This map shows the geographic impact of M Vanrumbeke'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 M Vanrumbeke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Vanrumbeke more than expected).
This network shows the impact of papers produced by M Vanrumbeke. 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 M Vanrumbeke. The network helps show where M Vanrumbeke may publish in the future.
Co-authorship network of co-authors of M Vanrumbeke
This figure shows the co-authorship network connecting the top 25 collaborators of M Vanrumbeke.
A scholar is included among the top collaborators of M Vanrumbeke 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 M Vanrumbeke. M Vanrumbeke is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Wattel, Eric, M Vanrumbeke, Nathalie Cambier, et al.. (1996). Differential efficacy of adenoviral mediated gene transfer into cells from hematological cell lines and fresh hematological malignancies.. PubMed. 10(1). 171–4.47 indexed citations
Laï, JL, Claude Preudhomme, Marc Zandecki, et al.. (1995). Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations.. PubMed. 9(3). 370–81.141 indexed citations
Quesnel, Bruno, Claude Preudhomme, M Vanrumbeke, et al.. (1994). Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia.. PubMed. 8(5). 878–80.12 indexed citations
12.
Preudhomme, Claude, Richard Lubin, Pascale Lepelley, M Vanrumbeke, & Pierre Fenaux. (1994). Detection of serum anti p53 antibodies and their correlation with p53 mutations in myelodysplastic syndromes and acute myeloid leukemia.. PubMed. 8(9). 1589–91.21 indexed citations
Lepelley, Pascale, Claude Preudhomme, M Vanrumbeke, et al.. (1994). Detection of p53 mutations in hematological malignancies: comparison between immunocytochemistry and DNA analysis.. PubMed. 8(8). 1342–9.68 indexed citations
15.
Fenaux, Pierre, Claude Preudhomme, JL Laï, et al.. (1992). Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis.. PubMed. 6(4). 246–50.122 indexed citations
Fenaux, Pierre, P Jonveaux, I. Quiquandon, et al.. (1992). Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases.. PubMed. 6(1). 42–6.49 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.