Aida Razi

1.2k total citations
20 papers, 941 citations indexed

About

Aida Razi is a scholar working on Molecular Biology, Genetics and Biomedical Engineering. According to data from OpenAlex, Aida Razi has authored 20 papers receiving a total of 941 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Biomedical Engineering. Recurrent topics in Aida Razi's work include RNA and protein synthesis mechanisms (7 papers), RNA modifications and cancer (6 papers) and Bacterial Genetics and Biotechnology (6 papers). Aida Razi is often cited by papers focused on RNA and protein synthesis mechanisms (7 papers), RNA modifications and cancer (6 papers) and Bacterial Genetics and Biotechnology (6 papers). Aida Razi collaborates with scholars based in Canada, United States and China. Aida Razi's co-authors include Jonathan F. Lovell, Joaquín Ortega, Jumin Geng, Joaquı́n Ortega, Kevin A. Carter, Shuai Shao, Dandan Luo, Ulaş Sunar, Gregory R. Steinberg and James G. Granneman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Aida Razi

19 papers receiving 935 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aida Razi Canada 13 437 310 188 177 172 20 941
Sonja Serafini Italy 15 391 0.9× 294 0.9× 329 1.8× 47 0.3× 192 1.1× 27 1.0k
Rafael Góngora Spain 16 362 0.8× 121 0.4× 66 0.4× 157 0.9× 82 0.5× 51 1.1k
Françoise Pons France 19 459 1.1× 145 0.5× 136 0.7× 60 0.3× 52 0.3× 39 1.0k
Carmen Gutiérrez Millán Spain 15 286 0.7× 218 0.7× 176 0.9× 40 0.2× 158 0.9× 20 736
Gregory R. Robbins United States 11 398 0.9× 180 0.6× 45 0.2× 130 0.7× 163 0.9× 12 960
Enayat Anvari Iran 17 358 0.8× 221 0.7× 58 0.3× 59 0.3× 228 1.3× 39 1.1k
Jian‐Ning Liu China 19 453 1.0× 95 0.3× 89 0.5× 120 0.7× 56 0.3× 79 1.1k
Yuefei Zhu United States 16 366 0.8× 278 0.9× 51 0.3× 32 0.2× 173 1.0× 27 837
Risako Onodera Japan 20 450 1.0× 126 0.4× 42 0.2× 75 0.4× 295 1.7× 64 1.0k
Ejaj Ahmad India 16 450 1.0× 189 0.6× 38 0.2× 46 0.3× 291 1.7× 37 1.0k

Countries citing papers authored by Aida Razi

Since Specialization
Citations

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

Fields of papers citing papers by Aida Razi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aida Razi

