Paul Coucke

19.2k citations

261 papers · 8.0k indexed · h-index 49

Genetics top 0.2%
Molecular Biology top 2%
Sensory Systems top 0.2%
Cell Biology top 1%
Rheumatology top 1%

Co-authors: Anne De Paepe Guy Van Camp Patrick J. Willems Bart Loeys Sofie Symoens Fransiska Malfait Bert Callewaert Andy Willaert
Topics: Connective tissue disorders research (90 papers)Dermatological and Skeletal Disorders (44 papers)Hearing, Cochlea, Tinnitus, Genetics (29 papers)
Cited by: Sensory Systems Genetics Otorhinolaryngology
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: Belgium United States Netherlands

In The Last Decade

Paul Coucke

253 papers receiving 7.8k citations

Peers

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

#	Work	Indexed citations
1	Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos 2023 ·Molecular Therapy ·(unknown),Annekatrien Boel,(unknown),(unknown),Mina Popovic,(unknown),(unknown),(unknown),(unknown),(unknown),Petra De Sutter,Dominic Stoop,Paul Coucke,Björn Menten,Björn Heindryckx	3
2	TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo 2022 ·Human Reproduction ·(unknown),(unknown),Annekatrien Boel,Björn Menten,Petra De Sutter,Dominic Stoop,Susana M. Chuva de Sousa Lopes,Frederic Lluı́s,Paul Coucke,Björn Heindryckx	23
3	Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? 2022 ·Genes ·(unknown),(unknown),Frederic Acke,Wim Wuyts,Kristof Van Schil,Paul Coucke,Sandra Janssens,Els De Leenheer	3
4	Serum Calcification Propensity T50 Associates with Disease Severity in Patients with Pseudoxanthoma Elasticum 2022 ·Journal of Clinical Medicine ·(unknown),(unknown),Suzanne Fischer,Laurence Campens,(unknown),Andreas Pasch,Julie De Zaeytijd,Bart P. Leroy,David Devos,Tine De Backer,Paul Coucke,Olivier Vanakker	7
5	CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping 2021 ·Proceedings of the National Academy of Sciences ·Thomas Naert,(unknown),(unknown),(unknown),(unknown),Matt van de Rijn,(unknown),Benjamin A. Alman,Paul Coucke,Kim De Leeneer,Christian Vanhove,Savvas N. Savvides,David Creytens,Kris Vleminckx	9
6	A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome 2021 ·Genes ·(unknown),Sarah Vergult,Annelies Dheedene,Björn Menten,Katya De Groote,Hans De Wilde,Laura Muiño Mosquera,Joseph Panzer,Kristof Vandekerckhove,Paul Coucke,Daniël De Wolf,Bert Callewaert	7
7	Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures 2021 ·PLoS Genetics ·(unknown),(unknown),(unknown),Franz‐Georg Hanisch,Geert Goeminne,Andreja Rajković,Paul Coucke,Patrick Sips,Bert Callewaert	6
8	Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects 2020 ·Human Molecular Genetics ·Annekatrien Boel,(unknown),(unknown),Aude Beyens,Marjolijn Renard,Sander Barnhoorn,Christophe Casteleyn,Dieter P. Reinhardt,Benedicte Descamps,Christian Vanhove,Ingrid van der Pluijm,Paul Coucke,Andy Willaert,Jeroen Essers,Bert Callewaert	4
9	Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR-Based Functional Screening of Osteoporosis Candidate Genes 2020 ·Journal of Bone and Mineral Research ·Jan Willem Bek,Chen Shochat,Adelbert De Clercq,(unknown),Annekatrien Boel,Juriaan R. Metz,(unknown),David Karasik,Andy Willaert,Paul Coucke	18
10	VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum 2020 ·Clinical Genetics ·(unknown),Mohammad Jakir Hosen,Ludovic Martin,Julie De Zaeytijd,Bart P. Leroy,(unknown),Paul Coucke,Anne De Paepe,Olivier Vanakker	9
