Robert Liefke

1.6k total citations
29 papers, 1.1k citations indexed

About

Robert Liefke is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Robert Liefke has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Immunology. Recurrent topics in Robert Liefke's work include Epigenetics and DNA Methylation (16 papers), RNA modifications and cancer (10 papers) and Cancer-related gene regulation (10 papers). Robert Liefke is often cited by papers focused on Epigenetics and DNA Methylation (16 papers), RNA modifications and cancer (10 papers) and Cancer-related gene regulation (10 papers). Robert Liefke collaborates with scholars based in Germany, United States and China. Robert Liefke's co-authors include Yang Shi, Tilman Borggrefe, Franz Oswald, Violetta Karwacki-Neisius, Zhanxin Wang, Gerhard Mittler, Junyi Jiang, Wei Tian, Martha L. Bulyk and María Domínguez and has published in prestigious journals such as Nature, Nucleic Acids Research and Genes & Development.

In The Last Decade

Robert Liefke

29 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Liefke Germany 15 949 124 119 69 57 29 1.1k
H. Irem Baymaz Netherlands 12 768 0.8× 121 1.0× 71 0.6× 73 1.1× 44 0.8× 12 851
Tomoyoshi Nakadai Japan 16 778 0.8× 101 0.8× 112 0.9× 85 1.2× 52 0.9× 36 939
Shannon Lauberth United States 11 892 0.9× 94 0.8× 231 1.9× 105 1.5× 108 1.9× 17 1.1k
Madeline Wong United States 13 601 0.6× 101 0.8× 162 1.4× 130 1.9× 63 1.1× 20 817
Nicki Gray United Kingdom 11 533 0.6× 66 0.5× 123 1.0× 46 0.7× 74 1.3× 12 704
Jit Kong Cheong Singapore 13 710 0.7× 82 0.7× 160 1.3× 109 1.6× 47 0.8× 24 925
Ik Soo Kim South Korea 12 759 0.8× 103 0.8× 156 1.3× 150 2.2× 83 1.5× 19 961
Charalampos Lazaris United States 11 782 0.8× 63 0.5× 76 0.6× 88 1.3× 75 1.3× 14 947
Susan L. Kloet Netherlands 14 697 0.7× 136 1.1× 59 0.5× 70 1.0× 54 0.9× 32 810
Jung S. Byun United States 14 554 0.6× 110 0.9× 108 0.9× 126 1.8× 56 1.0× 24 707

Countries citing papers authored by Robert Liefke

Since Specialization
Citations

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

Fields of papers citing papers by Robert Liefke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Liefke

