Sophie Vriz

3.7k total citations
72 papers, 2.4k citations indexed

About

Sophie Vriz is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sophie Vriz has authored 72 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 19 papers in Cell Biology and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sophie Vriz's work include Developmental Biology and Gene Regulation (15 papers), Zebrafish Biomedical Research Applications (14 papers) and Photoreceptor and optogenetics research (10 papers). Sophie Vriz is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Zebrafish Biomedical Research Applications (14 papers) and Photoreceptor and optogenetics research (10 papers). Sophie Vriz collaborates with scholars based in France, United States and Burundi. Sophie Vriz's co-authors include Michel Volovitch, Carole Gauron, Christine Rampon, Ludovic Jullien, David Bensimon, Arnaud Gautier, Mohamed Bouzaffour, Marcel Méchali, Thomas Le Saux and Jérémie Teillon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Sophie Vriz

72 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sophie Vriz France 29 1.4k 484 473 351 278 72 2.4k
Michel Volovitch France 32 2.1k 1.5× 950 2.0× 390 0.8× 503 1.4× 290 1.0× 71 3.4k
Lin Guo United States 24 2.5k 1.7× 380 0.8× 239 0.5× 393 1.1× 257 0.9× 71 3.5k
Pierre Neveu Germany 25 1.4k 0.9× 373 0.8× 535 1.1× 387 1.1× 171 0.6× 31 2.5k
Burkhard Wiesner Germany 40 3.3k 2.3× 632 1.3× 508 1.1× 413 1.2× 85 0.3× 103 5.0k
Joel Schwartz United States 17 1.6k 1.1× 793 1.6× 147 0.3× 365 1.0× 157 0.6× 17 2.7k
S. Karasawa Japan 17 1.2k 0.8× 375 0.8× 128 0.3× 212 0.6× 762 2.7× 21 2.0k
Carole Gauron France 15 726 0.5× 322 0.7× 331 0.7× 152 0.4× 190 0.7× 24 1.3k
Chandra L. Tucker United States 30 2.5k 1.8× 1.4k 2.9× 303 0.6× 349 1.0× 135 0.5× 51 3.6k
Edward M. Bonder United States 32 1.3k 0.9× 150 0.3× 238 0.5× 1.1k 3.1× 79 0.3× 76 3.0k
Eberhard Spieß Germany 30 1.4k 0.9× 328 0.7× 85 0.2× 546 1.6× 132 0.5× 92 2.7k

Countries citing papers authored by Sophie Vriz

Since Specialization
Citations

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

Fields of papers citing papers by Sophie Vriz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sophie Vriz

