Fré Arwert

4.7k total citations
65 papers, 3.7k citations indexed

About

Fré Arwert is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Fré Arwert has authored 65 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 19 papers in Genetics and 14 papers in Cancer Research. Recurrent topics in Fré Arwert's work include DNA Repair Mechanisms (43 papers), CRISPR and Genetic Engineering (16 papers) and Carcinogens and Genotoxicity Assessment (13 papers). Fré Arwert is often cited by papers focused on DNA Repair Mechanisms (43 papers), CRISPR and Genetic Engineering (16 papers) and Carcinogens and Genotoxicity Assessment (13 papers). Fré Arwert collaborates with scholars based in Netherlands, United States and United Kingdom. Fré Arwert's co-authors include Hans Joenje, Quinten Waisfisz, Johan P. de Winter, Martin A. Rooimans, Jan C. Pronk, Carola G.M. van Berkel, Christopher G. Mathew, Anneke B. Oostra, Manuel Buchwald and Aldur W. Eriksson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Fré Arwert

62 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fré Arwert Netherlands 28 3.3k 1.1k 889 465 405 65 3.7k
Anneke B. Oostra Netherlands 25 2.6k 0.8× 768 0.7× 632 0.7× 318 0.7× 389 1.0× 37 2.9k
Filippo Rosselli France 29 2.5k 0.8× 758 0.7× 364 0.4× 211 0.5× 712 1.8× 76 2.9k
Miria Stefanini Italy 42 4.8k 1.5× 1.3k 1.2× 868 1.0× 278 0.6× 717 1.8× 116 5.3k
Frédéric Coin France 36 3.8k 1.2× 733 0.7× 603 0.7× 157 0.3× 660 1.6× 65 4.1k
Maria Jasin United States 19 2.8k 0.9× 479 0.4× 860 1.0× 375 0.8× 720 1.8× 23 3.2k
Andrew J. Deans Australia 24 2.8k 0.9× 575 0.5× 447 0.5× 234 0.5× 684 1.7× 48 3.2k
Phillip B. Carpenter United States 23 3.6k 1.1× 610 0.5× 398 0.4× 213 0.5× 1.0k 2.6× 31 4.0k
Susan A. Harcourt United Kingdom 28 2.5k 0.8× 1.3k 1.2× 255 0.3× 247 0.5× 648 1.6× 37 3.2k
L A Donehower United States 24 3.0k 0.9× 585 0.5× 453 0.5× 217 0.5× 1.9k 4.6× 31 4.1k
N.C. Popescu United States 24 1.3k 0.4× 493 0.4× 515 0.6× 217 0.5× 426 1.1× 52 2.1k

Countries citing papers authored by Fré Arwert

Since Specialization
Citations

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

Fields of papers citing papers by Fré Arwert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fré Arwert

This figure shows the co-authorship network connecting the top 25 collaborators of Fré Arwert. A scholar is included among the top collaborators of Fré 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 Fré Arwert. Fré 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.
Barroca, Vilma, Marc‐André Mouthon, Daniel Lewandowski, et al.. (2011). Impaired functionality and homing of Fancg-deficient hematopoietic stem cells. Human Molecular Genetics. 21(1). 121–135. 18 indexed citations
2.
Sii-Felice, Karine, Etienne Olivier, Françoise Hoffschir, et al.. (2008). Fanconi DNA repair pathway is required for survival and long‐term maintenance of neural progenitors. The EMBO Journal. 27(5). 770–781. 41 indexed citations
3.
Godthelp, Barbara C., Paul P.W. van Buul, Nicolaas G.J. Jaspers, et al.. (2006). Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 601(1-2). 191–201. 38 indexed citations
4.
Levitus, Marieke, Quinten Waisfisz, Barbara C. Godthelp, et al.. (2005). The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nature Genetics. 37(9). 934–935. 338 indexed citations
5.
Yamada, Kaoru, Ali Ramezani, Robert G. Hawley, et al.. (2003). Phenotype correction of fanconi anemia group a hematopoietic stem cells using lentiviral vector. Molecular Therapy. 8(4). 600–610. 23 indexed citations
6.
Vrugt, Henri J. van de, Yne de Vries, Martin A. Rooimans, et al.. (2002). Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg. Genes to Cells. 7(3). 333–342. 16 indexed citations
7.
Blom, Eric, Henri J. van de Vrugt, Johan P. de Winter, Fré Arwert, & Hans Joenje. (2002). Evolutionary Clues to the Molecular Function of Fanconi Anemia Genes. Acta Haematologica. 108(4). 231–236. 13 indexed citations
8.
Winter, Johan P. de, France Léveillé, Carola G.M. van Berkel, et al.. (2000). Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene. The American Journal of Human Genetics. 67(5). 1306–1308. 175 indexed citations
9.
Waisfisz, Quinten, Çiğdem Altay, Peter A. J. Leegwater, et al.. (1999). The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p. The American Journal of Human Genetics. 64(5). 1400–1405. 41 indexed citations
10.
Waisfisz, Quinten, Neil V. Morgan, Michelangelo Savino, et al.. (1999). Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism. Nature Genetics. 22(4). 379–383. 153 indexed citations
11.
Abrahams, P. J., Ada Houweling, Paulien Cornelissen‐Steijger, et al.. (1998). Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromes. Mutation Research/DNA Repair. 407(2). 189–201. 19 indexed citations
12.
13.
Joenje, Hans, Anneke B. Oostra, Mario Wijker, et al.. (1997). Evidence for at Least Eight Fanconi Anemia Genes. The American Journal of Human Genetics. 61(4). 940–944. 238 indexed citations
14.
Foe, Jerome R. Lo Ten, et al.. (1996). Sequence variations in the Fanconi anaemia gene, FAC : pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant. Human Genetics. 98(5). 522–523. 18 indexed citations
15.
Foe, Jerome R. Lo Ten, Martin A. Rooimans, Hans Joenje, & Fré Arwert. (1996). Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia c gene,FAC. Human Mutation. 7(3). 264–265. 11 indexed citations
16.
Pronk, Jan C., Rachel A. Gibson, Anna Savoia, et al.. (1995). Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3. Nature Genetics. 11(3). 338–340. 78 indexed citations
17.
Li, Ning, et al.. (1993). Isolation and sequence analysis of variant forms of human transcobalamin II. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1172(1-2). 21–30. 53 indexed citations
18.
Bank, Ruud A., Ewald H. Hettema, Fré Arwert, Arie V. Nieuw Amerongen, & Jan C. Pronk. (1991). Electrophoretic characterization of posttranslational modifications of human parotid salivary α‐amylase. Electrophoresis. 12(1). 74–79. 26 indexed citations
19.
Groot, Peter C., Willem H. Mager, Niek V. Henriquez, et al.. (1990). Evolution of the human α-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossovers. Genomics. 8(1). 97–105. 25 indexed citations
20.
Groot, Peter C., Fré Arwert, Willem H. Mager, et al.. (1989). The human α-amylase multigene family consists of haplotypes with variable numbers of genes. Genomics. 5(1). 29–42. 72 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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