Jenneke van den Ende

3.8k citations

50 papers · 1.3k indexed · h-index 19

Co-authors: C. Sonneveld Frank Declau An Boudewyns Paul Van de Heyning Geert Mortier Annick Vogels J P Fryns Filip Vanhoenacker
Topics: Hearing, Cochlea, Tinnitus, Genetics (10 papers)Ear Surgery and Otitis Media (8 papers)Genomic variations and chromosomal abnormalities (5 papers)
Cited by: Sensory Systems Otorhinolaryngology Genetics
Journals: Brain PEDIATRICS The American Journal of Human Genetics
Partner nations: Belgium United States Netherlands

In The Last Decade

Jenneke van den Ende

45 papers receiving 1.2k citations

Peers

Countries citing papers authored by Jenneke van den Ende

Since Specialization

Citations

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

Fields of papers citing papers by Jenneke van den Ende

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jenneke van den Ende. 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 Jenneke van den Ende. The network helps show where Jenneke van den Ende may publish in the future.

Co-authorship network of co-authors of Jenneke van den Ende

This figure shows the co-authorship network connecting the top 25 collaborators of Jenneke van den Ende. A scholar is included among the top collaborators of Jenneke van den Ende 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 Jenneke van den Ende. Jenneke van den Ende 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	Paracentric inversion disrupting the SHANK2 gene 2025 ·European Journal of Medical Genetics ·(unknown),(unknown),Marjan De Rademaeker,Jenneke van den Ende,Geert Vandeweyer,R. Frank Kooy,Ligia Mateiu,(unknown)	0
2	Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia 2022 ·European Archives of Oto-Rhino-Laryngology ·(unknown),Jenneke van den Ende,Frank Declau,(unknown),Wim Wuyts,Guy Van Camp,Olivier M. Vanderveken,An Boudewyns	6
3	Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum 2022 ·Brain ·(unknown),Sara Van Mossevelde,Anne Sieben,Maria Bjerke,(unknown),Julie van der Zee,Peter Paul De Deyn,Jan De Bleecker,Jan Versijpt,Jenneke van den Ende,Olivier Deryck,Paul Bourgeois,(unknown),(unknown),Rik Vandenberghe,Sebastiaan Engelborghs,Christine Van Broeckhoven	4
4	Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children 2018 ·Otology & Neurotology ·An Boudewyns,Jenneke van den Ende,Manou Sommen,Wim Wuyts,Nils Peeters,Paul Van de Heyning,Guy Van Camp	9
5	Auditory neuropathy: a challenge for diagnosis and treatment. 2013 ·PubMed ·Frank Declau,A. Boudewyns,Jenneke van den Ende,Paul Van de Heyning	3
6	Identification of recurrent type-2NF1microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder 2012 ·Human Mutation ·J. Vogt,(unknown),(unknown),Kathleen Claes,Josef Högel,Nadia Chuzhanova,Chuanhua Fu,Jenneke van den Ende,Victor‐Felix Mautner,D.N. Cooper,Ludwine Messiaen,Hildegard Kehrer‐Sawatzki	24
7	Otitis Media With Effusion 2011 ·Otology & Neurotology ·An Boudewyns,Frank Declau,Jenneke van den Ende,Erwin Van Kerschaver,(unknown),(unknown),Paul Van de Heyning	52
8	Cytomegalovirus DNA Detection in Guthrie Cards 2009 ·Otology & Neurotology ·An Boudewyns,Frank Declau,Koenraad Smets,D. Ursi,François Eyskens,Jenneke van den Ende,Paul Van de Heyning	21
9	Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity 2009 ·Neuromuscular Disorders ·Jonathan Baets,Ines Dierick,Chantal Ceuterick‐de Groote,Jenneke van den Ende,(unknown),(unknown),Wim Robberecht,Eva Nelis,Vincent Timmerman,Peter De Jonghe	8