This figure shows the co-authorship network connecting the top 25 collaborators of Sophie Vriz. A scholar is included among the top collaborators of Sophie Vriz 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 Sophie Vriz. Sophie Vriz 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.
Plamont, Marie‐Aude, Christine Rampon, Sophie Vriz, et al.. (2023). A series of caged fluorophores for calibrating light intensity. Chemical Science. 14(47). 13799–13811. 2 indexed citations
2.
Thauvin, Marion, et al.. (2022). An early Shh–H2O2 reciprocal regulatory interaction controls the regenerative program during zebrafish fin regeneration. Journal of Cell Science. 135(6). 11 indexed citations
3.
Thauvin, Marion, Christine Rampon, Isabelle Quéguiner, et al.. (2022). Reciprocal Regulation of Shh Trafficking and H2O2 Levels via a Noncanonical BOC-Rac1 Pathway. Antioxidants. 11(4). 718–718. 4 indexed citations
4.
Kostyuk, Alexander I., Maria‐Armineh Tossounian, Marion Thauvin, et al.. (2022). Hypocrates is a genetically encoded fluorescent biosensor for (pseudo)hypohalous acids and their derivatives. Nature Communications. 13(1). 171–171. 16 indexed citations
5.
Thauvin, Marion, Yosuke Yoneyama, Yoichiro Kitani, et al.. (2022). NADPH-Oxidase Derived Hydrogen Peroxide and Irs2b Facilitate Re-oxygenation-Induced Catch-Up Growth in Zebrafish Embryo. Frontiers in Endocrinology. 13. 929668–929668. 6 indexed citations
6.
Zhang, Weiting, Isabelle Aujard, Thomas Le Saux, et al.. (2019). Optical control of protein activity and gene expression by photoactivation of caged cyclofen. Methods in enzymology on CD-ROM/Methods in enzymology. 624. 1–23. 4 indexed citations
7.
Albadri, Shahad, Marion Thauvin, Carole Gauron, et al.. (2019). Redox Signaling via Lipid Peroxidation Regulates Retinal Progenitor Cell Differentiation. Developmental Cell. 50(1). 73–89.e6. 31 indexed citations
8.
Labit, Elodie, Christine Rampon, Christophe Guissard, et al.. (2018). Opioids prevent regeneration in adult mammals through inhibition of ROS production. Scientific Reports. 8(1). 12170–12170. 17 indexed citations
9.
Vriz, Sophie. (2017). Redox signalling in development and regeneration. Seminars in Cell and Developmental Biology. 80. 1–2. 4 indexed citations
10.
Gauron, Carole, Francesca Meda, Edmond Dupont, et al.. (2016). Hydrogen peroxide (H2O2) controls axon pathfinding during zebrafish development. Developmental Biology. 414(2). 133–141. 66 indexed citations
11.
Plamont, Marie‐Aude, Emmanuelle Billon-Denis, Sylvie Maurin, et al.. (2015). Small fluorescence-activating and absorption-shifting tag for tunable protein imaging in vivo. Proceedings of the National Academy of Sciences. 113(3). 497–502. 192 indexed citations
12.
Rampon, Christine, Carole Gauron, Francesca Meda, Michel Volovitch, & Sophie Vriz. (2014). Adenosine enhances progenitor cell recruitment and nerve growth via its A2B receptor during adult fin regeneration. Purinergic Signalling. 10(4). 595–602. 11 indexed citations
13.
Feng, Zhiping, Weiting Zhang, Jianmin Xu, et al.. (2013). Optical control and study of biological processes at the single-cell level in a live organism. Reports on Progress in Physics. 76(7). 72601–72601. 14 indexed citations
14.
Ellertsdóttir, Elín, Peter Berthold, Mohamed Bouzaffour, et al.. (2012). Developmental Role of Zebrafish Protease-Activated Receptor 1 (PAR1) in the Cardio-Vascular System. PLoS ONE. 7(7). e42131–e42131. 12 indexed citations
15.
Sinha, Deepak K., Pierre Neveu, Nathalie Gagey‐Eilstein, et al.. (2010). Photoactivation of the CreER T2 Recombinase for Conditional Site-Specific Recombination with High Spatiotemporal Resolution. Zebrafish. 7(2). 199–204. 51 indexed citations
16.
Bouzaffour, Mohamed, Pascale Dufourcq, Virginie Lecaudey, Petra de Haas, & Sophie Vriz. (2009). Fgf and Sdf-1 Pathways Interact during Zebrafish Fin Regeneration. PLoS ONE. 4(6). e5824–e5824. 38 indexed citations
17.
Tawk, Marcel, Tamia K. Lapointe, Medea Imboden, et al.. (2001). Zebrafish keratin 8 is expressed at high levels in the epidermis of regenerating caudal fin. The International Journal of Developmental Biology. 45(2). 449–452. 25 indexed citations
18.
Tawk, Marcel, Catherine Joulie, & Sophie Vriz. (2000). Zebrafish Hsp40 and Hsc70 genes are both induced during caudal fin regeneration. Mechanisms of Development. 99(1-2). 183–186. 21 indexed citations
19.
Vriz, Sophie & Robin Lovell‐Badge. (1995). The zebrafish Zf-Sox 19 protein: a novel member of the Sox family which reveals highly conserved motifs outside of the DNA-binding domain. Gene. 153(2). 275–276. 40 indexed citations
20.
Méchali, Marcel, Geneviève Almouzni, J. Moreau, et al.. (1990). Genes and mechanisms involved in early embryonic development in Xenopus laevis.. PubMed. 34(1). 51–9. 3 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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