Christopher G. Parker

2.9k total citations · 1 hit paper
42 papers, 2.0k citations indexed

About

Christopher G. Parker is a scholar working on Molecular Biology, Organic Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Christopher G. Parker has authored 42 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 18 papers in Organic Chemistry and 9 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Christopher G. Parker's work include Click Chemistry and Applications (15 papers), Monoclonal and Polyclonal Antibodies Research (9 papers) and Chemical Synthesis and Analysis (8 papers). Christopher G. Parker is often cited by papers focused on Click Chemistry and Applications (15 papers), Monoclonal and Polyclonal Antibodies Research (9 papers) and Chemical Synthesis and Analysis (8 papers). Christopher G. Parker collaborates with scholars based in United States, Australia and Germany. Christopher G. Parker's co-authors include Matthew R. Pratt, David A. Spiegel, Benjamin F. Cravatt, Weichao Li, R. Michael Lawrence, Appaso Mahadev Jadhav, Yujia Wang, Andrea Galmozzi, Enrique Sáez and Patrick J. McEnaney and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Christopher G. Parker

39 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Click Chemistry in Proteomic Investigations

2020 265 citations Christopher G. Parker, Matthew R. Pratt Cell profile →

Peers

Christopher G. Parker

MB

OC

RNMI

ONCOL

IMMUN

Keriann M. Backus United States

Zhengqiu Li China

Marcos Hatada United States

Bent W. Sigurskjold Denmark

Jesús García Spain

Takayoshi Okabe Japan

Adel Nefzi United States

H.T. Wright United States

Claus‐Wilhelm von der Lieth Germany

Christian Hedberg Germany

Keriann M. Backus United States

Christopher G. Parker

1.9k ×1.4

MB

1.0k ×1.6

OC

150 ×0.6

RNMI

480 ×1.8

ONCOL

119 ×0.6

IMMUN

Citations per year, relative to Christopher G. Parker Christopher G. Parker (= 1×) peers Keriann M. Backus

Countries citing papers authored by Christopher G. Parker

Since Specialization

Citations

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

Fields of papers citing papers by Christopher G. Parker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher G. Parker. 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 Christopher G. Parker. The network helps show where Christopher G. Parker may publish in the future.

Co-authorship network of co-authors of Christopher G. Parker

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

All Works

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20 of 20 papers shown

1.

Conway, Louis P., Appaso Mahadev Jadhav, Kathy Sarris, et al.. (2025). Proteome-Wide Discovery of Degradable Proteins Using Bifunctional Molecules. ACS Central Science. 11(11). 2240–2256.

2.

Wang, Wei, et al.. (2025). Targeted Protein Acetylation Through Chemically Induced Proximity. Accounts of Chemical Research. 58(17). 2695–2707.

3.

Wozniak, Jacob M., Weichao Li, Paolo Governa, et al.. (2024). Enhanced mapping of small-molecule binding sites in cells. Nature Chemical Biology. 20(7). 823–834. 17 indexed citations

4.

Conway, Louis P., Appaso Mahadev Jadhav, Jason K. Dutra, et al.. (2024). Mechanistic differences between linear vs. spirocyclic dialkyldiazirine probes for photoaffinity labeling. Chemical Science. 15(37). 15463–15473.

5.

Lapek, John D., et al.. (2024). Photoaffinity labelling with small molecules. Nature Reviews Methods Primers. 4(1). 19 indexed citations

6.

Wozniak, Jacob M., Weichao Li, & Christopher G. Parker. (2024). Chemical proteomic mapping of reversible small molecule binding sites in native systems. Trends in Pharmacological Sciences. 45(11). 969–981. 2 indexed citations

7.

Parker, Christopher G., et al.. (2023). Proteome‐Wide Fragment‐Based Ligand and Target Discovery. Israel Journal of Chemistry. 63(3-4). 21 indexed citations

8.

Li, Weichao, Francisco Martínez‐Peña, Zengwei Luo, et al.. (2023). Synthesis of portimines reveals the basis of their anti-cancer activity. Nature. 622(7983). 507–513. 35 indexed citations

9.

Rimann, Ivo, Rosana González‐Quintial, Roberto Baccalà, et al.. (2022). The solute carrier SLC15A4 is required for optimal trafficking of nucleic acid–sensing TLRs and ligands to endolysosomes. Proceedings of the National Academy of Sciences. 119(14). e2200544119–e2200544119. 28 indexed citations

10.

Chen, Liyun, Wei Wang, Jacob M. Wozniak, & Christopher G. Parker. (2022). A heterobifunctional molecule system for targeted protein acetylation in cells. Methods in enzymology on CD-ROM/Methods in enzymology. 681. 287–323. 1 indexed citations

11.

Conway, Louis P., et al.. (2021). A Sos proteomimetic as a pan-Ras inhibitor. Proceedings of the National Academy of Sciences. 118(18). 26 indexed citations

12.

Wang, Wei, et al.. (2021). Targeted Protein Acetylation in Cells Using Heterobifunctional Molecules. Journal of the American Chemical Society. 143(40). 16700–16708. 70 indexed citations

13.

Conway, Louis P., Weichao Li, & Christopher G. Parker. (2021). Chemoproteomic-enabled phenotypic screening. Cell chemical biology. 28(3). 371–393. 32 indexed citations

14.

Li, Weichao, et al.. (2020). Mapping glycan-mediated galectin-3 interactions by live cell proximity labeling. Proceedings of the National Academy of Sciences. 117(44). 27329–27338. 49 indexed citations

15.

Parker, Christopher G. & Matthew R. Pratt. (2020). Click Chemistry in Proteomic Investigations. Cell. 180(4). 605–632. 265 indexed citations breakdown →

16.

Galmozzi, Andrea, Bernard P. Kok, Arthur S. Kim, et al.. (2019). PGRMC2 is an intracellular haem chaperone critical for adipocyte function. Nature. 576(7785). 138–142. 90 indexed citations

17.

Parker, Christopher G., Andrea Galmozzi, Yujia Wang, et al.. (2017). Ligand and Target Discovery by Fragment-Based Screening in Human Cells. Cell. 168(3). 527–541.e29. 313 indexed citations

18.

Parker, Christopher G., Robert A. Domaoal, Karen S. Anderson, & David A. Spiegel. (2009). An Antibody-Recruiting Small Molecule That Targets HIV gp120. Journal of the American Chemical Society. 131(45). 16392–16394. 78 indexed citations

19.

Garner, Philip, Jieyu Hu, Christopher G. Parker, Wiley J. Youngs, & Doug Medvetz. (2007). The CuI-catalyzed exo-selective asymmetric multicomponent [C+NC+CC] coupling reaction. Tetrahedron Letters. 48(22). 3867–3870. 15 indexed citations

20.

Mills, David, et al.. (2005). Genomic analysis of PSU-1 and its relevance to winemaking. FEMS Microbiology Reviews. 29(3). 465–475. 121 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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