Nathan Baird

1.0k total citations
19 papers, 811 citations indexed

About

Nathan Baird is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Nathan Baird has authored 19 papers receiving a total of 811 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Nathan Baird's work include RNA and protein synthesis mechanisms (18 papers), RNA modifications and cancer (15 papers) and RNA Research and Splicing (14 papers). Nathan Baird is often cited by papers focused on RNA and protein synthesis mechanisms (18 papers), RNA modifications and cancer (15 papers) and RNA Research and Splicing (14 papers). Nathan Baird collaborates with scholars based in United States, Japan and France. Nathan Baird's co-authors include A.R. Ferré-D′Amaré, Nadia Kulshina, Tobin R. Sosnick, Tao Pan, John S. Schneekloth, Stuart F.J. Le Grice, T. Kwaku Dayie, Fardokht A. Abulwerdi, David L. Spector and Wenbo Xu and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Nature Communications.

In The Last Decade

Nathan Baird

19 papers receiving 802 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathan Baird United States 14 772 143 120 42 37 19 811
Mikael Holm United States 13 528 0.7× 97 0.7× 96 0.8× 37 0.9× 22 0.6× 20 625
Ute Kothe Canada 18 1.2k 1.5× 224 1.6× 100 0.8× 52 1.2× 47 1.3× 30 1.2k
R.K. Montange United States 9 1.1k 1.5× 230 1.6× 43 0.4× 57 1.4× 48 1.3× 10 1.2k
P. Bieri Switzerland 10 1.1k 1.5× 70 0.5× 62 0.5× 35 0.8× 64 1.7× 10 1.2k
Matthias David Erlacher Austria 17 1.3k 1.6× 125 0.9× 366 3.0× 24 0.6× 14 0.4× 32 1.3k
Brent M. Znosko United States 20 863 1.1× 73 0.5× 46 0.4× 40 1.0× 28 0.8× 48 894
Scott P. Hennelly United States 18 1.4k 1.8× 152 1.1× 623 5.2× 33 0.8× 70 1.9× 28 1.5k
Mark A. Bayfield Canada 17 1.1k 1.5× 127 0.9× 76 0.6× 23 0.5× 19 0.5× 36 1.2k
Catherine D. Prescott United Kingdom 14 679 0.9× 191 1.3× 18 0.1× 66 1.6× 34 0.9× 18 761
Madalena Renouard France 12 583 0.8× 50 0.3× 97 0.8× 149 3.5× 22 0.6× 15 679

Countries citing papers authored by Nathan Baird

Since Specialization
Citations

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

Fields of papers citing papers by Nathan Baird

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathan Baird

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

All Works

19 of 19 papers shown
1.
Baird, Nathan, et al.. (2024). A Newly Identified Peripheral Duplex Anchors and Stabilizes the MALAT1 Triplex. Biochemistry. 63(18). 2280–2292. 1 indexed citations
2.
Swain, Monalisa, Wojciech K. Kasprzak, Mi Li, et al.. (2021). Dynamic bulge nucleotides in the KSHV PAN ENE triple helix provide a unique binding platform for small molecule ligands. Nucleic Acids Research. 49(22). 13179–13193. 12 indexed citations
3.
Abulwerdi, Fardokht A., Wenbo Xu, Gayatri Arun, et al.. (2019). Selective Small-Molecule Targeting of a Triple Helix Encoded by the Long Noncoding RNA, MALAT1. ACS Chemical Biology. 14(2). 223–235. 155 indexed citations
4.
Baird, Nathan, et al.. (2019). A highly ordered, nonprotective MALAT1 ENE structure is adopted prior to triplex formation. RNA. 25(8). 975–984. 11 indexed citations
5.
Baird, Nathan, et al.. (2019). Fluorescence-based investigations of RNA-small molecule interactions. Methods. 167. 54–65. 4 indexed citations
6.
Baird, Nathan, et al.. (2018). Finely tuned conformational dynamics regulate the protective function of the lncRNA MALAT1 triple helix. Nucleic Acids Research. 47(3). 1468–1481. 33 indexed citations
7.
Yu, Hao, Patricia Dranchak, Zhiru Li, et al.. (2017). Macrocycle peptides delineate locked-open inhibition mechanism for microorganism phosphoglycerate mutases. Nature Communications. 8(1). 14932–14932. 41 indexed citations
8.
Baird, Nathan, James Inglese, & A.R. Ferré-D′Amaré. (2015). Rapid RNA–ligand interaction analysis through high-information content conformational and stability landscapes. Nature Communications. 6(1). 8898–8898. 27 indexed citations
9.
Baird, Nathan & A.R. Ferré-D′Amaré. (2013). Analysis of Riboswitch Structure and Ligand Binding Using Small-Angle X-ray Scattering (SAXS). Methods in molecular biology. 1103. 211–225. 8 indexed citations
10.
Baird, Nathan & A.R. Ferré-D′Amaré. (2012). Modulation of quaternary structure and enhancement of ligand binding by the K-turn of tandem glycine riboswitches. RNA. 19(2). 167–176. 37 indexed citations
11.
Baird, Nathan, Jinwei Zhang, Tomoko Hamma, & A.R. Ferré-D′Amaré. (2012). YbxF and YlxQ are bacterial homologs of L7Ae and bind K-turns but not K-loops. RNA. 18(4). 759–770. 43 indexed citations
12.
Baird, Nathan & A.R. Ferré-D′Amaré. (2010). Idiosyncratically tuned switching behavior of riboswitch aptamer domains revealed by comparative small-angle X-ray scattering analysis. RNA. 16(3). 598–609. 89 indexed citations
13.
Baird, Nathan, et al.. (2010). Extended Structures in RNA Folding Intermediates Are Due to Nonnative Interactions Rather than Electrostatic Repulsion. Journal of Molecular Biology. 397(5). 1298–1306. 15 indexed citations
14.
Baird, Nathan, Nadia Kulshina, & A.R. Ferré-D′Amaré. (2010). Riboswitch function: Flipping the switch or tuning the dimmer?. RNA Biology. 7(3). 328–332. 57 indexed citations
15.
Baird, Nathan, Steven J. Ludtke, Htet A. Khant, et al.. (2010). Discrete Structure of an RNA Folding Intermediate Revealed by Cryo-electron Microscopy. Journal of the American Chemical Society. 132(46). 16352–16353. 21 indexed citations
16.
Kulshina, Nadia, Nathan Baird, & A.R. Ferré-D′Amaré. (2009). Recognition of the bacterial second messenger cyclic diguanylate by its cognate riboswitch. Nature Structural & Molecular Biology. 16(12). 1212–1217. 165 indexed citations
17.
Baird, Nathan, Xingwang Fang, Narayanan Srividya, Tao Pan, & Tobin R. Sosnick. (2007). Folding of a universal ribozyme: the ribonuclease P RNA. Quarterly Reviews of Biophysics. 40(2). 113–161. 24 indexed citations
18.
Baird, Nathan, Narayanan Srividya, Andrey S. Krasilnikov, et al.. (2006). Structural basis for altering the stability of homologous RNAs from a mesophilic and a thermophilic bacterium. RNA. 12(4). 598–606. 20 indexed citations
19.
Baird, Nathan, Éric Westhof, Hong Qin, Tao Pan, & Tobin R. Sosnick. (2005). Structure of a Folding Intermediate Reveals the Interplay Between Core and Peripheral Elements in RNA Folding. Journal of Molecular Biology. 352(3). 712–722. 48 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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