Hester Y. Kroes

3.9k total citations
38 papers, 1.5k citations indexed

About

Hester Y. Kroes is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hester Y. Kroes has authored 38 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 24 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hester Y. Kroes's work include Genetic and Kidney Cyst Diseases (12 papers), Retinal Development and Disorders (11 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Hester Y. Kroes is often cited by papers focused on Genetic and Kidney Cyst Diseases (12 papers), Retinal Development and Disorders (11 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Hester Y. Kroes collaborates with scholars based in Netherlands, United States and Germany. Hester Y. Kroes's co-authors include Frans P.M. Cremers, Annelien L. Bredenoord, Michael Parker, Edwin Cuppen, Johannes J. M. van Delden, Ronald Roepman, Stef J.F. Letteboer, Dan Doherty, Nicholas T. Gorden and Heleen H. Arts and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Hester Y. Kroes

37 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hester Y. Kroes Netherlands	19	1.0k	973	246	211	138	38	1.5k
Massimo Attanasio United States	20	1.1k 1.1×	1.3k 1.4×	331 1.3×	72 0.3×	41 0.3×	31	1.8k
Liesbeth Spruijt Netherlands	23	620 0.6×	1.0k 1.1×	143 0.6×	98 0.5×	47 0.3×	43	1.6k
Sibel Kantarci United States	15	1.0k 1.0×	821 0.8×	385 1.6×	33 0.2×	50 0.4×	23	1.8k
Louise Ocaka United Kingdom	19	420 0.4×	729 0.7×	36 0.1×	357 1.7×	58 0.4×	30	1.2k
A Seller United Kingdom	15	797 0.8×	940 1.0×	76 0.3×	60 0.3×	23 0.2×	24	1.7k
Jane S. Green Canada	19	1.2k 1.2×	1.1k 1.1×	69 0.3×	80 0.4×	17 0.1×	31	1.8k
Lauren Massingham United States	8	295 0.3×	365 0.4×	110 0.4×	64 0.3×	53 0.4×	19	845
Séverine Drunat France	21	443 0.4×	581 0.6×	144 0.6×	19 0.1×	100 0.7×	57	1.1k
Sachiko Nishina Japan	20	230 0.2×	533 0.5×	112 0.5×	481 2.3×	48 0.3×	82	1.2k
Nadia Sakati Saudi Arabia	22	546 0.5×	819 0.8×	160 0.7×	23 0.1×	25 0.2×	78	1.7k

Countries citing papers authored by Hester Y. Kroes

Since Specialization

Citations

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

Fields of papers citing papers by Hester Y. Kroes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hester Y. Kroes. 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 Hester Y. Kroes. The network helps show where Hester Y. Kroes may publish in the future.

Co-authorship network of co-authors of Hester Y. Kroes

This figure shows the co-authorship network connecting the top 25 collaborators of Hester Y. Kroes. A scholar is included among the top collaborators of Hester Y. Kroes 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 Hester Y. Kroes. Hester Y. Kroes 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

Haer‐Wigman, Lonneke, Ralph J. Florijn, Ronald van Beek, et al.. (2024). Utilization of automated cilia analysis to characterize novel INPP5E variants in patients with non-syndromic retinitis pigmentosa. European Journal of Human Genetics. 32(11). 1412–1418. 1 indexed citations

Born, L. Ingeborgh van den, Carel B. Hoyng, Jan Willem R. Pott, et al.. (2024). Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium. Investigative Ophthalmology & Visual Science. 65(10). 40–40.

Misceo, Doriana, Lisa Lirussi, Petter Strømme, et al.. (2023). A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis. Brain. 146(8). 3513–3527. 3 indexed citations

Duijkers, Lonneke, Michael Kwint, Hester Y. Kroes, et al.. (2022). The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner. Cells. 11(22). 3640–3640. 8 indexed citations

Kwint, Michael, Hester Y. Kroes, Sílvia Albert, et al.. (2022). Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65. Stem Cell Research. 60. 102689–102689. 1 indexed citations

Cauwenbergh, Caroline Van, Birgit Lorenz, Mette Bertelsen, et al.. (2018). Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation inCEP290. Investigative Ophthalmology & Visual Science. 59(11). 4384–4384. 18 indexed citations

Damme, Tim Van, Alain Colige, Delfien Syx, et al.. (2016). Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type. Genetics in Medicine. 18(9). 882–891. 34 indexed citations

Monroe, Glen R., G. W. J. Frederix, Sanne M. C. Savelberg, et al.. (2016). Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability. Genetics in Medicine. 18(9). 949–956. 125 indexed citations

Slaats, Gisela G., Marijn F. Stokman, Heleen H. Arts, et al.. (2015). Non-invasive sources of cells with primary cilia from pediatric and adult patients. PubMed. 4(1). 8–8. 27 indexed citations

10.

Kroes, Hester Y., Glen R. Monroe, Bert van der Zwaag, et al.. (2015). Joubert syndrome: genotyping a Northern European patient cohort. European Journal of Human Genetics. 24(2). 214–220. 50 indexed citations

11.

Booij, Judith C., Arne Bakker, H.J.M. Smeets, et al.. (2010). Simultaneous Mutation Detection in 90 Retinal Disease Genes in Multiple Patients Using a Custom-designed 300-kb Retinal Resequencing Chip. Ophthalmology. 118(1). 160–167.e3. 22 indexed citations

12.

Coppieters, Frauke, Ingele Casteels, Françoise Meire, et al.. (2010). Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes. Human Mutation. 31(10). E1709–E1766. 110 indexed citations

13.

Caliebe, Almuth, Hester Y. Kroes, Jasper J. van der Smagt, et al.. (2010). Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene. European Journal of Medical Genetics. 53(4). 179–185. 54 indexed citations

14.

Poot, Martin, Hester Y. Kroes, Marc J. Eleveld, et al.. (2007). Dandy‐Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33). American Journal of Medical Genetics Part A. 143A(10). 1038–1044. 31 indexed citations

15.

Arts, Heleen H., Dan Doherty, Sylvia E. C. van Beersum, et al.. (2007). Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome. Nature Genetics. 39(7). 882–888. 235 indexed citations

16.

Morava, Éva, Argirios Dinopoulos, Hester Y. Kroes, et al.. (2005). Mitochondrial Dysfunction in a Patient with Joubert Syndrome. Neuropediatrics. 36(3). 214–217. 7 indexed citations

17.

Kroes, Hester Y., Richard S. Olney, Aldo Rosano, et al.. (2004). Renal defects and limb deficiencies in 197 infants: Is it possible to define the “acrorenal syndrome”?. American Journal of Medical Genetics Part A. 129A(2). 149–155. 8 indexed citations

18.

Kroes, Hester Y., et al.. (2004). Hereditary fetal brain degeneration resembling fetal brain disruption sequence in two sibships. American Journal of Medical Genetics Part A. 127A(2). 172–182. 10 indexed citations

19.

Kroes, Hester Y., Jennita Reefhuis, & Martina C. Cornel. (2002). Is There an Association between Maternal Carbamazepine Use during Pregnancy and Eye Malformations in the Child?. Epilepsia. 43(8). 929–931. 12 indexed citations

20.

Rust, Stephan, Michael Walter, Harald Funke, et al.. (1998). Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy. Nature Genetics. 20(1). 96–98. 49 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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