Doris Lindner

2.0k total citations
20 papers, 1.4k citations indexed

About

Doris Lindner is a scholar working on Molecular Biology, Cell Biology and Computer Networks and Communications. According to data from OpenAlex, Doris Lindner has authored 20 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 3 papers in Cell Biology and 1 paper in Computer Networks and Communications. Recurrent topics in Doris Lindner's work include RNA Research and Splicing (12 papers), RNA modifications and cancer (10 papers) and RNA and protein synthesis mechanisms (7 papers). Doris Lindner is often cited by papers focused on RNA Research and Splicing (12 papers), RNA modifications and cancer (10 papers) and RNA and protein synthesis mechanisms (7 papers). Doris Lindner collaborates with scholars based in Germany, France and United Kingdom. Doris Lindner's co-authors include Elena Conti, J. Ebert, A. Arockia Jeyaprakash, Erich A. Nigg, Ulf Klein, Elisa Izaurralde, N. Fukuhara, Leonie Unterholzner, George H. Gauss and Stephen Desiderio and has published in prestigious journals such as Science, Cell and Journal of Biological Chemistry.

In The Last Decade

Doris Lindner

20 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Doris Lindner Germany 13 1.1k 311 227 191 164 20 1.4k
Khalid Ouararhni France 15 1.4k 1.3× 193 0.6× 117 0.5× 211 1.1× 158 1.0× 18 1.7k
Jia-Wei Wu United States 10 1.3k 1.2× 146 0.5× 205 0.9× 352 1.8× 102 0.6× 11 1.4k
Ian Gibbs‐Seymour United Kingdom 12 1.2k 1.1× 213 0.7× 167 0.7× 772 4.0× 90 0.5× 15 1.5k
Samantha G. Pattenden United States 16 1.2k 1.1× 161 0.5× 63 0.3× 182 1.0× 91 0.6× 25 1.4k
Mathieu Courcelles Canada 17 1.1k 1.0× 595 1.9× 91 0.4× 424 2.2× 93 0.6× 25 1.5k
Alexis Verger France 18 1.1k 1.1× 144 0.5× 76 0.3× 197 1.0× 191 1.2× 34 1.4k
Leslyn A. Hanakahi United States 17 1.3k 1.2× 168 0.5× 75 0.3× 237 1.2× 190 1.2× 22 1.5k
Jesse R. Raab United States 19 859 0.8× 275 0.9× 52 0.2× 145 0.8× 90 0.5× 26 1.3k
Christopher M. Hickey United States 14 1.1k 1.0× 140 0.5× 613 2.7× 229 1.2× 98 0.6× 20 1.3k
Julien Licchesi United States 15 1.1k 1.1× 195 0.6× 107 0.5× 266 1.4× 97 0.6× 17 1.3k

Countries citing papers authored by Doris Lindner

Since Specialization
Citations

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

Fields of papers citing papers by Doris Lindner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Doris Lindner

