Ilse Feenstra

4.6k citations

61 papers · 3.1k · 1 hit paper · h-index 26

Impact in

Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Dermatological and Skeletal Disorders

Papers in

Pediatrics, Perinatology and Child Health 21
- Prenatal Screening and Diagnostics 19
- Fetal and Pediatric Neurological Disorders 4
Genetics 26
- Genomic variations and chromosomal abnormalities 15
- Genomics and Rare Diseases 10
- Genetics and Neurodevelopmental Disorders 8

Co-authors: Helger G. Yntema (9 shared papers)Brigitte H. W. Faas (8 shared papers)Mireille N. Bekker (5 shared papers)Lean Beulen (6 shared papers)Lisenka E.L.M. Vissers (6 shared papers)Conny M.A. van Ravenswaaij‐Arts (5 shared papers)Egbert Bakker (2 shared papers)Han G. Brunner (5 shared papers)
Journals: Prenatal Diagnosis (7 papers)European Journal of Human Genetics (7 papers)The American Journal of Human Genetics (6 papers)Human Genetics (4 papers)Clinical Genetics (4 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Ilse Feenstra

60 papers receiving 3.0k citations

Ilse Feenstra's Hit Papers

align trajectories log scale

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands 2019 · 281 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2019 The American Journal of Human Genetics

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 61 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 L. MATTHIJS, Erika L. Souche, Marielle M. Alders, Anniek Corveleyn, Sebastian H. Eck, Ilse Feenstra, Valérie Race, Erik A. Sistermans	2015	401
2	A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases Human Mutation ·Kornelia Neveling, Ilse Feenstra, Christian Gilissen, Lies H. Hoefsloot, Erik‐Jan Kamsteeg, Arjen R. Mensenkamp, Richard J. Rodenburg, Helger G. Yntema	2013	283
3	TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands The American Journal of Human Genetics ·Karuna R. M. van der Meij, Erik A. Sistermans, Merryn V E Macville, Servi J.C. Stevens, Caroline J. Bax, Mireille N. Bekker, Caterina M. Bilardo, Elles M. J. Boon Hit paper breakdown →	2019	281
4	Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Can Be Caused by Mutations in Either ENPP1 or ABCC6 The American Journal of Human Genetics ·Yvonne Nitschke, Geneviève Baujat, Ulrike Botschen, Tanja Wittkampf, Marcel du Moulin, Jacqueline Stella, Martine Le Merrer, Geneviève Guest	2011	276
5	Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP Biological Psychiatry ·Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns, Ilse M. van der Werf, Grazia M. S. Mancini, Andreas Tzschach, Raphael Bernier, Illana Gozes	2018	123
6	The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands European Journal of Human Genetics ·Celia Zazo Seco, Mieke Wesdorp, Ilse Feenstra, Rolph Pfundt, Jayne Y. Hehir‐Kwa, Stefan H. Lelieveld, Steven Castelein, Christian Gilissen	2016	104
7	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	2007	103
8	Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins Human Genetics ·Przemysław Szafrański, Tomasz Gambin, Avinash V. Dharmadhikari, Kadir Caner Akdemir, Shalini N. Jhangiani, Jennifer J. Schuette, Nihal Godiwala, Svetlana A. Yatsenko	2016	97
9	Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study Genetics in Medicine ·Diane Van Opstal, Merel C. van Maarle, Klaske D. Lichtenbelt, Marjan M. Weiss, Heleen Schuring‐Blom, Shama L. Bhola, Mariëtte J.V. Hoffer, Karin Huijsdens–van Amsterdam	2017	94
10	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 Aljosja Koolen, A. Siezen, C. R. Evans, R M Winter, Melissa M. Lees, Mariluce Riegel	2005	85
11	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 H. M. Schuurs-Hoeijmakers, Ilse Feenstra, Ernie M.H.F. Bongers, Daniëlle G.M. Bosch, Nicole de Leeuw	2015	84
12	Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging Prenatal Diagnosis ·Chantal Deden, Kornelia Neveling, Dimitra Zafeiropopoulou, Christian Gilissen, Rolph Pfundt, Tuula Rinne, Nicole de Leeuw, Brigitte H. W. Faas	2020	71
13	Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study The American Journal of Human Genetics ·Lisanne van Prooyen Schuurman, Erik A. Sistermans, Diane Van Opstal, Lidewij Henneman, Mireille N. Bekker, Caroline J. Bax, Mijntje J. Pieters, Katelijne Bouman	2022	69
14	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	2008	67
15	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, Brigitte H. W. Faas, Ilse Feenstra, Michiel Hageman, J. M. van Vugt, Mireille N. Bekker +1 other	2016	59
16	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	2018	58
17	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, Andrew Green, Roel Hordijk	2011	53
18	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, John M. G. van Vugt, Mireille N. Bekker	2016	52
19	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, John M. G. van Vugt, Mireille N. Bekker	2014	50
20	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, John M. G. van Vugt, Mireille N. Bekker	2015	45

About Ilse Feenstra

Ilse Feenstra is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Sensory Systems, Molecular Biology and Cancer Research, having authored 61 papers that have together received 3.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (15 papers), Genomics and Rare Diseases (10 papers), Hearing, Cochlea, Tinnitus, Genetics (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (7 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Sensory Systems (254 citations), Genetics (1.3k citations), Pediatrics, Perinatology and Child Health (824 citations), Cancer Research (226 citations) and Otorhinolaryngology (54 citations). Ilse Feenstra has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Helger G. Yntema, Brigitte H. W. Faas, Mireille N. Bekker, Lean Beulen, Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij‐Arts, Egbert Bakker, Han G. Brunner, GERT L. MATTHIJS and Erika L. Souche. Their work appears in journals such as Prenatal Diagnosis, European Journal of Human Genetics, The American Journal of Human Genetics, Human Genetics and Clinical 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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Ilse Feenstra

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Ilse Feenstra

Ilse Feenstra's Hit Papers

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