Karen Duran

3.4k total citations
28 papers, 1.4k citations indexed

About

Karen Duran is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Karen Duran has authored 28 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Karen Duran's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Karen Duran is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Karen Duran collaborates with scholars based in Netherlands, United States and United Kingdom. Karen Duran's co-authors include Wigard P. Kloosterman, Edwin Cuppen, Gijs van Haaften, Mieke M. van Haelst, Ewart de Bruijn, Cisca Wijmenga, Isaäc J. Nijman, Ron Hochstenbach, Leo W. J. Klomp and Martin Poot and has published in prestigious journals such as Nature Genetics, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Karen Duran

28 papers receiving 1.3k citations

Peers

Karen Duran

GENET

PPCH

Tommaso Pippucci Italy

Cuiping Hou United States

Anas M. Alazami Saudi Arabia

Alex L. Nigg Netherlands

Lorena Travaglini Italy

Kanya Suphapeetiporn Thailand

Fides D. Lay United States

Barbara K. Goodman United States

Hidenori Kiyosawa Japan

Richard Sandford United Kingdom

Tommaso Pippucci Italy

Karen Duran

708 ×0.9

663 ×1.2

GENET

215 ×1.4

80 ×0.6

72 ×0.5

PPCH

Citations per year, relative to Karen Duran Karen Duran (= 1×) peers Tommaso Pippucci

Countries citing papers authored by Karen Duran

Since Specialization

Citations

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

Fields of papers citing papers by Karen Duran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Duran

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Duran. A scholar is included among the top collaborators of Karen Duran 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 Karen Duran. Karen Duran 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

Tessadori, Federico, Atteeq U. Rehman, Jacques C. Giltay, et al.. (2019). A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder. European Journal of Human Genetics. 28(5). 674–678. 11 indexed citations

Grange, Dorothy K., Helen I. Roessler, Conor McClenaghan, et al.. (2019). Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(4). 658–681. 44 indexed citations

Tessadori, Federico, Helen I. Roessler, Sanne M. C. Savelberg, et al.. (2018). Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders. Disease Models & Mechanisms. 11(10). 59 indexed citations

Tessadori, Federico, Jacques C. Giltay, Jane A. Hurst, et al.. (2017). Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control. Nature Genetics. 49(11). 1642–1646. 34 indexed citations

Houtman, Marien J. C., Karen Duran, Gijs van Haaften, et al.. (2017). PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function KIR2.1 channels, but increases channel protein expression. Journal of Biomedical Science. 24(1). 44–44. 12 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

Pagter, Mirjam S. de, Markus J. van Roosmalen, Annette F. Baas, et al.. (2015). Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring. The American Journal of Human Genetics. 96(4). 651–656. 80 indexed citations

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

Haelst, Mieke M. van, Glen R. Monroe, Karen Duran, et al.. (2014). Further confirmation of the MED13L haploinsufficiency syndrome. European Journal of Human Genetics. 23(1). 135–138. 31 indexed citations

10.

Hoogstraat, Marlous, Mirjam S. de Pagter, Geert A. Cirkel, et al.. (2013). Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer. Genome Research. 24(2). 200–211. 63 indexed citations

11.

Vergult, Sarah, Ellen van Binsbergen, Tom Sante, et al.. (2013). Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. European Journal of Human Genetics. 22(5). 652–659. 25 indexed citations

12.

Hochstenbach, Ron, Martin Poot, Isaäc J. Nijman, et al.. (2012). Discovery of variants unmasked by hemizygous deletions. European Journal of Human Genetics. 20(7). 748–753. 14 indexed citations

13.

Harakaľová, Magdaléna, Marie-José van den Boogaard, Richard J. Sinke, et al.. (2012). X-exome sequencing identifies a HDAC8 variant in a large pedigree with X-linked intellectual disability, truncal obesity, gynaecomastia, hypogonadism and unusual face. Journal of Medical Genetics. 49(8). 539–543. 50 indexed citations

14.

Eerde, Albertien M. van, Karen Duran, E. van Riel, et al.. (2012). Genes in the Ureteric Budding Pathway: Association Study on Vesico-Ureteral Reflux Patients. PLoS ONE. 7(4). e31327–e31327. 29 indexed citations

15.

Kloosterman, Wigard P., Victor Guryev, Karen Duran, et al.. (2011). Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†. Human Molecular Genetics. 20(10). 1916–1924. 225 indexed citations

16.

Harakaľová, Magdaléna, Michal Mokrý, Barbara Hrdličková, et al.. (2011). Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing. Nature Protocols. 6(12). 1870–1886. 51 indexed citations

17.

Duran, Karen, Wigard P. Kloosterman, Angelique J. Goverde, et al.. (2011). Limited contribution of NR5A1 (SF-1) mutations in women with primary ovarian insufficiency (POI). Fertility and Sterility. 97(1). 141–146.e2. 30 indexed citations

18.

Rozemuller, Erik H., et al.. (1999). Mutation in the β2m gene is not a frequent event in head and neck squamous cell carcinomas. Human Immunology. 60(8). 697–706. 27 indexed citations

19.

Duran, Karen, et al.. (1997). Two newly identified HLA-DRB1 alleles: DRB1 * 1322 and DRB1 * 1327. Immunogenetics. 46(5). 442–443. 2 indexed citations

20.

Rozemuller, Erik H., et al.. (1995). Ambiguous DPB1 allele combinations resolved by direct sequencing of selectively amplified alleles. Tissue Antigens. 46(4). 345–349. 31 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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