Julia E. Weigand

2.4k total citations
50 papers, 1.5k citations indexed

About

Julia E. Weigand is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Julia E. Weigand has authored 50 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 8 papers in Cancer Research and 5 papers in Genetics. Recurrent topics in Julia E. Weigand's work include RNA and protein synthesis mechanisms (35 papers), Advanced biosensing and bioanalysis techniques (16 papers) and RNA modifications and cancer (14 papers). Julia E. Weigand is often cited by papers focused on RNA and protein synthesis mechanisms (35 papers), Advanced biosensing and bioanalysis techniques (16 papers) and RNA modifications and cancer (14 papers). Julia E. Weigand collaborates with scholars based in Germany, United States and Iceland. Julia E. Weigand's co-authors include Beatrix Suess, Jens Wöhnert, Elke Duchardt‐Ferner, Marc Müller, Oliver Weichenrieder, Renée Schroeder, Stefanie Dimmeler, Oliver Ohlenschläger, Sandra E. Fischer and Marc Vogel and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Julia E. Weigand

48 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia E. Weigand Germany 22 1.4k 179 134 115 96 50 1.5k
Richard Štefl Czechia 28 2.3k 1.6× 84 0.5× 78 0.6× 27 0.2× 37 0.4× 47 2.4k
Aaron A. Hoskins United States 23 1.3k 1.0× 94 0.5× 52 0.4× 133 1.2× 27 0.3× 57 1.5k
Sheila S. Teves United States 12 1.3k 0.9× 103 0.6× 91 0.7× 83 0.7× 123 1.3× 20 1.6k
Kerry P. Mahon United States 10 1.1k 0.8× 157 0.9× 169 1.3× 17 0.1× 168 1.8× 10 1.3k
Vitaly Kuryavyi United States 19 4.5k 3.2× 131 0.7× 118 0.9× 23 0.2× 114 1.2× 23 4.6k
Adelene Y. L. Sim Singapore 17 907 0.6× 44 0.2× 92 0.7× 16 0.1× 86 0.9× 40 1.2k
Simone Kunzelmann United Kingdom 20 776 0.6× 64 0.4× 69 0.5× 36 0.3× 42 0.4× 41 1.0k
Nathan M. Belliveau United States 12 1.2k 0.9× 216 1.2× 93 0.7× 26 0.2× 383 4.0× 19 1.5k
Weria Pezeshkian Denmark 19 901 0.6× 64 0.4× 45 0.3× 18 0.2× 181 1.9× 38 1.1k
Rania Leventis Canada 21 1.8k 1.3× 221 1.2× 27 0.2× 25 0.2× 111 1.2× 30 1.9k

Countries citing papers authored by Julia E. Weigand

Since Specialization
Citations

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

Fields of papers citing papers by Julia E. Weigand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia E. Weigand. 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 Julia E. Weigand. The network helps show where Julia E. Weigand may publish in the future.

