Krysta Voesenek

1.5k total citations
11 papers, 1.0k citations indexed

About

Krysta Voesenek is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Krysta Voesenek has authored 11 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Ophthalmology. Recurrent topics in Krysta Voesenek's work include Retinal Development and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Retinal Diseases and Treatments (2 papers). Krysta Voesenek is often cited by papers focused on Retinal Development and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Retinal Diseases and Treatments (2 papers). Krysta Voesenek collaborates with scholars based in Netherlands, Germany and United States. Krysta Voesenek's co-authors include Frans P.M. Cremers, Han G. Brunner, Marijke N. Zonneveld, Klaus Rohrschneider, Anneke I. den Hollander, Carel B. Hoyng, Maarten Arends, Robert K. Koenekoop, L. Ingeborgh van den Born and Suzanne Yzer and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Soil Biology and Biochemistry.

In The Last Decade

Krysta Voesenek

10 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Krysta Voesenek Netherlands	9	863	524	228	154	93	11	1.0k
Penny Clouston United Kingdom	12	613 0.7×	452 0.9×	201 0.9×	56 0.4×	58 0.6×	34	850
Lawriston A. Wilson United States	10	1.0k 1.2×	210 0.4×	410 1.8×	142 0.9×	34 0.4×	12	1.3k
Mingchu Xu United States	19	623 0.7×	182 0.3×	184 0.8×	92 0.6×	18 0.2×	28	760
J. Bronwyn Bateman United States	16	460 0.5×	257 0.5×	206 0.9×	78 0.5×	17 0.2×	34	680
Katharina Steindl Switzerland	18	411 0.5×	323 0.6×	72 0.3×	52 0.3×	49 0.5×	50	698
Jeaneen L. Andorf United States	11	942 1.1×	397 0.8×	363 1.6×	105 0.7×	15 0.2×	17	1.0k
Sigrid Fuchs Germany	16	584 0.7×	148 0.3×	101 0.4×	69 0.4×	33 0.4×	35	790
Arif O. Khan Saudi Arabia	19	721 0.8×	299 0.6×	343 1.5×	114 0.7×	17 0.2×	74	960
Liesbeth M. Bleeker-Wagemakers Netherlands	10	415 0.5×	205 0.4×	63 0.3×	74 0.5×	29 0.3×	12	557
Ilaria Zito United Kingdom	10	449 0.5×	240 0.5×	117 0.5×	68 0.4×	26 0.3×	15	560

Countries citing papers authored by Krysta Voesenek

Since Specialization

Citations

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

Fields of papers citing papers by Krysta Voesenek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Krysta Voesenek

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

All Works

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11 of 11 papers shown

Brouwer, Arjan Pm de, Sander B. Nabuurs, Ingrid E.C. Verhaart, et al.. (2013). A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy. European Journal of Human Genetics. 22(4). 480–485. 29 indexed citations

Kalscheuer, Vera M., Zafar Iqbal, Han Hu, et al.. (2013). RAB40AL loss-of-function mutation does not cause X-linked intellectual disability. Adelaide Research & Scholarship (AR&S) (University of Adelaide). 3 indexed citations

Kühnisch, Jirko, Éva Morava, Joris H. Robben, et al.. (2011). A novel skeletal disorder characterized by progressive spondyloarthropathy is caused by a recessive ANKH mutation. Bone. 48. S154–S155.

Naranjo, Silvia, Krysta Voesenek, Elisa de la Calle‐Mustienes, et al.. (2010). Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing. Human Genetics. 128(4). 411–419. 31 indexed citations

Morava, Éva, Jirko Kühnisch, Jefte M. Drijvers, et al.. (2010). Autosomal Recessive Mental Retardation, Deafness, Ankylosis, and Mild Hypophosphatemia Associated with a NovelANKHMutation in a Consanguineous Family. The Journal of Clinical Endocrinology & Metabolism. 96(1). E189–E198. 31 indexed citations

Aller, Elena, Teresa Jaijo, Erwin van Wijk, et al.. (2010). Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin.. PubMed. 16. 495–500. 14 indexed citations

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

Hollander, Anneke I. den, Robert K. Koenekoop, Suzanne Yzer, et al.. (2006). Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis. The American Journal of Human Genetics. 79(3). 556–561. 488 indexed citations

Yzer, Suzanne, Bart P. Leroy, Elfride De Baere, et al.. (2006). Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 47(3). 1167–1167. 77 indexed citations

10.

Hurk, José A. J. M. van den, Penny Rashbass, Ronald Roepman, et al.. (2005). Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.. PubMed. 11. 263–73. 80 indexed citations

11.

Garbeva, Paolina, Krysta Voesenek, & Jan Dirk van Elsas. (2004). Quantitative detection and diversity of the pyrrolnitrin biosynthetic locus in soil under different treatments. Soil Biology and Biochemistry. 36(9). 1453–1463. 33 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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