Ilse Feenstra

4.5k citations
45 papers · 1.3k · h-index 19

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
  • Sensory Systems top 5%

Papers in

  • Genetics 22
    • Genomic variations and chromosomal abnormalities 15
    • Genomics and Rare Diseases 8
    • Genetics and Neurodevelopmental Disorders 7
  • Pediatrics, Perinatology and Child Health 18
    • Prenatal Screening and Diagnostics 17
    • Fetal and Pediatric Neurological Disorders 9
    • Ethics and Legal Issues in Pediatric Healthcare 4
Co-authors
Brigitte H. W. Faas (9 shared papers)Helger G. Yntema (9 shared papers)Lean Beulen (7 shared papers)Mireille N. Bekker (6 shared papers)Conny M.A. van Ravenswaaij‐Arts (5 shared papers)Lisenka E.L.M. Vissers (6 shared papers)Han G. Brunner (5 shared papers)Egbert Bakker (2 shared papers)
Journals
European Journal of Human Genetics (6 papers)Prenatal Diagnosis (5 papers)European Journal of Medical Genetics (4 papers)Clinical Genetics (3 papers)Ear and Hearing (2 papers)
Partner nations
NetherlandsUnited StatesGermany

In The Last Decade

Ilse Feenstra

43 papers receiving 1.3k citations

Peers

Ilse Feenstra
Comparison fields: 5 of 102
  • Genetics 731
  • Sensory Systems 97
  • Pediatrics, Perinatology and Child Health 377
  • Cancer Research 139
  • Otorhinolaryngology 35
Replace Barbara F. Crandall with:
Barbara F. Crandall United States
Patricia A. Ward United States
Sylvie Langlois Canada
Erin Rooney Riggs United States
Alina T. Midro Poland
Rima Slim Canada
Güven Lüleci Türkiye
Rena E. Falk United States
Hassan Rouba Morocco
Peter Miny Germany
Ilse Feenstra relative to Barbara F. Crandall United States Barbara F. Crandall's profile →
Citations per field
00.5×2×4×6.6×
Barbara F. Crandall · 1×
Citations per year

