Marion Drüsedau

812 total citations
11 papers, 525 citations indexed

About

Marion Drüsedau is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Marion Drüsedau has authored 11 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Marion Drüsedau's work include Prenatal Screening and Diagnostics (8 papers), Cancer Genomics and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Marion Drüsedau is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Cancer Genomics and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Marion Drüsedau collaborates with scholars based in Netherlands, United Kingdom and United States. Marion Drüsedau's co-authors include Jan G.M. Klijn, Frans B.L. Hogervorst, Peter Devilee, Hans F. A. Vasen, Marjolijn J. L. Ligtenberg, Renske Olmer, Ronald van Eijk, Tamara Peelen, Hanne Meijers-Heijboer and Egbert Bakker and has published in prestigious journals such as Nature Genetics, Human Reproduction and Journal of Medical Genetics.

In The Last Decade

Marion Drüsedau

10 papers receiving 505 citations

Peers

Marion Drüsedau

GENET

PPCH

PFM

Alba Sanchis‐Juan United Kingdom

Ahlem Amouri Tunisia

Matthew Lubin United States

Gregor Schlüter Germany

Shiyue Mei China

Ariella Weinberg‐Shukron Israel

Keiji Hirabayashi Japan

Elisabeth Syk Lundberg Sweden

Hila Fridman Israel

Emilie Ait‐Yahya France

Alba Sanchis‐Juan United Kingdom

Marion Drüsedau

224 ×0.7

GENET

234 ×0.7

48 ×0.5

PPCH

49 ×0.6

28 ×0.4

PFM

Citations per year, relative to Marion Drüsedau Marion Drüsedau (= 1×) peers Alba Sanchis‐Juan

Countries citing papers authored by Marion Drüsedau

Since Specialization

Citations

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

Fields of papers citing papers by Marion Drüsedau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marion Drüsedau

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

Dijk, W. van, Marion Drüsedau, Jos Dreesen, et al.. (2024). O-270 Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing. Human Reproduction. 39(Supplement_1).

Derks, Kasper, Marion Drüsedau, J. Dreesen, et al.. (2022). Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing. Human Reproduction. 37(11). 2700–2708. 3 indexed citations

Esteki, Masoud Zamani, Cindy Melotte, Edith Coonen, et al.. (2019). Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies. Reproductive BioMedicine Online. 38. e11–e12. 1 indexed citations

Otten, Auke B.C., Suzanne C.E.H. Sallevelt, Phillippa J. Carling, et al.. (2018). Mutation-specific effects in germline transmission of pathogenic mtDNA variants. Human Reproduction. 33(7). 1331–1341. 38 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Marion Drüsedau, et al.. (2016). PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy. Human Reproduction. 32(3). 698–703. 16 indexed citations

Drüsedau, Marion, Jos Dreesen, I. A. P. Derks-Smeets, et al.. (2013). PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers. European Journal of Human Genetics. 21(12). 1361–1368. 16 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Marion Drüsedau, et al.. (2013). Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success. Journal of Medical Genetics. 50(2). 125–132. 63 indexed citations

Stevens, Servi J.C., J. Dreesen, Marion Drüsedau, et al.. (2012). SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations. European Journal of Human Genetics. 20(9). 938–944. 33 indexed citations

Dreesen, J., Marion Drüsedau, Hubert J.M. Smeets, et al.. (2008). Validation of preimplantation genetic diagnosis by PCR analysis: genotype comparison of the blastomere and corresponding embryo, implications for clinical practice. Molecular Human Reproduction. 14(10). 573–579. 17 indexed citations

10.

Drüsedau, Marion. (2003). Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)n repeat detection. Molecular Human Reproduction. 10(1). 71–75. 17 indexed citations

11.

Peelen, Tamara, Margreethe van Vliet, Ronald van Eijk, et al.. (1997). BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nature Genetics. 17(3). 341–345. 321 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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