Willem Van de Ven

1.0k total citations
14 papers, 808 citations indexed

About

Willem Van de Ven is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Willem Van de Ven has authored 14 papers receiving a total of 808 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Pulmonary and Respiratory Medicine and 4 papers in Rheumatology. Recurrent topics in Willem Van de Ven's work include Sarcoma Diagnosis and Treatment (4 papers), Soft tissue tumor case studies (4 papers) and Tumors and Oncological Cases (3 papers). Willem Van de Ven is often cited by papers focused on Sarcoma Diagnosis and Treatment (4 papers), Soft tissue tumor case studies (4 papers) and Tumors and Oncological Cases (3 papers). Willem Van de Ven collaborates with scholars based in Belgium, Germany and United States. Willem Van de Ven's co-authors include Nils Mandahl, Bernd Kazmierczak, Sylke Wanschura, Herman Van den Berghe, Paola Dal Cin, Roberta Vanni, Juan Rosaí, Helena Willén, Felix Mitelman and Anders Rydholm and has published in prestigious journals such as Human Genetics, Histochemistry and Cell Biology and Genes Chromosomes and Cancer.

In The Last Decade

Willem Van de Ven

14 papers receiving 788 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Willem Van de Ven Belgium	11	304	277	175	175	157	14	808
C Mainguené France	14	356 1.2×	183 0.7×	169 1.0×	141 0.8×	166 1.1×	37	698
J. Bullerdiek Germany	22	367 1.2×	656 2.4×	254 1.5×	114 0.7×	216 1.4×	63	1.5k
Noriko Kato Japan	21	150 0.5×	485 1.8×	230 1.3×	63 0.4×	110 0.7×	64	1.3k
Mitsuhiko Kitaoka Japan	14	377 1.2×	297 1.1×	87 0.5×	130 0.7×	21 0.1×	35	922
Amanda J. Murphy Canada	14	182 0.6×	212 0.8×	156 0.9×	40 0.2×	32 0.2×	20	773
Brendan A.S. McIntyre Canada	18	192 0.6×	335 1.2×	84 0.5×	37 0.2×	42 0.3×	29	808
Deepali Jain India	13	121 0.4×	236 0.9×	77 0.4×	32 0.2×	49 0.3×	31	700
Nicolette S. den Hollander Netherlands	21	71 0.2×	510 1.8×	104 0.6×	61 0.3×	98 0.6×	43	1.6k
G. Petur Nielsen United States	17	294 1.0×	260 0.9×	201 1.1×	107 0.6×	53 0.3×	24	731
Anna P. Lam United States	13	428 1.4×	526 1.9×	71 0.4×	31 0.2×	171 1.1×	19	1.0k

Countries citing papers authored by Willem Van de Ven

Since Specialization

Citations

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

Fields of papers citing papers by Willem Van de Ven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Willem Van de Ven. 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 Willem Van de Ven. The network helps show where Willem Van de Ven may publish in the future.

Co-authorship network of co-authors of Willem Van de Ven

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

All Works

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14 of 14 papers shown

Esch, Hilde Van, C. Huysmans, Luc De Smet, et al.. (2005). Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD). European Journal of Medical Genetics. 48(4). 377–387. 35 indexed citations

Peeters, Hilde, Philippe Debeer, Amos Bairoch, et al.. (2003). PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse. Human Genetics. 112(5-6). 573–580. 98 indexed citations

Peeters, Hilde, Peter Groenen, Hilde Van Esch, et al.. (2001). Recurrent involvement of chromosomal region 6q21 in heterotaxy. American Journal of Medical Genetics. 103(1). 44–47. 8 indexed citations

Åström, Anna-Karin, Marianne L. Voz, Koen Kas, et al.. (1999). Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities: identification of SII as a new fusion partner gene.. PubMed. 59(4). 918–23. 132 indexed citations

Devriendt, Koenraad, Peter Groenen, Hilde Van Esch, et al.. (1998). Vesico-ureteral reflux: a genetic condition?. European Journal of Pediatrics. 157(4). 265–271. 28 indexed citations

Röijer, E., et al.. (1997). Mapping of the 8q 12 translocation breakpoint to a 40-kb region in a pleomorphic adenoma with an ins(8;3)(q12;p21.3p14.1). Cytogenetic and Genome Research. 76(1-2). 23–26. 4 indexed citations

Senden, Nicole H. M., Erika Timmer, Helgi van de Velde, et al.. (1997). Neuroendocrine-specific protein (NSP)-reticulons as independent markers for non-small cell lung cancer with neuroendocrine differentiation. Histochemistry and Cell Biology. 108(2). 155–165. 17 indexed citations

FLETCHER, C.D.M., Måns Åkerman, Paola Dal Cin, et al.. (1996). Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.. PubMed. 148(2). 623–30. 269 indexed citations

Kazmierczak, Bernd, et al.. (1995). Involvement of the MAR region in two rare benign mesenchymal tumors: A hamartoma of the breast and an aggressive angiomyxoma. Cancer Genetics and Cytogenetics. 84(2). 148–148. 3 indexed citations

10.

Wanschura, Sylke, Bernd Kazmierczak, Eric Schoenmakers, et al.. (1995). Regional fine mapping of the multiple‐aberration region involved in uterine leiomyoma, lipoma, and pleomorphic adenoma of the salivary gland to 12q15. Genes Chromosomes and Cancer. 14(1). 68–70. 36 indexed citations

11.

Kazmierczak, Bernd, Sylke Wanschura, Kerstin Meyer‐Bolte, et al.. (1995). Cytogenic and molecular analysis of an aggressive angiomyxoma.. PubMed. 147(3). 580–5. 54 indexed citations

12.

Cin, Paola Dal, Roberta Vanni, Susanna Marras, et al.. (1995). Four cytogenetic subgroups can be identified in endometrial polyps. Cancer Genetics and Cytogenetics. 84(2). 153–153. 26 indexed citations

13.

Kazmierczak, Bernd, Yvonne Hennig, Sylke Wanschura, et al.. (1995). Description of a novel fusion transcript between HMGI-C, a gene encoding for a member of the high mobility group proteins, and the mitochondrial aldehyde dehydrogenase gene.. PubMed. 55(24). 6038–9. 70 indexed citations

14.

Ven, Willem Van de, et al.. (1993). Detection of mucosal immune responses in chickens after immunization or infection. Veterinary Immunology and Immunopathology. 36(3). 281–291. 28 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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