Thomas H. Haines

3.6k total citations
38 papers, 2.8k citations indexed

About

Thomas H. Haines is a scholar working on Molecular Biology, Organic Chemistry and Renewable Energy, Sustainability and the Environment. According to data from OpenAlex, Thomas H. Haines has authored 38 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 6 papers in Organic Chemistry and 6 papers in Renewable Energy, Sustainability and the Environment. Recurrent topics in Thomas H. Haines's work include Lipid Membrane Structure and Behavior (14 papers), Photosynthetic Processes and Mechanisms (8 papers) and Algal biology and biofuel production (6 papers). Thomas H. Haines is often cited by papers focused on Lipid Membrane Structure and Behavior (14 papers), Photosynthetic Processes and Mechanisms (8 papers) and Algal biology and biofuel production (6 papers). Thomas H. Haines collaborates with scholars based in United States, Germany and Canada. Thomas H. Haines's co-authors include Norbert A. Dencher, Stefan Paula, David W. Deamer, Alexander G. Volkov, Alfred N. Van Hoek, Thomas Hauß, Silvia Dante, George L. Mayers, H. Z. Cummins and M. Kates and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Thomas H. Haines

36 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas H. Haines United States 27 1.9k 419 328 230 198 38 2.8k
G. Douglas Winget United States 13 1.6k 0.9× 197 0.5× 177 0.5× 303 1.3× 222 1.1× 21 3.1k
Norman E. Good United States 23 2.7k 1.4× 316 0.8× 461 1.4× 551 2.4× 282 1.4× 37 4.8k
Seikichi Izawa United States 18 2.2k 1.2× 202 0.5× 444 1.4× 546 2.4× 216 1.1× 27 3.7k
E. Wehrli Switzerland 27 1.6k 0.8× 375 0.9× 153 0.5× 191 0.8× 191 1.0× 60 2.8k
Flemming Steen Jørgensen Denmark 36 1.7k 0.9× 367 0.9× 171 0.5× 249 1.1× 135 0.7× 140 3.3k
A. Gambacorta Italy 37 2.4k 1.3× 758 1.8× 187 0.6× 93 0.4× 373 1.9× 127 3.9k
Elinor T. Adman United States 41 3.1k 1.7× 261 0.6× 203 0.6× 161 0.7× 110 0.6× 78 5.3k
Pill‐Soon Song United States 44 4.2k 2.2× 915 2.2× 318 1.0× 737 3.2× 214 1.1× 218 7.0k
John Gutknecht United States 29 1.6k 0.9× 147 0.4× 284 0.9× 279 1.2× 231 1.2× 47 3.1k
Kazuo Kobayashi Japan 41 3.0k 1.6× 534 1.3× 153 0.5× 365 1.6× 284 1.4× 186 5.5k

Countries citing papers authored by Thomas H. Haines

Since Specialization
Citations

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

Fields of papers citing papers by Thomas H. Haines

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas H. Haines. 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 Thomas H. Haines. The network helps show where Thomas H. Haines may publish in the future.

