Ellen Denayer

1.5k citations

30 papers · 809 indexed · h-index 15

Impact in

Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
Molecular Biology
- Protein Tyrosine Phosphatases
- PI3K/AKT/mTOR signaling in cancer

Papers in ⓘ

Neurology 7
- Neurofibromatosis and Schwannoma Cases 7
Endocrine and Autonomic Systems 2

Co-authors: Eric Legius (20 shared papers)Hilde Brems (10 shared papers)Thomy de Ravel (5 shared papers)Akihiko Yoshimura (2 shared papers)Magdalena Chmara (2 shared papers)Jan Cools (2 shared papers)Ludwine Messiaen (2 shared papers)Gilles Thomas (1 shared paper)
Journals: Human Reproduction (3 papers)European Journal of Medical Genetics (2 papers)European Journal of Pediatrics (2 papers)Nature Genetics (1 paper)Acta Dermato Venereologica (1 paper)
Partner nations: Belgium United States Netherlands

In The Last Decade

Ellen Denayer

27 papers receiving 778 citations

Peers

Countries citing papers authored by Ellen Denayer

Since Specialization

Citations

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

Fields of papers citing papers by Ellen Denayer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ellen Denayer. 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 Ellen Denayer. The network helps show where Ellen Denayer may publish in the future.

