Marieke Levitus

1.5k total citations
12 papers, 1.1k citations indexed

About

Marieke Levitus is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Marieke Levitus has authored 12 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Plant Science and 2 papers in Genetics. Recurrent topics in Marieke Levitus's work include DNA Repair Mechanisms (7 papers), CRISPR and Genetic Engineering (4 papers) and Chromosomal and Genetic Variations (3 papers). Marieke Levitus is often cited by papers focused on DNA Repair Mechanisms (7 papers), CRISPR and Genetic Engineering (4 papers) and Chromosomal and Genetic Variations (3 papers). Marieke Levitus collaborates with scholars based in Netherlands, United States and United Kingdom. Marieke Levitus's co-authors include Hans Joenje, Johan P. de Winter, Martin A. Rooimans, Fré Arwert, Quinten Waisfisz, Christopher G. Mathew, Gerard Pals, Jûrgen Steltenpool, Maureen E. Hoatlin and Anneke B. Oostra and has published in prestigious journals such as Nature Genetics, Blood and The American Journal of Human Genetics.

In The Last Decade

Marieke Levitus

12 papers receiving 1.1k citations

Peers

Marieke Levitus

GENET

ONCOL

Jörg Weimer Germany

Ulrike Schwarz‐Boeger Germany

Peter C. Verlander United States

Ángel Martínez‐Ramírez Spain

E. Cristy Ruteshouser United States

Gönül Oğur Türkiye

Axelle Loriot Belgium

Diha Freije United States

Huacheng Luo United States

Connie C. Cortez United States

Jörg Weimer Germany

Marieke Levitus

410 ×0.4

143 ×0.4

150 ×0.5

GENET

149 ×1.2

ONCOL

98 ×0.8

Citations per year, relative to Marieke Levitus Marieke Levitus (= 1×) peers Jörg Weimer

Countries citing papers authored by Marieke Levitus

Since Specialization

Citations

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

Fields of papers citing papers by Marieke Levitus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marieke Levitus

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

All Works

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12 of 12 papers shown

Vries, Yne de, Marieke Levitus, Sara J. Israels, et al.. (2012). A Dutch Fanconi AnemiaFANCCFounder Mutation in Canadian Manitoba Mennonites. Anemia. 2012. 1–6. 12 indexed citations

Hardeman, Max R., Marieke Levitus, Antonio Pelliccia, & A. Bouman. (2009). Test 1 analyser for determination of ESR. 1. Practical evaluation and comparison with the Westergren technique. Scandinavian Journal of Clinical and Laboratory Investigation. 70(1). 21–25. 23 indexed citations

Hardeman, Max R., Marieke Levitus, Antonio Pelliccia, & A. Bouman. (2009). Test 1 analyser for determination of ESR. 2. Experimental evaluation and comparison with RBC aggregometry. Scandinavian Journal of Clinical and Laboratory Investigation. 70(1). 26–32. 12 indexed citations

Levitus, Marieke, Antonio Pelliccia, R J van de Stadt, Alexandre E. Voskuyl, & A. Bouman. (2009). Is the Alifax Test-1TH useful to determine the Disease Activity Score (DAS28) in rheumatoid arthritis patients?. Clinical Rheumatology. 28(4). 469–474. 2 indexed citations

Linskens, Ingeborg H., Marieke Levitus, Peter C. J. I. Schielen, et al.. (2009). Performance of free β-human chorionic gonadotrophin (free β-hCG) and pregnancy associated plasma protein-A (PAPP-A) analysis between Delfia Xpress and AutoDelfia systems in The Netherlands. Clinical Chemistry and Laboratory Medicine (CCLM). 47(2). 222–6. 8 indexed citations

Heijboer, Annemieke C., Marieke Levitus, Marc Vervloet, et al.. (2009). Determination of fibroblast growth factor 23. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 46(4). 338–340. 63 indexed citations

Dorsman, Josephine C., Marieke Levitus, Davy Rockx, et al.. (2007). Identification of the Fanconi Anemia Complementation Group I Gene, FANCI. Analytical Cellular Pathology. 29(3). 211–218. 101 indexed citations

Levitus, Marieke, Hans Joenje, & Johan P. de Winter. (2006). The Fanconi Anemia Pathway of Genomic Maintenance. Analytical Cellular Pathology. 28(1-2). 3–29. 78 indexed citations

Levitus, Marieke, Quinten Waisfisz, Barbara C. Godthelp, et al.. (2005). The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nature Genetics. 37(9). 934–935. 338 indexed citations

10.

Meetei, Amom Ruhikanta, Marieke Levitus, Yutong Xue, et al.. (2004). X-linked inheritance of Fanconi anemia complementation group B. Nature Genetics. 36(11). 1219–1224. 229 indexed citations

11.

Levitus, Marieke, Martin A. Rooimans, Jûrgen Steltenpool, et al.. (2003). Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes. Blood. 103(7). 2498–2503. 177 indexed citations

12.

Joenje, Hans, Marieke Levitus, Quinten Waisfisz, et al.. (2000). Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A. The American Journal of Human Genetics. 67(3). 759–762. 99 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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