This figure shows the co-authorship network connecting the top 25 collaborators of Doris Lindner. A scholar is included among the top collaborators of Doris Lindner 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 Doris Lindner. Doris Lindner 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.
Lindner, Doris, Stefan M. Kallenberger, Johanna Schott, et al.. (2024). Turnover of PPP1R15A mRNA encoding GADD34 controls responsiveness and adaptation to cellular stress. Cell Reports. 43(4). 114069–114069. 9 indexed citations
2.
Lindner, Doris, et al.. (2024). E3 ubiquitin ligase RNF10 promotes dissociation of stalled ribosomes and responds to ribosomal subunit imbalance. Nature Communications. 15(1). 10350–10350. 7 indexed citations
3.
Schott, Johanna, Doris Lindner, Joris Messens, et al.. (2023). Stress-induced nuclear speckle reorganization is linked to activation of immediate early gene splicing. The Journal of Cell Biology. 222(12). 12 indexed citations
4.
Poetz, Fabian, Svetlana Lebedeva, Johanna Schott, et al.. (2022). Control of immediate early gene expression by CPEB4-repressor complex-mediated mRNA degradation. Genome biology. 23(1). 193–193. 11 indexed citations
5.
Hisaoka, Miharu, et al.. (2022). Preferential translation of p53 target genes. RNA Biology. 19(1). 437–452. 1 indexed citations
6.
Schott, Johanna, Sonja Reitter, Doris Lindner, et al.. (2021). Nascent Ribo-Seq measures ribosomal loading time and reveals kinetic impact on ribosome density. Nature Methods. 18(9). 1068–1074. 19 indexed citations
7.
Poetz, Fabian, Yevgen Levdansky, Doris Lindner, et al.. (2021). RNF219 attenuates global mRNA decay through inhibition of CCR4-NOT complex-mediated deadenylation. Nature Communications. 12(1). 7175–7175. 21 indexed citations
8.
Lindner, Doris, et al.. (2021). Expanding HLRS Academic HPC Simulation Training Programs to More Target Groups. 12(3). 13–26. 1 indexed citations
9.
Haneke, Katharina, Johanna Schott, Doris Lindner, et al.. (2020). CDK1 couples proliferation with protein synthesis. The Journal of Cell Biology. 219(3). 66 indexed citations
10.
Lindner, Doris & Ralf Dahm. (2018). Studienprogramm für die, die mehr wissen wollen. Biologie in unserer Zeit. 48(5). 279–279. 1 indexed citations
11.
Nowak, Agnieszka, Claudio Alfieri, Christian U. Stirnimann, et al.. (2011). Chromatin-modifying Complex Component Nurf55/p55 Associates with Histones H3 and H4 and Polycomb Repressive Complex 2 Subunit Su(z)12 through Partially Overlapping Binding Sites. Journal of Biological Chemistry. 286(26). 23388–23396. 51 indexed citations
12.
Lane, Laura A., Carlos Fernández‐Tornero, Min Zhou, et al.. (2011). Mass Spectrometry Reveals Stable Modules in holo and apo RNA Polymerases I and III. Structure. 19(1). 90–100. 47 indexed citations
13.
Fernández‐Tornero, Carlos, Bettina Böttcher, Umar Rashid, et al.. (2010). Conformational flexibility of RNA polymerase III during transcriptional elongation. The EMBO Journal. 29(22). 3762–3772. 57 indexed citations
14.
Grimm, Clemens, Nga Ly‐Hartig, Ulrich Steuerwald, et al.. (2009). Molecular recognition of histone lysine methylation by the Polycomb group repressor dSfmbt. The EMBO Journal. 28(13). 1965–1977. 66 indexed citations
15.
Lorentzen, Esben, Andrzej Dziembowski, Doris Lindner, Bertrand Séraphin, & Elena Conti. (2007). RNA channelling by the archaeal exosome. EMBO Reports. 8(5). 470–476. 93 indexed citations
16.
Jeyaprakash, A. Arockia, Ulf Klein, Doris Lindner, et al.. (2007). Structure of a Survivin–Borealin–INCENP Core Complex Reveals How Chromosomal Passengers Travel Together. Cell. 131(2). 271–285. 273 indexed citations
17.
Cook, Atlanta G., Elena Fernández Fernández, Doris Lindner, et al.. (2005). The Structure of the Nuclear Export Receptor Cse1 in Its Cytosolic State Reveals a Closed Conformation Incompatible with Cargo Binding. Molecular Cell. 18(3). 355–367. 58 indexed citations
18.
Fukuhara, N., J. Ebert, Leonie Unterholzner, et al.. (2005). SMG7 Is a 14-3-3-like Adaptor in the Nonsense-Mediated mRNA Decay Pathway. Molecular Cell. 17(4). 537–547. 192 indexed citations
19.
Bayliss, Richard, Teresa Sardón, J. Ebert, et al.. (2004). Determinants for Aurora-A Activation and Aurora-B Discrimination by TPX2. Cell Cycle. 3(4). 402–405. 48 indexed citations
20.
Schwarz, Klaus, George H. Gauss, Leopold Ludwig, et al.. (1996). RAG Mutations in Human B Cell-Negative SCID. Science. 274(5284). 97–99. 377 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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