Anne De Paepe

4.2k total citations
21 papers, 434 citations indexed

About

Anne De Paepe is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Anne De Paepe has authored 21 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Anne De Paepe's work include Connective tissue disorders research (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Dermatological and Skeletal Disorders (4 papers). Anne De Paepe is often cited by papers focused on Connective tissue disorders research (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Dermatological and Skeletal Disorders (4 papers). Anne De Paepe collaborates with scholars based in Belgium, United States and France. Anne De Paepe's co-authors include Fransiska Malfait, Alan J. Hakim, Rodney Grahame, Julie De Backer, Marc Dhont, H Laverge, Petra De Sutter, M.R. Verschraegen-Spae, Bart Loeys and Johan De Sutter and has published in prestigious journals such as Arteriosclerosis Thrombosis and Vascular Biology, Journal of Investigative Dermatology and Human Reproduction.

In The Last Decade

Anne De Paepe

21 papers receiving 418 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne De Paepe Belgium 12 298 85 77 73 70 21 434
Margo Whiteford United Kingdom 11 193 0.6× 194 2.3× 49 0.6× 43 0.6× 56 0.8× 15 398
Philip N. Mowrey United States 11 232 0.8× 162 1.9× 38 0.5× 134 1.8× 13 0.2× 22 436
Jolanta E. Pitera United Kingdom 9 173 0.6× 261 3.1× 150 1.9× 55 0.8× 22 0.3× 14 503
Hermine E. Veenstra‐Knol Netherlands 13 220 0.7× 276 3.2× 37 0.5× 71 1.0× 65 0.9× 20 561
Baiba Lāce Latvia 12 245 0.8× 215 2.5× 32 0.4× 22 0.3× 22 0.3× 50 474
Eva Maria Cutiongco Philippines 7 180 0.6× 168 2.0× 52 0.7× 36 0.5× 29 0.4× 7 327
Harinder Gill Canada 7 65 0.2× 189 2.2× 66 0.9× 40 0.5× 47 0.7× 21 346
Lisa Williams‐Simons United States 9 190 0.6× 436 5.1× 36 0.5× 122 1.7× 40 0.6× 9 551
Kristen Deak United States 13 194 0.7× 222 2.6× 70 0.9× 173 2.4× 19 0.3× 24 531
Susanne Zahn Germany 12 82 0.3× 215 2.5× 206 2.7× 24 0.3× 39 0.6× 14 402

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

20 of 20 papers shown
1.
Lenz, Barbara, Andreas Brink, Anne De Paepe, et al.. (2017). Application of Imaging Techniques to Cases of Drug-Induced Crystal Nephropathy in Preclinical Studies. Toxicological Sciences. 163(2). 409–419. 12 indexed citations
2.
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
3.
Campens, Laurence, Olivier Vanakker, Bram Trachet, et al.. (2013). Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum Families. Arteriosclerosis Thrombosis and Vascular Biology. 33(11). 2646–2652. 54 indexed citations
4.
Martens, Thomas, Isabelle Van Herzeele, Frédéric De Ryck, et al.. (2012). Multiple Aneurysms in a Patient With Aneurysms-Osteoarthritis Syndrome. The Annals of Thoracic Surgery. 95(1). 332–335. 14 indexed citations
5.
Meulen, Volker ter, Stefania Boccia, Martina C. Cornel, et al.. (2012). Direct-to-consumer genetic testing for health-related purposes in the European Union. 18. 11 indexed citations
6.
7.
Backer, Julie De, Bart Loeys, & Anne De Paepe. (2009). Marfan and Marfan-like syndromes. Artery Research. 3(1). 9–9. 6 indexed citations
8.
Maerken, Tom Van, Pieter Mestdagh, Sarah De Clercq, et al.. (2008). Real-time qPCR as a tool for evaluating RNAi-mediated gene silencing. Ghent University Academic Bibliography (Ghent University). 124. 1–7. 1 indexed citations
9.
Feys, Tom, Bruce Poppe, Katleen De Preter, et al.. (2007). A detailed inventory of DNA copy number alterations in four commonly used Hodgkin lymphoma cell lines. Ghent University Academic Bibliography (Ghent University). 1 indexed citations
10.
Malfait, Fransiska, Alan J. Hakim, Anne De Paepe, & Rodney Grahame. (2006). The genetic basis of the joint hypermobility syndromes. Lara D. Veeken. 45(5). 502–507. 105 indexed citations
11.
Backer, Julie De, et al.. (2006). A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndrome. Genetics in Medicine. 8(7). 401–408. 47 indexed citations
12.
Poppe, Bruce, Barbara Cauwelier, Heidi Van Limbergen, et al.. (2005). Novel cryptic chromosomal rearrangements in childhood acute lymphoblastic leukemia detected by multiple color fluorescent in situ hybridization.. PubMed. 90(9). 1179–85. 12 indexed citations
13.
14.
Limbergen, Heidi Van, H. Berna Beverloo, Ellen van Drunen, et al.. (2001). Molecular cytogenetic and clinical findings in ETV6ABL1‐positive leukemia. Genes Chromosomes and Cancer. 30(3). 274–282. 4 indexed citations
15.
Praeter, Claudine De, Ernst Bause, Lieve Nuytinck, et al.. (2000). A novel disorder in a newborn caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency. Glycobiology. 10(10). 1085–1085. 1 indexed citations
16.
Baere, Elfride De, Yoshimitsu Fukushima, Kent W. Small, et al.. (2000). Identification of BPESC1, a Novel Gene Disrupted by a Balanced Chromosomal Translocation, t(3;4)(q23;p15.2), in a Patient with BPES. Genomics. 68(3). 296–304. 19 indexed citations
17.
Verschraegen-Spae, M.R., B Quack, Sophie Rousseaux, et al.. (1998). Application of fluorescence in situ hybridization to the identification of different marker chromosomes.. PubMed. 41(1). 5–10. 1 indexed citations
18.
Laverge, H, Petra De Sutter, M.R. Verschraegen-Spae, Anne De Paepe, & Marc Dhont. (1997). Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryos. Human Reproduction. 12(4). 809–814. 71 indexed citations
19.
Contri, M. Baccarani, et al.. (1993). Cell-matrix interactions in cultured dermal fibroblasts from patients with an inherited connective-tissue disorder. Cytotechnology. 11(S1). S112–S114. 5 indexed citations
20.
Paepe, Anne De, Denis Viljoen, Peter Beighton, et al.. (1991). Pseudoxanthoma elasticum: Similar autosomal recessive subtype in Belgian and Afrikaner families. American Journal of Medical Genetics. 38(1). 16–20. 17 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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