Karin M. Greulich‐Bode

661 total citations
20 papers, 521 citations indexed

About

Karin M. Greulich‐Bode is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Karin M. Greulich‐Bode has authored 20 papers receiving a total of 521 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Plant Science. Recurrent topics in Karin M. Greulich‐Bode's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers) and DNA Repair Mechanisms (5 papers). Karin M. Greulich‐Bode is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers) and DNA Repair Mechanisms (5 papers). Karin M. Greulich‐Bode collaborates with scholars based in Germany, United States and United Kingdom. Karin M. Greulich‐Bode's co-authors include Petra Boukamp, Damir Krunic, Lynn Hlatky, Martina K. Brückner, Javier Arsuaga, Philip Hahnfeldt, Mariel Vázquez, David J. Brenner, Sabine M. Görisch and Peter Lichter and has published in prestigious journals such as The Journal of Cell Biology, PLoS ONE and Clinical Cancer Research.

In The Last Decade

Karin M. Greulich‐Bode

20 papers receiving 513 citations

Peers

Karin M. Greulich‐Bode
Nicki Gray United Kingdom
Jay F. Sarthy United States
Claire Heride United Kingdom
Elodie Hatchi France
Marieke Aarts Netherlands
Kinnimulki Vijayachandra United States
Chris van Oevelen Spain
Flavia Michelini United States
Susan L. Kloet Netherlands
Landon Wark Canada
Nicki Gray United Kingdom
Karin M. Greulich‐Bode
Citations per year, relative to Karin M. Greulich‐Bode Karin M. Greulich‐Bode (= 1×) peers Nicki Gray

Countries citing papers authored by Karin M. Greulich‐Bode

Since Specialization
Citations

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

Fields of papers citing papers by Karin M. Greulich‐Bode

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karin M. Greulich‐Bode. 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 Karin M. Greulich‐Bode. The network helps show where Karin M. Greulich‐Bode may publish in the future.

Co-authorship network of co-authors of Karin M. Greulich‐Bode

This figure shows the co-authorship network connecting the top 25 collaborators of Karin M. Greulich‐Bode. A scholar is included among the top collaborators of Karin M. Greulich‐Bode 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 Karin M. Greulich‐Bode. Karin M. Greulich‐Bode 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.
Krunic, Damir, et al.. (2013). The chromatin remodelling complex NoRC safeguards genome stability by heterochromatin formation at telomeres and centromeres. EMBO Reports. 14(8). 704–710. 51 indexed citations
2.
Krunic, Damir, et al.. (2013). The chromatin remodelling complex NoRC safeguards genome stability by heterochromatin formation at telomeres and centromeres. EMBO Reports. 14(9). 845–845. 2 indexed citations
3.
Greulich‐Bode, Karin M. & B Heinze. (2012). On the Power of Additional and Complex Chromosomal Aberrations in CML. Current Genomics. 13(6). 471–476. 8 indexed citations
4.
Fredebohm, Johannes, Michael Boettcher, Christian Eisen, et al.. (2012). Establishment and Characterization of a Highly Tumourigenic and Cancer Stem Cell Enriched Pancreatic Cancer Cell Line as a Well Defined Model System. PLoS ONE. 7(11). e48503–e48503. 37 indexed citations
5.
Greulich‐Bode, Karin M., et al.. (2012). Clinical, Molecular- and Cytogenetic Analysis of a Case of Severe Radio- Sensitivity. Current Genomics. 13(6). 426–432. 4 indexed citations
6.
Hampel, Sonja M., Antonella Pepe, Karin M. Greulich‐Bode, et al.. (2012). Mechanism of the Antiproliferative Activity of Some Naphthalene Diimide G-Quadruplex Ligands. Molecular Pharmacology. 83(2). 470–480. 28 indexed citations
7.
O’Brien, Benjamin, Gregg H. Jossart, Yuko Ito, et al.. (2010). ‘Chromosomal Rainbows’ Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors. PubMed Central. 6 indexed citations
8.
Krunic, Damir, Sharareh Moshir, Karin M. Greulich‐Bode, et al.. (2009). Tissue context-activated telomerase in human epidermis correlates with little age-dependent telomere loss. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792(4). 297–308. 33 indexed citations
9.
Weier, Heinz‐Ulrich G., Karin M. Greulich‐Bode, Jenny Wu, & Thomas Duell. (2009). Delineating Rearrangements in Single Yeast Artificial Chromosomes by Quantitative DNA Fiber Mapping. PubMed. 2(1). 15–23. 1 indexed citations
10.
Chung, Inn, Malte Wachsmuth, Sabine M. Görisch, et al.. (2009). Dynamics of Telomeres and Promyelocytic Leukemia Nuclear Bodies in a Telomerase-negative Human Cell Line. Molecular Biology of the Cell. 20(7). 2070–2082. 84 indexed citations
11.
Greulich‐Bode, Karin M., et al.. (2008). Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA. Molecular Cytogenetics. 1(1). 28–28. 6 indexed citations
12.
13.
Paschen, Annette, Norbert Arens, Antje Sucker, et al.. (2006). The Coincidence of Chromosome 15 Aberrations and β2-Microglobulin Gene Mutations Is Causative for the Total Loss of Human Leukocyte Antigen Class I Expression in Melanoma. Clinical Cancer Research. 12(11). 3297–3305. 28 indexed citations
14.
Lörch, Thomas, et al.. (2005). Automatic telomere length measurements in interphase nuclei by IQ‐FISH. Cytometry Part A. 68A(2). 113–120. 41 indexed citations
15.
Arsuaga, Javier, Karin M. Greulich‐Bode, Mariel Vázquez, et al.. (2004). Chromosome spatial clustering inferred from radiogenic aberrations. International Journal of Radiation Biology. 80(7). 507–515. 27 indexed citations
16.
Ermler, Sibylle, Damir Krunic, Tobias Knoch, et al.. (2004). Cell cycle-dependent 3D distribution of telomeres and telomere repeat-binding factor 2 (TRF2) in HaCaT and HaCaT-myc cells. European Journal of Cell Biology. 83(11-12). 681–690. 18 indexed citations
17.
MacLeod, Roderick A.F., Stefan Nagel, Maren Kaufmann, Karin M. Greulich‐Bode, & Hans G. Drexler. (2002). Multicolor-FISH analysis of a natural killer cell line (NK-92). Leukemia Research. 26(11). 1027–1033. 27 indexed citations
18.
Vázquez, Mariel, Karin M. Greulich‐Bode, Javier Arsuaga, et al.. (2002). Computer analysis of mFISH chromosome aberration data uncovers an excess of very complicated metaphases. International Journal of Radiation Biology. 78(12). 1103–1115. 15 indexed citations
19.
Cornforth, Michael N., Karin M. Greulich‐Bode, Bradford D. Loucas, et al.. (2002). Chromosomes are predominantly located randomly with respect to each other in interphase human cells. The Journal of Cell Biology. 159(2). 237–244. 75 indexed citations
20.
Weier, Heinz‐Ulrich G., Karin M. Greulich‐Bode, Yuko Ito, Robert Lersch, & Jingly Fung. (2002). FISH in cancer diagnosis and prognostication: from cause to course of disease. Expert Review of Molecular Diagnostics. 2(2). 109–119. 10 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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