10	Missense mutations to the TSC1 gene cause tuberous sclerosis complex 2008 ·European Journal of Human Genetics ·Mark Nellist,Diana van den Heuvel,(unknown),(unknown),Miriam Goedbloed,Anneke Maat‐Kievit,Ton van Essen,Karin van Spaendonck‐Zwarts,Floor E. Jansen,(unknown),G. Bartalini,Outi Vierimaa,Maila Penttinen,Jenneke van den Ende,Ans van den Ouweland,Dicky Halley	21
11	A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene 2006 ·The American Journal of Human Genetics ·Guy Van Camp,Rikkert L. Snoeckx,Nele Hilgert,Jenneke van den Ende,(unknown),(unknown),Hiroaki Suzuki,(unknown),Filip Vanhoenacker,Frank Declau,Paul Van de Heyning,Shin‐ichi Usami	120
12	N1303K and IVS8-5T, clinical presentation within a family with atypical cystic fibrosis 2006 ·Journal of Cystic Fibrosis ·Kim Van Hoorenbeeck,Katrien Storm,Jenneke van den Ende,Martine Biervliet,Kristine Desager	8
13	Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics 2005 ·Clinical Genetics ·Liesbeth Rooms,Edwin Reyniers,Wim Wuyts,Katrien Storm,Rob van Luijk,Stefaan Scheers,J. Wauters,Jenneke van den Ende,Martine Biervliet,François Eyskens,G. Van Goethem,Annick Laridon,Berten Ceulemans,Winnie Courtens,R. Frank Kooy	51
14	Stapes Ankylosis in a Family with a Novel NOG Mutation: Otologic Features of the Facioaudiosymphalangism Syndrome 2005 ·Otology & Neurotology ·Frank Declau,Jenneke van den Ende,Emiel Baten,(unknown)	12
15	Waardenburg syndrome: Clinical differentiation between types I and II 2003 ·American Journal of Medical Genetics Part A ·(unknown),Yolande van Bever,Jenneke van den Ende,(unknown),Paula Iughetti,(unknown),Orozimbo Alves Costa Filho,Antônio Richieri‐Costa,Oswaldo Frota‐Pessoa,Paulo Alberto Otto	41
16	Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders 2003 ·European Journal of Human Genetics ·Annick Vogels,Jenneke van den Ende,Kathelijn Keymolen,Geert Mortier,Koenraad Devriendt,Eric Legius,J P Fryns	135
17	Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) 2003 ·Human Mutation ·Liesbeth Rooms,Edwin Reyniers,Rob van Luijk,Stefaan Scheers,J. Wauters,Berten Ceulemans,Jenneke van den Ende,Yolande van Bever,R. Frank Kooy	79
18	Localization of the Gene for Sclerosteosis to the van Buchem Disease–Gene Region on Chromosome 17q12–q21 1999 ·The American Journal of Human Genetics ·Wendy Balemans,Jenneke van den Ende,(unknown),Frederik G. Dikkers,Patrick J. Willems,Filip Vanhoenacker,(unknown),(unknown),Constantine A. Stratakis,Suvimol Hill,Wim Van Hul	97
19	Sporadic, idiopathic MCA syndrome with mandibulofacial dysostosis and tibial hemimelia 1991 ·American Journal of Medical Genetics ·A. Richieri‐Costa,M. L. Guion‐Almeida,Jenneke van den Ende	1
20	De samenstelling van de zouten in het oppervlaktewater in het Zuidhollands glasdistrict 1967 ·Socio-Environmental Systems Modeling ·(unknown),Jenneke van den Ende	1

About Jenneke van den Ende

Jenneke van den Ende is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 50 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Ear Surgery and Otitis Media (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Sensory Systems (270 citations), Otorhinolaryngology (159 citations) and Genetics (479 citations). Jenneke van den Ende has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include C. Sonneveld, Frank Declau, An Boudewyns, Paul Van de Heyning, Geert Mortier, Annick Vogels, J P Fryns, Filip Vanhoenacker, Eric Legius and Kathelijn Keymolen. Their work appears in journals such as Brain, PEDIATRICS and The American Journal of Human 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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