Alanna Schepartz

9.9k total citations
180 papers, 7.4k citations indexed

About

Alanna Schepartz is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Alanna Schepartz has authored 180 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Molecular Biology, 40 papers in Organic Chemistry and 23 papers in Oncology. Recurrent topics in Alanna Schepartz's work include RNA and protein synthesis mechanisms (56 papers), Chemical Synthesis and Analysis (49 papers) and Advanced biosensing and bioanalysis techniques (40 papers). Alanna Schepartz is often cited by papers focused on RNA and protein synthesis mechanisms (56 papers), Chemical Synthesis and Analysis (49 papers) and Advanced biosensing and bioanalysis techniques (40 papers). Alanna Schepartz collaborates with scholars based in United States, France and United Kingdom. Alanna Schepartz's co-authors include Bernard Cuenoud, Joshua A. Kritzer, Douglas S. Daniels, E. James Petersson, Michael E. Hodsdon, Jade X. Qiu, Jacob Appelbaum, Derek Toomre, Jason W. Chin and Cody J. Craig and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Alanna Schepartz

176 papers receiving 7.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alanna Schepartz United States 51 6.1k 2.3k 731 615 609 180 7.4k
Christian Heinis Switzerland 37 4.3k 0.7× 1.8k 0.8× 687 0.9× 333 0.5× 194 0.3× 99 5.5k
Miquel Pons Spain 40 3.3k 0.5× 1.2k 0.5× 275 0.4× 214 0.3× 371 0.6× 173 5.2k
James D. Lear United States 48 6.1k 1.0× 621 0.3× 396 0.5× 170 0.3× 603 1.0× 87 7.8k
Christian P. R. Hackenberger Germany 40 4.2k 0.7× 3.0k 1.3× 860 1.2× 133 0.2× 261 0.4× 162 5.6k
Kathrin Lang Germany 40 4.7k 0.8× 2.6k 1.2× 524 0.7× 220 0.4× 111 0.2× 85 6.5k
Jennifer A. Prescher United States 41 8.4k 1.4× 7.4k 3.2× 949 1.3× 572 0.9× 609 1.0× 84 11.6k
George Bárány United States 46 5.8k 1.0× 3.0k 1.3× 718 1.0× 93 0.2× 213 0.3× 222 7.4k
Lynne Regan United States 52 7.7k 1.3× 520 0.2× 410 0.6× 373 0.6× 655 1.1× 173 9.2k
Nicholas J. Agard United States 17 4.2k 0.7× 3.9k 1.7× 542 0.7× 143 0.2× 379 0.6× 24 5.9k
Bradley L. Pentelute United States 40 4.6k 0.8× 2.6k 1.2× 927 1.3× 68 0.1× 306 0.5× 153 6.2k

Countries citing papers authored by Alanna Schepartz

Since Specialization
Citations

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

Fields of papers citing papers by Alanna Schepartz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alanna Schepartz