This figure shows the co-authorship network connecting the top 25 collaborators of Aida Razi. A scholar is included among the top collaborators of Aida Razi 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 Aida Razi. Aida Razi 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.
Razi, Aida, et al.. (2025). Evidence supporting a catalytic pentad mechanism for the proteasome and other N-terminal nucleophile enzymes. Nature Communications. 16(1). 2949–2949.
2.
Walsh, Richard M., Shaun Rawson, Aida Razi, et al.. (2024). Mechanism of autocatalytic activation during proteasome assembly. Nature Structural & Molecular Biology. 31(8). 1167–1175. 10 indexed citations
3.
Razi, Aida, Robert D. Hubbard, Richard M. Walsh, et al.. (2023). Rational design of proteasome inhibitors based on the structure of the endogenous inhibitor PI31/Fub1. Proceedings of the National Academy of Sciences. 120(51). e2308417120–e2308417120. 6 indexed citations
4.
Federizon, Jasmin, Wei‐Chiao Huang, Xuedan He, et al.. (2021). Experimental and Computational Observations of Immunogenic Cobalt Porphyrin Lipid Bilayers: Nanodomain-Enhanced Antigen Association. Pharmaceutics. 13(1). 98–98. 16 indexed citations
5.
Sun, Boyang, Upendra Chitgupi, Changning Li, et al.. (2020). Drug Delivery: Surfactant‐Stripped Cabazitaxel Micelles Stabilized by Clotrimazole or Mifepristone (Adv. Therap. 3/2020). Advanced Therapeutics. 3(3). 1 indexed citations
6.
Razi, Aida, Joseph H. Davis, Yumeng Hao, et al.. (2019). Role of Era in assembly and homeostasis of the ribosomal small subunit. Nucleic Acids Research. 47(15). 8301–8317. 27 indexed citations
7.
Sun, Boyang, Upendra Chitgupi, Changning Li, et al.. (2019). Surfactant‐Stripped Cabazitaxel Micelles Stabilized by Clotrimazole or Mifepristone. Advanced Therapeutics. 3(3). 8 indexed citations
8.
Shen, Y., Angela Huynh, Aida Razi, et al.. (2019). Streptomyces IHF uses multiple interfaces to bind DNA. Biochimica et Biophysica Acta (BBA) - General Subjects. 1863(11). 129405–129405. 4 indexed citations
9.
Miranda, Dyego, Haoyuan Huang, Homan Kang, et al.. (2019). Highly-Soluble Cyanine J-aggregates Entrapped by Liposomes for In Vivo Optical Imaging around 930 nm. Theranostics. 9(2). 381–390. 37 indexed citations
10.
Seffouh, Amal, Nikhil Jain, Dushyant Jahagirdar, et al.. (2019). Structural consequences of the interaction of RbgA with a 50S ribosomal subunit assembly intermediate. Nucleic Acids Research. 47(19). 10414–10425. 32 indexed citations
11.
Huang, Wei‐Chiao, Bingbing Deng, Cuiyan Lin, et al.. (2018). A malaria vaccine adjuvant based on recombinant antigen binding to liposomes. Nature Nanotechnology. 13(12). 1174–1181. 117 indexed citations
12.
Razi, Aida, Alba Guarné, & Joaquı́n Ortega. (2017). The cryo-EM structure of YjeQ bound to the 30S subunit suggests a fidelity checkpoint function for this protein in ribosome assembly. Proceedings of the National Academy of Sciences. 114(17). E3396–E3403. 26 indexed citations
13.
Mottillo, Emilio P., Eric M. Desjardins, Justin D. Crane, et al.. (2016). Lack of Adipocyte AMPK Exacerbates Insulin Resistance and Hepatic Steatosis through Brown and Beige Adipose Tissue Function. Cell Metabolism. 24(1). 118–129. 280 indexed citations
14.
Razi, Aida, Robert A. Britton, & Joaquı́n Ortega. (2016). The impact of recent improvements in cryo-electron microscopy technology on the understanding of bacterial ribosome assembly. Nucleic Acids Research. 45(3). 1027–1040. 12 indexed citations
15.
Ni, Xiaodan, Joseph H. Davis, Nikhil Jain, et al.. (2016). YphC and YsxC GTPases assist the maturation of the central protuberance, GTPase associated region and functional core of the 50S ribosomal subunit. Nucleic Acids Research. 44(17). 8442–8455. 37 indexed citations
16.
Carter, Kevin A., Dandan Luo, Aida Razi, et al.. (2016). Sphingomyelin Liposomes Containing Porphyrin-phospholipid for Irinotecan Chemophototherapy. Theranostics. 6(13). 2329–2336. 53 indexed citations
17.
Shao, Shuai, Aida Razi, Upendra Chitgupi, et al.. (2016). Design of Hydrated Porphyrin-Phospholipid Bilayers with Enhanced Magnetic Resonance Contrast. Small. 13(1). 1602505–1602505. 22 indexed citations
18.
Luo, Dandan, Kevin A. Carter, Aida Razi, et al.. (2015). Porphyrin-phospholipid liposomes with tunable leakiness. Journal of Controlled Release. 220(Pt A). 484–494. 48 indexed citations
19.
Luo, Dandan, Kevin A. Carter, Aida Razi, et al.. (2015). Doxorubicin encapsulated in stealth liposomes conferred with light-triggered drug release. Biomaterials. 75. 193–202. 192 indexed citations
20.

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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