Maria Bacia‐Verloop

480 total citations
17 papers, 341 citations indexed

About

Maria Bacia‐Verloop is a scholar working on Molecular Biology, Materials Chemistry and Biomaterials. According to data from OpenAlex, Maria Bacia‐Verloop has authored 17 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Materials Chemistry and 5 papers in Biomaterials. Recurrent topics in Maria Bacia‐Verloop's work include Clay minerals and soil interactions (5 papers), Enzyme Structure and Function (5 papers) and Bacteriophages and microbial interactions (3 papers). Maria Bacia‐Verloop is often cited by papers focused on Clay minerals and soil interactions (5 papers), Enzyme Structure and Function (5 papers) and Bacteriophages and microbial interactions (3 papers). Maria Bacia‐Verloop collaborates with scholars based in France, United Kingdom and Italy. Maria Bacia‐Verloop's co-authors include Antoine Thill, Erwan Paineau, Luc Belloni, Irina Gutsche, Pascale Launois, Ambroise Desfosses, Valérie Geertsen, Karine Huard, Mathew J. Boyer and Stéphan Rouzière 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

Maria Bacia‐Verloop

17 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Bacia‐Verloop France 12 114 112 93 59 46 17 341
Young Jae Kim South Korea 10 57 0.5× 18 0.2× 157 1.7× 59 1.0× 25 0.5× 21 356
Jasper Landman Netherlands 11 55 0.5× 173 1.5× 104 1.1× 16 0.3× 10 0.2× 27 458
Jiaqi Chen China 13 54 0.5× 23 0.2× 52 0.6× 27 0.5× 12 0.3× 35 348
Baolong Chen China 15 196 1.7× 30 0.3× 62 0.7× 4 0.1× 20 0.4× 50 603
Christoph Slouka Austria 16 365 3.2× 55 0.5× 165 1.8× 4 0.1× 30 0.7× 31 664
Hao Zong China 12 99 0.9× 16 0.1× 93 1.0× 7 0.1× 9 0.2× 62 451
Sojeong Lee South Korea 11 159 1.4× 22 0.2× 30 0.3× 6 0.1× 26 0.6× 45 344
Mark L. Wolfenden United States 7 246 2.2× 34 0.3× 114 1.2× 51 0.9× 4 0.1× 11 415
Т. Е. Пылаев Russia 12 258 2.3× 78 0.7× 209 2.2× 4 0.1× 9 0.2× 35 644
Mingxing Zhang China 10 89 0.8× 7 0.1× 65 0.7× 8 0.1× 9 0.2× 23 259

Countries citing papers authored by Maria Bacia‐Verloop

Since Specialization
Citations

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

Fields of papers citing papers by Maria Bacia‐Verloop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Bacia‐Verloop. 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 Maria Bacia‐Verloop. The network helps show where Maria Bacia‐Verloop may publish in the future.

