Hester Y. Kroes

3.9k citations

38 papers · 1.5k indexed · h-index 19

Genetics top 2%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 5%
Ophthalmology top 2%
Public Health, Environmental and Occupational Health

Co-authors: Frans P.M. Cremers Annelien L. Bredenoord Edwin Cuppen Michael Parker Johannes J. M. van Delden Ronald Roepman Nicholas T. Gorden Stef J.F. Letteboer
Topics: Genetic and Kidney Cyst Diseases (12 papers)Retinal Development and Disorders (11 papers)Fetal and Pediatric Neurological Disorders (9 papers)
Cited by: Genetics Ophthalmology Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Netherlands United States Germany

In The Last Decade

Hester Y. Kroes

37 papers receiving 1.5k citations

Peers

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

#	Work	Indexed citations
1	Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium 2024 ·Investigative Ophthalmology & Visual Science ·(unknown),L. Ingeborgh van den Born,(unknown),(unknown),Carel B. Hoyng,Jan Willem R. Pott,Hester Y. Kroes,Mary J. van Schooneveld,Camiel J. F. Boon,Maria M. van Genderen,Astrid S. Plomp,Yvonne de Jong‐Hesse,(unknown),Lies H. Hoefsloot,Arthur A. Bergen,Caroline C. W. Klaver,Magda A. Meester‐Smoor,Alberta A. H. J. Thiadens,Virginie J. M. Verhoeven	0
2	Utilization of automated cilia analysis to characterize novel INPP5E variants in patients with non-syndromic retinitis pigmentosa 2024 ·European Journal of Human Genetics ·(unknown),Lonneke Haer‐Wigman,Ralph J. Florijn,Ronald van Beek,Machteld M. Oud,Astrid S. Plomp,Camiel J. F. Boon,Hester Y. Kroes,Ronald Roepman	1
3	A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis 2023 ·Brain ·Doriana Misceo,Lisa Lirussi,Petter Strømme,Dulika Sumathipala,Andrea Guerin,Nicole I. Wolf,Andrés Server,Maria Stensland,Bjørn Dalhus,Aslıhan Tolun,Hester Y. Kroes,Tuula A. Nyman,Hilde Nilsen,Eirik Frengen	3
4	The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner 2022 ·Cells ·(unknown),Lonneke Duijkers,(unknown),(unknown),(unknown),(unknown),(unknown),Michael Kwint,(unknown),(unknown),Hester Y. Kroes,Christian Gilissen,Frans P.M. Cremers,Rob W.J. Collin,Susanne Roosing,Alejandro Garanto	8
5	Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA 2022 ·npj Genomic Medicine ·Lonneke Haer‐Wigman,(unknown),Maria M. van Genderen,Hester Y. Kroes,Joanne Verheij,(unknown),Attje S. Hoekstra,Raymon Vijzelaar,Jan Dirk Blom,Ronny Derks,(unknown),Helger G. Yntema,Marcel Nelen,Lisenka E.L.M. Vissers,Dorien Lugtenberg,Kornelia Neveling	7
6	Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65 2022 ·Stem Cell Research ·(unknown),Michael Kwint,Hester Y. Kroes,Sílvia Albert,(unknown),Christian Gilissen,Frans P.M. Cremers,Rob W.J. Collin,Susanne Roosing,Alejandro Garanto	1
7	Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability 2016 ·Genetics in Medicine ·Glen R. Monroe,G. W. J. Frederix,Sanne M. C. Savelberg,Tamar I. de Vries,Karen Duran,Jasper J. van der Smagt,Pauline Terhal,Peter M. van Hasselt,Hester Y. Kroes,Nanda M. Verhoeven‐Duif,Isaäc J. Nijman,Ellen C. Carbo,Koen L.I. van Gassen,Nine Knoers,Anke M. Hövels,Mieke M. van Haelst,Gepke Visser,Gijs van Haaften	125
8	Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type 2016 ·Genetics in Medicine ·Tim Van Damme,Alain Colige,Delfien Syx,Cecilia Giunta,Uschi Lindert,Marianne Rohrbach,Omid Aryani,Yasemin Alanay,Pelin Özlem Şimşek‐Kiper,Hester Y. Kroes,Koenraad Devriendt,Marc Thiry,Sofie Symoens,Anne De Paepe,Fransiska Malfait	34
9	Joubert syndrome: genotyping a Northern European patient cohort 2015 ·European Journal of Human Genetics ·Hester Y. Kroes,Glen R. Monroe,Bert van der Zwaag,Karen Duran,Carolien G. F. de Kovel,(unknown),Magdaléna Harakaľová,Isaäc J. Nijman,Wigard P. Kloosterman,Rachel H. Giles,Nine Knoers,Gijs van Haaften	50
10	Non-invasive sources of cells with primary cilia from pediatric and adult patients 2015 ·PubMed ·(unknown),Gisela G. Slaats,Marijn F. Stokman,Heleen H. Arts,Ive Logister,Hester Y. Kroes,Kirsten Y. Renkema,Mieke M. van Haelst,Pauline Terhal,Iris A.L.M. van Rooij,Mandy G. Keijzer‐Veen,Nine Knoers,Marc R. Liliën,Michael A.S. Jewett,Rachel H. Giles	27
