Andreas Gast

4.6k total citations · 2 hit papers
28 papers, 3.3k citations indexed

About

Andreas Gast is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Andreas Gast has authored 28 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Oncology and 8 papers in Genetics. Recurrent topics in Andreas Gast's work include Cutaneous Melanoma Detection and Management (6 papers), Melanoma and MAPK Pathways (4 papers) and Epigenetics and DNA Methylation (3 papers). Andreas Gast is often cited by papers focused on Cutaneous Melanoma Detection and Management (6 papers), Melanoma and MAPK Pathways (4 papers) and Epigenetics and DNA Methylation (3 papers). Andreas Gast collaborates with scholars based in Germany, Sweden and United States. Andreas Gast's co-authors include Rajiv Kumar, Kari Hemminki, Frauke Melchior, Dirk Schadendorf, Anne Dejean, Jacob-S. Seeler, Andrea Pichler, Antje Sucker, Adina Figl and Eduardo Nagore and has published in prestigious journals such as Science, Cell and The EMBO Journal.

In The Last Decade

Andreas Gast

28 papers receiving 3.2k citations

Hit Papers

TERT Promoter Mutations i... 2002 2026 2010 2018 2013 2002 400 800 1.2k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Andreas Gast 2.1k 957 607 517 462 28 3.3k
Karen Cerosaletti 2.7k 1.3× 1.2k 1.3× 960 1.6× 929 1.8× 1.1k 2.4× 65 4.2k
Christine Wasylyk 2.9k 1.4× 1.0k 1.1× 731 1.2× 630 1.2× 658 1.4× 52 4.0k
Cristina Montagna 3.0k 1.4× 1.4k 1.4× 811 1.3× 756 1.5× 505 1.1× 124 4.8k
Brigitte M. Pützer 2.9k 1.4× 1.9k 2.0× 491 0.8× 905 1.8× 404 0.9× 112 4.3k
Eric H. Westin 2.2k 1.0× 819 0.9× 631 1.0× 397 0.8× 759 1.6× 66 3.6k
Edward F. Fritsch 2.1k 1.0× 948 1.0× 532 0.9× 223 0.4× 1.1k 2.3× 25 4.1k
Wen-Lin Kuo 2.0k 1.0× 599 0.6× 1.7k 2.8× 813 1.6× 405 0.9× 33 3.7k
John F. Lyons 2.7k 1.3× 1.3k 1.4× 308 0.5× 551 1.1× 347 0.8× 81 4.3k
Perry D. Nisen 1.8k 0.8× 870 0.9× 491 0.8× 455 0.9× 274 0.6× 55 3.0k
Wendy Winckler 1.7k 0.8× 544 0.6× 775 1.3× 986 1.9× 213 0.5× 20 2.8k

