Anne De Paepe

25.5k citations

82 papers · 20.4k indexed · 1 hit paper · h-index 37

Cancer Research top 0.5%
Molecular Biology top 0.2%
- Cancer-related gene regulation 6
Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 5
Neurology top 0.5%
- Neuroblastoma Research and Treatments 25
- Neurofibromatosis and Schwannoma Cases 7
Aquatic Science top 0.5%
Oncology
- Cancer-related Molecular Pathways 7
Hematology
- Acute Myeloid Leukemia Research 6
Pulmonary and Respiratory Medicine
- Cystic Fibrosis Research Advances 5

Co-authors: Jo Vandesompele Nadine Van Roy Bruce Poppe Katleen De Preter Frank Speleman Filip Pattyn Ludwine Messiaen Geert Mortier
Cited by: Cancer Research Molecular Biology Genetics
Journals: Science (1 paper)Nucleic Acids Research (1 paper)Nature Genetics (1 paper)
Partner nations: Belgium United States France

In The Last Decade

Anne De Paepe

82 papers receiving 20.1k citations

Hit Papers

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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

The 25 scholars most cited alongside Anne De Paepe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anne De Paepe Line = papers co-authored together Anne De Paepe links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches European Journal of Human Genetics ·Mine Arslan‐Kirchner,Eloisa Arbustini,Cathérine Boileau,Philippe Charron,Anne H. Child,Gwenaëlle Collod‐Béroud,Julie De Backer,Anne De Paepe,Anna Dierking,Laurence Bonhomme‐Faivre,Sabine Hoffjan,Guillaume Jondeau,Britta Keyser,Bart Loeys,Karin Mayer,Peter N. Robinson,Jörg Schmidtke	2015	17
2	Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature Journal of Community Genetics ·Sandra Janssens,Anne De Paepe,Pascal Borry	2012	17
3	Functional Analysis of the p53 Pathway in Neuroblastoma Cells Using the Small-Molecule MDM2 Antagonist Nutlin-3 Molecular Cancer Therapeutics ·Tom Van Maerken,Ali Rihani,Daniel Dreidax,Sarah De Clercq,Nurten Yigit,Jean‐Christophe Marine,Frank Westermann,Anne De Paepe,Jo Vandesompele,Frank Speleman	2011	61
4	Dickkopf‐3 is regulated by the MYCN‐induced miR‐17‐92 cluster in neuroblastoma International Journal of Cancer ·Sara De Brouwer,Pieter Mestdagh,Irina Lambertz,Filip Pattyn,Anne De Paepe,Frank Westermann,Christina I. Schroeder,Johannes H. Schulte,Alexander Schramm,Katleen De Preter,Jo Vandesompele,Frank Speleman	2011	32
5	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) ·Anne De Paepe,Marie-Geneviève Pinsart,M Bonduelle,Gilles Genicot,M. Roelandt,Arnaud Dieudonné,M. Dumont,E. Eggermont,Ernst Heinen,G. Kiebooms,Guido Pennings,Jacques Stiennon,Paul Devroey	2009	1
6	Antitumor Activity of the Selective MDM2 Antagonist Nutlin-3 Against Chemoresistant Neuroblastoma With Wild-Type p53 JNCI Journal of the National Cancer Institute ·Tom Van Maerken,Liesbeth Ferdinande,Jasmien Taildeman,Irina Lambertz,Nurten Yigit,Liesbeth Vercruysse,Ali Rihani,Martin Michaelis,Jindřich Činátl,Claude Cuvelier,Jean‐Christophe Marine,Anne De Paepe,Marc Bracke,Frank Speleman,Jo Vandesompele	2009	99
7	Aberrant methylation of candidate tumor suppressor genes in neuroblastoma Cancer Letters ·Jasmien Hoebeeck,Evi Michels,Filip Pattyn,Valérie Combaret,Joëlle Vermeulen,Nurten Yigit,Claire Hoyoux,Geneviève Laureys,Anne De Paepe,Frank Speleman,Jo Vandesompele	2008	48
8	CADM1 is a strong neuroblastoma candidate gene that maps within a 3.72 Mb critical region of loss on 11q23 BMC Cancer ·Evi Michels,Jasmien Hoebeeck,Katleen De Preter,Alexander Schramm,Bénédicte Brichard,Anne De Paepe,Angelika Eggert,Geneviève Laureys,Jo Vandesompele,Frank Speleman	2008	26
