Gregg Fields

8.6k total citations · 3 hit papers
92 papers, 6.9k citations indexed

About

Gregg Fields is a scholar working on Cancer Research, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Gregg Fields has authored 92 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Cancer Research, 43 papers in Molecular Biology and 30 papers in Immunology and Allergy. Recurrent topics in Gregg Fields's work include Protease and Inhibitor Mechanisms (43 papers), Cell Adhesion Molecules Research (30 papers) and Peptidase Inhibition and Analysis (29 papers). Gregg Fields is often cited by papers focused on Protease and Inhibitor Mechanisms (43 papers), Cell Adhesion Molecules Research (30 papers) and Peptidase Inhibition and Analysis (29 papers). Gregg Fields collaborates with scholars based in United States, United Kingdom and Sweden. Gregg Fields's co-authors include Richard L. Noble, Cynthia G. Fields, Janelle L. Lauer‐Fields, David S. King, Matthias P. Lütolf, Franz E. Weber, Hugo G. Schmoekel, Jeffrey A. Hubbell, Andrew T. Metters and Matthew Tirrell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Gregg Fields

89 papers receiving 6.7k citations

Hit Papers

Solid phase peptide synthesis utilizing 9‐fluorenylmethox... 1990 2026 2002 2014 1990 2003 1990 500 1000 1.5k 2.0k

Peers

Gregg Fields
Gregg B. Fields United States
Douglas A. Steeber United States
Kazuki N. Sugahara United States
Lesley G. Ellies United States
Achim Aigner Germany
Arwyn T. Jones United Kingdom
Martin C. Woodle United States
Gregg B. Fields United States
Gregg Fields
Citations per year, relative to Gregg Fields Gregg Fields (= 1×) peers Gregg B. Fields

Countries citing papers authored by Gregg Fields

Since Specialization
Citations

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

Fields of papers citing papers by Gregg Fields

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gregg Fields

This figure shows the co-authorship network connecting the top 25 collaborators of Gregg Fields. A scholar is included among the top collaborators of Gregg Fields 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 Gregg Fields. Gregg Fields 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.
Tokmina‐Roszyk, Dorota, Chandani Singh, Fei Chen, et al.. (2025). Heat inactivation of proteins: implications for the Mars Sample Campaign and other extraterrestrial sample return missions. International Journal of Astrobiology. 24.
2.
4.
Xu, Zhongwei, Bingze Xu, Susanna L. Lundström, et al.. (2023). A subset of type-II collagen-binding antibodies prevents experimental arthritis by inhibiting FCGR3 signaling in neutrophils. Nature Communications. 14(1). 5949–5949. 9 indexed citations
5.
Fuerst, Rita, Anna M. Knapinska, Michael D. Cameron, et al.. (2022). Development of a putative Zn2+-chelating but highly selective MMP-13 inhibitor. Bioorganic & Medicinal Chemistry Letters. 76. 129014–129014. 8 indexed citations
6.
Lo, Chen Hao, Gemma Shay, Jeremy McGuire, et al.. (2021). Host-Derived Matrix Metalloproteinase-13 Activity Promotes Multiple Myeloma–Induced Osteolysis and Reduces Overall Survival. Cancer Research. 81(9). 2415–2428. 13 indexed citations
7.
Khamoui, Andy V., Dorota Tokmina‐Roszyk, Harry B. Rossiter, Gregg Fields, & Nishant P. Visavadiya. (2020). Hepatic proteome analysis reveals altered mitochondrial metabolism and suppressed acyl-CoA synthetase-1 in colon-26 tumor-induced cachexia. Physiological Genomics. 52(5). 203–216. 18 indexed citations
8.
Rodríguez, María C., et al.. (2020). TF-containing MUC1 glycopeptides fail to entice Galectin-1 recognition of tumor-associated Thomsen-Freidenreich (TF) antigen (CD176) in solution. Glycoconjugate Journal. 37(6). 657–666. 8 indexed citations
9.
Karabencheva‐Christova, Tatyana G., Christo Christov, & Gregg Fields. (2017). Collagenolytic Matrix Metalloproteinase Structure–Function Relationships: Insights From Molecular Dynamics Studies. Advances in protein chemistry and structural biology. 109. 1–24. 8 indexed citations
10.
Fields, Gregg. (2015). New strategies for targeting matrix metalloproteinases. Matrix Biology. 44-46. 239–246. 88 indexed citations
11.
Bhowmick, Manishabrata, Roma Stawikowska, Dorota Tokmina‐Roszyk, & Gregg Fields. (2015). Matrix Metalloproteinase Inhibition by Heterotrimeric Triple‐Helical Peptide Transition State Analogues. ChemBioChem. 16(7). 1084–1092. 19 indexed citations
12.
Fields, Gregg. (2014). Biophysical Studies of Matrix Metalloproteinase/Triple-Helix Complexes. Advances in protein chemistry and structural biology. 97. 37–48. 9 indexed citations
13.
Stawikowski, Maciej, et al.. (2014). Glycosylation Modulates Melanoma Cell α2β1 and α3β1 Integrin Interactions with Type IV Collagen. Journal of Biological Chemistry. 289(31). 21591–21604. 32 indexed citations
14.
Fields, Cynthia G., Gregg Fields, Richard L. Noble, & Timothy A. Cross. (2009). Solid phase peptide synthesis of 15N-gramicidins A, B, and C and high performance liquid chromatographic purification. International journal of peptide & protein research. 33(4). 298–303. 9 indexed citations
15.
Lauer‐Fields, Janelle L., et al.. (2005). Improved synthesis of 5‐hydroxylysine (Hyl) derivatives*. Journal of Peptide Research. 65(2). 272–283. 12 indexed citations
16.
Lütolf, Matthias P., Janelle L. Lauer‐Fields, Hugo G. Schmoekel, et al.. (2003). Synthetic matrix metalloproteinase-sensitive hydrogels for the conduction of tissue regeneration: Engineering cell-invasion characteristics. Proceedings of the National Academy of Sciences. 100(9). 5413–5418. 1170 indexed citations breakdown →
17.
Lauer‐Fields, Janelle L., et al.. (2000). Hydrolysis of Triple-helical Collagen Peptide Models by Matrix Metalloproteinases. Journal of Biological Chemistry. 275(18). 13282–13290. 105 indexed citations
18.
Fields, Gregg, et al.. (1998). Proteinlike molecular architecture: Biomaterial applications for inducing cellular receptor binding and signal transduction. Biopolymers. 47(2). 143–151. 121 indexed citations
19.
Fields, Gregg. (1995). The Collagen Triple-Helix: Correlation of Conformation with Biological Activities. Connective Tissue Research. 31(3). 235–243. 36 indexed citations
20.
Fields, Cynthia G., Albert Loffet, Steven A. Kates, & Gregg Fields. (1992). The development of high-performance liquid chromatographic analysis of allyl and allyloxycarbonyl side-chain-protected phenylthiohydantoin amino acids. Analytical Biochemistry. 203(2). 245–251. 11 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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