Marina Chekulaeva

4.2k total citations · 2 hit papers
23 papers, 3.1k citations indexed

About

Marina Chekulaeva is a scholar working on Molecular Biology, Cancer Research and Infectious Diseases. According to data from OpenAlex, Marina Chekulaeva has authored 23 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 8 papers in Cancer Research and 1 paper in Infectious Diseases. Recurrent topics in Marina Chekulaeva's work include RNA Research and Splicing (19 papers), RNA modifications and cancer (13 papers) and RNA and protein synthesis mechanisms (12 papers). Marina Chekulaeva is often cited by papers focused on RNA Research and Splicing (19 papers), RNA modifications and cancer (13 papers) and RNA and protein synthesis mechanisms (12 papers). Marina Chekulaeva collaborates with scholars based in Germany, United States and Israel. Marina Chekulaeva's co-authors include Witold Filipowicz, Nikolaus Rajewsky, Markus Landthaler, Nagarjuna Reddy Pamudurti, Mor Hanan, Marvin Jens, Daniel Pérez-Hernández, Shlomo Shenzis, Osnat Bartok and Evelyn Ramberger and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Communications.

In The Last Decade

Marina Chekulaeva

22 papers receiving 3.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Translation of CircRNAs

2017 1.4k citations Nagarjuna Reddy Pamudurti, Osnat Bartok et al. Molecular Cell profile →
Mechanisms of miRNA-mediated post-transcriptional regulation in animal cells

2009 564 citations Marina Chekulaeva, Witold Filipowicz Current Opinion in Cell Biology profile →

Peers

Marina Chekulaeva

IMMUN

GENET

Zhuo Fang Germany

Kevin Czaplinski United States

Erika Lasda United States

Gabriel A. Pratt United States

Yingchun Tong United States

Isabelle Behm‐Ansmant France

Pietro Laneve Italy

Haidi Zhang China

Shawn M. Lyons United States

Zhuo Fang Germany

Marina Chekulaeva

2.5k ×0.9

2.2k ×1.2

308 ×2.2

IMMUN

95 ×0.9

124 ×1.4

GENET

Citations per year, relative to Marina Chekulaeva Marina Chekulaeva (= 1×) peers Zhuo Fang

Countries citing papers authored by Marina Chekulaeva

Since Specialization

Citations

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

Fields of papers citing papers by Marina Chekulaeva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Chekulaeva

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

All Works

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20 of 20 papers shown

Römer, Christine, M A Strauch, B. M. Zuckerman, et al.. (2025). Neuromuscular dysfunction in patient-derived FUSR244RR–ALS iPSC model via axonal downregulation of neuromuscular junction proteins. PubMed. 2(2). ugaf005–ugaf005.

Chekulaeva, Marina. (2024). Mechanistic insights into the basis of widespread RNA localization. Nature Cell Biology. 26(7). 1037–1046. 13 indexed citations

Lödige, Inga, et al.. (2023). Massively parallel identification of mRNA localization elements in primary cortical neurons. Nature Neuroscience. 26(3). 394–405. 23 indexed citations

Loedige, Inga, Niko Popitsch, В. В. Черепанов, et al.. (2023). mRNA stability and m6A are major determinants of subcellular mRNA localization in neurons. Molecular Cell. 83(15). 2709–2725.e10. 36 indexed citations

Калинина, А. М., et al.. (2022). The key features of SARS-CoV-2 leader and NSP1 required for viral escape of NSP1-mediated repression. RNA. 28(5). 766–779. 35 indexed citations

Witte, Franziska, Jorge Ruiz‐Orera, Camilla Ciolli Mattioli, et al.. (2021). A trans locus causes a ribosomopathy in hypertrophic hearts that affects mRNA translation in a protein length-dependent fashion. Genome biology. 22(1). 191–191. 7 indexed citations

Chekulaeva, Marina, et al.. (2021). Charcot–Marie–Tooth mutation in glycyl-tRNA synthetase stalls ribosomes in a pre-accommodation state and activates integrated stress response. Nucleic Acids Research. 49(17). 10007–10017. 25 indexed citations

Chekulaeva, Marina, et al.. (2019). Genome-wide analysis of RNA and protein localization and local translation in mESC-derived neurons. Methods. 162-163. 31–41. 12 indexed citations

Chekulaeva, Marina & Nikolaus Rajewsky. (2018). Roles of Long Noncoding RNAs and Circular RNAs in Translation. Cold Spring Harbor Perspectives in Biology. 11(6). a032680–a032680. 33 indexed citations

10.

Mattioli, Camilla Ciolli, Vedran Franke, Koshi Imami, et al.. (2017). RNA localization is a key determinant of neurite-enriched proteome. Nature Communications. 8(1). 583–583. 146 indexed citations

11.

Pamudurti, Nagarjuna Reddy, Osnat Bartok, Marvin Jens, et al.. (2017). Translation of CircRNAs. Molecular Cell. 66(1). 9–21.e7. 1399 indexed citations breakdown →

12.

Kirchner, Marieluise, Reuven Aharoni, Camilla Ciolli Mattioli, et al.. (2016). Conservation of miRNA-mediated silencing mechanisms across 600 million years of animal evolution. Nucleic Acids Research. 45(2). 938–950. 21 indexed citations

13.

Chekulaeva, Marina & Markus Landthaler. (2016). Eyes on Translation. Molecular Cell. 63(6). 918–925. 21 indexed citations

14.

Chekulaeva, Marina, et al.. (2011). miRNA repression involves GW182-mediated recruitment of CCR4–NOT through conserved W-containing motifs. Nature Structural & Molecular Biology. 18(11). 1218–1226. 279 indexed citations

15.

Chekulaeva, Marina, Roy Parker, & Witold Filipowicz. (2010). The GW/WG repeats of Drosophila GW182 function as effector motifs for miRNA-mediated repression. Nucleic Acids Research. 38(19). 6673–6683. 28 indexed citations

16.

Ozgur, Sevim, Marina Chekulaeva, & Georg Stoecklin. (2010). Human Pat1b Connects Deadenylation with mRNA Decapping and Controls the Assembly of Processing Bodies. Molecular and Cellular Biology. 30(17). 4308–4323. 114 indexed citations

17.

Chekulaeva, Marina, Witold Filipowicz, & Roy Parker. (2009). Multiple independent domains of dGW182 function in miRNA-mediated repression in Drosophila. RNA. 15(5). 794–803. 61 indexed citations

18.

Chekulaeva, Marina & Witold Filipowicz. (2009). Mechanisms of miRNA-mediated post-transcriptional regulation in animal cells. Current Opinion in Cell Biology. 21(3). 452–460. 564 indexed citations breakdown →

19.

Chekulaeva, Marina, Matthias W. Hentze, & Anne Ephrussi. (2006). Bruno Acts as a Dual Repressor of oskar Translation, Promoting mRNA Oligomerization and Formation of Silencing Particles. Cell. 124(3). 521–533. 175 indexed citations

20.

Chekulaeva, Marina & Anne Ephrussi. (2004). Drosophila Development: RNA Interference ab ovo. Current Biology. 14(11). R428–R430. 5 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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