Allan M. Weissman

21.8k total citations · 10 hit papers
129 papers, 18.0k citations indexed

About

Allan M. Weissman is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Allan M. Weissman has authored 129 papers receiving a total of 18.0k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Molecular Biology, 46 papers in Oncology and 41 papers in Immunology. Recurrent topics in Allan M. Weissman's work include Ubiquitin and proteasome pathways (70 papers), Cancer-related Molecular Pathways (27 papers) and T-cell and B-cell Immunology (27 papers). Allan M. Weissman is often cited by papers focused on Ubiquitin and proteasome pathways (70 papers), Cancer-related Molecular Pathways (27 papers) and T-cell and B-cell Immunology (27 papers). Allan M. Weissman collaborates with scholars based in United States, Israel and United Kingdom. Allan M. Weissman's co-authors include Jane P. Jensen, Shengyun Fang, Claudio A.P. Joazeiro, Juan S. Bonifacino, Yien Che Tsai, Richard D. Klausner, Meredith B. Metzger, Kevin L. Lorick, Yili Yang and Jonathan D. Ashwell and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Allan M. Weissman

127 papers receiving 17.8k citations

Hit Papers

Themes and variations on ... 1997 2026 2006 2016 2001 2000 1999 2000 2000 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Allan M. Weissman United States 65 13.4k 4.2k 3.7k 3.7k 2.3k 129 18.0k
Ulf R. Rapp Germany 85 18.9k 1.4× 5.1k 1.2× 3.0k 0.8× 3.7k 1.0× 1.2k 0.5× 325 24.8k
Sara A. Courtneidge United States 65 11.2k 0.8× 4.0k 1.0× 4.1k 1.1× 2.5k 0.7× 727 0.3× 125 17.4k
Bart Vanhaesebroeck United Kingdom 68 14.4k 1.1× 4.1k 1.0× 2.6k 0.7× 5.7k 1.6× 1.3k 0.6× 194 22.4k
Zhou Songyang United States 69 15.1k 1.1× 2.8k 0.7× 2.8k 0.8× 3.1k 0.8× 696 0.3× 193 19.9k
Tullia Lindsten United States 58 13.2k 1.0× 4.2k 1.0× 1.9k 0.5× 8.4k 2.3× 3.8k 1.7× 98 22.8k
Martin Rechsteiner United States 62 12.3k 0.9× 3.0k 0.7× 3.9k 1.0× 1.7k 0.5× 1.7k 0.8× 148 14.5k
Len Stephens United Kingdom 67 13.3k 1.0× 2.1k 0.5× 4.7k 1.2× 3.9k 1.1× 785 0.3× 177 19.1k
Alan L. Schwartz United States 66 9.2k 0.7× 2.4k 0.6× 3.5k 0.9× 1.7k 0.5× 1.3k 0.6× 176 14.3k
Tetsu Akiyama Japan 67 13.0k 1.0× 4.7k 1.1× 3.0k 0.8× 1.8k 0.5× 684 0.3× 264 20.0k
Brian Raught Canada 60 13.9k 1.0× 2.2k 0.5× 2.7k 0.7× 1.7k 0.5× 1.0k 0.4× 172 17.3k

Countries citing papers authored by Allan M. Weissman

Since Specialization
Citations

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

Fields of papers citing papers by Allan M. Weissman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Allan M. Weissman