9	Integrative genomics in neuroblastoma research Ghent University Academic Bibliography (Ghent University) ·Frank Speleman,Katleen De Preter,Evi Michels,Jasmien Hoebeeck,Filip Pattyn,Joëlle Vermeulen,Nadine Van Roy,Anne De Paepe,Geneviève Laureys,Jo Vandesompele	2007	1
10	Small-Molecule MDM2 Antagonists as a New Therapy Concept for Neuroblastoma Cancer Research ·Tom Van Maerken,Frank Speleman,Joëlle Vermeulen,Irina Lambertz,Sarah De Clercq,Els De Smet,Nurten Yigit,Vicky Coppens,Jan Philippé,Anne De Paepe,Jean‐Christophe Marine,Jo Vandesompele	2006	120
11	methBLAST and methPrimerDB: web-tools for PCR based methylation analysis BMC Bioinformatics ·Filip Pattyn,Jasmien Hoebeeck,Piet Robbrecht,Evi Michels,Anne De Paepe,Guy Bottu,David Coornaert,Robert Herzog,Frank Speleman,Jo Vandesompele	2006	28
12	HOXA gene cluster rearrangement in a t(7;9)(p15;q34) in a child with MDS Cancer Genetics and Cytogenetics ·Bruce Poppe,Nurten Yigit,Barbara De Moerloose,Anne De Paepe,Yves Benoît,Frank Speleman	2005	3
13	The humanFOXL2 mutation database Human Mutation ·Diane Beysen,Jo Vandesompele,Ludwine Messiaen,Anne De Paepe,Elfride De Baere	2004	42
14	Elimination of Primer–Dimer Artifacts and Genomic Coamplification Using a Two-Step SYBR Green I Real-Time RT-PCR Analytical Biochemistry ·Jo Vandesompele,Anne De Paepe,Frank Speleman	2002	189
15	Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia Leukemia ·Heidi Van Limbergen,Bruce Poppe,Ann Janssens,R. De Bock,Anne De Paepe,L. Noens,Frank Speleman	2002	40
16	Quantification of NF1 transcripts reveals novel highly expressed splice variants FEBS Letters ·Ina Vandenbroucke,Jo Vandesompele,Anne De Paepe,Ludwine Messiaen	2002	36
17	Molecular characterization of a t(2;3)(p23;q26): A recurrent translocation involving the EVI1 gene Ghent University Academic Bibliography (Ghent University) ·Bruce Poppe,Nurten Yigit,Peter Marynen,A Hagemeijer,Heidi Van Limbergen,Barbara Smet,Anne De Paepe,Frank Speleman	2001	2
18	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 ·Nadine Van Roy,Anna Jauch,Mireille Van Gele,Geneviève Laureys,Rogier Versteeg,Anne De Paepe,Thomas Cremer,Frank Speleman	1997	38
19	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) ·Anne De Paepe,Lieve Nuytinck,A C Nicholls,P Narcisi,J De Roose,M. Matton	1992	1
20	Pallister‐killian syndrome: Characterization of the isochromosome 12p by fluorescent In Situ hybridization American Journal of Medical Genetics ·Frank Speleman,Jules G. Leroy,Nadine Van Roy,Anne De Paepe,Ron F. Suijkerbuijk,Han G. Brunner,Leendert H. J. Looijenga,Marie‐Rose Verschraegen‐Spae,E. Orye	1991	50

About Anne De Paepe

Anne De Paepe is a scholar working on Neurology, Hematology and Oncology, having authored 82 papers that have together received 20.4k indexed citations. Recurring topics across this work include Neuroblastoma Research and Treatments (25 papers), Cancer-related Molecular Pathways (7 papers), Neurofibromatosis and Schwannoma Cases (7 papers), Cancer-related gene regulation (6 papers), Acute Myeloid Leukemia Research (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Connective tissue disorders research (5 papers) and Cystic Fibrosis Research Advances (5 papers). The work is most often cited by research in Cancer Research (2.6k citations), Molecular Biology (10.7k citations) and Genetics (2.8k citations). Anne De Paepe has collaborated with scholars based in Belgium, United States and France. Frequent 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. Their work appears in journals such as Science, Nucleic Acids Research and Nature Genetics.

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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