Anne De Paepe

21.4k total citations · 3 hit papers
188 papers, 11.4k citations indexed

About

Anne De Paepe is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Anne De Paepe has authored 188 papers receiving a total of 11.4k indexed citations (citations by other indexed papers that have themselves been cited), including 167 papers in Genetics, 57 papers in Molecular Biology and 39 papers in Rheumatology. Recurrent topics in Anne De Paepe's work include Connective tissue disorders research (136 papers), Dermatological and Skeletal Disorders (58 papers) and Skin and Cellular Biology Research (23 papers). Anne De Paepe is often cited by papers focused on Connective tissue disorders research (136 papers), Dermatological and Skeletal Disorders (58 papers) and Skin and Cellular Biology Research (23 papers). Anne De Paepe collaborates with scholars based in Belgium, United States and Netherlands. Anne De Paepe's co-authors include Fransiska Malfait, Paul Coucke, Richard Wenstrup, Harry C. Dietz, Beat Steinmann, Peter Beighton, Petros Tsipouras, Raoul C. M. Hennekam, Richard B. Devereux and Reed E. Pyeritz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Genetics.

In The Last Decade

Anne De Paepe

187 papers receiving 11.0k 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.

Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997

1998 1.2k citations Peter Beighton, Anne De Paepe et al. American Journal of Medical Genetics profile →
Revised diagnostic criteria for the Marfan syndrome

1996 1.1k citations Anne De Paepe et al. American Journal of Medical Genetics profile →
Osteogenesis imperfecta

2017 494 citations Anne De Paepe et al. profile →

Peers

Countries citing papers authored by Anne De Paepe

Since Specialization

Citations

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

Fields of papers citing papers by Anne De Paepe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne De Paepe. 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 Anne De Paepe. The network helps show where Anne De Paepe may publish in the future.

Co-authorship network of co-authors of Anne De Paepe

This figure shows the co-authorship network connecting the top 25 collaborators of Anne De Paepe. A scholar is included among the top collaborators of Anne De Paepe 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 Anne De Paepe. Anne De Paepe 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	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
2	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
3	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
4	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
5	Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type 2016 ·Genetics in Medicine ·Tim Van Damme, Alain Colige, Delfien Syx, Cecilia Giunta, Uschi Lindert, Marianne Rohrbach, Omid Aryani, Yasemin Alanay, Pelin Özlem Şimşek‐Kiper, Hester Y. Kroes, Koenraad Devriendt, Marc Thiry, Sofie Symoens, Anne De Paepe, Fransiska Malfait	34
6	Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability 2013 ·American Journal of Medical Genetics Part A ·Barbara Oehl‐Jaschkowitz, Olivier Vanakker, Anne De Paepe, Björn Menten, Thomas G. Martin, Georg F. Weber, Alexander Christmann, (unknown), (unknown), Susan McNerlan, Shane McKee, Andreas Tzschach	17
7	New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections 2013 ·Polskie Archiwum Medycyny Wewnętrznej ·Laurence Campens, Marjolijn Renard, Bert Callewaert, Paul Coucke, Julie De Backer, Anne De Paepe	4
8	Balance and gait and risk of falling in females with the Ehlers-Danlos syndrome 2011 ·Ghent University Academic Bibliography (Ghent University) ·Lies Rombaut, Fransiska Malfait, Inge De Wandele, Anne De Paepe, Patrick Calders	0
9	GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling 2011 ·Human Molecular Genetics ·Andy Willaert, (unknown), Bert Callewaert, Paul Coucke, Seth D. Crosby, (unknown), Elaine C. Davis, Sruti Shiva, Michael Tsang, Anne De Paepe, Zsolt Urbán	45
10	Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial 2010 ·The Lancet ·Kim-Thanh Ong, Jérôme Perdu, Julie De Backer, Erwan Bozec, Patrick Collignon, Joseph Emmerich, Anne‐Laure Fauret, Jean‐Noël Fiessinger, Dominique P. Germain, G. Georgesco, Jean‐Sébastien Hulot, Anne De Paepe, Henri Plauchu, Xavier Jeunemaı̂tre, Stéphane Laurent, Pierre Boutouyrie	217
11	A hotspot splicing mutation in LEPREI affects prolyl 3-hydroxylation and causes recessive osteogenesis imperfecta 2008 ·Ghent University Academic Bibliography (Ghent University) ·Fransiska Malfait, Andy Willaert, Sofie Symoens, Paul Coucke, Anne De Paepe	1
12	A Hotspot Splicing Mutation in LEPREI Affects Prolyl 3-hydroxylation and Causes Recessive Osteogenesis Imperfecta 2008 ·Journal of Bone and Mineral Research ·Andy Willaert, Sofie Symoens, Fransiska Malfait, Kris Gevaert, Paul Coucke, Anne De Paepe	1
13	Pseudoxanthoma Elasticum with Generalized Retinal Dysfunction, a Common Finding? 2007 ·Investigative Ophthalmology & Visual Science ·Isabelle Audo, Olivier Vanakker, (unknown), Bart P. Leroy, Anthony G. Robson, Sharon Jenkins, Paul Coucke, Alan C. Bird, Anne De Paepe, Graham E. Holder, Andrew R. Webster	21
14	Novel clinico-molecular insights in pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchart 2007 ·Human Mutation ·Olivier Vanakker, Bart P. Leroy, Paul Coucke, Lionel Bercovitch, Jouni Uitto, (unknown), Sharon F. Terry, Petra Van Acker, Dirk Matthys, Bart Loeys, Anne De Paepe	72
15	Emerging patterns of cryptic chromosomal imbalances in patients with idiopathic mental retardation and multiple congenital anomalies 2006 ·European Journal of Human Genetics ·Joris Vermeesch, (unknown), Bernard Thienpont, Thomy de Ravel, Irina Balikova, Jean‐Pierre Fryns, Koenraad Devriendt, Yves Moreau, (unknown), Frank Speleman, Geert Mortier, Anne De Paepe	1
16	Orofacial manifestations of congenital fibrillin deficiency: pathogenesis and clinical diagnostics. 2005 ·PubMed ·P. J. De Coster, Luc Martens, Anne De Paepe	15
17	Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations 2005 ·European Journal of Human Genetics ·(unknown), Björn Menten, Cindy Melotte, Bernard Thienpont, Karen Buysse, (unknown), Peter Marynen, Anne De Paepe, Jean‐Pierre Fryns, Geert Mortier, Koenraad Devriendt, Frank Speleman, Joris Vermeesch	2
18	Oral manifestations of patients with Marfan syndrome: A case-control study 2002 ·Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology ·(unknown), Luc Martens, Anne De Paepe	55
19	The vascular type of the Ehlers-Danlos syndrome: update on the correlation between molecular and phenotypic findings 1998 ·Ghent University Academic Bibliography (Ghent University) ·Lieve Nuytinck, Michel De Vos, Anne De Paepe	4
20	Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 breakdown → 1998 ·American Journal of Medical Genetics ·Peter Beighton, Anne De Paepe, Beat Steinmann, Petros Tsipouras, Richard Wenstrup	1192

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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