Mong-Shang Lin

400 total citations
17 papers, 308 citations indexed

About

Mong-Shang Lin is a scholar working on Pathology and Forensic Medicine, Genetics and Rheumatology. According to data from OpenAlex, Mong-Shang Lin has authored 17 papers receiving a total of 308 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pathology and Forensic Medicine, 9 papers in Genetics and 8 papers in Rheumatology. Recurrent topics in Mong-Shang Lin's work include Autoimmune Bullous Skin Diseases (12 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (9 papers) and Urticaria and Related Conditions (8 papers). Mong-Shang Lin is often cited by papers focused on Autoimmune Bullous Skin Diseases (12 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (9 papers) and Urticaria and Related Conditions (8 papers). Mong-Shang Lin collaborates with scholars based in United States, Italy and Germany. Mong-Shang Lin's co-authors include Janet A. Fairley, George J. Giudice, Marleen M. Janson, Yung‐Wu Chen, Valerie K. Salato, Zelmira Lazarova, Mei Chen, Animesh A. Sinha, Detlef Zillikens and David T. Woodley and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Investigative Dermatology and Journal of the American Academy of Dermatology.

In The Last Decade

Mong-Shang Lin

16 papers receiving 293 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mong-Shang Lin United States 10 231 164 164 44 40 17 308
Stephen Kacir United States 7 264 1.1× 227 1.4× 184 1.1× 97 2.2× 31 0.8× 9 400
Yask Gupta Germany 8 201 0.9× 174 1.1× 150 0.9× 12 0.3× 32 0.8× 10 267
Ryosuke Sogame Japan 9 278 1.2× 179 1.1× 181 1.1× 56 1.3× 12 0.3× 11 322
D. Zillikens Germany 5 314 1.4× 253 1.5× 237 1.4× 26 0.6× 11 0.3× 5 346
V. Hébert France 9 155 0.7× 111 0.7× 109 0.7× 35 0.8× 10 0.3× 34 229
Mónica Olague-Marchan United States 8 431 1.9× 362 2.2× 349 2.1× 42 1.0× 13 0.3× 9 459
Reine Moriuchi Japan 8 222 1.0× 194 1.2× 193 1.2× 10 0.2× 7 0.2× 16 266
M. T. Vatutin Ukraine 4 54 0.2× 71 0.4× 68 0.4× 46 1.0× 19 0.5× 12 212
Adriana T. Lopez United States 7 149 0.6× 83 0.5× 57 0.3× 7 0.2× 65 1.6× 22 347
L. Gusdorf France 8 60 0.3× 27 0.2× 123 0.8× 63 1.4× 116 2.9× 20 273

Countries citing papers authored by Mong-Shang Lin

Since Specialization
Citations

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

Fields of papers citing papers by Mong-Shang Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mong-Shang Lin. 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 Mong-Shang Lin. The network helps show where Mong-Shang Lin may publish in the future.

Co-authorship network of co-authors of Mong-Shang Lin

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

All Works

17 of 17 papers shown
1.
2.
Denoncourt, Alix, et al.. (2019). A synthetic non-histone substrate to study substrate targeting by the Gcn5 HAT and sirtuin HDACs. Journal of Biological Chemistry. 294(16). 6227–6239. 7 indexed citations
3.
Liao, Wen‐Chieh, et al.. (2011). Overview of the Generation, Validation, and Application of Phosphosite-Specific Antibodies. Methods in molecular biology. 3–43. 18 indexed citations
4.
Cavacini, Lisa A., Kailash C. Bhol, Mong-Shang Lin, et al.. (2006). Pathogenic human monoclonal antibody against desmoglein 3. Clinical Immunology. 120(1). 68–75. 39 indexed citations
5.
Salato, Valerie K., et al.. (2005). Role of intramolecular epitope spreading in pemphigus vulgaris. Clinical Immunology. 116(1). 54–64. 44 indexed citations
6.
Bonamonte, Domenico, Mong-Shang Lin, Alberta Lucchese, et al.. (2005). Characterization of polyclonal antibodies raised against a linear peptide determinant of desmoglein-3.. PubMed. 5(1). 1–7. 6 indexed citations
7.
Fairley, Janet A., David T. Woodley, Mei Chen, George J. Giudice, & Mong-Shang Lin. (2004). A patient with both bullous pemphigoid and epidermolysis bullosa acquisita: an example of intermolecular epitope spreading. Journal of the American Academy of Dermatology. 51(1). 118–122. 34 indexed citations
8.
Zillikens, Detlef, et al.. (2004). T cell receptor gene usage of BP180-specific T lymphocytes from patients with bullous pemphigoid and pemphigoid gestationis. Clinical Immunology. 113(2). 179–186. 9 indexed citations
9.
Lucchese, Alberta, Abraham Mittelman, Mong-Shang Lin, Darja Kanduc, & Animesh A. Sinha. (2004). Epitope definition by proteomic similarity analysis: identification of the linear determinant of the anti-Dsg3 MAb 5H10. Journal of Translational Medicine. 2(1). 43–43. 18 indexed citations
10.
Fairley, Janet A., et al.. (2003). T Cell Receptor Gene Usage in Desmoglein-3-Specific T Lymphocytes from Patients with Pemphigus Vulgaris. Journal of Investigative Dermatology. 121(6). 1365–1372. 16 indexed citations
11.
Moesta, Achim K., Animesh A. Sinha, Mong-Shang Lin, & Luis A. Díaz. (2002). T Cell Receptor β Chain Gene Usage in Endemic Pemphigus Foliaceus (Fogo Selvagem). Journal of Investigative Dermatology. 119(2). 377–383. 11 indexed citations
12.
13.
Janson, Marleen M., et al.. (2002). Isotypes and Antigenic Profiles of Pemphigus Foliaceus and Pemphigus Vulgaris Autoantibodies. Clinical Immunology. 105(1). 64–74. 47 indexed citations
14.
Lin, Mong-Shang, et al.. (1998). Autoimmune responses of linear IgA disease: Both T cells and autoantibodies recognize the NC16A domain of BP180. Journal of Dermatological Science. 16. S11–S11. 2 indexed citations
15.
Lin, Mong-Shang, Susan J. Swartz, George J. Giudice, & Luis A. Díaz. (1998). Development and characterization of BP180-specific T cells from patients with bullous pemphigoid. Journal of Dermatological Science. 16. S11–S11. 1 indexed citations
16.
Lin, Mong-Shang & Yung‐Wu Chen. (1993). B Cell Differentiation. Cellular Immunology. 150(2). 343–352. 18 indexed citations
17.
Chen, Yung‐Wu, Mong-Shang Lin, & Kalpit A. Vora. (1992). B cell differentiation: I. Development and functional analysis of murine B cells immortalized by a recombinant retrovirus. International Immunology. 4(11). 1293–1302. 6 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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