Lorraine M. Deck

3.9k total citations · 1 hit paper
44 papers, 3.2k citations indexed

About

Lorraine M. Deck is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Lorraine M. Deck has authored 44 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 13 papers in Organic Chemistry and 8 papers in Plant Science. Recurrent topics in Lorraine M. Deck's work include Research in Cotton Cultivation (6 papers), Curcumin's Biomedical Applications (6 papers) and Chemical Synthesis and Analysis (4 papers). Lorraine M. Deck is often cited by papers focused on Research in Cotton Cultivation (6 papers), Curcumin's Biomedical Applications (6 papers) and Chemical Synthesis and Analysis (4 papers). Lorraine M. Deck collaborates with scholars based in United States and Germany. Lorraine M. Deck's co-authors include David L. Vander Jagt, Robert E. Royer, Lucy A. Hunsaker, Anirban Maitra, Chi V. Dang, Ramani Dinavahi, Charles R. Cooper, Anne Le, Arvin M. Gouw and Gregg L. Semenza and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Lorraine M. Deck

42 papers receiving 3.1k citations

Hit Papers

Inhibition of lactate dehydrogenase A induces oxidative s... 2010 2026 2015 2020 2010 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lorraine M. Deck United States 25 1.6k 1000 503 323 306 44 3.2k
Alena Líšková Slovakia 34 1.9k 1.2× 806 0.8× 197 0.4× 380 1.2× 156 0.5× 52 3.8k
Lucy A. Hunsaker United States 31 1.3k 0.8× 247 0.2× 397 0.8× 231 0.7× 265 0.9× 51 3.3k
Xianzhang Bu China 31 2.0k 1.2× 560 0.6× 608 1.2× 69 0.2× 271 0.9× 103 3.3k
Kodappully Sivaraman Siveen United States 38 2.7k 1.7× 951 1.0× 386 0.8× 282 0.9× 208 0.7× 74 4.7k
Ilaria Lampronti Italy 39 1.9k 1.2× 645 0.6× 856 1.7× 566 1.8× 48 0.2× 144 4.3k
Shousong Cao United States 39 2.5k 1.5× 677 0.7× 259 0.5× 251 0.8× 92 0.3× 113 4.7k
Panayotis Pantazis United States 36 2.5k 1.6× 421 0.4× 192 0.4× 165 0.5× 392 1.3× 93 3.7k
Huiqing Yuan China 36 1.6k 1.0× 506 0.5× 630 1.3× 461 1.4× 74 0.2× 117 3.5k
Sushil Kumar India 22 1.8k 1.1× 509 0.5× 293 0.6× 292 0.9× 182 0.6× 67 3.4k
Hye Jin Jung South Korea 26 1.3k 0.8× 332 0.3× 217 0.4× 250 0.8× 133 0.4× 118 2.3k

Countries citing papers authored by Lorraine M. Deck

Since Specialization
Citations

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

Fields of papers citing papers by Lorraine M. Deck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lorraine M. Deck. 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 Lorraine M. Deck. The network helps show where Lorraine M. Deck may publish in the future.