Co-authorship network of co-authors of Maria Bacia‐Verloop

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

All Works

17 of 17 papers shown
1.
Paineau, Erwan, Franck Bourdelle, Laurent Truche, et al.. (2024). Nonclassical Growth Mechanism of Double‐Walled Metal‐Oxide Nanotubes Implying Transient Single‐Walled Structures. Small. 20(24). e2308665–e2308665. 2 indexed citations
2.
Acajjaoui, Samira, Ambroise Desfosses, Maria Bacia‐Verloop, et al.. (2023). The assembly of the Mitochondrial Complex I Assembly complex uncovers a redox pathway coordination. Nature Communications. 14(1). 8248–8248. 15 indexed citations
3.
Desfosses, Ambroise, Maria Bacia‐Verloop, Didier Chevret, et al.. (2023). Structural landscape of the respiratory syncytial virus nucleocapsids. Nature Communications. 14(1). 5732–5732. 10 indexed citations
4.
Huard, Karine, Ambroise Desfosses, Guillaume Tetreau, et al.. (2022). Structural and biochemical characterisation of the Providencia stuartii arginine decarboxylase shows distinct polymerisation and regulation. Communications Biology. 5(1). 317–317. 3 indexed citations
5.
Liesche, Clarissa, Jan Félix, Ambroise Desfosses, et al.. (2020). Supramolecular assembly of the Escherichia coli LdcI upon acid stress. Proceedings of the National Academy of Sciences. 118(2). 9 indexed citations
6.
Burt, Alister, C. Keith Cassidy, Peter Ames, et al.. (2020). Complete structure of the chemosensory array core signalling unit in an E. coli minicell strain. Nature Communications. 11(1). 743–743. 49 indexed citations
7.
Blum, Thorsten B., Dominique Housset, Max T. B. Clabbers, et al.. (2020). Statistically correcting dynamical electron scattering improves the refinement of protein nanocrystals, including charge refinement of coordinated metals. Acta Crystallographica Section D Structural Biology. 77(1). 75–85. 15 indexed citations
8.
Bonechi, Claudia, et al.. (2020). Lipids from algal biomass provide new (nonlamellar) nanovectors with high carrier potentiality for natural antioxidants. European Journal of Pharmaceutics and Biopharmaceutics. 158. 410–416. 16 indexed citations
9.
Wagemans, Jeroen, Dominique Holtappels, Jean-Pierre Hernálsteens, et al.. (2020). Structural Analysis of Jumbo Coliphage phAPEC6. International Journal of Molecular Sciences. 21(9). 3119–3119. 14 indexed citations
10.
Miras, Roger, Karine Huard, Maria Bacia‐Verloop, et al.. (2020). Structural insights into ATP hydrolysis by the MoxR ATPase RavA and the LdcI-RavA cage-like complex. Communications Biology. 3(1). 46–46. 23 indexed citations
11.
Giachin, Gabriele, Samira Acajjaoui, Maria Bacia‐Verloop, et al.. (2020). Assembly of The Mitochondrial Complex I Assembly Complex Suggests a Regulatory Role for Deflavination. Angewandte Chemie International Edition. 60(9). 4689–4697. 19 indexed citations
12.
Kandiah, Eaazhisai, Pierre Garcia, Jan Félix, et al.. (2019). Structure, Function, and Evolution of the Pseudomonas aeruginosa Lysine Decarboxylase LdcA. Structure. 27(12). 1842–1854.e4. 11 indexed citations
13.
Falsini, Sara, Emanuela Di Cola, Giulia C. Fadda, et al.. (2019). Green Nanovectors for Phytodrug Delivery: In-Depth Structural and Morphological Characterization. ACS Sustainable Chemistry & Engineering. 7(15). 12838–12846. 10 indexed citations
14.
Amara, Mohamed, Stéphan Rouzière, Erwan Paineau, et al.. (2014). Hexagonalization of Aluminogermanate Imogolite Nanotubes Organized into Closed-Packed Bundles. The Journal of Physical Chemistry C. 118(17). 9299–9306. 33 indexed citations
15.
Boyer, Mathew J., Erwan Paineau, Maria Bacia‐Verloop, & Antoine Thill. (2014). Aqueous dispersion state of amphiphilic hybrid aluminosilicate nanotubes. Applied Clay Science. 96. 45–49. 27 indexed citations
16.
Paineau, Erwan, Maria Bacia‐Verloop, Patrick Davidson, et al.. (2013). Single-step formation of micron long (OH)3Al2O3Ge(OH) imogolite-like nanotubes. Chemical Communications. 49(96). 11284–11284. 51 indexed citations
17.
Thill, Antoine, et al.. (2012). How the Diameter and Structure of (OH)3Al2O3SixGe1–xOH Imogolite Nanotubes Are Controlled by an Adhesion versus Curvature Competition. The Journal of Physical Chemistry C. 116(51). 26841–26849. 34 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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