Beatrice Renault

3.0k total citations · 1 hit paper
22 papers, 2.3k citations indexed

About

Beatrice Renault is a scholar working on Oncology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Beatrice Renault has authored 22 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Oncology, 8 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Beatrice Renault's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and Cancer-related Molecular Pathways (4 papers). Beatrice Renault is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (5 papers) and Cancer-related Molecular Pathways (4 papers). Beatrice Renault collaborates with scholars based in United States, Italy and Netherlands. Beatrice Renault's co-authors include Guglielmina Nadia Ranzani, Raju Kucherlapati, Natalia S. Pellegata, Riccardo Fodde, Enrico Solcia, Janine LeBlanc-Straceski, David M. Grayzel, David R. Bachinsky, Tatjana Levi and Craig T. Basson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Genetics.

In The Last Decade

Beatrice Renault

22 papers receiving 2.2k citations

Hit Papers

Mutations in human cause limb and cardiac malformation in... 1997 2026 2006 2016 1997 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
    1997 787 citations Craig T. Basson, David R. Bachinsky et al. Nature Genetics profile →

Peers

Beatrice Renault
Kevin Barton United States
J. Schütte Germany
Hui C. Tsou United States
Jene Choi South Korea
Janet M. Cowan United States
Isamu Nishisho Japan
Sylvain Fisson France
Suzanne Jordan United Kingdom
Kenji Okami Japan
Ken Yagi Japan
Kevin Barton United States
Beatrice Renault
Citations per year, relative to Beatrice Renault Beatrice Renault (= 1×) peers Kevin Barton

Countries citing papers authored by Beatrice Renault

Since Specialization
Citations

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

Fields of papers citing papers by Beatrice Renault

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beatrice Renault

This figure shows the co-authorship network connecting the top 25 collaborators of Beatrice Renault. A scholar is included among the top collaborators of Beatrice Renault 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 Beatrice Renault. Beatrice Renault 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.
Bala, Shashi, George R. Oliver, Beatrice Renault, et al.. (2000). Genetic analysis of theAPAF1 gene in male germ cell tumors. Genes Chromosomes and Cancer. 28(3). 258–268. 20 indexed citations
2.
Murty, Vundavalli V., Kate Montgomery, Shashi Bala, et al.. (1999). A 3-Mb High-Resolution BAC/PAC Contig of 12q22 Encompassing the 830-kb Consensus Minimal Deletion in Male Germ Cell Tumors. Genome Research. 9(7). 662–671. 17 indexed citations
3.
Renault, Beatrice & Karen Birmingham. (1999). Call to buy nevirapine for developing countries. Nature Medicine. 5(10). 1093–1093. 2 indexed citations
4.
Pasche, Boris, Yan Luo, Pulivarthi H. Rao, et al.. (1998). Type I transforming growth factor beta receptor maps to 9q22 and exhibits a polymorphism and a rare variant within a polyalanine tract.. PubMed. 58(13). 2727–32. 77 indexed citations
5.
Basson, Craig T., David R. Bachinsky, Robert C. Lin, et al.. (1997). Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome. Nature Genetics. 15(1). 30–35. 787 indexed citations breakdown →
6.
Renault, Beatrice, Alain Hovnanian, S Bryce, et al.. (1997). A Sequence-Ready Physical Map of a Region of 12q24.1. Genomics. 45(2). 271–278. 7 indexed citations
7.
Amadori, Dino, Marco Maltoni, Annalisa Volpi, et al.. (1997). Gene amplification and proliferative kinetics in relation to prognosis of patients with gastric carcinoma. Cancer. 79(2). 226–232. 24 indexed citations
8.
9.
Barnes, Kathleen C., John D. Neely, David L. Duffy, et al.. (1996). Linkage of Asthma and Total Serum IgE Concentration to Markers on Chromosome 12q: Evidence from Afro-Caribbean and Caucasian Populations. Genomics. 37(1). 41–50. 174 indexed citations
10.
11.
Renault, Beatrice, et al.. (1996). Microsatellite instability and mutations of p53 and TGF-‚ RII genes in gastric cancer. Human Genetics. 98(5). 601–607. 70 indexed citations
12.
Marondel, Ivonne, et al.. (1996). Physical Mapping of the Human Neurotensin Gene (NTS) between Markers D12S1444 and D12S81 on Chromosome 12q21. Genomics. 38(2). 243–245. 9 indexed citations
13.
14.
Miller, Perry L., P. Nadkarni, Kenneth K. Kídd, et al.. (1995). Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12. Journal of the American Medical Informatics Association. 2(6). 351–364. 11 indexed citations
15.
Ranzani, Guglielmina Nadia, Ombretta Luinetti, Daniele Calistri, et al.. (1995). p53 gene mutations and protein nuclear accumulation are early events in intestinal type gastric cancer but late events in diffuse type.. PubMed. 4(3). 223–31. 91 indexed citations
16.
Pellegata, Natalia S., Fausto Sessa, Beatrice Renault, et al.. (1994). K-ras and p53 gene mutations in pancreatic cancer: ductal and nonductal tumors progress through different genetic lesions.. PubMed. 54(6). 1556–60. 334 indexed citations
17.
Ranzani, Guglielmina Nadia, Beatrice Renault, Natalia S. Pellegata, et al.. (1993). Loss of heterozygosity and K-ras gene mutations in gastric cancer. Human Genetics. 92(3). 244–9. 47 indexed citations
18.
Renault, Beatrice, Marcel van den Broek, Riccardo Fodde, et al.. (1993). Base transitions are the most frequent genetic changes at P53 in gastric cancer.. PubMed. 53(11). 2614–7. 97 indexed citations
19.
Renault, Beatrice, et al.. (1993). Sites and types of p53 mutations in an unselected series of colorectal cancers in The Netherlands.. PubMed. 13(3). 587–92. 6 indexed citations
20.
Gaetani, Paolo, et al.. (1990). High-dose methylprednisolone and 'ex vivo' release of eicosanoids after experimental subarachnoid haemorrhage. Neurological Research. 12(2). 111–116. 13 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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