11	Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies 2018 ·Proceedings of the National Academy of Sciences ·Charlotte Gistelinck,Ronald Y. Kwon,Fransiska Malfait,Sofie Symoens,Matthew P. Harris,Katrin Henke,M. Brent Hawkins,Shannon Fisher,Patrick Sips,Brecht Guillemyn,Jan Willem Bek,Petra Vermassen,(unknown),P. Eckhard Witten,MaryAnn Weis,Anne De Paepe,David R. Eyre,Andy Willaert,Paul Coucke	69
12	CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragments 2018 ·Disease Models & Mechanisms ·Annekatrien Boel,(unknown),Wouter Steyaert,Bert Callewaert,Anne De Paepe,Paul Coucke,Andy Willaert	68
13	MicroCT-Based Phenomics in the Zebrafish Skeleton Reveals Virtues of Deep Phenotyping in a Distributed Organ System 2017 ·Zebrafish ·(unknown),Charlotte Gistelinck,(unknown),Jane Lee,(unknown),(unknown),(unknown),Sarah K. McMenamin,Andy Willaert,David M. Parichy,Paul Coucke,Ronald Y. Kwon	7
14	Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected families 2017 ·Molecular Genetics & Genomic Medicine ·(unknown),Sofie Symoens,(unknown),(unknown),(unknown),Andy Willaert,Tamer Essawi,Bert Callewaert,Anne De Paepe,Fransiska Malfait,Paul Coucke	25
15	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 2016 ·Ghent University Academic Bibliography (Ghent University) ·(unknown),Andy Willaert,Kris Vleminckx,Petra Vermassen,(unknown),Paul Coucke,Anne Vral,Kathleen Claes	1
16	Congenital Fixed Dilated Pupils Due to ACTA2– Multisystemic Smooth Muscle Dysfunction Syndrome 2014 ·Journal of Neuro-Ophthalmology ·(unknown),(unknown),Patricia Delbeke,Patrick Van Bogaert,Georges Rodesch,Julie De Zaeytijd,Fanny Depasse,Paul Coucke,Françoise Meire	17
17	Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline 2010 ·BMC Bioinformatics ·(unknown),Kim De Leeneer,Steve Lefever,(unknown),Filip Pattyn,Filip Van Nieuwerburgh,Paul Coucke,Dieter Deforce,Jo Vandesompele,Sofie Bekaert,Jan Hellemans,Wim Van Criekinge	14
18	Mutation analysis in the FBN1 gene in patients with Marfan Syndrome 2006 ·Ghent University Academic Bibliography (Ghent University) ·Paul Coucke,(unknown),(unknown)	5
19	Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome 1999 ·Journal of Medical Genetics ·Paul Coucke,Peter Van Hauwe,Lorraine A. Everett,Osman Demırhan,(unknown),Nicole Dietrich,Richard J. Smith,Beth Coyle,William Reardon,Richard C. Trembath,P J Willems,(unknown),Guy Van Camp	40
20	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. 1998 ·PubMed ·(unknown),Guy Van Camp,(unknown),Ed Green,Margriet Verstreken,Isabelle Schatteman,Paul Van de Heyning,Wendy Balemans,Paul Coucke,(unknown),Richard J. Smith,E. H. Huizing,Patrick J. Willems	18

About Paul Coucke

Paul Coucke is a scholar working on Sensory Systems, Genetics and Cell Biology, having authored 261 papers that have together received 8.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (90 papers), Dermatological and Skeletal Disorders (44 papers) and Hearing, Cochlea, Tinnitus, Genetics (29 papers). The work is most often cited by research in Sensory Systems (1.4k citations), Genetics (3.7k citations) and Otorhinolaryngology (422 citations). Paul Coucke has collaborated with scholars based in Belgium, United States and Netherlands. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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