Nicholas V. Hud

11.8k total citations · 1 hit paper
148 papers, 9.1k citations indexed

About

Nicholas V. Hud is a scholar working on Molecular Biology, Astronomy and Astrophysics and Biomaterials. According to data from OpenAlex, Nicholas V. Hud has authored 148 papers receiving a total of 9.1k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Molecular Biology, 53 papers in Astronomy and Astrophysics and 13 papers in Biomaterials. Recurrent topics in Nicholas V. Hud's work include DNA and Nucleic Acid Chemistry (74 papers), RNA and protein synthesis mechanisms (60 papers) and Origins and Evolution of Life (53 papers). Nicholas V. Hud is often cited by papers focused on DNA and Nucleic Acid Chemistry (74 papers), RNA and protein synthesis mechanisms (60 papers) and Origins and Evolution of Life (53 papers). Nicholas V. Hud collaborates with scholars based in United States, Spain and Slovenia. Nicholas V. Hud's co-authors include Juli Feigon, Jie Zheng, Robert M. Dickson, Jeffrey T. Petty, Loren Dean Williams, Brian J. Cafferty, Igor D. Vilfan, Kenneth H. Downing, Ramanarayanan Krishnamurthy and Irena Mamajanov and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Nicholas V. Hud

147 papers receiving 9.0k citations

Hit Papers

DNA-Templated Ag Nanocluster Formation 2004 2026 2011 2018 2004 250 500 750

Peers

Nicholas V. Hud
Gerald F. Joyce United States
Loren Dean Williams United States
M. Reza Ghadiri United States
Christine D. Keating United States
Ole Buchardt Denmark
Eric T. Kool United States
Nicholas V. Hud
Citations per year, relative to Nicholas V. Hud Nicholas V. Hud (= 1×) peers Thomas Carell

Countries citing papers authored by Nicholas V. Hud

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas V. Hud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas V. Hud. 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 Nicholas V. Hud. The network helps show where Nicholas V. Hud may publish in the future.

Co-authorship network of co-authors of Nicholas V. Hud

This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas V. Hud. A scholar is included among the top collaborators of Nicholas V. Hud 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 Nicholas V. Hud. Nicholas V. Hud 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.
Martin, C, Moran Frenkel‐Pinter, Loren Dean Williams, et al.. (2022). Water-Based Dynamic Depsipeptide Chemistry: Building Block Recycling and Oligomer Distribution Control Using Hydration–Dehydration Cycles. JACS Au. 2(6). 1395–1404. 11 indexed citations
2.
Frenkel‐Pinter, Moran, et al.. (2022). Differential Oligomerization of Alpha versus Beta Amino Acids and Hydroxy Acids in Abiotic Proto-Peptide Synthesis Reactions. Life. 12(2). 265–265. 10 indexed citations
3.
Schuster, Gary B., Nicholas V. Hud, & Asem Alenaizan. (2022). Structural and Thermodynamic Control of Supramolecular Polymers and DNA Assemblies with Cyanuric Acid: Influence of Substituents and Intermolecular Interactions. The Journal of Physical Chemistry B. 126(50). 10758–10767. 4 indexed citations
4.
Fialho, David M., et al.. (2022). A Plausible Prebiotic Path to Nucleosides: Ribosides and Related Aldosides Generated from Ribulose, Fructose, and Similar Abiotic Precursors. Chemistry - A European Journal. 29(6). e202203036–e202203036. 13 indexed citations
5.
Grover, Martha A., et al.. (2021). Urea and Acetamide Rich Solutions Circumvent the Strand Inhibition Problem to Allow Multiple Rounds of DNA and RNA Copying. ChemBioChem. 23(1). e202100495–e202100495. 7 indexed citations
6.
Fialho, David M., et al.. (2021). Depsipeptide Nucleic Acids: Prebiotic Formation, Oligomerization, and Self-Assembly of a New Proto-Nucleic Acid Candidate. Journal of the American Chemical Society. 143(34). 13525–13537. 17 indexed citations
7.
Alenaizan, Asem, Carlos H. Borca, Suneesh C. Karunakaran, et al.. (2021). X-ray Fiber Diffraction and Computational Analyses of Stacked Hexads in Supramolecular Polymers: Insight into Self-Assembly in Water by Prospective Prebiotic Nucleobases. Journal of the American Chemical Society. 143(16). 6079–6094. 17 indexed citations
8.
Krishnamurthy, Ramanarayanan & Nicholas V. Hud. (2020). Introduction: Chemical Evolution and the Origins of Life. Chemical Reviews. 120(11). 4613–4615. 38 indexed citations
9.
Frenkel‐Pinter, Moran, C Martin, Anton S. Petrov, et al.. (2020). Mutually stabilizing interactions between proto-peptides and RNA. Nature Communications. 11(1). 3137–3137. 74 indexed citations
10.
Alenaizan, Asem, et al.. (2020). The proto-Nucleic Acid Builder: a software tool for constructing nucleic acid analogs. Nucleic Acids Research. 49(1). 79–89. 13 indexed citations
12.
Burcar, Bradley T., Alma D. Castañeda, Matthew A. Pasek, et al.. (2019). A Stark Contrast to Modern Earth: Phosphate Mineral Transformation and Nucleoside Phosphorylation in an Iron‐ and Cyanide‐Rich Early Earth Scenario. Angewandte Chemie. 131(47). 17137–17143. 6 indexed citations
13.
Burcar, Bradley T., Alma D. Castañeda, Matthew A. Pasek, et al.. (2019). A Stark Contrast to Modern Earth: Phosphate Mineral Transformation and Nucleoside Phosphorylation in an Iron‐ and Cyanide‐Rich Early Earth Scenario. Angewandte Chemie International Edition. 58(47). 16981–16987. 24 indexed citations
14.
Bowman, Jessica C., Anton S. Petrov, Amit R. Reddi, et al.. (2018). Multiple prebiotic metals mediate translation. Proceedings of the National Academy of Sciences. 115(48). 12164–12169. 43 indexed citations
15.
Saydjari, Andrew K., et al.. (2018). A Possible Path to Prebiotic Peptides Involving Silica and Hydroxy Acid‐Mediated Amide Bond Formation. ChemBioChem. 19(18). 1913–1917. 18 indexed citations
16.
Fialho, David M., et al.. (2017). Glycosylation of a model proto-RNA nucleobase with non-ribose sugars: implications for the prebiotic synthesis of nucleosides. Organic & Biomolecular Chemistry. 16(8). 1263–1271. 27 indexed citations
17.
Yu, Shengsheng, Ramanarayanan Krishnamurthy, Facundo M. Fernández, et al.. (2017). Elongation of Model Prebiotic Proto-Peptides by Continuous Monomer Feeding. Macromolecules. 50(23). 9286–9294. 29 indexed citations
18.
Cafferty, Brian J., et al.. (2016). Spontaneous formation and base pairing of plausible prebiotic nucleotides in water. Nature Communications. 7(1). 11328–11328. 98 indexed citations
19.
Petrov, Anton S., Burak Gulen, Ashlyn Norris, et al.. (2015). History of the ribosome and the origin of translation. Proceedings of the National Academy of Sciences. 112(50). 15396–15401. 195 indexed citations
20.
Joung, In Suk, Özgül Persil Çetinkol, Nicholas V. Hud, & Thomas E. Cheatham. (2009). Molecular dynamics simulations and coupled nucleotide substitution experiments indicate the nature of A·A base pairing and a putative structure of the coralyne-induced homo-adenine duplex. Nucleic Acids Research. 37(22). 7715–7727. 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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