Anne De Paepe

25.5k total citations · 1 hit paper
82 papers, 20.4k citations indexed

About

Anne De Paepe is a scholar working on Molecular Biology, Neurology and Oncology. According to data from OpenAlex, Anne De Paepe has authored 82 papers receiving a total of 20.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 29 papers in Neurology and 18 papers in Oncology. Recurrent topics in Anne De Paepe's work include Neuroblastoma Research and Treatments (25 papers), Cancer-related Molecular Pathways (7 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Anne De Paepe is often cited by papers focused on Neuroblastoma Research and Treatments (25 papers), Cancer-related Molecular Pathways (7 papers) and Neurofibromatosis and Schwannoma Cases (7 papers). Anne De Paepe collaborates with scholars based in Belgium, United States and France. Anne De Paepe's co-authors include Jo Vandesompele, Nadine Van Roy, Bruce Poppe, Katleen De Preter, Frank Speleman, Filip Pattyn, Frank Speleman, Ludwine Messiaen, Frank Speleman and Geert Mortier and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Anne De Paepe

82 papers receiving 20.1k citations

Hit Papers

align trajectories sort by overperformance

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.

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

2002 16.7k citations Jo Vandesompele, Katleen De Preter et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne De Paepe Belgium	37	10.7k	2.8k	2.6k	2.5k	1.9k	82	20.4k
Frank Speleman Belgium	28	10.6k 1.0×	2.6k 0.9×	2.5k 1.0×	2.5k 1.0×	1.9k 1.0×	67	19.4k
Nadine Van Roy Belgium	41	11.8k 1.1×	3.1k 1.1×	3.1k 1.2×	2.8k 1.1×	2.1k 1.1×	167	22.1k
Katleen De Preter Belgium	36	11.6k 1.1×	2.5k 0.9×	3.4k 1.3×	2.4k 1.0×	2.1k 1.1×	117	20.6k
Filip Pattyn Belgium	25	10.3k 1.0×	2.3k 0.8×	2.4k 0.9×	2.4k 0.9×	1.9k 1.0×	42	18.5k
Akira Kikuchi Japan	88	20.4k 1.9×	2.3k 0.8×	1.7k 0.7×	1.9k 0.8×	1.8k 1.0×	463	26.8k
Bruce Poppe Belgium	33	10.4k 1.0×	2.6k 0.9×	2.6k 1.0×	2.4k 0.9×	1.9k 1.0×	83	19.1k
Sonali Jha United Kingdom	4	17.6k 1.6×	3.4k 1.2×	4.4k 1.7×	3.5k 1.4×	4.3k 2.3×	7	29.0k
Jeremy A. Garson United Kingdom	41	8.1k 0.8×	1.7k 0.6×	1.5k 0.6×	2.1k 0.8×	1.9k 1.0×	118	18.4k
Jean Weissenbach France	66	13.8k 1.3×	7.1k 2.5×	1.1k 0.4×	2.1k 0.8×	1.2k 0.6×	183	24.5k
Marijke J. van Baren United States	14	9.1k 0.8×	1.7k 0.6×	2.4k 0.9×	3.4k 1.3×	1.1k 0.6×	18	14.7k

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

Janssens, Sandra, et al.. (2015). Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issues. European Journal of Human Genetics. 24(4). 506–512. 25 indexed citations

Maerken, Tom Van, Ali Rihani, Daniel Dreidax, et al.. (2011). Functional Analysis of the p53 Pathway in Neuroblastoma Cells Using the Small-Molecule MDM2 Antagonist Nutlin-3. Molecular Cancer Therapeutics. 10(6). 983–993. 61 indexed citations

Fieuw, Annelies, Candy Kumps, Alexander Schramm, et al.. (2011). Identification of a novel recurrent 1q42.2‐1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas. International Journal of Cancer. 130(11). 2599–2606. 34 indexed citations

Paepe, Anne De, M Bonduelle, Arnaud Dieudonné, et al.. (2009). Avis n° 49 du 20 avril 2009 relatif à l'utilisation du diagnostic génétique préimplantatoire (DPI) pour détecter les porteurs sains d'une mutation causant une affection héréditaire grave qui peut entraîner un risque élevé pour les descendants. Open Repository and Bibliography (University of Liège). 1 indexed citations