Co-authorship network of co-authors of Lorraine M. Deck

This figure shows the co-authorship network connecting the top 25 collaborators of Lorraine M. Deck. A scholar is included among the top collaborators of Lorraine M. Deck 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 Lorraine M. Deck. Lorraine M. Deck 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.
Deck, Lorraine M., Lisa J. Whalen, Lucy A. Hunsaker, Robert E. Royer, & David L. Vander Jagt. (2017). Activation of anti-oxidant Nrf2 signaling by substituted trans stilbenes. Bioorganic & Medicinal Chemistry. 25(4). 1423–1430. 13 indexed citations
2.
Orlando, Robert A., Amanda M. Gonzales, Robert E. Royer, Lorraine M. Deck, & David L. Vander Jagt. (2012). A Chemical Analog of Curcumin as an Improved Inhibitor of Amyloid Abeta Oligomerization. PLoS ONE. 7(3). e31869–e31869. 56 indexed citations
3.
Le, Anne, Charles R. Cooper, Arvin M. Gouw, et al.. (2010). Inhibition of lactate dehydrogenase A induces oxidative stress and inhibits tumor progression. Proceedings of the National Academy of Sciences. 107(5). 2037–2042. 1169 indexed citations breakdown →
4.
Hunsaker, Lucy A., et al.. (2008). Isocoumarin-based inhibitors of pancreatic cholesterol esterase. Bioorganic & Medicinal Chemistry. 16(9). 5285–5294. 56 indexed citations
5.
Hunsaker, Lucy A., et al.. (2006). Uncharged isocoumarin-based inhibitors of urokinase-type plasminogen activator. SHILAP Revista de lepidopterología. 6(1). 1–1. 17 indexed citations
6.
Weber, Waylon, Lucy A. Hunsaker, Amanda M. Gonzales, et al.. (2006). Substituted trans-Stilbenes, Including Analogues of the Natural Product Resveratrol, Inhibit the Human Tumor Necrosis Factor Alpha-Induced Activation of Transcription Factor Nuclear Factor KappaB. Journal of Medicinal Chemistry. 49(24). 7182–7189. 140 indexed citations
7.
Weber, Waylon, Lucy A. Hunsaker, Amanda M. Gonzales, et al.. (2006). TPA-induced up-regulation of activator protein-1 can be inhibited or enhanced by analogs of the natural product curcumin. Biochemical Pharmacology. 72(8). 928–940. 62 indexed citations
8.
Heidrich, John E., et al.. (2004). Inhibition of pancreatic cholesterol esterase reduces cholesterol absorption in the hamster. BMC Pharmacology. 4(1). 5–5. 61 indexed citations
9.
Brown, William M., Charles A. Yowell, Thomas A. Vander Jagt, et al.. (2004). Comparative Structural Analysis and Kinetic Properties of Lactate Dehydrogenases from the Four Species of Human Malarial Parasites. Biochemistry. 43(20). 6219–6229. 75 indexed citations
10.
Brown, William M., Louis E. Metzger, Lucy A. Hunsaker, et al.. (2003). 17-β-Hydroxysteroid dehydrogenase type 1: computational design of active site inhibitors targeted to the Rossmann fold. Chemico-Biological Interactions. 143-144. 481–491. 26 indexed citations
11.
Brown, William M., et al.. (2002). Inhibition of yeast lipase (CRL1) and cholesterol esterase (CRL3) by 6-chloro-2-pyrones: comparison with porcine cholesterol esterase. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1596(2). 381–391. 21 indexed citations
12.
Hunsaker, Lucy A., et al.. (2001). The kinetic properties and sensitivities to inhibitors of lactate dehydrogenases (LDH1 and LDH2) from Toxoplasma gondii: comparisons with pLDH from Plasmodium falciparum. Molecular and Biochemical Parasitology. 118(1). 23–32. 54 indexed citations
13.
Jagt, David L. Vander, Lorraine M. Deck, & Robert E. Royer. (2000). Gossypol Prototype of Inhibitors Targeted to Dinucleotide Folds. Current Medicinal Chemistry. 7(4). 479–498. 86 indexed citations
14.
Deck, Lorraine M., et al.. (1999). 3-Alkyl-6-Chloro-2-pyrones:  Selective Inhibitors of Pancreatic Cholesterol Esterase. Journal of Medicinal Chemistry. 42(20). 4250–4256. 38 indexed citations
15.
Hunsaker, Lucy A., et al.. (1996). Physiological Substrates of Human Aldose and Aldehyde Reductases. Advances in experimental medicine and biology. 414. 491–497. 15 indexed citations
16.
Royer, Robert E., et al.. (1995). Synthesis and Anti-HIV Activity of 1,1'-Dideoxygossypol and Related Compounds. Journal of Medicinal Chemistry. 38(13). 2427–2432. 88 indexed citations
17.
Deck, Lorraine M., David L. Vander Jagt, & Robert E. Royer. (1991). Gossypol and derivatives: a new class of aldose reductase inhibitors. Journal of Medicinal Chemistry. 34(11). 3301–3305. 39 indexed citations
18.
Royer, Robert E., et al.. (1988). Binding of Gossypol Derivatives to Human Serum Albumin. Journal of Pharmaceutical Sciences. 77(3). 237–240. 13 indexed citations
19.
Daub, Guido H., et al.. (1987). SYNTHESIS OF 6,7,12-TRIMETHYLBENZ[a]ANTHRACENE 6,7-, AND 6,12-DIHETHYLBENZ[a]ANTHRACENE. Organic Preparations and Procedures International. 19(4-5). 269–276. 1 indexed citations
20.
Royer, Robert E., et al.. (1986). Biologically active derivatives of gossypol: synthesis and antimalarial activities of peri-acylated gossylic nitriles. Journal of Medicinal Chemistry. 29(9). 1799–1801. 91 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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