Andreas W. Kuß

6.5k total citations
87 papers, 3.2k citations indexed

About

Andreas W. Kuß is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Andreas W. Kuß has authored 87 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 36 papers in Genetics and 12 papers in Cancer Research. Recurrent topics in Andreas W. Kuß's work include Genetics and Neurodevelopmental Disorders (18 papers), RNA modifications and cancer (11 papers) and RNA and protein synthesis mechanisms (7 papers). Andreas W. Kuß is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), RNA modifications and cancer (11 papers) and RNA and protein synthesis mechanisms (7 papers). Andreas W. Kuß collaborates with scholars based in Germany, Iran and United States. Andreas W. Kuß's co-authors include Masoud Garshasbi, Andreas Tzschach, Kimia Kahrizi, Hossein Najmabadi, Hans‐Hilger Ropers, Michael Nerlich, Klaus von der Mark, Thorsten Kirsch, G. Weseloh and H Stöß and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Environmental Science & Technology.

In The Last Decade

Andreas W. Kuß

85 papers receiving 3.2k citations

Peers

Andreas W. Kuß
Bernd Wollnik Germany
Miyuki Suzawa Japan
Atsushi Watanabe Japan
Nathalie Drouot France
Xizhi Guo China
J. Douglas Coffin United States
Maurizio D’Esposito Italy
Andreas Winterpacht Germany
Jorge Laborda Spain
Catherine E. Ovitt United States
Bernd Wollnik Germany
Andreas W. Kuß
Citations per year, relative to Andreas W. Kuß Andreas W. Kuß (= 1×) peers Bernd Wollnik

Countries citing papers authored by Andreas W. Kuß

Since Specialization
Citations

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

Fields of papers citing papers by Andreas W. Kuß

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas W. Kuß. 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 Andreas W. Kuß. The network helps show where Andreas W. Kuß may publish in the future.

Co-authorship network of co-authors of Andreas W. Kuß

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas W. Kuß. A scholar is included among the top collaborators of Andreas W. Kuß 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 Andreas W. Kuß. Andreas W. Kuß 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.
Klockmann, Michael, Andreas W. Kuß, Lars R. Jensen, et al.. (2025). Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range‐Expanding Spider. Ecology and Evolution. 15(12). e72507–e72507.
2.
Schwabe, Michael, Andreas W. Kuß, Katharina Schaufler, et al.. (2023). Natural phenolic compounds as biofilm inhibitors of multidrug-resistant Escherichia coli – the role of similar biological processes despite structural diversity. Frontiers in Microbiology. 14. 1232039–1232039. 17 indexed citations
3.
Jensen, Lars R., et al.. (2023). MncR: Late Integration Machine Learning Model for Classification of ncRNA Classes Using Sequence and Structural Encoding. International Journal of Molecular Sciences. 24(10). 8884–8884. 4 indexed citations
4.
Cordellier, Mathilde, Katharina Hoffmann, Corinna Jensen, et al.. (2022). Identification of sex chromosomes using genomic and cytogenetic methods in a range-expanding spider, Argiope bruennichi (Araneae: Araneidae). Biological Journal of the Linnean Society. 136(3). 405–416. 2 indexed citations
5.
Krehenwinkel, Henrik, George R. Uhl, Andreas W. Kuß, et al.. (2021). Chromosome-level reference genome of the European wasp spider Argiope bruennichi : a resource for studies on range expansion and evolutionary adaptation. GigaScience. 10(1). 36 indexed citations
6.
Thumberger, Thomas, Stefan Weiß, Lars R. Jensen, et al.. (2021). The C-Mannosylome of Human Induced Pluripotent Stem Cells Implies a Role for ADAMTS16 C-Mannosylation in Eye Development. Molecular & Cellular Proteomics. 20. 100092–100092. 7 indexed citations
7.
8.
Bertelsen, Birgitte, Linea Cecilie Melchior, Lars R. Jensen, et al.. (2014). A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD. Psychiatry Research. 225(3). 268–275. 13 indexed citations
9.
Weißmann, Robert, Allan Lind-Thomsen, Matthias Peiser, et al.. (2014). Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. BMC Genomics. 15(1). 537–537. 5 indexed citations
10.
Bouter, Yvonne, Tim Kacprowski, Robert Weißmann, et al.. (2014). Deciphering the Molecular Profile of Plaques, Memory Decline and Neuron Loss in Two Mouse Models for Alzheimer’s Disease by Deep Sequencing. Frontiers in Aging Neuroscience. 6. 75–75. 70 indexed citations
11.
Starokadomskyy, Petro, Nathan Gluck, Haiying Li, et al.. (2013). CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling. Journal of Clinical Investigation. 123(5). 2244–2256. 77 indexed citations
12.
Kelly, Seth M., ChangHui Pak, Masoud Garshasbi, et al.. (2012). New kid on the ID block. RNA Biology. 9(5). 555–562. 17 indexed citations
13.
Mertel, Sara, Kimia Kahrizi, Sebahattin Çirak, et al.. (2012). Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability. The American Journal of Human Genetics. 90(5). 847–855. 218 indexed citations
14.
Garshasbi, Masoud, Kimia Kahrizi, Masoumeh Hosseini, et al.. (2011). A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family. American Journal of Medical Genetics Part A. 155(8). 1976–1980. 39 indexed citations
15.
Kahrizi, Kimia, Masoud Garshasbi, Seyedeh Sedigheh Abedini, et al.. (2010). Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. European Journal of Human Genetics. 19(1). 115–117. 49 indexed citations
16.
Kahrizi, Kimia, Hossein Najmabadi, Roxana Kariminejad, et al.. (2008). An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4. European Journal of Human Genetics. 17(1). 125–128. 16 indexed citations
17.
Motazacker, Mohammad Mahdi, Benjamin R. Rost, Tim Hucho, et al.. (2007). A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 81(4). 792–798. 112 indexed citations
18.
Jensen, Lars Riff, Steffen Lenzner, Bettina A. Moser, et al.. (2006). X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11. European Journal of Human Genetics. 15(1). 68–75. 12 indexed citations
19.
Kuß, Andreas W., et al.. (2003). Associations of a Polymorphic AP-2 Binding Site in the 5′-Flanking Region of the Bovine β-Lactoglobulin Gene with Milk Proteins. Journal of Dairy Science. 86(6). 2213–2218. 38 indexed citations
20.
Herold, Marco J., et al.. (2002). Mitochondria-Dependent Caspase-9 Activation Is Necessary for Antigen Receptor-Mediated Effector Caspase Activation and Apoptosis in WEHI 231 Lymphoma Cells. The Journal of Immunology. 168(8). 3902–3909. 41 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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