Countries citing papers authored by Ilse Feenstra

Since Specialization
Citations

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

Fields of papers citing papers by Ilse Feenstra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Guidelines for diagnostic next-generation sequencing
European Journal of Human Genetics ·Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik A. Sistermans, Marc Sturm, Marjan M. Weiss, Helger G. Yntema, Egbert Bakker, Hans Scheffer, Peter Bauer
2015337
2
Genotype–phenotype mapping of chromosome 18q deletions by high‐resolution array CGH: An update of the phenotypic map
American Journal of Medical Genetics Part A ·Ilse Feenstra, Lisenka E.L.M. Vissers, Mirjam Orsel, Ad Geurts van Kessel, Han G. Brunner, Joris A. Veltman, Conny M.A. van Ravenswaaij‐Arts
200798
3
TRIOloss of function is associated with mild intellectual disability and affects dendritic branching and synapse function
Human Molecular Genetics ·Wei Ba, Yan Yan, Margot R.F. Reijnders, Janneke Schuurs-Hoeijmakers, Ilse Feenstra, Ernie M.H.F. Bongers, Daniëlle G.M. Bosch, Nicole de Leeuw, Rolph Pfundt, Christian Gilissen, Petra F. de Vries, Joris A. Veltman, Alexander Hoischen, Heather C. Mefford, Evan E. Eichler, Lisenka E.L.M. Vissers, Nael Nadif Kasri, Bert B.A. de Vries
201568
4
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities
European Journal of Medical Genetics ·Ilse Feenstra, Jiayi Fang, David A. Koolen, A. Siezen, C. R. Evans, R M Winter, Melissa Lees, Mariluce Riegel, Bert B.A. de Vries, Conny M.A. van Ravenswaaij, Albert Schinzel
200559
5
Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt–Hopkins syndrome
American Journal of Medical Genetics Part A ·Vera M. Kalscheuer, Ilse Feenstra, Conny M.A. van Ravenswaaij‐Arts, Dominique Smeets, Corinna Menzel, Reinhard Ullmann, Luciana Musante, Hans‐Hilger Ropers
200858
6
The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial
European Journal of Human Genetics ·Lean Beulen, M. van den Berg, Brigitte H. W. Faas, Ilse Feenstra, Michiel Hageman, J. M. van Vugt, Mireille N. Bekker
201653
7
1 in 38 individuals at risk of a dominant medically actionable disease
European Journal of Human Genetics ·Lonneke Haer‐Wigman, Vyne van der Schoot, Ilse Feenstra, Anneke T. Vulto‐van Silfhout, Christian Gilissen, Han G. Brunner, Lisenka E.L.M. Vissers, Helger G. Yntema
201848
8
The consequences of implementing non-invasive prenatal testing in Dutch national health care: a cost-effectiveness analysis
European Journal of Obstetrics & Gynecology and Reproductive Biology ·Lean Beulen, Janneke P.C. Grutters, Brigitte H. W. Faas, Ilse Feenstra, J. M. G. van Vugt, Mireille N. Bekker
201447
9
Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies
Ultrasound in Obstetrics and Gynecology ·Lean Beulen, Brigitte H. W. Faas, Ilse Feenstra, J. M. G. van Vugt, Mireille N. Bekker
201646
10
Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment
Prenatal Diagnosis ·Lean Beulen, Janneke P.C. Grutters, Brigitte H. W. Faas, Ilse Feenstra, Hans Groenewoud, J. M. G. van Vugt, Mireille N. Bekker
201544
11
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis
European Journal of Human Genetics ·Ilse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema‐Raddatz, Helger G. Yntema, Trijnie Dijkhuizen, Dorien Lugtenberg, Joanne Verheij, Andrew Green, Roel Hordijk, William Reardon, Bert de Vries, Han G. Brunner, Ernie M.H.F. Bongers, Nicole de Leeuw, Conny M.A. van Ravenswaaij‐Arts
201141
12
TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction
Journal of Clinical Investigation ·Daniela Ragancokova, Elena Rocca, Anne M.M. Oonk, Herbert Schulz, E Rohde, Jan Bednarsch, Ilse Feenstra, Ronald J. E. Pennings, Hagen Wende, Alistair N. Garratt
201437
13
Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans
The American Journal of Human Genetics ·Ilse Feenstra, Lisenka E.L.M. Vissers, Ronald J. E. Pennings, Willy Nillessen, Rolph Pfundt, Henricus P. M. Kunst, R.J.C. Admiraal, Joris A. Veltman, Conny M.A. van Ravenswaaij‐Arts, Han G. Brunner, Cor W. R. J. Cremers
201132
14
Non‐targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one‐year experience
Prenatal Diagnosis ·Brigitte H. W. Faas, Ilse Feenstra, Alex J. Eggink, Angelique J. A. Kooper, Rolph Pfundt, John MG van Vugt, Nicole de Leeuw
201230
15
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Human Genetics ·Jeroen J. Smits, Jaap Oostrik, Andy J. Beynon, Sarina G. Kant, Pia A. M. de Koning Gans, Liselotte J. C. Rotteveel, Jolien S. Klein Wassink‐Ruiter, Rolien H. Free, Saskia M. Maas, Jiddeke van de Kamp, Paul Merkus, Wouter Koole, Ilse Feenstra, R.J.C. Admiraal, Cris Lanting, Margit Schraders, Helger G. Yntema, Ronald J. E. Pennings, Hannie Kremer
201825
16
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature
European Journal of Medical Genetics ·Ilse Feenstra, David A. Koolen, J. Van der Pas, Ben C.J. Hamel, Hanneke Mieloo, Dominique Smeets, Conny M.A. van Ravenswaaij
200623
17
Cardiac anomalies in individuals with the 18q deletion syndrome; report of a child with Ebstein anomaly and review of the literature
European Journal of Medical Genetics ·Dorothée C. van Trier, Ilse Feenstra, P. T. G. Bot, Nicole de Leeuw, Jos Draaisma
201321
18
Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature
American Journal of Medical Genetics Part A ·Tjitske Kleefstra, Nicole de Leeuw, Roy Wolf, Willy M. Nillesen, Gaby Schobers, Hanneke Mieloo, Marjolein H. Willemsen, Concetta Simona Perrotta, Pino J. Poddighe, Ilse Feenstra, Jos Draaisma, Conny M.A. van Ravenswaaij‐Arts
201021
19
Similar Phenotypes Caused by Mutations in OTOG and OTOGL
Ear and Hearing ·Anne M.M. Oonk, Joop M. Leijendeckers, P.L.M. Huygen, Margit Schraders, Miguel Del Campo, Ignacio del Castillo, Mustafa Tekin, Ilse Feenstra, Andy J. Beynon, Henricus P. M. Kunst, A.F.M. Snik, Hannie Kremer, R.J.C. Admiraal, Ronald J. E. Pennings
201418
20
Noninvasive prenatal diagnosis of Huntington disease: detection of the paternally inherited expanded CAG repeat in maternal plasma
Prenatal Diagnosis ·Jessica M.E. van den Oever, Emilia K. Bijlsma, Ilse Feenstra, N. D. Muntjewerff, Inge B. Mathijssen, Egbert Bakker, Martine J. van Belzen, Elles M. J. Boon
201518

About Ilse Feenstra

Ilse Feenstra is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Sensory Systems and Surgery, having authored 45 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Fetal and Pediatric Neurological Disorders (9 papers), Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Ethics and Legal Issues in Pediatric Healthcare (4 papers). The work is most often cited by research in Genetics (731 citations), Sensory Systems (97 citations), Pediatrics, Perinatology and Child Health (377 citations), Cancer Research (139 citations) and Otorhinolaryngology (35 citations). Ilse Feenstra has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Brigitte H. W. Faas, Helger G. Yntema, Lean Beulen, Mireille N. Bekker, Conny M.A. van Ravenswaaij‐Arts, Lisenka E.L.M. Vissers, Han G. Brunner, Egbert Bakker, J. M. G. van Vugt and Mariëlle Alders. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, European Journal of Medical Genetics, Clinical Genetics and Ear and Hearing.

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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