This figure shows the co-authorship network connecting the top 25 collaborators of Alanna Schepartz. A scholar is included among the top collaborators of Alanna Schepartz 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 Alanna Schepartz. Alanna Schepartz 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.
Schissel, Carly K., et al.. (2025). Monitoring monomer-specific acyl–tRNA levels in cells with PARTI. Nucleic Acids Research. 53(8).
2.
Wasko, Kevin, et al.. (2025). Packaged delivery of CRISPR–Cas9 ribonucleoproteins accelerates genome editing. Nucleic Acids Research. 53(5). 9 indexed citations
3.
Schissel, Carly K., Bhavana Shah, Shuai Zheng, et al.. (2025). Site-selective protein editing by backbone extension acyl rearrangements. Nature Chemical Biology. 21(10). 1621–1630. 1 indexed citations
4.
Schissel, Carly K., et al.. (2025). Peptide Backbone Editing via Post-Translational O to C Acyl Shift. Journal of the American Chemical Society. 147(8). 6503–6513. 5 indexed citations
5.
Griffin, Wezley C., José Luís Pérez Alejo, Ryan A. Brady, et al.. (2024). β-Amino Acids Reduce Ternary Complex Stability and Alter the Translation Elongation Mechanism. ACS Central Science. 10(6). 1262–1275. 5 indexed citations
6.
Palo, Michael Z., et al.. (2024). Minimization of the E. coli ribosome, aided and optimized by community science. Nucleic Acids Research. 52(3). 1027–1042. 3 indexed citations
7.
Walker, Joshua A., et al.. (2023). Aminobenzoic Acid Derivatives Obstruct Induced Fit in the Catalytic Center of the Ribosome. ACS Central Science. 9(6). 1160–1169. 6 indexed citations
8.
Zheng, Shuai, et al.. (2023). Long-term super-resolution inner mitochondrial membrane imaging with a lipid probe. Nature Chemical Biology. 20(1). 83–92. 41 indexed citations
9.
Ad, Omer, Kyle Hoffman, Andrew G. Cairns, et al.. (2019). Translation of Diverse Aramid- and 1,3-Dicarbonyl-peptides by Wild Type Ribosomes in Vitro. ACS Central Science. 5(7). 1289–1294. 55 indexed citations
10.
Steinauer, Angela, et al.. (2019). HOPS-dependent endosomal fusion required for efficient cytosolic delivery of therapeutic peptides and small proteins. Proceedings of the National Academy of Sciences. 116(2). 512–521. 40 indexed citations
11.
Walker, Allison S., et al.. (2018). Mechanism of Allosteric Coupling into and through the Plasma Membrane by EGFR. Cell chemical biology. 25(7). 857–870.e7. 27 indexed citations
12.
Bottanelli, Francesca, Nicole Kilian, Andreas M. Ernst, et al.. (2017). A novel physiological role for ARF1 in the formation of bidirectional tubules from the Golgi. Molecular Biology of the Cell. 28(12). 1676–1687. 52 indexed citations
13.
Scheck, Rebecca A., et al.. (2015). Growth Factor Identity Is Encoded by Discrete Coiled-Coil Rotamers in the EGFR Juxtamembrane Region. Chemistry & Biology. 22(6). 776–784. 36 indexed citations
14.
Erdmann, Roman S., Hideo Takakura, Alexander D. Thompson, et al.. (2014). Super‐Resolution Imaging of the Golgi in Live Cells with a Bioorthogonal Ceramide Probe. Angewandte Chemie International Edition. 53(38). 10242–10246. 142 indexed citations
15.
Craig, Cody J., et al.. (2012). Relationship between side-chain branching and stoichiometry in β3-peptide bundles. Tetrahedron. 68(23). 4342–4345. 6 indexed citations
16.
Appelbaum, Jacob, et al.. (2012). Arginine Topology Controls Escape of Minimally Cationic Proteins from Early Endosomes to the Cytoplasm. Chemistry & Biology. 19(7). 819–830. 144 indexed citations
17.
Schepartz, Alanna, et al.. (2010). Direct Visualization of Protein Association in Living Cells with Complex‐Edited Electron Microscopy. Angewandte Chemie International Edition. 49(43). 7952–7954. 8 indexed citations
18.
Schepartz, Alanna, et al.. (1998). Interaction, assembly and processing at the chemistry—biology interface. Current Opinion in Chemical Biology. 2(1). 9–10. 9 indexed citations
19.
Tsai, Francis, Otis Littlefield, Péter Kósa, et al.. (1998). Polarity of Transcription on Pol II and Archaeal Promoters: Where Is the "One-way Sign" and How Is It Read?. Cold Spring Harbor Symposia on Quantitative Biology. 63(0). 53–62. 4 indexed citations
20.
Cox, Julia, et al.. (1998). Preinitiation complex assembly: potentially a bumpy path. Current Opinion in Chemical Biology. 2(1). 11–17. 4 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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