Eric Agius

3.7k total citations · 1 hit paper
29 papers, 2.9k citations indexed

About

Eric Agius is a scholar working on Molecular Biology, Developmental Neuroscience and Cell Biology. According to data from OpenAlex, Eric Agius has authored 29 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 10 papers in Developmental Neuroscience and 4 papers in Cell Biology. Recurrent topics in Eric Agius's work include Developmental Biology and Gene Regulation (15 papers), Neurogenesis and neuroplasticity mechanisms (10 papers) and Epigenetics and DNA Methylation (5 papers). Eric Agius is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Neurogenesis and neuroplasticity mechanisms (10 papers) and Epigenetics and DNA Methylation (5 papers). Eric Agius collaborates with scholars based in France, United States and United Kingdom. Eric Agius's co-authors include Edward M. De Robertis, Stefano Piccolo, Tewis Bouwmeester, Philippe Cochard, Luc Leyns, Horst Grunz, Bin Lü, Oliver Wessely, Michael Oelgeschläger and Caroline Kemp and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Eric Agius

29 papers receiving 2.8k citations

Hit Papers

The head inducer Cerberus is a multifunctional antagonist... 1999 2026 2008 2017 1999 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Agius France 19 2.5k 396 342 324 294 29 2.9k
Nobue Itasaki United Kingdom 25 2.9k 1.2× 608 1.5× 700 2.0× 453 1.4× 245 0.8× 41 3.4k
Carol Hicks United States 13 1.6k 0.7× 277 0.7× 237 0.7× 410 1.3× 358 1.2× 14 2.3k
Ken W.Y. Cho United States 27 2.6k 1.0× 391 1.0× 532 1.6× 166 0.5× 77 0.3× 50 3.0k
Shuichi Kani Japan 16 1.8k 0.7× 387 1.0× 350 1.0× 292 0.9× 129 0.4× 20 2.3k
Paul Scherz United States 11 2.0k 0.8× 466 1.2× 602 1.8× 343 1.1× 174 0.6× 36 2.6k
Edgar M. Pera Sweden 17 1.8k 0.7× 312 0.8× 379 1.1× 190 0.6× 129 0.4× 28 2.0k
Estelle Hirsinger France 16 1.9k 0.8× 358 0.9× 332 1.0× 150 0.5× 234 0.8× 25 2.2k
Martin Cheung Hong Kong 19 1.6k 0.6× 187 0.5× 499 1.5× 183 0.6× 254 0.9× 41 2.2k
Christophe Marcelle France 32 3.6k 1.5× 610 1.5× 873 2.6× 500 1.5× 195 0.7× 62 4.4k
Brian A. Parr United States 16 2.2k 0.9× 209 0.5× 584 1.7× 300 0.9× 330 1.1× 20 2.8k

Countries citing papers authored by Eric Agius

Since Specialization
Citations

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

Fields of papers citing papers by Eric Agius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Agius

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Agius. A scholar is included among the top collaborators of Eric Agius 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 Eric Agius. Eric Agius 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.
Molina, Angie, Valérie Lobjois, Sophie Bel-Vialar, et al.. (2022). Single-cell imaging of the cell cycle reveals CDC25B-induced heterogeneity of G1 phase length in neural progenitor cells. Development. 149(11). 9 indexed citations
2.
Agius, Eric, et al.. (2019). Timing the spinal cord development with neural progenitor cells losing their proliferative capacity: a theoretical analysis. Neural Development. 14(1). 7–7. 3 indexed citations
3.
Agius, Eric, Sophie Bel-Vialar, Nathalie Escalas, et al.. (2018). FGF signaling controls Shh-dependent oligodendroglial fate specification in the ventral spinal cord. Neural Development. 13(1). 3–3. 18 indexed citations
4.
Ohayon, David, Alain Garcès, Chadi Soukkarieh, et al.. (2016). Onset of Spinal Cord Astrocyte Precursor Emigration from the Ventricular Zone Involves the Zeb1 Transcription Factor. Cell Reports. 17(6). 1473–1481. 14 indexed citations
5.
Agius, Eric, et al.. (2014). Cell cycle and cell fate in the developing nervous system: the role of CDC25B phosphatase. Cell and Tissue Research. 359(1). 201–213. 14 indexed citations
6.
Agius, Eric, Yann Decker, Chadi Soukkarieh, Cathy Soula, & Philippe Cochard. (2010). Role of BMPs in controlling the spatial and temporal origin of GFAP astrocytes in the embryonic spinal cord. Developmental Biology. 344(2). 611–620. 15 indexed citations
7.
Nguyen‐Chi, Mai, Frédéric Chalmel, Eric Agius, et al.. (2009). Temporally Regulated Traffic of HuR and Its Associated ARE-Containing mRNAs from the Chromatoid Body to Polysomes during Mouse Spermatogenesis. PLoS ONE. 4(3). e4900–e4900. 43 indexed citations
8.
Soukkarieh, Chadi, Eric Agius, Cathy Soula, & Philippe Cochard. (2006). Pax2 regulates neuronal–glial cell fate choice in the embryonic optic nerve. Developmental Biology. 303(2). 800–813. 40 indexed citations
9.
Agius, Eric, et al.. (2006). Familial factors in diabetic nephropathy: an offspring study. Diabetic Medicine. 23(3). 331–334. 27 indexed citations
10.
11.
Braquart‐Varnier, Christine, Cathy Danesin, Eric Agius, et al.. (2004). A subtractive approach to characterize genes with regionalized expression in the gliogenic ventral neuroepithelium: identification of chick Sulfatase 1 as a new oligodendrocyte lineage gene. Molecular and Cellular Neuroscience. 25(4). 612–628. 25 indexed citations
12.
Agius, Eric, Chadi Soukkarieh, Cathy Danesin, et al.. (2004). Converse control of oligodendrocyte and astrocyte lineage development by Sonic hedgehog in the chick spinal cord. Developmental Biology. 270(2). 308–321. 63 indexed citations
13.
Wessely, Oliver, Eric Agius, Michael Oelgeschläger, Edgar M. Pera, & Edward M. De Robertis. (2001). Neural Induction in the Absence of Mesoderm: β-Catenin-Dependent Expression of Secreted BMP Antagonists at the Blastula Stage in Xenopus. Developmental Biology. 234(1). 161–173. 99 indexed citations
14.
Daluiski, Aaron, Thomas Engstrand, Matthew E. Bahamonde, et al.. (2001). Bone morphogenetic protein-3 is a negative regulator of bone density. Nature Genetics. 27(1). 84–88. 328 indexed citations
15.
Belo, José António, Daniel Bachiller, Eric Agius, et al.. (2000). Cerberus-like is a secreted BMP and nodal antagonist not essential for mouse development. genesis. 26(4). 265–265. 9 indexed citations
16.
Agius, Eric, Michael Oelgeschläger, Oliver Wessely, Caroline Kemp, & Edward M. De Robertis. (2000). Endodermal Nodal-related signals and mesoderm induction in Xenopus. Development. 127(6). 1173–1183. 345 indexed citations
17.
Piccolo, Stefano, Eric Agius, Luc Leyns, et al.. (1999). The head inducer Cerberus is a multifunctional antagonist of Nodal, BMP and Wnt signals. Nature. 397(6721). 707–710. 666 indexed citations breakdown →
19.
Robertis, Edward M. De, Luc Leyns, Stefano Piccolo, et al.. (1997). . Cold Spring Harbor Symposia on Quantitative Biology. 62(1). 169–175. 27 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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