11	The clinical utility of MRI in patients with neurodevelopmental disorders of unknown origin 2010 ·European Journal of Neurology ·(unknown),Rutger A. J. Nievelstein,R. H. J. M. Gooskens,Hester Y. Kroes,R. van Empelen,Olga Braams,D. Wittebol‐Post,Margriet M. W. B. Hendriks,Gepke Visser	7
12	Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes 2010 ·Human Mutation ·Frauke Coppieters,Ingele Casteels,Françoise Meire,Sarah De Jaegere,(unknown),Nicole Van Regemorter,Hilde Van Esch,Aušra Matulevičienė,Luís Nunes,(unknown),Sophie Walraedt,(unknown),Paul Coucke,(unknown),Hester Y. Kroes,Johan Vande Walle,Thomy de Ravel,Bart P. Leroy,Elfride De Baere	110
13	Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene 2010 ·European Journal of Medical Genetics ·Almuth Caliebe,Hester Y. Kroes,Jasper J. van der Smagt,José I. Martı́n-Subero,Holger Tönnies,Ruben van ‘t Slot,Rutger A. J. Nievelstein,Hiltrud Muhle,Ulrich Stephani,Karsten Alfke,Irina Stefanova,Yorck Hellenbroich,Gabriele Gillessen‐Kaesbach,Ron Hochstenbach,Reiner Siebert,Martin Poot	54
14	Yield of additional metabolic studies in neurodevelopmental disorders 2008 ·Annals of Neurology ·(unknown),Ruud Berger,Peter van Hasselt,(unknown),Monique G.M. de Sain–van der Velden,Hester Y. Kroes,Gepke Visser	26
15	Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature 2008 ·Human Mutation ·Bert Callewaert,Bart Loeys,Anna Ficcadenti,Sascha Vermeer,Magnus Landgren,Hester Y. Kroes,Yuval Yaron,Michael Pope,Nicola Foulds,Odile Boute,Francisco Galán,Helen Kingston,Nathalie Van der Aa,(unknown),Mariëlle E.M. Swinkels,Carina Wallgren‐Pettersson,Orazio Gabrielli,Julie De Backer,Paul Coucke,Anne M. De Paepe	62
16	Dandy‐Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33) 2007 ·American Journal of Medical Genetics Part A ·Martin Poot,Hester Y. Kroes,(unknown),Marc J. Eleveld,Liesbeth Rooms,Rutger A. J. Nievelstein,Daniël Olde Weghuis,René C. F. M. Vreuls,G. Hageman,R. Frank Kooy,Ron Hochstenbach	31
17	Mitochondrial Dysfunction in a Patient with Joubert Syndrome 2005 ·Neuropediatrics ·Éva Morava,Argirios Dinopoulos,Hester Y. Kroes,Richard J. Rodenburg,Hans van Bokhoven,Lambertus P. van den Heuvel,Jan Smeıtınk	7
18	Renal defects and limb deficiencies in 197 infants: Is it possible to define the “acrorenal syndrome”? 2004 ·American Journal of Medical Genetics Part A ·Hester Y. Kroes,Richard S. Olney,Aldo Rosano,Yecai Liu,Eduardo E. Castilla,Guido Cocchi,Catherine De Vigan,María Luisa Martínez‐Frías,Pierpaolo Mastroiacovo,Paul Merlob,Osvaldo M. Mutchinick,Annukka Ritvanen,Claude Stoll,Anthonie J. van Essen,Jan Maarten Cobben,Martina C. Cornel	8
19	Is There an Association between Maternal Carbamazepine Use during Pregnancy and Eye Malformations in the Child? 2002 ·Epilepsia ·Hester Y. Kroes,Jennita Reefhuis,Martina C. Cornel	12
20	Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy 1998 ·Nature Genetics ·Stephan Rust,Michael Walter,Harald Funke,Arnold von Eckardstein,Paul Cullen,Hester Y. Kroes,Roel Hordijk,Jürgen Geisel,J. Kastelein,Henri O.F. Molhuizen,(unknown),(unknown),Harry Hahmann,Gerd Assmann	49

About Hester Y. Kroes

Hester Y. Kroes is a scholar working on Genetics, Ophthalmology and Pediatrics, Perinatology and Child Health, having authored 38 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Retinal Development and Disorders (11 papers) and Fetal and Pediatric Neurological Disorders (9 papers). The work is most often cited by research in Genetics (1.0k citations), Ophthalmology (211 citations) and Molecular Biology (973 citations). Hester Y. Kroes has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Frans P.M. Cremers, Annelien L. Bredenoord, Edwin Cuppen, Michael Parker, Johannes J. M. van Delden, Ronald Roepman, Nicholas T. Gorden, Stef J.F. Letteboer, Dan Doherty and Heleen H. Arts. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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