Bernard Peers

4.2k total citations
58 papers, 3.0k citations indexed

About

Bernard Peers is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Bernard Peers has authored 58 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 34 papers in Surgery and 21 papers in Genetics. Recurrent topics in Bernard Peers's work include Pancreatic function and diabetes (34 papers), Congenital heart defects research (17 papers) and Zebrafish Biomedical Research Applications (12 papers). Bernard Peers is often cited by papers focused on Pancreatic function and diabetes (34 papers), Congenital heart defects research (17 papers) and Zebrafish Biomedical Research Applications (12 papers). Bernard Peers collaborates with scholars based in Belgium, United Kingdom and United States. Bernard Peers's co-authors include Marc Montminy, Joseph Martial, Marianne L. Voz, Frédéric Biemar, James Leonard, Ted W. Johnson, Alexandra Belayew, Isabelle Manfroid, Francesco Argenton and Kevin Ferreri and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Bernard Peers

56 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernard Peers Belgium 32 1.9k 1.4k 1.2k 646 560 58 3.0k
Maike Sander United States 18 1.5k 0.8× 1.6k 1.1× 891 0.8× 431 0.7× 223 0.4× 23 2.7k
Simona Chera Norway 23 1.4k 0.8× 1.7k 1.2× 1.2k 1.0× 955 1.5× 315 0.6× 53 3.1k
Beatriz Sosa‐Pineda United States 28 2.2k 1.2× 2.8k 2.0× 1.9k 1.6× 1.1k 1.7× 210 0.4× 36 4.5k
Catherine Carrière United States 18 1.5k 0.8× 368 0.3× 714 0.6× 602 0.9× 192 0.3× 23 2.4k
Paolo Chieffi Italy 38 1.6k 0.9× 865 0.6× 601 0.5× 162 0.3× 514 0.9× 110 3.3k
Michael Ray United States 9 1.4k 0.8× 2.2k 1.5× 1.4k 1.2× 651 1.0× 141 0.3× 10 2.8k
Joan‐Marc Servitja Spain 22 1.0k 0.6× 644 0.5× 389 0.3× 205 0.3× 258 0.5× 42 1.9k
Fong Cheng Pan United States 16 995 0.5× 1.3k 0.9× 633 0.5× 372 0.6× 131 0.2× 19 2.0k
Anthony Antonellis United States 30 2.4k 1.3× 634 0.4× 716 0.6× 271 0.4× 539 1.0× 75 3.8k
Frédéric Clotman Belgium 26 1.3k 0.7× 1.0k 0.7× 457 0.4× 105 0.2× 315 0.6× 57 2.6k

Countries citing papers authored by Bernard Peers

Since Specialization
Citations

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

Fields of papers citing papers by Bernard Peers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Peers