This figure shows the co-authorship network connecting the top 25 collaborators of Allan M. Weissman. A scholar is included among the top collaborators of Allan M. Weissman 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 Allan M. Weissman. Allan M. Weissman 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.
Yang, Mei, Jennifer Mariano, R. Su, et al.. (2023). SARS-CoV-2 papain-like protease plays multiple roles in regulating cellular proteins in the endoplasmic reticulum. Journal of Biological Chemistry. 299(12). 105346–105346. 4 indexed citations
2.
Tsai, Yien Che, Yu‐He Liang, Jennifer Mariano, et al.. (2021). A structurally conserved site in AUP1 binds the E2 enzyme UBE2G2 and is essential for ER-associated degradation. PLoS Biology. 19(12). e3001474–e3001474. 11 indexed citations
3.
Ahmed, Syed Feroj, Gary Sibbet, Ventzislava A. Hristova, et al.. (2020). Structural basis for DNA damage-induced phosphoregulation of MDM2 RING domain. Nature Communications. 11(1). 2094–2094. 28 indexed citations
4.
Metzger, Meredith B., et al.. (2020). A protein quality control pathway at the mitochondrial outer membrane. eLife. 9. 50 indexed citations
5.
Cavellini, Laetitia, et al.. (2017). An ubiquitin-dependent balance between mitofusin turnover and fatty acids desaturation regulates mitochondrial fusion. Nature Communications. 8(1). 15832–15832. 20 indexed citations
6.
Balch, William E., Jacob I. Sznajder, Daniel Finley, et al.. (2013). Malfolded Protein Structure and Proteostasis in Lung Diseases. American Journal of Respiratory and Critical Care Medicine. 189(1). 96–103. 44 indexed citations
7.
Metzger, Meredith B., Jonathan N. Pruneda, Rachel E. Klevit, & Allan M. Weissman. (2013). RING-type E3 ligases: Master manipulators of E2 ubiquitin-conjugating enzymes and ubiquitination. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1843(1). 47–60. 462 indexed citations breakdown →
8.
Metzger, Meredith B., Ventzislava A. Hristova, & Allan M. Weissman. (2012). HECT and RING finger families of E3 ubiquitin ligases at a glance. Journal of Cell Science. 125(3). 531–537. 472 indexed citations breakdown →
9.
Weissman, Allan M., Nitzan Shabek, & Aaron Ciechanover. (2011). The predator becomes the prey: regulating the ubiquitin system by ubiquitylation and degradation. Nature Reviews Molecular Cell Biology. 12(9). 605–620. 246 indexed citations
10.
Weissman, Allan M., et al.. (2008). Inhibiting Hdm2 and Ubiquitin-Activating Enzyme: Targeting the Ubiquitin Conjugating System in Cancer. PubMed. 171–190. 11 indexed citations
11.
Cohen, Mickaël M., et al.. (2008). Ubiquitin–Proteasome-dependent Degradation of a Mitofusin, a Critical Regulator of Mitochondrial Fusion. Molecular Biology of the Cell. 19(6). 2457–2464. 145 indexed citations
12.
Yang, Yili, Jirouta Kitagaki, Ren‐Ming Dai, et al.. (2007). Inhibitors of Ubiquitin-Activating Enzyme (E1), a New Class of Potential Cancer Therapeutics. Cancer Research. 67(19). 9472–9481. 372 indexed citations
13.
Yang, Yili, Robert L. Ludwig, Jane P. Jensen, et al.. (2005). Small molecule inhibitors of HDM2 ubiquitin ligase activity stabilize and activate p53 in cells. Cancer Cell. 7(6). 547–559. 263 indexed citations
14.
Plafker, Scott M., Kendra S. Plafker, Allan M. Weissman, & Ian G. Macara. (2004). Ubiquitin charging of human class III ubiquitin-conjugating enzymes triggers their nuclear import. The Journal of Cell Biology. 167(4). 649–659. 76 indexed citations
15.
Magnifico, Alessandra, Seth A. Ettenberg, Cuihong Yang, et al.. (2003). WW Domain HECT E3s Target Cbl RING Finger E3s for Proteasomal Degradation. Journal of Biological Chemistry. 278(44). 43169–43177. 144 indexed citations
16.
Weissman, Allan M.. (2003). Detecting Ubiquitinated T-Cell Antigen Receptor Subunits by Immunoblotting. Humana Press eBooks. 134. 283–287. 1 indexed citations
17.
Cohen, Shaul, et al.. (1992). Epidural Patient-Controlled Analgesia After Cesarean Section. Anesthesia & Analgesia. 74(2). 226–230. 38 indexed citations
18.
Kosugi, Atsushi, Allan M. Weissman, M Ogata, Takafumi Hamaoka, & H Fujiwara. (1992). Instability of assembled T-cell receptor complex that is associated with rapid degradation of zeta chains in immature CD4+CD8+ thymocytes.. Proceedings of the National Academy of Sciences. 89(20). 9494–9498. 19 indexed citations
19.
Klausner, Richard D., Allan M. Weissman, Michal Baniyash, Juan S. Bonifacino, & Lawrence E. Samelson. (1989). The Role of the Zeta Chain in the Expression, Structure and Function of the T Cell Receptor. PubMed. 254. 21–24. 8 indexed citations
20.
Weissman, Allan M., P Ross, Pilar García-Morales, et al.. (1988). Tyrosine phosphorylation of the human T cell antigen receptor zeta -chain: activation via CD3 but not CD2.. The Journal of Immunology. 141(10). 3532–3536. 48 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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