Daniëlle Bodmer

2.3k total citations · 1 hit paper
21 papers, 1.2k citations indexed

About

Daniëlle Bodmer is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Daniëlle Bodmer has authored 21 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Pulmonary and Respiratory Medicine and 11 papers in Cancer Research. Recurrent topics in Daniëlle Bodmer's work include Renal cell carcinoma treatment (12 papers), Renal and related cancers (11 papers) and Cancer Genomics and Diagnostics (11 papers). Daniëlle Bodmer is often cited by papers focused on Renal cell carcinoma treatment (12 papers), Renal and related cancers (11 papers) and Cancer Genomics and Diagnostics (11 papers). Daniëlle Bodmer collaborates with scholars based in Netherlands, Australia and Croatia. Daniëlle Bodmer's co-authors include Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, Ad Geurts van Kessel, J. Han van Krieken, Han G. Brunner, Konnie M. Hebeda, Monique Goossens, Roland P. Kuiper, Tsun Leung Chan and Suet Yi Leung and has published in prestigious journals such as Nature Genetics, JNCI Journal of the National Cancer Institute and Kidney International.

In The Last Decade

Daniëlle Bodmer

21 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

2008 546 citations Marjolijn J. L. Ligtenberg, Roland P. Kuiper et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniëlle Bodmer Netherlands	14	599	522	485	437	263	21	1.2k
Anna‐Maria Björkqvist Finland	6	377 0.6×	472 0.9×	272 0.6×	310 0.7×	143 0.5×	10	973
Nils Rahner Germany	17	658 1.1×	310 0.6×	331 0.7×	445 1.0×	86 0.3×	35	1.0k
Viviana Gismondi Italy	17	692 1.2×	297 0.6×	253 0.5×	472 1.1×	132 0.5×	45	1.0k
Erin Salo‐Mullen United States	15	355 0.6×	331 0.6×	588 1.2×	886 2.0×	151 0.6×	44	1.3k
Stéphanie Baert‐Desurmont France	15	376 0.6×	596 1.1×	421 0.9×	419 1.0×	115 0.4×	38	1.2k
Denisa Ilenčíková Slovakia	15	438 0.7×	301 0.6×	257 0.5×	227 0.5×	96 0.4×	40	851
T Aoki Japan	7	389 0.6×	298 0.6×	267 0.6×	546 1.2×	123 0.5×	7	821
Anke Schwendel Germany	12	166 0.3×	553 1.1×	301 0.6×	343 0.8×	115 0.4×	21	1.0k
Marjo van Puijenbroek Netherlands	22	878 1.5×	359 0.7×	479 1.0×	814 1.9×	67 0.3×	33	1.4k
Barbro Werelius Sweden	15	514 0.9×	444 0.9×	299 0.6×	519 1.2×	37 0.1×	23	1.1k

Countries citing papers authored by Daniëlle Bodmer

Since Specialization

Citations

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

Fields of papers citing papers by Daniëlle Bodmer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniëlle Bodmer

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

Baas, Annette F., Michael T. Gabbett, Martine Raphaël, et al.. (2012). Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome. European Journal of Human Genetics. 21(1). 55–61. 34 indexed citations

Manders, Peggy, Liesbeth Spruijt, C. Marleen Kets, et al.. (2011). Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. European Journal of Cancer. 47(9). 1407–1413. 11 indexed citations

Post, Rachel S. van der, Lambertus A. Kiemeney, Marjolijn J. L. Ligtenberg, et al.. (2010). Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers. Journal of Medical Genetics. 47(7). 464–470. 137 indexed citations

Vermeer, Sascha, Rowdy Meijer, Tom Hofste, et al.. (2009). Design and Validation of a Conformation Sensitive Capillary Electrophoresis-Based Mutation Scanning System and Automated Data Analysis of the More than 15 kbp-Spanning Coding Sequence of the SACS Gene. Journal of Molecular Diagnostics. 11(6). 514–523. 6 indexed citations