Co-authorship network of co-authors of Thomas H. Haines

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas H. Haines. A scholar is included among the top collaborators of Thomas H. Haines 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 Thomas H. Haines. Thomas H. Haines 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.
Haines, Thomas H., et al.. (2023). SoK: Secure E-Voting with Everlasting Privacy. Proceedings on Privacy Enhancing Technologies. 2023(1). 279–293. 5 indexed citations
2.
Haines, Thomas H., et al.. (2017). Anionic H-Bonds in the Chlorosulfolipid Surface Bilayer of O. danica the Strength of a Bacterial Cell Wall. Biophysical Journal. 112(3). 223a–223a.
3.
Haines, Thomas H.. (2013). Are Phospholipids Stabilized by Short, Strong H-Bonds?. Biophysical Journal. 104(2). 549a–549a.
4.
Rodríguez-Capote, Karina, Dahís Manzanares, Thomas H. Haines, & Fred Possmayer. (2006). Reactive Oxygen Species Inactivation of Surfactant Involves Structural and Functional Alterations to Surfactant Proteins SP-B and SP-C. Biophysical Journal. 90(8). 2808–2821. 85 indexed citations
5.
Hauß, Thomas, Silvia Dante, Thomas H. Haines, & Norbert A. Dencher. (2005). Localization of coenzyme Q10 in the center of a deuterated lipid membrane by neutron diffraction. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1710(1). 57–62. 69 indexed citations
6.
Hauß, Thomas, Silvia Dante, Norbert A. Dencher, & Thomas H. Haines. (2002). Squalane is in the midplane of the lipid bilayer: implications for its function as a proton permeability barrier. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1556(2-3). 149–154. 104 indexed citations
7.
Haines, Thomas H. & Norbert A. Dencher. (2002). Cardiolipin: a proton trap for oxidative phosphorylation. FEBS Letters. 528(1-3). 35–39. 323 indexed citations
8.
Haines, Thomas H.. (2001). Do sterols reduce proton and sodium leaks through lipid bilayers?. Progress in Lipid Research. 40(4). 299–324. 302 indexed citations
9.
Mileykovskaya, Eugenia, et al.. (2001). Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces. FEBS Letters. 507(2). 187–190. 111 indexed citations
10.
Paula, Stefan, Alexander G. Volkov, Alfred N. Van Hoek, Thomas H. Haines, & David W. Deamer. (1996). Permeation of protons, potassium ions, and small polar molecules through phospholipid bilayers as a function of membrane thickness. Biophysical Journal. 70(1). 339–348. 486 indexed citations
11.
Mas‐Oliva, Jaime, et al.. (1996). Receptor Pattern Formation as a Signal for the Capture of Lipoproteins. Biochemical and Biophysical Research Communications. 224(1). 212–218. 5 indexed citations
12.
Haines, Thomas H.. (1994). Water transport across biological membranes. FEBS Letters. 346(1). 115–122. 86 indexed citations
13.
Haines, Thomas H., et al.. (1991). The elasticity of synthetic phospholipid vesicles obtained by photon correlation spectroscopy. Biochemistry. 30(23). 5688–5696. 54 indexed citations
14.
Haines, Thomas H., Wei Li, Michael Green, & H. Z. Cummins. (1987). The elasticity of uniform, unilamellar vesicles of acidic phospholipids during osmotic swelling is dominated by the ionic strength of the media. Biochemistry. 26(17). 5439–5447. 28 indexed citations
15.
Mooney, Carolyn L. & Thomas H. Haines. (1973). Chlorination and sulfation reactions in the biosynthesis of chlorosulfolipids in Ochromonas danica, in vivo. Biochemistry. 12(22). 4469–4472. 20 indexed citations
16.
Haines, Thomas H.. (1973). Halogen- and Sulfur-Containing Lipids of Ochromonas. Annual Review of Microbiology. 27(1). 403–412. 55 indexed citations
17.
Aaronson, S., et al.. (1971). Ultrastructure of intracellular and extracellular vesicles, membranes, and myelin figures produced by Ochromonas danica. Journal of Ultrastructure Research. 35(5-6). 418–430. 73 indexed citations
18.
Haines, Thomas H., et al.. (1969). Microbial sulpholipids: (R)-13-chloro-1-(R)-14-docosanediol disulphate and polychlorosulpholipids in Ochromonas danica. Biochemical Journal. 113(3). 565–566. 48 indexed citations
19.
Mayers, George L., et al.. (1969). Microbial sulfolipids. III. Disulfate of (+)-1,14-docosanediol in Ochromonas danica. Biochemistry. 8(7). 2981–2986. 41 indexed citations
20.
Haines, Thomas H., S. Aaronson, Joanne L. Gellerman, & Hermann Schlenk. (1962). Occurrence of Arachidonic and Related Acids in the Protozoon Ochromonas danica. Nature. 194(4835). 1282–1283. 38 indexed citations

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