Co-authors

The 25 scholars most cited alongside Ellen Denayer, 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 Ellen Denayer Line = papers co-authored together Ellen Denayer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype Nature Genetics ·Hilde Brems, Magdalena Chmara, Mourad Sahbatou, Ellen Denayer, Koji Taniguchi, Reiko Kato, Riet Somers, Ludwine Messiaen, Sofie De Schepper, Jean‐Pierre Fryns, Jan Cools, Peter Marynen, Gilles Thomas, Akihiko Yoshimura, Eric Legius	2007	291
2	Spred1Is Required for Synaptic Plasticity and Hippocampus-Dependent Learning Journal of Neuroscience ·Ellen Denayer, Tariq Ahmed, Hilde Brems, Geeske M. van Woerden, Nils Z. Borgesius, Zsuzsanna Callaerts‐Vegh, Akihiko Yoshimura, Dieter Hartmann, Ype Elgersma, Rudi D’Hooge, Eric Legius, Detlef Balschun	2008	77
3	Clinical and molecular aspects of RAS related disorders Journal of Medical Genetics ·Ellen Denayer, Thomy de Ravel, Eric Legius	2008	60
4	Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations Genes Chromosomes and Cancer ·Ellen Denayer, Koenraad Devriendt, Thomy de Ravel, Griet Van Buggenhout, Eric Smeets, Inge François, Yves Sznajer, Margarita Craen, Georgios Leventopoulos, Léon Mutesa, W. Vandecasseye, Guy Massa, Hülya Kayserili, Raf Sciot, J P Fryns, Eric Legius	2009	46
5	Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M Human Reproduction ·Aspasia Destouni, Eftychia Dimitriadou, Heleen Masset, Sophie Debrock, Cindy Melotte, Kris Van Den Bogaert, Masoud Zamani Esteki, Jia Ding, Thierry Voet, Ellen Denayer, Thomy de Ravel, Eric Legius, Christel Meuleman, Karen Peeraer, Joris Vermeesch	2018	45
6	Mutation analysis in Costello syndrome: functional and structural characterization of theHRASp.Lys117Arg mutation Human Mutation ·Ellen Denayer, Annabel Parret, Magdalena Chmara, Suzanne Schubbert, Annick Vogels, Koenraad Devriendt, Jean‐Pierre Frijns, Vladimir Rybin, Thomy de Ravel, Kevin Shannon, Jan Cools, Klaus Scheffzek, Eric Legius	2007	38
7	What’s new in the neuro-cardio-facial-cutaneous syndromes? European Journal of Pediatrics ·Ellen Denayer, Eric Legius	2007	28
8	Pathogenesis of vestibular schwannoma in ring chromosome 22 BMC Medical Genetics ·Ellen Denayer, Hilde Brems, Paul De Cock, D. Gareth Evans, Frank Van Calenbergh, Naomi L. Bowers, Raf Sciot, Maria Dêbiec‐Rychter, Joris Vermeesch, Jean‐Pierre Fryns, Eric Legius	2009	27
9	Noonan syndrome and systemic lupus erythematosus in a patient with a novel KRAS mutation. PubMed ·Georgios Leventopoulos, Ellen Denayer, Periklis Makrythanasis, C Papapolychroniou, Helen Fryssira	2010	26
10	A preliminary report on the efficacy of the Multicare AR-Bed in 3-week-3-month-old infants on regurgitation, associated symptoms and acid reflux Archives of Disease in Childhood ·Yvan Vandenplas, Jean De Schepper, Stefanie Verheyden, Thierry Devreker, Johan Franckx, M Peelman, Ellen Denayer, Bruno Hauser	2009	25
11	Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation npj Genomic Medicine ·Olga Tšuiko, Michiel Vanneste, Cindy Melotte, Jia Ding, Sophie Debrock, Heleen Masset, Maire Peters, Andres Salumets, Anne De Leener, Céline Pirard, Candice Kluyskens, Katleen Hostens, Arne van de Vijver, Karen Peeraer, Ellen Denayer, Joris Vermeesch, Eftychia Dimitriadou	2021	21
12	<b><i>NRAS</i></b> Mutations in Noonan Syndrome Molecular Syndromology ·Ellen Denayer, Hilde Peeters, L. Sevenants, Murat Derbent, J. P. Fryns, Eric Legius	2012	21
13	Observations on intelligence and behavior in 15 patients with Legius syndrome American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Ellen Denayer, Mie‐Jef Descheemaeker, Douglas R. Stewart, Kathelijn Keymolen, Ellen Plasschaert, Sarah L. Ruppert, Joseph Snow, Audrey Thurm, Lisa Joseph, Jean‐Pierre Fryns, Eric Legius	2011	19
14	The cardiofaciocutaneous syndrome: prenatal findings in two patients Prenatal Diagnosis ·Ingrid Witters, Ellen Denayer, Hilde Brems, J. P. Fryns, Eric Legius	2007	16
15	Next-generation sequencing in prenatal setting: Some examples of unexpected variant association European Journal of Medical Genetics ·Berardo Rinaldi, Valérie Race, Anniek Corveleyn, Elke Van Hoof, Marijke Bauters, Kris Van Den Bogaert, Ellen Denayer, Thomy de Ravel, Eric Legius, Marcella Baldewijns, Michaël Aertsen, Liesbeth Lewi, Luc De Catte, Jeroen Breckpot, Koenraad Devriendt	2020	16
16	Legius Syndrome and its Relationship with Neurofibromatosis Type 1 Acta Dermato Venereologica ·Ellen Denayer, Eric Legius	2020	12
17	Preclinical workup using long-read amplicon sequencing provides families withde novopathogenic variants access to universal preimplantation genetic testing Human Reproduction ·Olga Tšuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Jia Ding, Sophie Debrock, Karen Peeraer, Arne Vanhie, Anne De Leener, Céline Pirard, Candice Kluyskens, Ellen Denayer, Eric Legius, Joris Vermeesch, Hilde Brems, Eftychia Dimitriadou	2023	9
18	Sleep apnoea in babies born after in vitro fertilization European Journal of Pediatrics ·H. Audiens, Ellen Denayer, N. Ahlenajafie, E. Troch, M Bonduelle, José Ramet, Yvan Vandenplas	1995	5
19	Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findings Ophthalmic Genetics ·Dorien Herijgers, Ellen Denayer, Irina Balikova, Peter Witters, Julie A. Jacob, Ingele Casteels	2021	5
20	Multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus: a new syndrome European Journal of Human Genetics ·Dusica Babovic‐Vuksanovic, Ludwine Messiaen, Christoph Nagel, Hilde Brems, Bernd Scheithauer, Ellen Denayer, Rong Mao, Raf Sciot, Karen M. Janowski, Martin U. Schuhmann, Kathleen Claes, Eline Beert, James A. Garrity, Robert J. Spinner, Anat Stemmer‐Rachamimov, Ralitza H. Gavrilova, Frank Van Calenbergh, Victor Mautner, Eric Legius	2012	4

About Ellen Denayer

Ellen Denayer is a scholar working on Neurology, Endocrine and Autonomic Systems, Genetics, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 30 papers that have together received 809 indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (10 papers), Neurofibromatosis and Schwannoma Cases (7 papers), Galectins and Cancer Biology (5 papers), Prenatal Screening and Diagnostics (5 papers), Neonatal Respiratory Health Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Cardiomyopathy and Myosin Studies (2 papers). The work is most often cited by research in Neurology (224 citations), Molecular Biology (462 citations), Immunology (141 citations), Rheumatology (100 citations) and Gastroenterology (30 citations). Ellen Denayer has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Eric Legius, Hilde Brems, Thomy de Ravel, Akihiko Yoshimura, Magdalena Chmara, Jan Cools, Ludwine Messiaen, Gilles Thomas, Koji Taniguchi and Jean‐Pierre Fryns. Their work appears in journals such as Human Reproduction, European Journal of Medical Genetics, European Journal of Pediatrics, Nature Genetics and Acta Dermato Venereologica.

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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