Andreas Schönegger

3.5k total citations
5 papers, 537 citations indexed

About

Andreas Schönegger is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Andreas Schönegger has authored 5 papers receiving a total of 537 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Hematology. Recurrent topics in Andreas Schönegger's work include Acute Myeloid Leukemia Research (2 papers), Epigenetics and DNA Methylation (2 papers) and Genomics and Chromatin Dynamics (2 papers). Andreas Schönegger is often cited by papers focused on Acute Myeloid Leukemia Research (2 papers), Epigenetics and DNA Methylation (2 papers) and Genomics and Chromatin Dynamics (2 papers). Andreas Schönegger collaborates with scholars based in Austria, Germany and Italy. Andreas Schönegger's co-authors include Christoph Bock, Nathan C. Sheffield, Paul Datlinger, Matthias Farlik, Johanna Klughammer, Angelo Nuzzo, Michael Schuster, Stefan Kubicek, Heinrich Kovar and Eleni M. Tomazou and has published in prestigious journals such as Blood, Genome biology and Cell Reports.

In The Last Decade

Andreas Schönegger

5 papers receiving 530 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Schönegger Austria 4 432 128 75 71 70 5 537
Erik L. Bao United States 10 314 0.7× 68 0.5× 120 1.6× 74 1.0× 34 0.5× 14 538
Nikki A. Evensen United States 8 212 0.5× 107 0.8× 34 0.5× 19 0.3× 109 1.6× 18 352
Kimberly R. Blahnik United States 7 691 1.6× 104 0.8× 15 0.2× 83 1.2× 33 0.5× 7 782
Gerald L. Arthur United States 10 272 0.6× 54 0.4× 46 0.6× 51 0.7× 46 0.7× 12 359
Yong Sam Shin South Korea 12 278 0.6× 69 0.5× 58 0.8× 60 0.8× 106 1.5× 18 501
Elisa Lavarone Italy 10 642 1.5× 100 0.8× 28 0.4× 97 1.4× 65 0.9× 13 729
Roel Vandepoel Belgium 12 264 0.6× 61 0.5× 13 0.2× 38 0.5× 72 1.0× 14 439
Rosalind Codrington United Kingdom 7 185 0.4× 26 0.2× 31 0.4× 33 0.5× 86 1.2× 8 339
Paul Guilhamon United Kingdom 10 361 0.8× 135 1.1× 88 1.2× 103 1.5× 36 0.5× 13 480
Sarina Sulong Malaysia 10 157 0.4× 64 0.5× 20 0.3× 73 1.0× 42 0.6× 48 378

Countries citing papers authored by Andreas Schönegger

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Schönegger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Schönegger

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Schönegger. A scholar is included among the top collaborators of Andreas Schönegger 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 Schönegger. Andreas Schönegger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

5 of 5 papers shown
1.
Frech, Christian, Andreas Schönegger, Cornelia Eckert, et al.. (2015). KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia. Leukemia. 29(8). 1656–1667. 73 indexed citations
2.
Feenstra, Jelena D. Milosevic, Elisa Rumi, Daniela Pietra, et al.. (2015). Whole Exome Sequencing Reveals Clonal Evolution of Myeloproliferative Neoplasms to Acute Myeloid Leukemia. Blood. 126(23). 1626–1626. 1 indexed citations
3.
Farlik, Matthias, Nathan C. Sheffield, Angelo Nuzzo, et al.. (2015). Single-Cell DNA Methylome Sequencing and Bioinformatic Inference of Epigenomic Cell-State Dynamics. Cell Reports. 10(8). 1386–1397. 317 indexed citations
4.
Tomazou, Eleni M., Nathan C. Sheffield, Christian Schmidl, et al.. (2015). Epigenome Mapping Reveals Distinct Modes of Gene Regulation and Widespread Enhancer Reprogramming by the Oncogenic Fusion Protein EWS-FLI1. Cell Reports. 10(7). 1082–1095. 140 indexed citations
5.
Dürnberger, Gerhard, Tilmann Bürckstümmer, K. Huber, et al.. (2013). Experimental characterization of the human non-sequence-specific nucleic acid interactome. Genome biology. 14(7). R81–R81. 6 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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