Co-authorship network of co-authors of Julia E. Weigand

This figure shows the co-authorship network connecting the top 25 collaborators of Julia E. Weigand. A scholar is included among the top collaborators of Julia E. Weigand 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 Julia E. Weigand. Julia E. Weigand 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.
Vögele, Jennifer, Elke Duchardt‐Ferner, Jasleen Kaur Bains, et al.. (2024). Structure of an internal loop motif with three consecutive U•U mismatches from stem–loop 1 in the 3′-UTR of the SARS-CoV-2 genomic RNA. Nucleic Acids Research. 52(11). 6687–6706. 5 indexed citations
2.
Tants, Jan‐Niklas, et al.. (2024). Comprehensive Profiling of Roquin Binding Preferences for RNA Stem‐Loops. Angewandte Chemie International Edition. 63(50). e202412596–e202412596.
3.
Tants, Jan‐Niklas, et al.. (2024). Structure and RNA-binding of the helically extended Roquin CCCH-type zinc finger. Nucleic Acids Research. 52(16). 9838–9853. 7 indexed citations
4.
Vögele, Jennifer, Daniel Hymon, Jan Ferner, et al.. (2023). High-resolution structure of stem-loop 4 from the 5′-UTR of SARS-CoV-2 solved by solution state NMR. Nucleic Acids Research. 51(20). 11318–11331. 16 indexed citations
5.
Vogel, Marc, Bettina Appel, Julia E. Weigand, et al.. (2023). Magnesium Ion-Driven Folding and Conformational Switching Kinetics of Tetracycline Binding Aptamer: Implications for in vivo Riboswitch Engineering. Journal of Molecular Biology. 435(20). 168253–168253. 5 indexed citations
6.
Korn, Sophie Marianne, Karthikeyan Dhamotharan, Boris Fürtig, et al.. (2020). 1H, 13C, and 15N backbone chemical shift assignments of the nucleic acid-binding domain of SARS-CoV-2 non-structural protein 3e. Biomolecular NMR Assignments. 14(2). 329–333. 4 indexed citations
7.
Binas, Oliver, Jan‐Niklas Tants, Robert Janowski, et al.. (2020). Structural basis for the recognition of transiently structured AU-rich elements by Roquin. Nucleic Acids Research. 48(13). 7385–7403. 15 indexed citations
8.
Korn, Sophie Marianne, Boris Fürtig, Martin Hengesbach, et al.. (2020). 1H, 13C, and 15N backbone chemical shift assignments of the C-terminal dimerization domain of SARS-CoV-2 nucleocapsid protein. Biomolecular NMR Assignments. 15(1). 129–135. 15 indexed citations
9.
Grünewald, Christian, et al.. (2018). Structure guided fluorescence labeling reveals a two-step binding mechanism of neomycin to its RNA aptamer. Nucleic Acids Research. 47(1). 15–28. 15 indexed citations
10.
Vogel, Marc, et al.. (2018). Influence of Mg2+ on the conformational flexibility of a tetracycline aptamer. RNA. 25(1). 158–167. 27 indexed citations
11.
Fischer, Sandra E., et al.. (2017). Auto- and cross-regulation of the hnRNPs D and DL. RNA. 24(3). 324–331. 35 indexed citations
12.
Duchardt‐Ferner, Elke, Florian Groher, Julia E. Weigand, et al.. (2014). Building a stable RNA U-turn with a protonated cytidine. RNA. 20(8). 1163–1172. 22 indexed citations
13.
Weigand, Julia E., et al.. (2014). Sequence Elements Distal to the Ligand Binding Pocket Modulate the Efficiency of a Synthetic Riboswitch. ChemBioChem. 15(11). 1627–1637. 14 indexed citations
14.
Weigand, Julia E., et al.. (2011). Conformational dynamics of the tetracycline-binding aptamer. Nucleic Acids Research. 40(4). 1807–1817. 46 indexed citations
15.
Weigand, Julia E., et al.. (2011). RNA-Based Networks: Using RNA Aptamers and Ribozymes as Synthetic Genetic Devices. Methods in molecular biology. 813. 157–168. 12 indexed citations
16.
Suess, Beatrix, Karl‐Dieter Entian, Peter Kötter, & Julia E. Weigand. (2011). Aptamer-Regulated Expression of Essential Genes in Yeast. Methods in molecular biology. 824. 381–391. 3 indexed citations
17.
Duchardt‐Ferner, Elke, et al.. (2010). NMR resonance assignments of an engineered neomycin-sensing riboswitch RNA bound to ribostamycin and tobramycin. Biomolecular NMR Assignments. 4(1). 115–118. 18 indexed citations
18.
Suess, Beatrix & Julia E. Weigand. (2009). Aptamers as Artificial Gene Regulation Elements. Methods in molecular biology. 535. 201–208. 6 indexed citations
19.
Weigand, Julia E., et al.. (2007). Screening for engineered neomycin riboswitches that control translation initiation. RNA. 14(1). 89–97. 173 indexed citations
20.
Weigand, Julia E. & Beatrix Suess. (2007). Tetracycline aptamer-controlled regulation of pre-mRNA splicing in yeast. Nucleic Acids Research. 35(12). 4179–4185. 102 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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