Birgitta Beatrix

2.3k total citations
29 papers, 1.7k citations indexed

About

Birgitta Beatrix is a scholar working on Molecular Biology, Rheumatology and Oncology. According to data from OpenAlex, Birgitta Beatrix has authored 29 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 7 papers in Rheumatology and 5 papers in Oncology. Recurrent topics in Birgitta Beatrix's work include RNA and protein synthesis mechanisms (15 papers), Porphyrin Metabolism and Disorders (9 papers) and RNA modifications and cancer (9 papers). Birgitta Beatrix is often cited by papers focused on RNA and protein synthesis mechanisms (15 papers), Porphyrin Metabolism and Disorders (9 papers) and RNA modifications and cancer (9 papers). Birgitta Beatrix collaborates with scholars based in Germany, United States and Japan. Birgitta Beatrix's co-authors include Roland Beckmann, Otto Berninghausen, Thomas Becker, Wolfgang Buckel, Oskar Zelder, Martin Wiedmann, Jean‐Paul Armache, Thomas Spreter, Thorsten Mielke and Hideaki Sakai and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Birgitta Beatrix

28 papers receiving 1.7k citations

Peers

Birgitta Beatrix
Justin C. Deme United Kingdom
Ewa Folta‐Stogniew United States
Carilee Denison United States
Valerie E. Pye United Kingdom
Kelly R. Molloy United States
Basil J. Greber United States
Jan P. Erzberger United States
Justin C. Deme United Kingdom
Birgitta Beatrix
Citations per year, relative to Birgitta Beatrix Birgitta Beatrix (= 1×) peers Justin C. Deme

Countries citing papers authored by Birgitta Beatrix

Since Specialization
Citations

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

Fields of papers citing papers by Birgitta Beatrix

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgitta Beatrix

This figure shows the co-authorship network connecting the top 25 collaborators of Birgitta Beatrix. A scholar is included among the top collaborators of Birgitta Beatrix 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 Birgitta Beatrix. Birgitta Beatrix 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.
Denk, Timo, et al.. (2026). Structural basis of co-translational N-myristoylation in humans. Nature Communications. 17(1). 1191–1191.
2.
Mackens‐Kiani, Timur, et al.. (2023). The dynamic architecture of Map1- and NatB-ribosome complexes coordinates the sequential modifications of nascent polypeptide chains. PLoS Biology. 21(4). e3001995–e3001995. 14 indexed citations
3.
Steinchen, Wieland, Birgitta Beatrix, Otto Berninghausen, et al.. (2020). Architecture of the active post‐translational Sec translocon. The EMBO Journal. 40(3). e105643–e105643. 32 indexed citations
4.
Těšina, Petr, Jingdong Cheng, Micheline Fromont‐Racine, et al.. (2019). Structure of the 80S ribosome–Xrn1 nuclease complex. Nature Structural & Molecular Biology. 26(4). 275–280. 60 indexed citations
5.
Schmidt, Christian, Petr Těšina, Otto Berninghausen, et al.. (2018). Ribosome–NatA architecture reveals that rRNA expansion segments coordinate N-terminal acetylation. Nature Structural & Molecular Biology. 26(1). 35–39. 84 indexed citations
6.
Sluis, Eli O. van der, Otto Berninghausen, Wei Han, et al.. (2016). Dynamic Behavior of Trigger Factor on the Ribosome. Journal of Molecular Biology. 428(18). 3588–3602. 24 indexed citations
7.
Becker, Thomas, Birgitta Beatrix, Jean‐Paul Armache, et al.. (2014). Structures of the Sec61 complex engaged in nascent peptide translocation or membrane insertion. Nature. 506(7486). 107–110. 166 indexed citations
8.
Frauenfeld, Jens, James C. Gumbart, Eli O. van der Sluis, et al.. (2011). Cryo-EM structure of the ribosome–SecYE complex in the membrane environment. Nature Structural & Molecular Biology. 18(5). 614–621. 230 indexed citations
9.
Pech, Markus, Thomas Spreter, Roland Beckmann, & Birgitta Beatrix. (2010). Dual Binding Mode of the Nascent Polypeptide-associated Complex Reveals a Novel Universal Adapter Site on the Ribosome. Journal of Biological Chemistry. 285(25). 19679–19687. 44 indexed citations
10.
Armache, Jean‐Paul, A. Jarasch, Andreas M. Anger, et al.. (2010). Cryo-EM structure and rRNA model of a translating eukaryotic 80S ribosome at 5.5-Å resolution. Proceedings of the National Academy of Sciences. 107(46). 19748–19753. 172 indexed citations
11.
Hotokezaka, Yuka, Klaus van Leyen, Eng H. Lo, et al.. (2009). αNAC depletion as an initiator of ER stress-induced apoptosis in hypoxia. Cell Death and Differentiation. 16(11). 1505–1514. 42 indexed citations
12.
Heroven, Ann Kathrin, et al.. (2005). Analysis of RovA, a Transcriptional Regulator of Yersinia pseudotuberculosis Virulence That Acts through Antirepression and Direct Transcriptional Activation. Journal of Biological Chemistry. 280(51). 42423–42432. 45 indexed citations
13.
Spreter, Thomas, Markus Pech, & Birgitta Beatrix. (2005). The Crystal Structure of Archaeal Nascent Polypeptide-associated Complex (NAC) Reveals a Unique Fold and the Presence of a Ubiquitin-associated Domain. Journal of Biological Chemistry. 280(16). 15849–15854. 56 indexed citations
14.
Hotokezaka, Yuka, Hitoshi Hotokezaka, Klaus van Leyen, et al.. (2002). Interaction of the Eukaryotic Elongation Factor 1A with Newly Synthesized Polypeptides. Journal of Biological Chemistry. 277(21). 18545–18551. 70 indexed citations
15.
Möller, Ines, Birgitta Beatrix, Gert Kreibich, et al.. (1998). Unregulated exposure of the ribosomal M‐site caused by NAC depletion results in delivery of non‐secretory polypeptides to the Sec61 complex. FEBS Letters. 441(1). 1–5. 31 indexed citations
17.
Zelder, Oskar, Birgitta Beatrix, & Wolfgang Buckel. (1994). Cloning, sequencing and expression inEscherichia coliof the gene encoding component S of the coenzyme B12-dependent glutamate mutase fromClostridium cochlearium. FEMS Microbiology Letters. 118(1-2). 15–21. 15 indexed citations
18.
Beatrix, Birgitta, Oskar Zelder, Dietmar Linder, & Wolfgang Buckel. (1994). Cloning, sequencing and expression of the gene encoding the coenzyme B12‐dependent 2‐methyleneglutarate mutase from Clostridium barkeri in Escherichia coli. European Journal of Biochemistry. 221(1). 101–109. 44 indexed citations
19.
Zelder, Oskar, et al.. (1994). Characterization of the Coenzyme‐B12–Dependent Glutamate Mutase from Clostridium cochlearium Produced in Escherichia coli. European Journal of Biochemistry. 226(2). 577–585. 62 indexed citations
20.
Beatrix, Birgitta, Klaus Bendrat, Sabine Rospert, & Wolfgang Buckel. (1990). The biotin-dependent sodium ion pump glutaconyl-CoA decarboxylase from Fusobacterium nucleatum (subsp. nucleatum). Archives of Microbiology. 154(4). 362–369. 39 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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