Countries citing papers authored by Andreas Gast

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Gast

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Gast

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Gast. A scholar is included among the top collaborators of Andreas Gast 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 Gast. Andreas Gast 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.
Horn, Susanne, Adina Figl, P. Sivaramakrishna Rachakonda, et al.. (2013). TERT Promoter Mutations in Familial and Sporadic Melanoma. Science. 339(6122). 959–961. 1267 indexed citations breakdown →
2.
Arab, Khelifa, Laura T. Smith, Andreas Gast, et al.. (2011). Epigenetic deregulation of TCF21 inhibits metastasis suppressor KISS1 in metastatic melanoma. Carcinogenesis. 32(10). 1467–1473. 56 indexed citations
3.
Gast, Andreas, Justo Lorenzo Bermejo, Rainer Claus, et al.. (2011). Association of Inherited Variation in Toll-Like Receptor Genes with Malignant Melanoma Susceptibility and Survival. PLoS ONE. 6(9). e24370–e24370. 56 indexed citations
4.
Lenci, Romina, P. Sivaramakrishna Rachakonda, A. V. Kubarenko, et al.. (2011). Integrin genes and susceptibility to human melanoma. Mutagenesis. 27(3). 367–373. 18 indexed citations
5.
Gast, Andreas, Dominique Scherer, Bowang Chen, et al.. (2010). Somatic alterations in the melanoma genome: A high‐resolution array‐based comparative genomic hybridization study. Genes Chromosomes and Cancer. 49(8). 733–745. 71 indexed citations
6.
Figl, Adina, Dominique Scherer, Eduardo Nagore, et al.. (2010). Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 702(1). 8–16. 26 indexed citations
7.
Prasad, Rashmi B., Fay J. Hosking, Jayaram Vijayakrishnan, et al.. (2009). Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. Blood. 115(9). 1765–1767. 91 indexed citations
8.
Dai, Liping, Andreas Gast, Alexandra Horská, et al.. (2009). A case–control study of childhood acute lymphoblastic leukaemia and polymorphisms in the TGF‐β and receptor genes. Pediatric Blood & Cancer. 52(7). 819–823. 9 indexed citations
9.
Figl, Adina, Dominique Scherer, Eduardo Nagore, et al.. (2008). Single nucleotide polymorphisms in DNA repair genes XRCC1 and APEX1 in progression and survival of primary cutaneous melanoma patients. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 661(1-2). 78–84. 20 indexed citations
10.
Figl, Adina, Ranjit K. Thirumaran, Selma Ugurel, et al.. (2007). Multiple Melanomas After Treatment for Hodgkin Lymphoma in a Non-Dutch p16-Leiden Mutation Carrier With 2 MC1R High-Risk Variants. Archives of Dermatology. 143(4). 495–9. 5 indexed citations
11.
Gast, Andreas, Péter Rudnai, Eugen Gurzău, et al.. (2007). ARLTS1 polymorphisms and basal cell carcinoma of the skin. Hereditary Cancer in Clinical Practice. 5(1). 25–25. 1 indexed citations
12.
Ugurel, Selma, Ranjit K. Thirumaran, Sandra Bloethner, et al.. (2007). B-RAF and N-RAS Mutations Are Preserved during Short Time In Vitro Propagation and Differentially Impact Prognosis. PLoS ONE. 2(2). e236–e236. 103 indexed citations
13.
Bloethner, Sandra, Erna Snellman, Justo Lorenzo Bermejo, et al.. (2007). Differential gene expression in melanocytic nevi with the V600E BRAF mutation. Genes Chromosomes and Cancer. 46(11). 1019–1027. 14 indexed citations
14.
Frank, Bernd, Peter Meyer, Melanie Barbara Boettger, et al.. (2006). ARLTS1 variants and melanoma risk. International Journal of Cancer. 119(7). 1736–1737. 19 indexed citations
15.
Sun, Baohua, Min Liang, Yao-Yun Liang, et al.. (2003). Opposed Regulation of Corepressor CtBP by SUMOylation and PDZ Binding. Molecular Cell. 12(3). 791–791. 3 indexed citations
16.
Lin, Xia, Baohua Sun, Min Liang, et al.. (2003). Opposed Regulation of Corepressor CtBP by SUMOylation and PDZ Binding. Molecular Cell. 11(5). 1389–1396. 140 indexed citations
17.
Pichler, Andrea, Andreas Gast, Jacob-S. Seeler, Anne Dejean, & Frauke Melchior. (2002). The Nucleoporin RanBP2 Has SUMO1 E3 Ligase Activity. Cell. 108(1). 109–120. 660 indexed citations breakdown →
18.
Motro, Uzi, et al.. (2002). Allele frequencies of nine STR loci of Jewish and Arab populations in Israel. International Journal of Legal Medicine. 116(3). 184–186. 8 indexed citations
19.
Gast, Andreas, Jean Schneikert, & Andrew C.B. Cato. (1998). N-terminal sequences of the human androgen receptor in DNA binding and transrepressing functions. The Journal of Steroid Biochemistry and Molecular Biology. 65(1-6). 117–123. 20 indexed citations
20.
Gast, Andreas, et al.. (1995). A single amino acid exchange abolishes dimerization of the androgen receptor and causes Reifenstein syndrome. Molecular and Cellular Endocrinology. 111(1). 93–98. 31 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026