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard Peers. A scholar is included among the top collaborators of Bernard Peers 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 Bernard Peers. Bernard Peers 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
2.
Nepal, Chirag, Yavor Hadzhiev, Piotr J. Balwierz, et al.. (2020). Dual-initiation promoters with intertwined canonical and TCT/TOP transcription start sites diversify transcript processing. Nature Communications. 11(1). 168–168. 29 indexed citations
3.
Flasse, Lydie, et al.. (2013). Ascl1b and Neurod1, instead of Neurog3, control pancreatic endocrine cell fate in zebrafish. BMC Biology. 11(1). 78–78. 29 indexed citations
4.
Manfroid, Isabelle, Luyuan Pan, P. Taylur, et al.. (2012). Zebrafish sox9b is crucial for hepatopancreatic duct development and pancreatic endocrine cell regeneration. Developmental Biology. 366(2). 268–278. 64 indexed citations
5.
Voz, Marianne L., et al.. (2012). Essential roles of zebrafishbmp2a,fgf10, andfgf24in the specification of the ventral pancreas. Molecular Biology of the Cell. 23(5). 945–954. 21 indexed citations
6.
Giacomotto, Jean, et al.. (2012). Pax4 is not essential for beta-cell differentiation in zebrafish embryos but modulates alpha-cell generation by repressing arx gene expression. BMC Developmental Biology. 12(1). 37–37. 22 indexed citations
7.
Marée, Raphaël, et al.. (2010). Zebrafish as model in toxicology/pharmacology.. Open Repository and Bibliography (University of Liège). 2 indexed citations
8.
Manfroid, Isabelle, Lydie Flasse, Marie Winandy, et al.. (2010). Nkx6.1 and nkx6.2 regulate α- and β-cell formation in zebrafish by acting on pancreatic endocrine progenitor cells. Developmental Biology. 340(2). 397–407. 34 indexed citations
9.
Pendeville, Hélène, Marie Winandy, Olivier Nivelles, et al.. (2008). Zebrafish Sox7 and Sox18 function together to control arterial–venous identity. Developmental Biology. 317(2). 405–416. 100 indexed citations
10.
Mavropoulos, Anastasia, Nathalie Devos, Frédéric Biemar, et al.. (2005). sox4b is a key player of pancreatic α cell differentiation in zebrafish. Developmental Biology. 285(1). 211–223. 65 indexed citations
11.
Zecchin, Elisabetta, Anastasia Mavropoulos, Nathalie Devos, et al.. (2004). Evolutionary conserved role of ptf1a in the specification of exocrine pancreatic fates. Developmental Biology. 268(1). 174–184. 91 indexed citations
12.
Devos, Nathalie, Gianluca Deflorian, Frédéric Biemar, et al.. (2002). Differential expression of two somatostatin genes during zebrafish embryonic development. Mechanisms of Development. 115(1-2). 133–137. 56 indexed citations
13.
Biemar, Frédéric, et al.. (2001). Cloning and expression of the TALE superclass homeobox Meis2 gene during zebrafish embryonic development. Mechanisms of Development. 109(2). 427–431. 20 indexed citations
14.
Goudet, Ghylène, Sylvie Delhalle, Frédéric Biemar, Joseph Martial, & Bernard Peers. (1999). Functional and Cooperative Interactions between the Homeodomain PDX1, Pbx, and Prep1 Factors on the Somatostatin Promoter. Journal of Biological Chemistry. 274(7). 4067–4073. 85 indexed citations
15.
Peers, Bernard, Seema Sharma, Ted W. Johnson, Mark P. Kamps, & Marc Montminy. (1995). The Pancreatic Islet Factor STF-1 Binds Cooperatively with Pbx to a Regulatory Element in the Somatostatin Promoter: Importance of the FPWMK Motif and of the Homeodomain. Molecular and Cellular Biology. 15(12). 7091–7097. 135 indexed citations
16.
Jacquemin, Patrick, Cécile Oury, Bernard Peers, et al.. (1994). Characterization of a single strong tissue-specific enhancer downstream from the three human genes encoding placental lactogen. Molecular and Cellular Biology. 14(1). 93–103. 41 indexed citations
17.
Peers, Bernard, James Leonard, Surangama Sharma, Gladys Teitelman, & Marc Montminy. (1994). Insulin expression in pancreatic islet cells relies on cooperative interactions between the helix loop helix factor E47 and the homeobox factor STF-1.. Molecular Endocrinology. 8(12). 1798–1806. 179 indexed citations
18.
Voz, Marianne L., Bernard Peers, Murielle Wiedig, et al.. (1992). Transcriptional Regulation by Triiodothyronine Requires Synergistic Action of the Thyroid Receptor with Another trans -Acting Factor. Molecular and Cellular Biology. 12(9). 3991–3997. 32 indexed citations
19.
Peers, Bernard, Marianne L. Voz, Philippe Monget, et al.. (1990). Regulatory Elements Controlling Pituitary-Specific Expression of the Human Prolactin Gene. Molecular and Cellular Biology. 10(9). 4690–4700. 19 indexed citations
20.
Lemaigre, Frédéric P., Bernard Peers, Dominique A. Lafontaine, et al.. (1989). Pituitary-Specific Factor Binding to the Human Prolactin, Growth Hormone, and Placental Lactogen Genes. DNA. 8(3). 149–159. 54 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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