Hwai‐Chen Guo

1.7k total citations
33 papers, 1.4k citations indexed

About

Hwai‐Chen Guo is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Hwai‐Chen Guo has authored 33 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Immunology and 7 papers in Oncology. Recurrent topics in Hwai‐Chen Guo's work include Glycosylation and Glycoproteins Research (8 papers), Lysosomal Storage Disorders Research (6 papers) and Bacterial Genetics and Biotechnology (6 papers). Hwai‐Chen Guo is often cited by papers focused on Glycosylation and Glycoproteins Research (8 papers), Lysosomal Storage Disorders Research (6 papers) and Bacterial Genetics and Biotechnology (6 papers). Hwai‐Chen Guo collaborates with scholars based in United States, Poland and Canada. Hwai‐Chen Guo's co-authors include J L Strominger, Don C. Wiley, Theodore S. Jardetzky, William S. Lane, D. C. Wiley, Chudi Guan, Jeffrey W. Roberts, Deirdre A. Buckley, Xuhong Qian and Richard A. Collins and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Hwai‐Chen Guo

33 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hwai‐Chen Guo United States 19 831 615 174 167 145 33 1.4k
Larry J. Ross United States 21 737 0.9× 425 0.7× 201 1.2× 129 0.8× 104 0.7× 32 1.6k
Pascale Duplay Canada 19 643 0.8× 603 1.0× 284 1.6× 176 1.1× 219 1.5× 31 1.3k
Lance M. Hellman United States 20 1.1k 1.3× 426 0.7× 235 1.4× 177 1.1× 252 1.7× 31 1.7k
Charles Belunis United States 16 693 0.8× 505 0.8× 153 0.9× 230 1.4× 102 0.7× 21 1.2k
Kuslima Shogen United States 23 1.2k 1.5× 295 0.5× 201 1.2× 90 0.5× 160 1.1× 47 1.7k
Stanislaw M. Mikulski United States 21 1.2k 1.5× 374 0.6× 195 1.1× 162 1.0× 291 2.0× 41 1.8k
R. Crowther United States 18 927 1.1× 491 0.8× 375 2.2× 192 1.1× 165 1.1× 23 1.8k
Ira Palmer United States 17 986 1.2× 209 0.3× 117 0.7× 114 0.7× 128 0.9× 24 1.6k
Hannes Uchtenhagen Sweden 15 640 0.8× 417 0.7× 83 0.5× 101 0.6× 78 0.5× 24 1.4k
Corinne Vivès France 17 782 0.9× 356 0.6× 82 0.5× 134 0.8× 54 0.4× 38 1.2k

Countries citing papers authored by Hwai‐Chen Guo

Since Specialization
Citations

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

Fields of papers citing papers by Hwai‐Chen Guo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hwai‐Chen Guo. 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 Hwai‐Chen Guo. The network helps show where Hwai‐Chen Guo may publish in the future.

