Ilse Feenstra

4.5k total citations
45 papers, 1.3k citations indexed

About

Ilse Feenstra is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ilse Feenstra has authored 45 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 18 papers in Pediatrics, Perinatology and Child Health and 16 papers in Molecular Biology. Recurrent topics in Ilse Feenstra's work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (15 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Ilse Feenstra is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (15 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Ilse Feenstra collaborates with scholars based in Netherlands, United States and Germany. Ilse Feenstra's 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 Hans Scheffer and has published in prestigious journals such as Journal of Clinical Investigation, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Ilse Feenstra

43 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilse Feenstra Netherlands 19 731 479 377 139 97 45 1.3k
Güven Lüleci Türkiye 21 808 1.1× 750 1.6× 286 0.8× 111 0.8× 59 0.6× 110 1.7k
Patricia A. Ward United States 25 1.2k 1.7× 1.0k 2.2× 627 1.7× 129 0.9× 59 0.6× 65 2.5k
Erin Rooney Riggs United States 14 950 1.3× 462 1.0× 377 1.0× 153 1.1× 16 0.2× 21 1.3k
Barbara F. Crandall United States 25 719 1.0× 704 1.5× 740 2.0× 127 0.9× 69 0.7× 88 2.0k
Hassan Rouba Morocco 22 739 1.0× 762 1.6× 116 0.3× 58 0.4× 176 1.8× 83 1.4k
P. Sistonen Finland 25 906 1.2× 643 1.3× 111 0.3× 90 0.6× 82 0.8× 52 2.2k
Neeme Tõnisson Estonia 16 305 0.4× 937 2.0× 97 0.3× 241 1.7× 47 0.5× 38 1.3k
Sylvie Langlois Canada 32 1.6k 2.2× 1.1k 2.2× 1.5k 3.9× 122 0.9× 38 0.4× 107 2.8k
Peter Miny Germany 21 629 0.9× 437 0.9× 844 2.2× 40 0.3× 14 0.1× 88 1.5k
Tsang‐Ming Ko Taiwan 18 463 0.6× 483 1.0× 409 1.1× 14 0.1× 96 1.0× 83 1.3k

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-authorship network of co-authors of Ilse Feenstra

This figure shows the co-authorship network connecting the top 25 collaborators of Ilse Feenstra. A scholar is included among the top collaborators of Ilse Feenstra 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 Ilse Feenstra. Ilse Feenstra is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Schoot, Vyne van der, Lonneke Haer‐Wigman, Ilse Feenstra, et al.. (2021). Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals. European Journal of Human Genetics. 30(2). 170–177. 17 indexed citations
2.
Verbakel, Sanne K., B. Jeroen Klevering, Maria M. van Genderen, et al.. (2019). The identification of a RNA splice variant in TULP1 in two siblings with early‐onset photoreceptor dystrophy. Molecular Genetics & Genomic Medicine. 7(6). e660–e660. 12 indexed citations
3.
Oostrik, Jaap, Andy J. Beynon, Sarina G. Kant, et al.. (2018). De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Human Genetics. 138(1). 61–72. 25 indexed citations
4.
Lefeber, Dirk J., et al.. (2017). ALG13-CDG with Infantile Spasms in a Male Patient Due to a De Novo ALG13 Gene Mutation. JIMD Reports. 40. 11–16. 14 indexed citations
5.
Beulen, Lean, et al.. (2016). P01.07: The clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies. Ultrasound in Obstetrics and Gynecology. 48(S1). 169–169. 1 indexed citations
6.
Oonk, Anne M.M., Ronald J. E. Pennings, Ilse Feenstra, et al.. (2015). Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment. Ear and Hearing. 37(1). 103–111. 14 indexed citations
7.
Matthijs, Gert, Erika Souche, Mariëlle Alders, et al.. (2015). Guidelines for diagnostic next-generation sequencing. European Journal of Human Genetics. 24(1). 2–5. 337 indexed citations
8.
Oonk, Anne M.M., P.L.M. Huygen, Margit Schraders, et al.. (2014). Similar Phenotypes Caused by Mutations in OTOG and OTOGL. Ear and Hearing. 35(3). e84–e91. 18 indexed citations
9.
Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations
10.
Beulen, Lean, Janneke P.C. Grutters, Brigitte H. W. Faas, et al.. (2014). 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. 182. 53–61. 47 indexed citations
11.
Feenstra, Ilse, et al.. (2013). 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. 56(8). 426–431. 21 indexed citations
12.
Kooper, Angelique J. A., A.J. Eggink, Thijs Feuth, et al.. (2012). Why Do Parents Prefer to Know the Fetal Sex as Part of Invasive Prenatal Testing. Obstetrics and Gynecology. 2012. 524537–524537. 1 indexed citations
13.
Verhoeven, W.M.A., J.I.M. Egger, Ilse Feenstra, & Nicole de Leeuw. (2011). A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy. European Journal of Medical Genetics. 55(5). 358–361. 5 indexed citations
14.
Feenstra, Ilse, Birgit Sikkema‐Raddatz, Helger G. Yntema, et al.. (2011). 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. 19(11). 1152–1160. 41 indexed citations
15.
Bon, Bregje W.M. van, David A. Koolen, Ilse Feenstra, et al.. (2007). Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and review. Clinical Dysmorphology. 16(4). 279–282. 1 indexed citations
16.
Feenstra, Ilse, Lisenka E.L.M. Vissers, Ad Geurts van Kessel, et al.. (2007). 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. 143A(16). 1858–1867. 98 indexed citations
17.
Feenstra, Ilse, Conny van Ravenswaaij, Marjo S. van der Knaap, & Michèl A.A.P. Willemsen. (2006). Neuroimaging in Nine Patients with Inversion Duplication of the Short Arm of Chromosome 8. Neuropediatrics. 37(2). 83–87. 3 indexed citations
18.
Feenstra, Ilse, HG Brunner, & Conny M.A. van Ravenswaaij. (2006). Cytogenetic genotype-phenotype studies: Improving genotyping, phenotyping and data storage. Cytogenetic and Genome Research. 115(3-4). 231–239. 10 indexed citations
19.
Feenstra, Ilse, et al.. (2006). 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. 49(5). 384–395. 23 indexed citations
20.
Feenstra, Ilse, Jiayi Fang, David A. Koolen, et al.. (2005). European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities. European Journal of Medical Genetics. 49(4). 279–291. 59 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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