Marianne Quaas

1.2k total citations
18 papers, 931 citations indexed

About

Marianne Quaas is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Marianne Quaas has authored 18 papers receiving a total of 931 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Oncology and 5 papers in Cell Biology. Recurrent topics in Marianne Quaas's work include Cancer-related Molecular Pathways (8 papers), Epigenetics and DNA Methylation (5 papers) and DNA Repair Mechanisms (3 papers). Marianne Quaas is often cited by papers focused on Cancer-related Molecular Pathways (8 papers), Epigenetics and DNA Methylation (5 papers) and DNA Repair Mechanisms (3 papers). Marianne Quaas collaborates with scholars based in Germany, United States and United Kingdom. Marianne Quaas's co-authors include Kurt Engeland, Martin Fischer, Gerd A. Müller, Lydia Steiner, Andrew D. Sharrocks, Xi Chen, Ben Stutchbury, Namshik Han, Gabriela Aust and James A. DeCaprio and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and PLoS ONE.

In The Last Decade

Marianne Quaas

16 papers receiving 926 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marianne Quaas Germany 13 730 402 148 145 64 18 931
Geun‐Hyoung Ha South Korea 18 631 0.9× 268 0.7× 187 1.3× 201 1.4× 89 1.4× 32 899
Zhen Cai China 13 731 1.0× 302 0.8× 132 0.9× 94 0.6× 59 0.9× 21 963
Antony Letai United States 11 545 0.7× 303 0.8× 163 1.1× 81 0.6× 56 0.9× 11 840
Toshinori Hyodo Japan 21 781 1.1× 225 0.6× 171 1.2× 193 1.3× 91 1.4× 47 1.1k
Weibin Wang China 20 949 1.3× 355 0.9× 193 1.3× 71 0.5× 54 0.8× 54 1.2k
Nicole L. Collins United States 6 498 0.7× 355 0.9× 116 0.8× 230 1.6× 41 0.6× 11 844
Liliana Krasińska France 12 561 0.8× 234 0.6× 135 0.9× 235 1.6× 96 1.5× 18 910
Monideepa Roy United States 11 779 1.1× 251 0.6× 113 0.8× 206 1.4× 53 0.8× 18 1.1k
Ricardo E. Perez United States 16 602 0.8× 375 0.9× 168 1.1× 88 0.6× 97 1.5× 42 960
Silvia Pandolfi Italy 14 676 0.9× 361 0.9× 140 0.9× 72 0.5× 41 0.6× 19 870

Countries citing papers authored by Marianne Quaas

Since Specialization
Citations

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

Fields of papers citing papers by Marianne Quaas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marianne Quaas

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

All Works

18 of 18 papers shown
1.
Quaas, Marianne, et al.. (2025). BRCA1 and BRCA2 gene expression: p53- and cell cycle-dependent repression requires RB and DREAM. Cell Death and Differentiation. 33(1). 51–63.
2.
Aust, Gabriela, et al.. (2022). To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer. Cells. 11(9). 1538–1538. 17 indexed citations
3.
Quaas, Marianne, Uwe Wolfrum, Torsten Thalheim, et al.. (2022). The Adhesion G-Protein-Coupled Receptor GPR115/ADGRF4 Regulates Epidermal Differentiation and Associates with Cytoskeletal KRT1. Cells. 11(19). 3151–3151. 3 indexed citations
4.
Hofmann, Felix, Torsten Thalheim, Karen Rother, et al.. (2021). How to Obtain a Mega-Intestine with Normal Morphology: In Silico Modelling of Postnatal Intestinal Growth in a Cd97-Transgenic Mouse. International Journal of Molecular Sciences. 22(14). 7345–7345.
5.
Morawski, Markus, Knut Krohn, Nada Rayes, et al.. (2021). Adhesion GPCR GPR56 Expression Profiling in Human Tissues. Cells. 10(12). 3557–3557. 7 indexed citations
6.
Thalheim, Torsten, Marianne Quaas, Maria Herberg, et al.. (2021). Epigenetic Drifts during Long-Term Intestinal Organoid Culture. Cells. 10(7). 1718–1718. 13 indexed citations
7.
Thalheim, Torsten, Lydia Hopp, Maria Herberg, et al.. (2020). Fighting Against Promoter DNA Hyper-Methylation: Protective Histone Modification Profiles of Stress-Resistant Intestinal Stem Cells. International Journal of Molecular Sciences. 21(6). 1941–1941. 4 indexed citations
8.
Herberg, Maria, Marianne Quaas, Torsten Thalheim, et al.. (2019). Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestine. Clinical Epigenetics. 11(1). 65–65. 18 indexed citations
9.
Hoffmann, Franz, Sven Rothemund, Marianne Quaas, et al.. (2018). Mechano-Dependent Phosphorylation of the PDZ-Binding Motif of CD97/ADGRE5 Modulates Cellular Detachment. Cell Reports. 24(8). 1986–1995. 31 indexed citations
10.
Thalheim, Torsten, Marianne Quaas, Maria Herberg, et al.. (2017). Linking stem cell function and growth pattern of intestinal organoids. Developmental Biology. 433(2). 254–261. 31 indexed citations
11.
12.
Klein, Ditte Kjærsgaard, Saskia Hoffmann, Johanna K. Ahlskog, et al.. (2015). Cyclin F suppresses B-Myb activity to promote cell cycle checkpoint control. Nature Communications. 6(1). 5800–5800. 60 indexed citations
13.
Fischer, Martin, Marianne Quaas, Lydia Steiner, & Kurt Engeland. (2015). The p53-p21-DREAM-CDE/CHR pathway regulates G2/M cell cycle genes. Nucleic Acids Research. 44(1). 164–174. 246 indexed citations
14.
Fischer, Martin, Marianne Quaas, Axel Wintsche, Gerd A. Müller, & Kurt Engeland. (2013). Polo-like kinase 4 transcription is activated via CRE and NRF1 elements, repressed by DREAM through CDE/CHR sites and deregulated by HPV E7 protein. Nucleic Acids Research. 42(1). 163–180. 52 indexed citations
15.
16.
Chen, Xi, Gerd A. Müller, Marianne Quaas, et al.. (2012). The Forkhead Transcription Factor FOXM1 Controls Cell Cycle-Dependent Gene Expression through an Atypical Chromatin Binding Mechanism. Molecular and Cellular Biology. 33(2). 227–236. 185 indexed citations
17.
Quaas, Marianne, Gerd A. Müller, & Kurt Engeland. (2012). p53 can repress transcription of cell cycle genes through a p21WAF1/CIP1-dependent switch from MMB to DREAM protein complex binding at CHR promoter elements. Cell Cycle. 11(24). 4661–4672. 85 indexed citations
18.
Müller, Gerd A., Marianne Quaas, Michael Schümann, et al.. (2011). The CHR promoter element controls cell cycle-dependent gene transcription and binds the DREAM and MMB complexes. Nucleic Acids Research. 40(4). 1561–1578. 89 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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