F. Arwert
Impact in
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
- Molecular Biology top 5%
- DNA Repair Mechanisms
- PI3K/AKT/mTOR signaling in cancer
- CRISPR and Genetic Engineering
Papers in
-
- DNA Repair Mechanisms 19
- DNA and Nucleic Acid Chemistry 5
- CRISPR and Genetic Engineering 5
- RNA and protein synthesis mechanisms 4
- Genetics 14
- Bacterial Genetics and Biotechnology 4
- Co-authors
- Hans Joenje (15 shared papers)Aldur W. Eriksson (7 shared papers)Leo P. de Waal (1 shared paper)G. G. de Lange (1 shared paper)J.P.W. van der Veen (1 shared paper)Th. M. Starink (1 shared paper)Gerard Venema (3 shared papers)Martin A. Rooimans (7 shared papers)
- Journals
- Human Genetics (7 papers)Neurology (2 papers)Annals of Neurology (2 papers)Clinical Genetics (2 papers)Scandinavian Journal of Clinical and Laboratory Investigation (2 papers)
- Partner nations
- NetherlandsUnited StatesPoland
In The Last Decade
F. Arwert
47 papers receiving 2.2k citations
F. Arwert's Hit Papers
Peers
Comparison fields: 5 of 103
- Cancer Research 428
- Molecular Biology 1.5k
- Otorhinolaryngology 75
- Genetics 518
- Neurology 238
Countries citing papers authored by F. Arwert
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
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-authors
The 25 scholars most cited alongside F. Arwert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Cowden syndrome: a clinical and genetic study in 21 patients Hit paper breakdown → | 1986 | 402 |
| 2 | Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. | 1997 | 159 |
| 3 | 1995 | 158 | |
| 4 | 1992 | 147 | |
| 5 | 1997 | 145 | |
| 6 | 1999 | 109 | |
| 7 | Integrated human papillomavirus type 16 and loss of heterozygosity at 11q22 and 18q21 in an oral carcinoma and its derivative cell line. | 1995 | 105 |
| 8 | 1996 | 95 | |
| 9 | 1985 | 94 | |
| 10 | 1973 | 81 | |
| 11 | 1985 | 67 | |
| 12 | 1984 | 58 | |
| 13 | 1998 | 46 | |
| 14 | 1997 | 44 | |
| 15 | 1979 | 44 | |
| 16 | 1987 | 39 | |
| 17 | 1999 | 35 | |
| 18 | Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase. | 1997 | 34 |
| 19 | 2000 | 31 | |
| 20 | 1984 | 31 |
About F. Arwert
F. Arwert is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Plant Science, having authored 48 papers that have together received 2.3k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (19 papers), Carcinogens and Genotoxicity Assessment (8 papers), Microtubule and mitosis dynamics (5 papers), DNA and Nucleic Acid Chemistry (5 papers), Chromosomal and Genetic Variations (5 papers), CRISPR and Genetic Engineering (5 papers), Bacterial Genetics and Biotechnology (4 papers) and RNA and protein synthesis mechanisms (4 papers). The work is most often cited by research in Cancer Research (428 citations), Molecular Biology (1.5k citations), Otorhinolaryngology (75 citations), Genetics (518 citations) and Neurology (238 citations). F. Arwert has collaborated with scholars based in Netherlands, United States and Poland. Frequent co-authors include Hans Joenje, Aldur W. Eriksson, Leo P. de Waal, G. G. de Lange, J.P.W. van der Veen, Th. M. Starink, Gerard Venema, Martin A. Rooimans, M. L. Kwee and Gerard Pals. Their work appears in journals such as Human Genetics, Neurology, Annals of Neurology, Clinical Genetics and Scandinavian Journal of Clinical and Laboratory Investigation.
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.