Arthur Wüster

2.6k total citations
25 papers, 1.5k citations indexed

About

Arthur Wüster is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Arthur Wüster has authored 25 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Immunology. Recurrent topics in Arthur Wüster's work include Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (4 papers) and Bioinformatics and Genomic Networks (3 papers). Arthur Wüster is often cited by papers focused on Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (4 papers) and Bioinformatics and Genomic Networks (3 papers). Arthur Wüster collaborates with scholars based in United States, United Kingdom and France. Arthur Wüster's co-authors include M. Madan Babu, Matthew E. Hurles, Marc Torrent, Raheleh Rahbari, Natalia Sánchez de Groot, Guilhem Chalancon, Ludmil B. Alexandrov, Sarah Lindsay, Saeed Al Turki and David J. Porteous and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Arthur Wüster

24 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
Arthur Wüster United States 16 992 456 214 133 111 25 1.5k
Andrew J. Holloway Australia 10 1.3k 1.3× 271 0.6× 293 1.4× 159 1.2× 93 0.8× 14 1.8k
Alex Rolfe United States 11 1.1k 1.1× 536 1.2× 97 0.5× 190 1.4× 113 1.0× 18 1.8k
Ann S. Zweig United States 12 1.8k 1.8× 428 0.9× 399 1.9× 148 1.1× 247 2.2× 16 2.3k
Walter Santana-Garcia France 4 1.1k 1.1× 195 0.4× 260 1.2× 161 1.2× 176 1.6× 4 1.4k
Matthias Harbers Japan 21 1.7k 1.7× 365 0.8× 315 1.5× 129 1.0× 156 1.4× 43 2.0k
Eugene Kulesha United Kingdom 13 1.4k 1.4× 432 0.9× 131 0.6× 70 0.5× 169 1.5× 13 1.8k
A. Kasprzyk United Kingdom 6 1.3k 1.3× 400 0.9× 489 2.3× 169 1.3× 80 0.7× 9 1.9k
Maciej Kotecki United States 13 1.0k 1.0× 272 0.6× 130 0.6× 165 1.2× 52 0.5× 23 1.4k

Countries citing papers authored by Arthur Wüster

Since Specialization
Citations

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

Fields of papers citing papers by Arthur Wüster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arthur Wüster

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur Wüster. A scholar is included among the top collaborators of Arthur Wüster 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 Arthur Wüster. Arthur Wüster 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.
Yu, Ketian, Karol Estrada, Tõnu Esko, et al.. (2025). Plasma Metabolic Outliers Identified in Estonian Human Knockouts. Metabolites. 15(5). 323–323.
2.
Jaagura, Madis, Jaanika Kronberg, Anu Reigo, et al.. (2024). Comorbidities confound metabolomics studies of human disease. Scientific Reports. 14(1). 24810–24810. 2 indexed citations
3.
Trinidad, Marena, Alicia Ljungdahl, Geoffrey Y. Berguig, et al.. (2024). Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants. The American Journal of Human Genetics. 111(6). 1222–1238. 7 indexed citations
4.
Stockwell, Amy, Simon S. Gao, Ivaylo Stoilov, et al.. (2023). Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects. PLoS ONE. 18(4). e0280484–e0280484. 4 indexed citations
5.
Estrada, Karol, Steven Froelich, Arthur Wüster, et al.. (2021). Identifying therapeutic drug targets using bidirectional effect genes. Nature Communications. 12(1). 2224–2224. 18 indexed citations
6.
Simpfendorfer, Kim R., Wentian Li, Andrew Shih, et al.. (2019). Influence of genetic copy number variants of the human GLUT3 glucose transporter gene SLC2A3 on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study. Molecular Genetics and Metabolism Reports. 19. 100470–100470. 5 indexed citations
7.
Tom, Jennifer, Diana Chang, Arthur Wüster, et al.. (2018). Enabling genome-wide association testing with multiple diseases and no healthy controls. Gene. 684. 118–123. 3 indexed citations
8.
Haug-Baltzell, Asher, Tushar Bhangale, Diana Chang, et al.. (2018). Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms. Genes and Immunity. 20(2). 172–179. 2 indexed citations
9.
Rathore, Nisha, Sree R. Ramani, Homer Pantua, et al.. (2018). Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease. PLoS Genetics. 14(11). e1007427–e1007427. 47 indexed citations
10.
Torrent, Marc, Guilhem Chalancon, Natalia Sánchez de Groot, Arthur Wüster, & M. Madan Babu. (2018). Cells alter their tRNA abundance to selectively regulate protein synthesis during stress conditions. Science Signaling. 11(546). 178 indexed citations
11.
Narasimhan, Vagheesh M., Raheleh Rahbari, Aylwyn Scally, et al.. (2017). Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes. Nature Communications. 8(1). 303–303. 54 indexed citations
12.
Yang, Chiao-Wen, Meijuan Zhou, Xiumin Wu, et al.. (2016). Regulation of T Cell Receptor Signaling by DENND1B in T H 2 Cells and Allergic Disease. Cell. 164(1-2). 141–155. 47 indexed citations
13.
Rouhani, Foad J., Serena Nik‐Zainal, Arthur Wüster, et al.. (2016). Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells. PLoS Genetics. 12(4). e1005932–e1005932. 78 indexed citations
14.
Rahbari, Raheleh, Arthur Wüster, Sarah Lindsay, et al.. (2015). Timing, rates and spectra of human germline mutation. Nature Genetics. 48(2). 126–133. 381 indexed citations
15.
Ramu, Avinash, Michiel J. Noordam, Rachel S. Schwartz, et al.. (2013). DeNovoGear: de novo indel and point mutation discovery and phasing. Nature Methods. 10(10). 985–987. 95 indexed citations
16.
Beltrão, Pedro, N.C. Gassner, Chunshui Zhou, et al.. (2010). Cross‐species chemogenomic profiling reveals evolutionarily conserved drug mode of action. Molecular Systems Biology. 6(1). 451–451. 121 indexed citations
17.
Wüster, Arthur, AJ Venkatakrishnan, Gebhard F. X. Schertler, & M. Madan Babu. (2010). Spial: analysis of subtype-specific features in multiple sequence alignments of proteins. Bioinformatics. 26(22). 2906–2907. 6 indexed citations
18.
Wüster, Arthur & M. Madan Babu. (2009). Transcriptional control of the quorum sensing response in yeast. Molecular BioSystems. 6(1). 134–141. 51 indexed citations
19.
Wüster, Arthur & M. Madan Babu. (2008). Chemogenomics and biotechnology. Trends in biotechnology. 26(5). 252–258. 23 indexed citations
20.
Wüster, Arthur & M. Madan Babu. (2007). Conservation and Evolutionary Dynamics of the agr Cell-to-Cell Communication System across Firmicutes. Journal of Bacteriology. 190(2). 743–746. 74 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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