Yaser Hashem

3.3k total citations
53 papers, 2.2k citations indexed

About

Yaser Hashem is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Yaser Hashem has authored 53 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in Yaser Hashem's work include RNA and protein synthesis mechanisms (45 papers), RNA modifications and cancer (29 papers) and RNA Research and Splicing (11 papers). Yaser Hashem is often cited by papers focused on RNA and protein synthesis mechanisms (45 papers), RNA modifications and cancer (29 papers) and RNA Research and Splicing (11 papers). Yaser Hashem collaborates with scholars based in France, United States and Russia. Yaser Hashem's co-authors include Joachim Frank, Pascal Auffinger, Lauriane Kühn, Amédée des Georges, Christopher U.T. Hellen, Tatyana V. Pestova, Vidya Dhote, Hstau Y. Liao, Robert A. Grassucci and Angelita Simonetti and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Yaser Hashem

51 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yaser Hashem France 29 1.9k 228 176 142 139 53 2.2k
Alexey Petrov United States 30 1.9k 1.0× 241 1.1× 219 1.2× 61 0.4× 157 1.1× 43 2.2k
Peter V. Cornish United States 16 1.3k 0.7× 171 0.8× 181 1.0× 51 0.4× 129 0.9× 29 1.7k
I.S. Fernandez United Kingdom 24 2.2k 1.1× 340 1.5× 235 1.3× 70 0.5× 154 1.1× 33 2.8k
Anke M. Mulder United States 10 833 0.4× 106 0.5× 146 0.8× 120 0.8× 91 0.7× 15 1.3k
Josué Gómez-Blanco Spain 18 1.1k 0.6× 200 0.9× 89 0.5× 133 0.9× 274 2.0× 31 1.9k
Andrey L. Konevega Russia 27 2.5k 1.3× 474 2.1× 98 0.6× 40 0.3× 207 1.5× 81 2.8k
J. Loerke Germany 21 1.5k 0.8× 267 1.2× 165 0.9× 33 0.2× 90 0.6× 29 1.7k
Scott Bailey United States 28 2.0k 1.1× 539 2.4× 132 0.8× 287 2.0× 201 1.4× 39 2.4k
M. Selmer Sweden 21 2.3k 1.2× 593 2.6× 145 0.8× 51 0.4× 205 1.5× 42 2.6k
Ambroise Desfosses France 22 810 0.4× 158 0.7× 44 0.3× 294 2.1× 180 1.3× 34 1.4k

Countries citing papers authored by Yaser Hashem

Since Specialization
Citations

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

Fields of papers citing papers by Yaser Hashem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yaser Hashem

This figure shows the co-authorship network connecting the top 25 collaborators of Yaser Hashem. A scholar is included among the top collaborators of Yaser Hashem 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 Yaser Hashem. Yaser Hashem 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.
Erath, Jessey, et al.. (2025). A rapid, simple, and economical method for the isolation of ribosomes and translational machinery for structural and functional studies. Nature Communications. 16(1). 7185–7185. 1 indexed citations
2.
Wolff, Philippe, David Pflieger, Todd Blevins, et al.. (2025). Structural insights into cauliflower mitoribosome in translation state and in association with a late assembly factor. Nature Communications. 16(1). 10839–10839.
3.
Wang, Chaoyue, Rafael E. O. Rocha, Joachim Kloehn, et al.. (2024). Apicomplexan mitoribosome from highly fragmented rRNAs to a functional machine. Nature Communications. 15(1). 10689–10689. 2 indexed citations
4.
Sweeney, Trevor R., et al.. (2021). Functional role and ribosomal position of the unique N-terminal region of DHX29, a factor required for initiation on structured mammalian mRNAs. Nucleic Acids Research. 49(22). 12955–12969. 9 indexed citations
5.
Waltz, Florent, Thalia Salinas‐Giegé, Heddy Soufari, et al.. (2021). How to build a ribosome from RNA fragments in Chlamydomonas mitochondria. Nature Communications. 12(1). 7176–7176. 35 indexed citations
6.
Khusainov, Iskander, Heddy Soufari, Stefano Marzi, et al.. (2021). Stabilization of Ribosomal RNA of the Small Subunit by Spermidine in Staphylococcus aureus. Frontiers in Molecular Biosciences. 8. 738752–738752. 10 indexed citations
7.
Moulinier, Luc, et al.. (2021). Peculiarities of aminoacyl-tRNA synthetases from trypanosomatids. Journal of Biological Chemistry. 297(2). 100913–100913. 10 indexed citations
8.
Sissler, Marie & Yaser Hashem. (2021). Mitoribosome assembly comes into view. Nature Structural & Molecular Biology. 28(8). 631–633. 4 indexed citations
9.
Soufari, Heddy, et al.. (2020). Specific features and assembly of the plant mitochondrial complex I revealed by cryo-EM. Nature Communications. 11(1). 5195–5195. 65 indexed citations
10.
Abaeva, Irina S., Quentin Vicens, Anthony Bochler, et al.. (2020). The Halastavi árva Virus Intergenic Region IRES Promotes Translation by the Simplest Possible Initiation Mechanism. Cell Reports. 33(10). 108476–108476. 13 indexed citations
11.
Simonetti, Angelita, et al.. (2020). Structural Insights into the Mammalian Late-Stage Initiation Complexes. Cell Reports. 31(1). 107497–107497. 53 indexed citations
12.
Vicens, Quentin, et al.. (2020). Interaction Networks of Ribosomal Expansion Segments in Kinetoplastids. Sub-cellular biochemistry. 96. 433–450. 6 indexed citations
13.
Hashem, Yaser, et al.. (2018). Major structural rearrangements of the canonical eukaryotic translation initiation complex. Current Opinion in Structural Biology. 53. 151–158. 7 indexed citations
14.
Pellegrino, Simone, N. Demeshkina, Eder Mancera-Martínez, et al.. (2018). Structural Insights into the Role of Diphthamide on Elongation Factor 2 in mRNA Reading-Frame Maintenance. Journal of Molecular Biology. 430(17). 2677–2687. 37 indexed citations
15.
Khusainov, Iskander, Quentin Vicens, Konstantin S. Usachev, et al.. (2017). Structures and dynamics of hibernating ribosomes from Staphylococcus aureus mediated by intermolecular interactions of HPF. The EMBO Journal. 36(14). 2073–2087. 57 indexed citations
16.
Doniger, Tirza, K. Shanmugha Rajan, Osnat Bartok, et al.. (2016). A pseudouridylation switch in rRNA is implicated in ribosome function during the life cycle of Trypanosoma brucei. Scientific Reports. 6(1). 25296–25296. 37 indexed citations
17.
Liao, Hstau Y., Yaser Hashem, & Joachim Frank. (2015). Efficient Estimation of Three-Dimensional Covariance and its Application in the Analysis of Heterogeneous Samples in Cryo-Electron Microscopy. Structure. 23(6). 1129–1137. 23 indexed citations
18.
Sun, Ming, et al.. (2015). Dynamical features of thePlasmodium falciparumribosome during translation. Nucleic Acids Research. 43(21). gkv991–gkv991. 37 indexed citations
19.
Boël, Grégory, Paul Smith, Michael T. Englander, et al.. (2014). The ABC-F protein EttA gates ribosome entry into the translation elongation cycle. Nature Structural & Molecular Biology. 21(2). 143–151. 95 indexed citations
20.
Georges, Amédée des, Yaser Hashem, Anett Unbehaun, et al.. (2013). Structure of the mammalian ribosomal pre-termination complex associated with eRF1•eRF3•GDPNP. Nucleic Acids Research. 42(5). 3409–3418. 63 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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