F. Arwert

3.2k total citations
47 papers, 2.2k citations indexed

About

F. Arwert is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, F. Arwert has authored 47 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Cancer Research. Recurrent topics in F. Arwert's work include DNA Repair Mechanisms (19 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Microtubule and mitosis dynamics (5 papers). F. Arwert is often cited by papers focused on DNA Repair Mechanisms (19 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Microtubule and mitosis dynamics (5 papers). F. Arwert collaborates with scholars based in Netherlands, United States and France. F. Arwert's co-authors include Hans Joenje, Aldur W. Eriksson, Gilles Thomas, G. G. de Lange, J.P.W. van der Veen, Th. M. Starink, Leo P. de Waal, Gerard Venema, Gerard Pals and J.W.I.M. Simons and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Neurology.

In The Last Decade

F. Arwert

46 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F. Arwert Netherlands 25 1.5k 519 425 299 251 47 2.2k
Jan C. Pronk Netherlands 31 3.4k 2.3× 553 1.1× 644 1.5× 217 0.7× 131 0.5× 77 4.1k
Claude Gazin France 11 2.2k 1.5× 325 0.6× 294 0.7× 252 0.8× 105 0.4× 13 2.9k
Sandra Schneider Germany 22 1.1k 0.8× 394 0.8× 361 0.8× 269 0.9× 162 0.6× 40 1.9k
Yael Bernstein Israel 20 1.6k 1.1× 189 0.4× 325 0.8× 377 1.3× 123 0.5× 27 2.6k
Ayelet Erez United States 31 1.6k 1.1× 705 1.4× 796 1.9× 244 0.8× 230 0.9× 60 3.0k
Kazue Hattori United States 10 2.3k 1.6× 462 0.9× 463 1.1× 585 2.0× 49 0.2× 13 3.2k
M.G. Byers United States 30 2.1k 1.5× 732 1.4× 349 0.8× 453 1.5× 52 0.2× 54 3.6k
Motoko Unoki Japan 29 2.8k 1.9× 395 0.8× 468 1.1× 319 1.1× 144 0.6× 51 3.4k
R. E. K. Fournier United States 34 3.0k 2.1× 1.2k 2.3× 301 0.7× 310 1.0× 102 0.4× 91 3.9k
Giuseppe Raschellà Italy 29 1.8k 1.2× 238 0.5× 660 1.6× 681 2.3× 670 2.7× 68 2.7k

Countries citing papers authored by F. Arwert

Since Specialization
Citations

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

Fields of papers citing papers by F. Arwert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Arwert

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

All Works

20 of 20 papers shown
1.
Vrugt, Henri J. van de, Ngan Ching Cheng, Yne de Vries, et al.. (2000). Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary. Mammalian Genome. 11(4). 326–331. 29 indexed citations
2.
Limburg, M., et al.. (1998). The role of type III collagen in spontaneous cervical arterial dissections. Annals of Neurology. 43(4). 494–498. 39 indexed citations
3.
Foe, Jerome R. Lo Ten, M. L. Kwee, Anneke B. Oostra, et al.. (1997). Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.. PubMed. 5(3). 137–48. 149 indexed citations
4.
Savoia, Anna, Maria Rosaria Piemontese, Michelangelo Savino, et al.. (1996). Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene. Human Genetics. 99(1). 93–97. 8 indexed citations
5.
Wijker, Mario, Zbigniew K. Wszołek, Martin A. Rooimans, et al.. (1996). Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21. Human Molecular Genetics. 5(1). 151–154. 88 indexed citations
6.
Kwee, M. L., Jerome R. Lo Ten Foe, F. Arwert, et al.. (1996). EARLY PRENATAL DIAGNOSIS OF FANCONI ANAEMIA IN A TWIN PREGNANCY, USING DNA ANALYSIS. Prenatal Diagnosis. 16(4). 345–348. 7 indexed citations
7.
Pals, Gerard, J. Défize, Jan Paul Bebelman, et al.. (1995). Transcription Regulation of Human and Porcine Pepsinogen A. Advances in experimental medicine and biology. 362. 67–75. 3 indexed citations
8.
Rooimans, Martin A., et al.. (1993). Genetic diversity of mitomycin C-hypersensitive Chinese hamster cell mutants: A new complementation group with chromosomal instability. Somatic Cell and Molecular Genetics. 19(5). 431–437. 29 indexed citations
9.
Wszołek, Zbigniew K., Ronald F. Pfeiffer, Mohit Bhatt, et al.. (1992). Rapidly progressive autosomal dominant parkinsonism and dementia with pallido‐ponto‐nigral degeneration. Annals of Neurology. 32(3). 312–320. 138 indexed citations
10.
Bebelman, Jan Paul, Gerard Pals, F. Arwert, et al.. (1991). Analysis of the Promoter of a Human Pepsinogen a Gene. Advances in experimental medicine and biology. 306. 87–90. 4 indexed citations
11.
Arwert, F., Martin A. Rooimans, A. Westerveld, J.W.I.M. Simons, & M.Z. Zdzienicka. (1991). The Chinese hamster cell mutant V-H4 is homologous to Fanconi anemia (complementation group A). Cytogenetic and Genome Research. 56(1). 23–26. 17 indexed citations
12.
Arwert, F., et al.. (1990). Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossovers. UCL Discovery (University College London). 8 indexed citations
13.
Zdzienicka, M.Z., et al.. (1990). The Chinese hamster V79 cell mutant V-H4 is phenotypically like Fanconi anemia cells. Somatic Cell and Molecular Genetics. 16(6). 575–581. 26 indexed citations
14.
Thomas, Gilles, Erik Mullaart, Jan Vijg, et al.. (1989). Chromosomal instability in an oxygen-tolerant variant of Chinese hamster ovary cells. Mutation Research/DNAging. 219(1). 17–28. 24 indexed citations
15.
Lindemans, Jan, J. Van Kapel, F. Arwert, & J. Abels. (1988). Separation of transcobalamin II isoproteins by means of chromatofocusing. Journal of Chromatography B Biomedical Sciences and Applications. 432. 103–111. 2 indexed citations
16.
Lafleur, M.V.M., et al.. (1987). Dna Damage by Chemically Generated Singlet Oxygen. Free Radical Research Communications. 2(4-6). 343–350. 36 indexed citations
17.
Starink, Th. M., J.P.W. van der Veen, F. Arwert, et al.. (1986). The Cowden syndrome: a clinical and genetic study in 21 patients. Clinical Genetics. 29(3). 222–233. 371 indexed citations
18.
Zelle, B., Ad Geurts van Kessel, Jan de Wit, et al.. (1985). Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11. Human Genetics. 70(4). 337–340. 25 indexed citations
19.
Nieuwint, Aggie, et al.. (1985). Inability of Chemically Generated Singlet Oxygen to Break the DNA Backbone. Free Radical Research Communications. 1(1). 1–9. 66 indexed citations
20.
Arwert, F., Gunnar Bjursell, & Lars Rutberg. (1976). Induction of prophage SPO2 in Bacillus subtilis: isolation of excised prophage DNA as a covently closed circle. Journal of Virology. 17(2). 492–502. 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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