Natalia de Val

7.6k total citations · 2 hit papers
56 papers, 3.9k citations indexed

About

Natalia de Val is a scholar working on Molecular Biology, Virology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Natalia de Val has authored 56 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 28 papers in Virology and 20 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Natalia de Val's work include HIV Research and Treatment (27 papers), Monoclonal and Polyclonal Antibodies Research (19 papers) and Glycosylation and Glycoproteins Research (11 papers). Natalia de Val is often cited by papers focused on HIV Research and Treatment (27 papers), Monoclonal and Polyclonal Antibodies Research (19 papers) and Glycosylation and Glycoproteins Research (11 papers). Natalia de Val collaborates with scholars based in United States, United Kingdom and Netherlands. Natalia de Val's co-authors include Andrew B. Ward, Ian A. Wilson, John P. Moore, Rogier W. Sanders, Albert Cupo, Dennis R. Burton, Jean‐Philippe Julien, Dmitry Lyumkis, Richard T. Wyatt and Javier Guenaga and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Natalia de Val

56 papers receiving 3.8k citations

Hit Papers

A Next-Generation Cleaved... 2013 2026 2017 2021 2013 2013 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
Natalia de Val United States 32 2.3k 2.1k 1.1k 964 914 56 3.9k
Ping Zhu China 32 1.9k 0.8× 2.6k 1.3× 1.2k 1.1× 763 0.8× 950 1.0× 93 4.9k
Devin Sok United States 33 2.9k 1.3× 2.1k 1.0× 1.8k 1.7× 1.5k 1.5× 1.4k 1.5× 51 4.6k
Celia C. LaBranche United States 33 2.8k 1.2× 1.2k 0.6× 1.8k 1.6× 629 0.7× 1.3k 1.4× 149 3.9k
Katie J. Doores United Kingdom 32 1.4k 0.6× 1.6k 0.8× 866 0.8× 691 0.7× 931 1.0× 78 3.3k
Christopher N. Scanlan United Kingdom 24 1.6k 0.7× 3.1k 1.5× 1.3k 1.2× 1.4k 1.4× 478 0.5× 31 4.4k
Debra M. Eckert United States 23 1.4k 0.6× 1.8k 0.9× 586 0.5× 411 0.4× 1.0k 1.1× 40 3.4k
Elena Chertova United States 32 2.8k 1.3× 1.4k 0.7× 1.5k 1.4× 411 0.4× 1.3k 1.4× 51 4.2k
Gabriel Ozorowski United States 27 1.7k 0.7× 1.3k 0.6× 860 0.8× 771 0.8× 825 0.9× 63 2.8k
Erik A. Whitehorn United States 14 1.5k 0.7× 1.9k 0.9× 883 0.8× 552 0.6× 924 1.0× 17 3.7k
Gilad Ofek United States 15 1.8k 0.8× 952 0.5× 990 0.9× 821 0.9× 591 0.6× 20 2.4k

Countries citing papers authored by Natalia de Val

Since Specialization
Citations

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

Fields of papers citing papers by Natalia de Val

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalia de Val. 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 Natalia de Val. The network helps show where Natalia de Val may publish in the future.