Co-authorship network of co-authors of Hwai‐Chen Guo

This figure shows the co-authorship network connecting the top 25 collaborators of Hwai‐Chen Guo. A scholar is included among the top collaborators of Hwai‐Chen Guo 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 Hwai‐Chen Guo. Hwai‐Chen Guo 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.
Guo, Hwai‐Chen, et al.. (2023). Structure‐guided discovery of aminopeptidase ERAP1 variants capable of processing antigens with novel PC anchor specificities. Immunology. 171(1). 131–145. 1 indexed citations
2.
Guo, Hwai‐Chen, et al.. (2021). ERAP1 binds peptide C-termini of different sequences and/or lengths by a common recognition mechanism. Immunobiology. 226(4). 152112–152112. 4 indexed citations
3.
Guo, Hwai‐Chen, et al.. (2019). The T99K variant of glycosylasparaginase shows a new structural mechanism of the genetic disease aspartylglucosaminuria. Protein Science. 28(6). 1013–1023. 1 indexed citations
4.
Damodharan, L., et al.. (2017). Crystal structure of a mutant glycosylasparaginase shedding light on aspartylglycosaminuria-causing mechanism as well as on hydrolysis of non-chitobiose substrate. Molecular Genetics and Metabolism. 121(2). 150–156. 5 indexed citations
5.
Damodharan, L., et al.. (2014). Structural Basis of a Point Mutation that Causes the Genetic Disease Aspartylglucosaminuria. Structure. 22(12). 1855–1861. 9 indexed citations
6.
Gandhi, Amit, L. Damodharan, Yixin Sun, & Hwai‐Chen Guo. (2011). Structural insights into the molecular ruler mechanism of the endoplasmic reticulum aminopeptidase ERAP1. Scientific Reports. 1(1). 186–186. 36 indexed citations
7.
Wang, Yeming & Hwai‐Chen Guo. (2010). Crystallographic Snapshot of Glycosylasparaginase Precursor Poised for Autoprocessing. Journal of Molecular Biology. 403(1). 120–130. 22 indexed citations
8.
Wang, Yeming & Hwai‐Chen Guo. (2006). Crystallographic Snapshot of a Productive Glycosylasparaginase–Substrate Complex. Journal of Molecular Biology. 366(1). 82–92. 15 indexed citations
9.
Meyer, Rosana, Xiaofeng Qian, Hwai‐Chen Guo, & Nader Rahimi. (2006). Leucine Motif-dependent Tyrosine Autophosphorylation of Type III Receptor Tyrosine Kinases. Journal of Biological Chemistry. 281(13). 8620–8627. 5 indexed citations
10.
Xu, Qian, Richard J. Roberts, & Hwai‐Chen Guo. (2005). Two crystal forms of the restriction enzyme MspI–DNA complex show the same novel structure. Protein Science. 14(10). 2590–2600. 18 indexed citations
11.
Kucera, Rebecca, et al.. (2004). An Asymmetric Complex of Restriction Endonuclease MspI on Its Palindromic DNA Recognition Site. Structure. 12(9). 1741–1747. 37 indexed citations
12.
Xu, Qian, et al.. (2000). Crystallization and preliminary X-ray diffraction analysis ofMspI restriction endonuclease in complex with its cognate DNA. Acta Crystallographica Section D Biological Crystallography. 56(12). 1652–1655. 4 indexed citations
13.
Liao, Pei‐Yu, et al.. (2000). Mutagenesis and expression of the E3-19k lumenal domain of adenovirus type 2.. PubMed. 16(4). 181–6. 1 indexed citations
14.
Qian, Xuhong, Deirdre A. Buckley, Chudi Guan, & Hwai‐Chen Guo. (1999). Structural Insights into the Mechanism of Intramolecular Proteolysis. Cell. 98(5). 651–661. 111 indexed citations
15.
Cui, Tao, et al.. (1999). Purification and crystallization of precursors and autoprocessed enzymes of Flavobacterium glycosylasparaginase: an N-terminal nucleophile hydrolase. Acta Crystallographica Section D Biological Crystallography. 55(11). 1961–1964. 10 indexed citations
16.
Guo, Hwai‐Chen, Xuhong Qian, Deirdre A. Buckley, & Chudi Guan. (1998). Crystal Structures of FlavobacteriumGlycosylasparaginase. Journal of Biological Chemistry. 273(32). 20205–20212. 54 indexed citations
17.
Bouvier, Marlène, Hwai‐Chen Guo, Kathrine J. Smith, & Don C. Wiley. (1998). Crystal structures of HLA-A*0201 complexed with antigenic peptides with either the amino- or carboxyl-terminal group substituted by a methyl group. Proteins Structure Function and Bioinformatics. 33(1). 97–106. 36 indexed citations
18.
Guo, Hwai‐Chen, et al.. (1992). Different length peptides bind to HLA-Aw68 similarly at their ends but bulge out in the middle. Nature. 360(6402). 364–366. 341 indexed citations
19.
Guo, Hwai‐Chen, et al.. (1992). Atomic structure of a human MHC molecule presenting an influenza virus peptide. Nature. 360(6402). 367–369. 209 indexed citations
20.
Guo, Hwai‐Chen & Jeffrey W. Roberts. (1990). Heterogeneous initiation due to slippage at the bacteriophage 82 late gene promoter in vitro. Biochemistry. 29(47). 10702–10709. 44 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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