Freek Manders

1.6k total citations
14 papers, 202 citations indexed

About

Freek Manders is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, Freek Manders has authored 14 papers receiving a total of 202 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Cancer Research and 4 papers in Hematology. Recurrent topics in Freek Manders's work include Cancer Genomics and Diagnostics (11 papers), Acute Myeloid Leukemia Research (4 papers) and CRISPR and Genetic Engineering (3 papers). Freek Manders is often cited by papers focused on Cancer Genomics and Diagnostics (11 papers), Acute Myeloid Leukemia Research (4 papers) and CRISPR and Genetic Engineering (3 papers). Freek Manders collaborates with scholars based in Netherlands, Switzerland and Germany. Freek Manders's co-authors include Ruben van Boxtel, Mark Verheul, Rurika Oka, Markus J. van Roosmalen, Arianne M. Brandsma, Jurrian K. de Kanter, Edwin Cuppen, Arne van Hoeck, Bastiaan van der Roest and Sjors Middelkamp and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Scientific Reports.

In The Last Decade

Freek Manders

13 papers receiving 201 citations

Peers

Freek Manders

ONCOL

PFM

HEMAT

T. Peretz Israel

Nozomi Yachida Japan

Marta Llop Spain

Nicholas Hickson United Kingdom

Manon Ouimet Canada

Lenka Stolařová Czechia

Alexandra Clipson United Kingdom

Jelle ten Hoeve Netherlands

Jeremy B. Samon United States

Cecelia Miller United States

T. Peretz Israel

Freek Manders

122 ×1.0

76 ×0.7

67 ×1.5

ONCOL

66 ×1.7

PFM

78 ×2.2

HEMAT

Citations per year, relative to Freek Manders Freek Manders (= 1×) peers T. Peretz

Countries citing papers authored by Freek Manders

Since Specialization

Citations

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

Fields of papers citing papers by Freek Manders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Freek Manders

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

All Works

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14 of 14 papers shown

Tsaalbi‐Shtylik, Anastasia, Rurika Oka, Freek Manders, et al.. (2024). DNA mismatch repair controls the mutagenicity of Polymerase ζ-dependent translesion synthesis at methylated guanines. DNA repair. 142. 103755–103755. 2 indexed citations

Wang, Cheng, Freek Manders, Laszlo Groh, Roel Oldenkamp, & Colin Logie. (2023). Corticosteroid‐induced chromatin loop dynamics at the FKBP5 gene. Annals of the New York Academy of Sciences. 1529(1). 109–119.

Middelkamp, Sjors, Freek Manders, Markus J. van Roosmalen, et al.. (2023). Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox. Cell Genomics. 3(9). 100389–100389. 7 indexed citations

Manders, Freek, et al.. (2022). Mutation accumulation in mtDNA of cancers resembles mutagenesis in normal stem cells. iScience. 25(12). 105610–105610. 1 indexed citations

Manders, Freek, Arianne M. Brandsma, Jurrian K. de Kanter, et al.. (2022). MutationalPatterns: the one stop shop for the analysis of mutational processes. BMC Genomics. 23(1). 134–134. 88 indexed citations

Manders, Freek, Mark Verheul, Markus J. van Roosmalen, et al.. (2022). Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo. iScience. 25(2). 103736–103736. 7 indexed citations

Yu, Yun, Freek Manders, Guy C. M. Grinwis, Martien A. M. Groenen, & R.P.M.A. Crooijmans. (2022). A recurrent somatic missense mutation in GNAS gene identified in familial thyroid follicular cell carcinomas in German longhaired pointer dogs. BMC Genomics. 23(1). 669–669. 1 indexed citations

Middelkamp, Sjors, Freek Manders, Arianne M. Brandsma, et al.. (2022). Retrospective Lineage Tracing of Pediatric Acute Myeloid Leukemia Using Single-Cell Whole Genome Sequencing. Blood. 140(Supplement 1). 8725–8726. 1 indexed citations

Brandsma, Arianne M., Markus J. van Roosmalen, Rurika Oka, et al.. (2021). Mutation Signatures of Pediatric Acute Myeloid Leukemia and Normal Blood Progenitors Associated with Differential Patient Outcomes. Blood Cancer Discovery. 2(5). 484–499. 18 indexed citations

10.

Manders, Freek, Ruben van Boxtel, & Sjors Middelkamp. (2021). The Dynamics of Somatic Mutagenesis During Life in Humans. SHILAP Revista de lepidopterología. 2. 802407–802407. 19 indexed citations

11.

Manders, Freek, et al.. (2021). Increased risk of leukaemia in children with Down syndrome: a somatic evolutionary view. Expert Reviews in Molecular Medicine. 23. e5–e5. 8 indexed citations

12.

Kanter, Jurrian K. de, Axel Rosendahl Huber, Markus J. van Roosmalen, et al.. (2021). Antiviral treatment causes a unique mutational signature in cancers of transplantation recipients. Cell stem cell. 28(10). 1726–1739.e6. 23 indexed citations

13.

Manders, Freek, Marie‐Louise van der Hoorn, Mark Verheul, et al.. (2020). Mutation accumulation and developmental lineages in normal and Down syndrome human fetal haematopoiesis. Scientific Reports. 10(1). 12991–12991. 22 indexed citations

14.

Huber, Axel Rosendahl, Freek Manders, Rurika Oka, & Ruben van Boxtel. (2019). Characterizing Mutational Load and Clonal Composition of Human Blood. Journal of Visualized Experiments. 5 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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