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Liefke. A scholar is included among the top collaborators of Robert Liefke 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 Robert Liefke. Robert Liefke 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.
Stielow, Bastian, et al.. (2025). Cooperation of a polymerizing SAM domain and an intrinsically disordered region enables full SAMD1 function on chromatin. Nucleic Acids Research. 53(6). 1 indexed citations
2.
Stielow, Bastian, Ignasi Forné, Andrea Nist, et al.. (2024). SAMD1 suppresses epithelial–mesenchymal transition pathways in pancreatic ductal adenocarcinoma. PLoS Biology. 22(8). e3002739–e3002739. 2 indexed citations
3.
Stielow, Bastian, Florian Finkernagel, Ignasi Forné, et al.. (2024). IRF2BP2 counteracts the ATF7/JDP2 AP-1 heterodimer to prevent inflammatory overactivation in acute myeloid leukemia (AML) cells. Nucleic Acids Research. 52(13). 7590–7609. 2 indexed citations
4.
Liefke, Robert, et al.. (2023). Polycomb-like Proteins in Gene Regulation and Cancer. Genes. 14(4). 938–938. 11 indexed citations
5.
Forné, Ignasi, Andrea Nist, Gert Bange, et al.. (2023). Peptide-mediated inhibition of the transcriptional regulator Elongin BC induces apoptosis in cancer cells. Cell chemical biology. 30(7). 766–779.e11. 2 indexed citations
6.
Stielow, Bastian, et al.. (2022). The CpG Island-Binding Protein SAMD1 Contributes to an Unfavorable Gene Signature in HepG2 Hepatocellular Carcinoma Cells. Biology. 11(4). 557–557. 9 indexed citations
7.
Jia, Yulin, Bastian Stielow, Stephen S. Gisselbrecht, et al.. (2022). The histone acetyltransferase KAT6A is recruited to unmethylated CpG islands via a DNA binding winged helix domain. Nucleic Acids Research. 51(2). 574–594. 19 indexed citations
8.
Liefke, Robert, et al.. (2022). Evolutionary adaptation of the Polycomb repressive complex 2. Epigenetics & Chromatin. 15(1). 7–7. 23 indexed citations
9.
Jiang, Junyi, Kun Yan, Robert Liefke, et al.. (2022). A TRIM66/DAX1/Dux axis suppresses the totipotent 2-cell-like state in murine embryonic stem cells. Cell stem cell. 29(6). 948–961.e6. 16 indexed citations
10.
Liefke, Robert, Andrea Nist, Thorsten Stiewe, et al.. (2021). Ush regulates hemocyte-specific gene expression, fatty acid metabolism and cell cycle progression and cooperates with dNuRD to orchestrate hematopoiesis. PLoS Genetics. 17(2). e1009318–e1009318. 6 indexed citations
11.
Wang, Ying, Andrea Nist, Thorsten Stiewe, et al.. (2021). IRF8 Is an AML-Specific Susceptibility Factor That Regulates Signaling Pathways and Proliferation of AML Cells. Cancers. 13(4). 764–764. 13 indexed citations
12.
Stielow, Bastian, Hans‐Martin Pogoda, Junyi Jiang, et al.. (2021). The SAM domain-containing protein 1 (SAMD1) acts as a repressive chromatin regulator at unmethylated CpG islands. Science Advances. 7(20). 24 indexed citations
13.
Liefke, Robert, et al.. (2021). SUMOylated non-canonical polycomb PRC1.6 complex as a prerequisite for recruitment of transcription factor RBPJ. Epigenetics & Chromatin. 14(1). 38–38. 1 indexed citations
14.
Liefke, Robert, et al.. (2018). Enhancer-driven transcriptional regulation is a potential key determinant for human visceral and subcutaneous adipocytes. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1861(9). 826–840. 1 indexed citations
15.
Liefke, Robert, Violetta Karwacki-Neisius, & Yang Shi. (2016). EPOP Interacts with Elongin BC and USP7 to Modulate the Chromatin Landscape. Molecular Cell. 64(4). 659–672. 87 indexed citations
16.
Liefke, Robert & Yang Shi. (2015). The PRC2-associated factor C17orf96 is a novel CpG island regulator in mouse ES cells. Cell Discovery. 1(1). 15008–15008. 26 indexed citations
17.
Liefke, Robert, Jochen Gaedcke, Gabriela Salinas-Riester, et al.. (2015). The oxidative demethylase ALKBH3 marks hyperactive gene promoters in human cancer cells. Genome Medicine. 7(1). 66–66. 14 indexed citations
18.
Borggrefe, Tilman & Robert Liefke. (2012). Fine-tuning of the intracellular canonical Notch signaling pathway. Cell Cycle. 11(2). 264–276. 81 indexed citations
19.
Liefke, Robert, Franz Oswald, Cristóbal Alvarado, et al.. (2010). Histone demethylase KDM5A is an integral part of the core Notch–RBP-J repressor complex. Genes & Development. 24(6). 590–601. 145 indexed citations
20.
Liefke, Robert, et al.. (2008). ETO, but Not Leukemogenic Fusion Protein AML1/ETO, Augments RBP-Jκ/SHARP-Mediated Repression of Notch Target Genes. Molecular and Cellular Biology. 28(10). 3502–3512. 36 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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