Ligtenberg, Marjolijn J. L., Roland P. Kuiper, Tsun Leung Chan, et al.. (2008). Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1. Nature Genetics. 41(1). 112–117. 546 indexed citations breakdown →

Overbeek, Lucy, C. Marleen Kets, Konnie M. Hebeda, et al.. (2007). Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer. British Journal of Cancer. 96(10). 1605–1612. 40 indexed citations

Vreede, Lilian, Roland P. Kuiper, Daniëlle Bodmer, et al.. (2007). Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene. Cancer Genetics and Cytogenetics. 179(1). 11–18. 17 indexed citations

Kets, Carolien M., Nicoline Hoogerbrugge, Daniëlle Bodmer, et al.. (2006). Unfavorable pathological characteristics in familial colorectal cancer with low-level microsatellite instability. Modern Pathology. 19(12). 1624–1630. 10 indexed citations

Bodmer, Daniëlle, et al.. (2006). Optimal selection for BRCA1 and BRCA2 mutation testing using a combination of ‘easy to apply’ probability models. British Journal of Cancer. 95(6). 757–762. 10 indexed citations

10.

Bodmer, Daniëlle, et al.. (2004). Chromosome 3 Translocations and Familial Renal Cell Cancer. Current Molecular Medicine. 4(8). 849–854. 20 indexed citations

11.

Bodmer, Daniëlle, Marga Schepens, Marc J. Eleveld, Eric Schoenmakers, & Ad Geurts van Kessel. (2003). Disruption of a novel gene, DIRC3, and expression of DIRC3‐HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21). Genes Chromosomes and Cancer. 38(2). 107–116. 40 indexed citations

12.

Bodmer, Daniëlle. (2002). Understanding familial and nonfamilial renal cell cancer. Human Molecular Genetics. 20. 2489–2498. 4 indexed citations

13.

Bodmer, Daniëlle. (2002). Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21). Human Molecular Genetics. 11(6). 641–649. 36 indexed citations

14.

Bodmer, Daniëlle, Marc J. Eleveld, Marjolijn J. L. Ligtenberg, et al.. (2002). Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21). Cancer Genetics and Cytogenetics. 134(1). 6–12. 16 indexed citations

15.

Bodmer, Daniëlle, Irene M. Janssen, Yvonne M.H. Versleijen‐Jonkers, et al.. (2002). Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13∼q22 breakpoints. Cancer Genetics and Cytogenetics. 136(2). 95–100. 6 indexed citations

16.

Bodmer, Daniëlle. (2002). Understanding familial and non-familial renal cell cancer. Human Molecular Genetics. 11(20). 2489–2498. 61 indexed citations

17.

Eleveld, Marc J., Daniëlle Bodmer, Gerard Merkx, et al.. (2001). Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15). Genes Chromosomes and Cancer. 31(1). 23–32. 29 indexed citations

18.

Kessel, Ad Geurts van, Hanneke A. H. Wijnhoven, Daniëlle Bodmer, et al.. (1999). Renal Cell Cancer: Chromosome 3 Translocations as Risk Factors. JNCI Journal of the National Cancer Institute. 91(13). 1159–1160. 43 indexed citations

19.

Koolen, M. I., Daniëlle Bodmer, Marc J. Eleveld, et al.. (1998). A familial case of renal cell carcinoma and a t(2;3) chromosome translocation. Kidney International. 53(2). 273–275. 37 indexed citations

20.

Bodmer, Daniëlle, Marc J. Eleveld, Marjolijn J. L. Ligtenberg, et al.. (1998). An Alternative Route for Multistep Tumorigenesis in a Novel Case of Hereditary Renal Cell Cancer and a t(2;3)(q35;q21) Chromosome Translocation. The American Journal of Human Genetics. 62(6). 1475–1483. 58 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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