Maerken, Tom Van, Liesbeth Ferdinande, Irina Lambertz, et al.. (2009). Antitumor Activity of the Selective MDM2 Antagonist Nutlin-3 Against Chemoresistant Neuroblastoma With Wild-Type p53. JNCI Journal of the National Cancer Institute. 101(22). 1562–1574. 99 indexed citations

Trachet, Bram, Abigaïl Swillens, Denis Van Loo, et al.. (2009). The influence of aortic dimensions on calculated wall shear stress in the mouse aortic arch. Computer Methods in Biomechanics & Biomedical Engineering. 12(5). 491–499. 22 indexed citations

Hoebeeck, Jasmien, Evi Michels, Filip Pattyn, et al.. (2008). Aberrant methylation of candidate tumor suppressor genes in neuroblastoma. Cancer Letters. 273(2). 336–346. 48 indexed citations

Michels, Evi, Jasmien Hoebeeck, Katleen De Preter, et al.. (2008). CADM1 is a strong neuroblastoma candidate gene that maps within a 3.72 Mb critical region of loss on 11q23. BMC Cancer. 8(1). 173–173. 26 indexed citations

Speleman, Frank, Katleen De Preter, Evi Michels, et al.. (2007). Integrative genomics in neuroblastoma research. Ghent University Academic Bibliography (Ghent University). 1 indexed citations

10.

Maerken, Tom Van, Frank Speleman, Joëlle Vermeulen, et al.. (2006). Small-Molecule MDM2 Antagonists as a New Therapy Concept for Neuroblastoma. Cancer Research. 66(19). 9646–9655. 120 indexed citations

11.

Pattyn, Filip, Jasmien Hoebeeck, Evi Michels, et al.. (2006). methBLAST and methPrimerDB: web-tools for PCR based methylation analysis. BMC Bioinformatics. 7(1). 496–496. 28 indexed citations

12.

Cauwelier, Barbara, Nicole Dastugue, Jan Cools, et al.. (2006). Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCRβ locus rearrangements and putative new T-cell oncogenes. Leukemia. 20(7). 1238–1244. 44 indexed citations

13.

Poppe, Bruce, Nurten Yigit, Barbara De Moerloose, et al.. (2005). HOXA gene cluster rearrangement in a t(7;9)(p15;q34) in a child with MDS. Cancer Genetics and Cytogenetics. 162(1). 82–84. 3 indexed citations

14.

Beysen, Diane, Jo Vandesompele, Ludwine Messiaen, Anne De Paepe, & Elfride De Baere. (2004). The humanFOXL2 mutation database. Human Mutation. 24(3). 189–193. 42 indexed citations

15.

Vandesompele, Jo, Anne De Paepe, & Frank Speleman. (2002). Elimination of Primer–Dimer Artifacts and Genomic Coamplification Using a Two-Step SYBR Green I Real-Time RT-PCR. Analytical Biochemistry. 303(1). 95–98. 189 indexed citations

16.

Claes, Kathleen, Jo Vandesompele, Bruce Poppe, et al.. (2002). Pathological splice mutations outside the invariant AG/GT splice sites of BRCA1 exon 5 increase alternative transcript levels in the 5′ end of the BRCA1 gene. Oncogene. 21(26). 4171–4175. 32 indexed citations

17.

Vermeulen, Stefan, et al.. (2002). Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion. American Journal of Medical Genetics. 108(4). 315–318. 26 indexed citations

18.

Poppe, Bruce, Nurten Yigit, Peter Marynen, et al.. (2001). Molecular characterization of a t(2;3)(p23;q26): A recurrent translocation involving the EVI1 gene. Ghent University Academic Bibliography (Ghent University). 2 indexed citations

19.

Roy, Nadine Van, Anna Jauch, Mireille Van Gele, et al.. (1997). Comparative genomic hybridization analysis of human neuroblastomas: Detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines. Cancer Genetics and Cytogenetics. 97(2). 135–142. 38 indexed citations

20.

Paepe, Anne De, et al.. (1992). Study of a type III collagen protein defect in a patient with ecchymotic EDS: importance of the analysis of non-cutaneous connective tissues. Ghent University Academic Bibliography (Ghent University). 1 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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