Co-authorship network of co-authors of Natalia de Val

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia de Val. A scholar is included among the top collaborators of Natalia de Val 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 Natalia de Val. Natalia de Val 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.
Kanai, Tapan, Zongyi Hu, Renbin Yang, et al.. (2022). Three-Dimensional Reconstruction of the Hepatitis C Virus Envelope Glycoprotein E1E2 Heterodimer by Electron Microscopic Analysis. Journal of Virology. 97(1). e0178822–e0178822. 1 indexed citations
2.
Puri, Anu, André O’Reilly Beringhs, Paul Zakrevsky, et al.. (2022). Stealth oxime ether lipid vesicles promote delivery of functional DsiRNA in human lung cancer A549 tumor bearing mouse xenografts. Nanomedicine Nanotechnology Biology and Medicine. 44. 102572–102572. 6 indexed citations
3.
Lita, Adrian, Artem Pliss, Andrey N. Kuzmin, et al.. (2021). IDH1 mutations induce organelle defects via dysregulated phospholipids. Nature Communications. 12(1). 614–614. 52 indexed citations
4.
Zakrevsky, Paul, Wojciech K. Kasprzak, William F. Heinz, et al.. (2020). Truncated tetrahedral RNA nanostructures exhibit enhanced features for delivery of RNAi substrates. Nanoscale. 12(4). 2555–2568. 14 indexed citations
5.
Seabright, Gemma E., Christopher A. Cottrell, Marit J. van Gils, et al.. (2020). Networks of HIV-1 Envelope Glycans Maintain Antibody Epitopes in the Face of Glycan Additions and Deletions. Structure. 28(8). 897–909.e6. 36 indexed citations
6.
Gao, Yang, Yanxiang Cui, Tara Fox, et al.. (2019). Structures and operating principles of the replisome. Science. 363(6429). 107 indexed citations
7.
Botos, Istvan, G.T. Lountos, Weimin Wu, et al.. (2019). Cryo-EM structure of substrate-free E. coli Lon protease provides insights into the dynamics of Lon machinery. SHILAP Revista de lepidopterología. 1. 13–20. 19 indexed citations
8.
Yuan, Meng, Christopher A. Cottrell, Gabriel Ozorowski, et al.. (2019). Conformational Plasticity in the HIV-1 Fusion Peptide Facilitates Recognition by Broadly Neutralizing Antibodies. Cell Host & Microbe. 25(6). 873–883.e5. 26 indexed citations
9.
Aldon, Yoann, Paul F. McKay, Joel D. Allen, et al.. (2018). Rational Design of DNA-Expressed Stabilized Native-Like HIV-1 Envelope Trimers. Cell Reports. 24(12). 3324–3338.e5. 33 indexed citations
10.
Voss, James E., Raiees Andrabi, Laura E. McCoy, et al.. (2017). Elicitation of Neutralizing Antibodies Targeting the V2 Apex of the HIV Envelope Trimer in a Wild-Type Animal Model. Cell Reports. 21(1). 222–235. 42 indexed citations
11.
Pallesen, Jesper, Charles D. Murin, Natalia de Val, et al.. (2016). Structures of Ebola virus GP and sGP in complex with therapeutic antibodies. Nature Microbiology. 1(9). 16128–16128. 87 indexed citations
12.
He, Linling, Natalia de Val, Charles D. Morris, et al.. (2016). Presenting native-like trimeric HIV-1 antigens with self-assembling nanoparticles. Nature Communications. 7(1). 12041–12041. 131 indexed citations
13.
Pugach, Pavel, Gabriel Ozorowski, Albert Cupo, et al.. (2015). A Native-Like SOSIP.664 Trimer Based on an HIV-1 Subtype B env Gene. Journal of Virology. 89(6). 3380–3395. 177 indexed citations
14.
Sharma, S. K., Natalia de Val, Shridhar Bale, et al.. (2015). Cleavage-Independent HIV-1 Env Trimers Engineered as Soluble Native Spike Mimetics for Vaccine Design. Cell Reports. 11(4). 539–550. 161 indexed citations
15.
Guenaga, Javier, Natalia de Val, Karen Tran, et al.. (2015). Well-Ordered Trimeric HIV-1 Subtype B and C Soluble Spike Mimetics Generated by Negative Selection Display Native-like Properties. PLoS Pathogens. 11(1). e1004570–e1004570. 72 indexed citations
16.
Tran, Karen, Christian Poulsen, Javier Guenaga, et al.. (2014). Vaccine-elicited primate antibodies use a distinct approach to the HIV-1 primary receptor binding site informing vaccine redesign. Proceedings of the National Academy of Sciences. 111(7). E738–47. 58 indexed citations
17.
Matho, Michael H., Natalia de Val, Gregory M. Miller, et al.. (2014). Murine Anti-vaccinia Virus D8 Antibodies Target Different Epitopes and Differ in Their Ability to Block D8 Binding to CS-E. PLoS Pathogens. 10(12). e1004495–e1004495. 17 indexed citations
18.
Lyumkis, Dmitry, Jean‐Philippe Julien, Natalia de Val, et al.. (2013). Cryo-EM Structure of a Fully Glycosylated Soluble Cleaved HIV-1 Envelope Trimer. Science. 342(6165). 1484–1490. 527 indexed citations breakdown →
19.
Val, Natalia de, Wilfred R. Hagen, & Robert R. Crichton. (2006). EPR Studies of Recombinant Horse L-Chain Apoferritin and its Mutant (E 53,56,57,60 Q) with Haemin. BioMetals. 20(1). 21–26. 1 indexed citations
20.
Val, Natalia de, et al.. (2006). Mass spectrometry studies of demetallation of haemin by recombinant horse L chain apoferritin and its mutant (E 53,56,57,60 Q). FEBS Letters. 580(26). 6275–6280. 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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