Harma Feitsma

1.2k total citations
19 papers, 810 citations indexed

About

Harma Feitsma is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Harma Feitsma has authored 19 papers receiving a total of 810 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 4 papers in Genetics. Recurrent topics in Harma Feitsma's work include DNA Repair Mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Harma Feitsma is often cited by papers focused on DNA Repair Mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Harma Feitsma collaborates with scholars based in Netherlands, Finland and Germany. Harma Feitsma's co-authors include Edwin Cuppen, Frits Meijlink, Ewart de Bruijn, Isaäc J. Nijman, Sanne Kuijper, C.C.M. Kroon, Marcelo C. Leal, Rüdiger Schulz, Carolien Wansleeben and Jeroen Korving and has published in prestigious journals such as Nucleic Acids Research, Circulation and PLoS ONE.

In The Last Decade

Harma Feitsma

18 papers receiving 800 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Harma Feitsma Netherlands 11 578 209 152 94 89 19 810
Ben D. Cox United States 10 627 1.1× 176 0.8× 93 0.6× 60 0.6× 46 0.5× 12 776
Nannan Chang China 11 918 1.6× 154 0.7× 212 1.4× 124 1.3× 58 0.7× 15 1.1k
Greg Runke United States 9 596 1.0× 151 0.7× 136 0.9× 61 0.6× 48 0.5× 9 727
Nuno Miguel Luis France 13 442 0.8× 124 0.6× 108 0.7× 46 0.5× 46 0.5× 18 712
Antonella Galli United Kingdom 17 1.0k 1.8× 134 0.6× 232 1.5× 62 0.7× 48 0.5× 32 1.2k
Emily S. Noël Netherlands 12 716 1.2× 223 1.1× 84 0.6× 82 0.9× 85 1.0× 18 904
Odile Bronchain France 15 621 1.1× 125 0.6× 159 1.0× 35 0.4× 68 0.8× 28 778
Fatma O. Kok United States 9 711 1.2× 303 1.4× 129 0.8× 131 1.4× 29 0.3× 13 904
Jennifer N. Cech United States 10 892 1.5× 182 0.9× 201 1.3× 115 1.2× 85 1.0× 13 1.2k
Suk-Won Jin United States 13 456 0.8× 117 0.6× 90 0.6× 85 0.9× 40 0.4× 18 733

Countries citing papers authored by Harma Feitsma

Since Specialization
Citations

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

Fields of papers citing papers by Harma Feitsma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harma Feitsma

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

All Works

19 of 19 papers shown
1.
2.
Stelloo, Ellen, Ruud W. J. Meijers, Joost F. Swennenhuis, et al.. (2023). Formalin-Fixed, Paraffin-Embedded–Targeted Locus Capture. Journal of Molecular Diagnostics. 25(10). 758–770. 3 indexed citations
3.
Stelloo, Ellen, Miangela M. Laclé, Joost F. Swennenhuis, et al.. (2023). Comparison of NTRK fusion detection methods in microsatellite-instability-high metastatic colorectal cancer. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 482(6). 983–992. 8 indexed citations
4.
Zogchel, Lieke M. J. van, Ellen Stelloo, Joost F. Swennenhuis, et al.. (2023). Targeted locus amplification to develop robust patient-specific assays for liquid biopsies in pediatric solid tumors. Frontiers in Oncology. 13. 1124737–1124737. 2 indexed citations
5.
Kuiper, Roland P., Patricia G. Hoogeveen, Reno S. Bladergroen, et al.. (2021). Minimal residual disease (MRD) detection in acute lymphoblastic leukaemia based on fusion genes and genomic deletions: towards MRD for all. British Journal of Haematology. 194(5). 888–892. 5 indexed citations
6.
Feitsma, Harma, et al.. (2011). Protein biomarker enrichment by biomarker antibody complex elution for immunoassay biosensing. Biosensors and Bioelectronics. 29(1). 18–22. 3 indexed citations
7.
Wansleeben, Carolien, Léon van Gurp, Harma Feitsma, et al.. (2011). An ENU-Mutagenesis Screen in the Mouse: Identification of Novel Developmental Gene Functions. PLoS ONE. 6(4). e19357–e19357. 27 indexed citations
8.
Wansleeben, Carolien, Harma Feitsma, Mireille Montcouquiol, et al.. (2010). Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b. Development. 137(7). 1067–1073. 78 indexed citations
9.
Wansleeben, Carolien, Harma Feitsma, C.C.M. Kroon, et al.. (2010). A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction. The International Journal of Developmental Biology. 54(10). 1465–1470. 8 indexed citations
10.
Mokrý, Michal, Harma Feitsma, Isaäc J. Nijman, et al.. (2010). Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries. Nucleic Acids Research. 38(10). e116–e116. 67 indexed citations
11.
Bruijn, Ewart de, Edwin Cuppen, & Harma Feitsma. (2009). Highly Efficient ENU Mutagenesis in Zebrafish. Methods in molecular biology. 546. 3–12. 40 indexed citations
12.
Feitsma, Harma, Ewart de Bruijn, José van de Belt, Isaäc J. Nijman, & Edwin Cuppen. (2008). Mismatch repair deficiency does not enhance ENU mutagenesis in the zebrafish germ line. Mutagenesis. 23(4). 325–329. 8 indexed citations
13.
Leal, Marcelo C., Harma Feitsma, Edwin Cuppen, Luiz R. França, & Rüdiger Schulz. (2008). Completion of meiosis in male zebrafish (Danio rerio) despite lack of DNA mismatch repair gene mlh1. Cell and Tissue Research. 332(1). 133–139. 17 indexed citations
14.
Feitsma, Harma & Edwin Cuppen. (2008). Zebrafish as a Cancer Model. Molecular Cancer Research. 6(5). 685–694. 186 indexed citations
15.
Feitsma, Harma, Alper Akay, & Edwin Cuppen. (2008). Alkylation damage causes MMR-dependent chromosomal instability in vertebrate embryos. Nucleic Acids Research. 36(12). 4047–4056. 16 indexed citations
16.
Feitsma, Harma, Raoul Kuiper, Jeroen Korving, Isaäc J. Nijman, & Edwin Cuppen. (2008). Zebrafish with Mutations in Mismatch Repair Genes Develop Neurofibromas and Other Tumors. Cancer Research. 68(13). 5059–5066. 45 indexed citations
17.
Feitsma, Harma, Marcelo C. Leal, Peter B. Møens, Edwin Cuppen, & Rüdiger Schulz. (2007). Mlh1 Deficiency in Zebrafish Results in Male Sterility and Aneuploid as Well as Triploid Progeny in Females. Genetics. 175(4). 1561–1569. 66 indexed citations
18.
Blaschke, Rüdiger J., Nathan D. Hahurij, Sanne Kuijper, et al.. (2007). Targeted Mutation Reveals Essential Functions of the Homeodomain Transcription Factor Shox2 in Sinoatrial and Pacemaking Development. Circulation. 115(14). 1830–1838. 189 indexed citations
19.
Kuijper, Sanne, Harma Feitsma, Rushikesh Sheth, et al.. (2005). Function and regulation of Alx4 in limb development: Complex genetic interactions with Gli3 and Shh. Developmental Biology. 285(2). 533–544. 42 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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