2). 137–143. 17 indexed citations

17.

Leeneer, Kim De, Steve Lefever, Filip Pattyn, et al.. (2010). Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline. BMC Bioinformatics. 11(1). 269–269. 14 indexed citations

18.

Coucke, Paul, et al.. (2006). Mutation analysis in the FBN1 gene in patients with Marfan Syndrome. Ghent University Academic Bibliography (Ghent University). 5 indexed citations

19.

Coucke, Paul, Peter Van Hauwe, Lorraine A. Everett, et al.. (1999). Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome. Journal of Medical Genetics. 36(6). 475–477. 40 indexed citations

20.

Camp, Guy Van, Ed Green, Margriet Verstreken, et al.. (1998). Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea.. PubMed. 5(6). 397–405. 18 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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