Valerie Booth

1.5k total citations
52 papers, 952 citations indexed

About

Valerie Booth is a scholar working on Molecular Biology, Microbiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Valerie Booth has authored 52 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 21 papers in Microbiology and 13 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Valerie Booth's work include Lipid Membrane Structure and Behavior (22 papers), Antimicrobial Peptides and Activities (21 papers) and Neonatal Respiratory Health Research (13 papers). Valerie Booth is often cited by papers focused on Lipid Membrane Structure and Behavior (22 papers), Antimicrobial Peptides and Activities (21 papers) and Neonatal Respiratory Health Research (13 papers). Valerie Booth collaborates with scholars based in Canada, United States and France. Valerie Booth's co-authors include Brian D. Sykes, Ian Clark‐Lewis, Michael R. Morrow, Alan J. Waring, Monique B. Kamphuis, David W. Keizer, C.H. Arrowsmith, Frans J. Walther, Muzaddid Sarker and Carolyn M. Slupsky and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Valerie Booth

50 papers receiving 934 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valerie Booth Canada 18 552 234 185 144 99 52 952
Natàlia Jiménez Spain 19 386 0.7× 49 0.2× 190 1.0× 213 1.5× 126 1.3× 47 906
William R. Kearney United States 13 684 1.2× 337 1.4× 147 0.8× 47 0.3× 53 0.5× 18 1.0k
Tanya R. Mealy United States 17 842 1.5× 50 0.2× 116 0.6× 145 1.0× 38 0.4× 17 1.2k
Celestine J. Thomas India 21 687 1.2× 131 0.6× 261 1.4× 22 0.2× 40 0.4× 32 1.0k
Magali Soyer France 9 277 0.5× 226 1.0× 109 0.6× 35 0.2× 112 1.1× 17 706
David W. Keizer Australia 18 591 1.1× 64 0.3× 158 0.9× 34 0.2× 109 1.1× 41 1.1k
Chahrazade El Amri France 19 722 1.3× 334 1.4× 126 0.7× 12 0.1× 104 1.1× 52 1.1k
Robert J. A. Goode Australia 18 636 1.2× 38 0.2× 105 0.6× 27 0.2× 54 0.5× 31 1.0k
Juan Pérez-Vilar United States 17 724 1.3× 26 0.1× 200 1.1× 220 1.5× 34 0.3× 19 1.2k
Mira Glibowicka Canada 10 691 1.3× 41 0.2× 46 0.2× 37 0.3× 44 0.4× 12 971

Countries citing papers authored by Valerie Booth

Since Specialization
Citations

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

Fields of papers citing papers by Valerie Booth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valerie Booth

This figure shows the co-authorship network connecting the top 25 collaborators of Valerie Booth. A scholar is included among the top collaborators of Valerie Booth 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 Valerie Booth. Valerie Booth 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.
Yethiraj, Anand, et al.. (2024). The effects of biological crowders on fibrillization, structure, diffusion, and conformational dynamics of α‐synuclein. Protein Science. 33(3). e4894–e4894. 4 indexed citations
2.
Booth, Valerie, et al.. (2022). Interaction between Antimicrobial Peptide Magainin 2 and Nonlipid Components in the Bacterial Outer Envelope. The Journal of Physical Chemistry B. 126(29). 5473–5480. 4 indexed citations
3.
Kumari, Sarika, Michael R. Morrow, & Valerie Booth. (2022). Role of lipopolysaccharide in antimicrobial and cell penetrating peptide membrane interactions probed by deuterium NMR of whole cells. SHILAP Revista de lepidopterología. 2. 100057–100057. 2 indexed citations
4.
Morrow, Michael R., et al.. (2020). Effect of AMPs MSI-78 and BP100 on the lipid acyl chains of 2H-labeled intact Gram positive bacteria. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1862(5). 183199–183199. 13 indexed citations
5.
Morrow, Michael R., et al.. (2016). Protocols for Studying the Interaction of MSI-78 with the Membranes of Whole Gram-Positive and Gram-Negative Bacteria by NMR. Methods in molecular biology. 1548. 217–230. 8 indexed citations
6.
7.
Mannion, Michael R., Laurence Madera, Melanie R. Power Coombs, et al.. (2015). Structure–function relationships in histidine-rich antimicrobial peptides from Atlantic cod. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1848(7). 1451–1461. 39 indexed citations
8.
Saika‐Voivod, Ivan, et al.. (2014). Molecular dynamics simulations of histidine-containing cod antimicrobial peptide paralogs in self-assembled bilayers. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1838(11). 2778–2787. 27 indexed citations
9.
Bertani, Philippe, et al.. (2012). Orientation and depth of surfactant protein B C-terminal helix in lung surfactant bilayers. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818(5). 1165–1172. 10 indexed citations
10.
Booth, Valerie, et al.. (2011). Orientation and Dynamics of Synthetic Transbilayer Polypeptides Containing GpATM Dimerization Motifs. Biophysical Journal. 100(3). 656–664. 1 indexed citations
11.
Booth, Valerie, et al.. (2011). Self-Association of an Activating Natural Killer Cell Receptor, KIR2DS1. PLoS ONE. 6(8). e23052–e23052. 12 indexed citations
12.
13.
Booth, Valerie, et al.. (2009). Structure-Activity Relationships in Two Antimicrobial Peptides Based on Chemokine Helical Segments: RP-1 and IL-8α. Biophysical Journal. 96(3). 409a–410a. 1 indexed citations
14.
Morrow, Michael R., et al.. (2009). The Effect of a C-Terminal Peptide of Surfactant Protein B (SP-B) on Oriented Lipid Bilayers, Characterized by Solid-State 2H- and 31P-NMR. Biophysical Journal. 96(9). 3762–3771. 12 indexed citations
15.
Booth, Valerie, et al.. (2009). Perturbation of DPPC/POPG bilayers by the N-terminal helix of lung surfactant protein SP-B: a 2H NMR study. European Biophysics Journal. 38(5). 613–624. 10 indexed citations
16.
Waring, Alan J., et al.. (2009). Structure of Chemokine-Derived Antimicrobial Peptide Interleukin-8α and Interaction with Detergent Micelles and Oriented Lipid Bilayers. Biochemistry. 48(44). 10509–10521. 15 indexed citations
17.
Gulliver, Wayne, et al.. (2009). Peptide T exhibits a well‐defined structure in fluorinated solvent at low temperature. Journal of Peptide Science. 15(12). 818–823. 1 indexed citations
18.
Booth, Valerie, Carolyn M. Slupsky, Ian Clark‐Lewis, & Brian D. Sykes. (2003). Unmasking Ligand Binding Motifs: Identification of a Chemokine Receptor Motif by NMR Studies of Antagonist Peptides. Journal of Molecular Biology. 327(2). 329–334. 13 indexed citations
19.
Booth, Valerie, Christopher M. Koth, A.M. Edwards, & C.H. Arrowsmith. (2000). Structure of a Conserved Domain Common to the Transcription Factors TFIIS, Elongin A, and CRSP70. Journal of Biological Chemistry. 275(40). 31266–31268. 51 indexed citations
20.
Booth, Valerie, et al.. (2000). Radioprotective Thiolamines WR-1065 and WR-33278 Selectively Denature Nonhistone Nuclear Proteins. Radiation Research. 153(6). 813–822. 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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