Susann Schweiger

4.8k total citations
58 papers, 2.6k citations indexed

About

Susann Schweiger is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Susann Schweiger has authored 58 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 11 papers in Genetics. Recurrent topics in Susann Schweiger's work include Ubiquitin and proteasome pathways (13 papers), RNA modifications and cancer (11 papers) and Congenital heart defects research (5 papers). Susann Schweiger is often cited by papers focused on Ubiquitin and proteasome pathways (13 papers), RNA modifications and cancer (11 papers) and Congenital heart defects research (5 papers). Susann Schweiger collaborates with scholars based in Germany, Austria and United Kingdom. Susann Schweiger's co-authors include Rainer Schneider, Sybille Krauß, Vanessa Suckow, John Foerster, Jennifer Winter, Hans‐Hilger Ropers, Andrea Köhler, Thomas Haaf, Désirée Rutschow and Karen Stout and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Susann Schweiger

57 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susann Schweiger Germany 27 1.9k 479 419 356 285 58 2.6k
Olivia Wendling France 23 1.8k 1.0× 265 0.6× 564 1.3× 317 0.9× 297 1.0× 37 2.6k
Michał Dąbrowski Poland 30 1.3k 0.7× 377 0.8× 255 0.6× 367 1.0× 199 0.7× 70 2.4k
Benoît Bilanges United Kingdom 20 2.0k 1.1× 323 0.7× 300 0.7× 183 0.5× 378 1.3× 27 2.9k
Jean Charron Canada 30 2.1k 1.1× 343 0.7× 481 1.1× 177 0.5× 508 1.8× 63 3.3k
Erich F. Greiner Germany 17 1.2k 0.6× 349 0.7× 428 1.0× 265 0.7× 213 0.7× 22 2.3k
Antonio Feliciello Italy 37 2.4k 1.3× 219 0.5× 283 0.7× 351 1.0× 234 0.8× 67 3.5k
Sung‐Il Yang South Korea 14 1.8k 0.9× 285 0.6× 315 0.8× 148 0.4× 395 1.4× 20 2.6k
Keyong Du United States 24 2.3k 1.2× 363 0.8× 334 0.8× 394 1.1× 358 1.3× 35 3.4k
Dorothea Rudolph Austria 14 1.7k 0.9× 419 0.9× 211 0.5× 615 1.7× 465 1.6× 28 2.8k
Lars Grøntved Denmark 25 1.4k 0.8× 458 1.0× 417 1.0× 295 0.8× 499 1.8× 40 2.5k

Countries citing papers authored by Susann Schweiger

Since Specialization
Citations

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

Fields of papers citing papers by Susann Schweiger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susann Schweiger

This figure shows the co-authorship network connecting the top 25 collaborators of Susann Schweiger. A scholar is included among the top collaborators of Susann Schweiger 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 Susann Schweiger. Susann Schweiger 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.
Heese, Raoul, et al.. (2022). The Big Picture of Neurodegeneration: A Meta Study to Extract the Essential Evidence on Neurodegenerative Diseases in a Network-Based Approach. Frontiers in Aging Neuroscience. 14. 866886–866886. 4 indexed citations
2.
Hewel, Charlotte, Hristo Todorov, Susann Schweiger, et al.. (2021). Reliability of genomic variants across different next-generation sequencing platforms and bioinformatic processing pipelines. BMC Genomics. 22(1). 62–62. 6 indexed citations
3.
Jagannath, Somanath, Junaid Akhtar, Konstantin Radyushkin, et al.. (2020). Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndrome. Nature Communications. 11(1). 480–480. 18 indexed citations
4.
Gucev, Zoran, Velibor Tasić, Momir Polenaković, et al.. (2019). Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation. European Journal of Medical Genetics. 63(1). 103613–103613. 3 indexed citations
5.
Monteiro, Olivia, Changwei Chen, Ryan P. Bingham, et al.. (2018). Pharmacological disruption of the MID1/α4 interaction reduces mutant Huntingtin levels in primary neuronal cultures. Neuroscience Letters. 673. 44–50. 8 indexed citations
6.
Komlósi, Katalin, Stefan Diederich, Oliver Bartsch, et al.. (2018). Targeted next-generation sequencing analysis in couples at increased risk for autosomal recessive disorders. Orphanet Journal of Rare Diseases. 13(1). 23–23. 7 indexed citations
7.
Schweiger, Susann, Frank Matthes, Karen L. Posey, et al.. (2017). Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex. Scientific Reports. 7(1). 13753–13753. 74 indexed citations
8.
9.
Köhler, Andrea, Sybille Krauß, J. Aigner, et al.. (2014). A hormone-dependent feedback-loop controls androgen receptor levels by limiting MID1, a novel translation enhancer and promoter of oncogenic signaling. Molecular Cancer. 13(1). 146–146. 35 indexed citations
10.
Krauß, Sybille, Paul Thornhill, Désirée Rutschow, et al.. (2010). Biguanide metformin acts on tau phosphorylation via mTOR/protein phosphatase 2A (PP2A) signaling. Proceedings of the National Academy of Sciences. 107(50). 21830–21835. 368 indexed citations
11.
Krauß, Sybille, John Foerster, Rainer Schneider, & Susann Schweiger. (2008). Protein Phosphatase 2A and Rapamycin Regulate the Nuclear Localization and Activity of the Transcription Factor GLI3. Cancer Research. 68(12). 4658–4665. 48 indexed citations
12.
Aranda-Orgillés, Beatriz, J. Aigner, Melanie Kunath, et al.. (2008). Active Transport of the Ubiquitin Ligase MID1 along the Microtubules Is Regulated by Protein Phosphatase 2A. PLoS ONE. 3(10). e3507–e3507. 35 indexed citations
13.
Al‐Yacoub, Nadya, Małgorzata Romanowska, Sybille Krauß, Susann Schweiger, & John Foerster. (2008). PPARδ Is a Type 1 IFN Target Gene and Inhibits Apoptosis in T Cells. Journal of Investigative Dermatology. 128(8). 1940–1949. 25 indexed citations
14.
Winter, Jennifer, et al.. (2007). Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1. BMC Molecular Biology. 8(1). 105–105. 18 indexed citations
15.
Minina, Eleonora, et al.. (2005). Characterization of FBX25, encoding a novel brain-expressed F-box protein. Biochimica et Biophysica Acta (BBA) - General Subjects. 1760(1). 110–118. 20 indexed citations
16.
Foerster, John, Ilja M. Nolte, Marcel Bruinenberg, et al.. (2005). Haplotype Sharing Analysis Identifies a Retroviral dUTPase as Candidate Susceptibility Gene for Psoriasis. Journal of Investigative Dermatology. 124(1). 99–102. 27 indexed citations
17.
Foerster, John, Ilja M. Nolte, Susann Schweiger, et al.. (2004). Evaluation of the IRF-2 Gene as a Candidate for PSORS3. Journal of Investigative Dermatology. 122(1). 61–64. 30 indexed citations
18.
Schweiger, Susann & Rainer Schneider. (2003). The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome. BioEssays. 25(4). 356–366. 61 indexed citations
19.
Trockenbacher, Alexander, Vanessa Suckow, John Foerster, et al.. (2001). MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation. Nature Genetics. 29(3). 287–294. 240 indexed citations
20.

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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