Barbara Klink

6.3k total citations · 1 hit paper
73 papers, 2.5k citations indexed

About

Barbara Klink is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Barbara Klink has authored 73 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 23 papers in Cancer Research and 22 papers in Genetics. Recurrent topics in Barbara Klink's work include Glioma Diagnosis and Treatment (21 papers), Cancer Genomics and Diagnostics (13 papers) and Genomic variations and chromosomal abnormalities (9 papers). Barbara Klink is often cited by papers focused on Glioma Diagnosis and Treatment (21 papers), Cancer Genomics and Diagnostics (13 papers) and Genomic variations and chromosomal abnormalities (9 papers). Barbara Klink collaborates with scholars based in Germany, Luxembourg and Norway. Barbara Klink's co-authors include Gabriele Schackert, Evelin Schröck, Dietmar Krex, Michael Seifert, Michael Sabel, Andreas von Deimling, Oliver Heese, Christian Hartmann, Guido Reifenberger and Torsten Pietsch and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Barbara Klink

70 papers receiving 2.5k citations

Hit Papers

Long-term survival with g... 2007 2026 2013 2019 2007 200 400 600

Author Peers

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

Author Last Decade Papers Cites
Barbara Klink 1.0k 855 775 530 370 73 2.5k
David P. Noske 1.5k 1.5× 641 0.7× 728 0.9× 706 1.3× 299 0.8× 69 2.7k
Naoki Shinojima 1.3k 1.2× 1.3k 1.5× 602 0.8× 682 1.3× 283 0.8× 80 3.0k
Yu Yao 1.1k 1.0× 1.1k 1.3× 772 1.0× 893 1.7× 563 1.5× 112 3.0k
Clark C. Chen 1.1k 1.1× 693 0.8× 450 0.6× 581 1.1× 572 1.5× 131 2.7k
Logan A. Walsh 1.7k 1.7× 868 1.0× 1.1k 1.4× 979 1.8× 429 1.2× 55 3.4k
Frits Thorsen 1.6k 1.6× 1.2k 1.4× 972 1.3× 955 1.8× 648 1.8× 84 4.0k
Benoît Lhermitte 821 0.8× 1.1k 1.3× 647 0.8× 710 1.3× 702 1.9× 77 2.5k
Sameer Agnihotri 1.9k 1.8× 1.0k 1.2× 1.3k 1.6× 443 0.8× 271 0.7× 74 3.2k
Masayuki Nitta 1.9k 1.9× 734 0.9× 444 0.6× 950 1.8× 497 1.3× 94 3.7k
Ruihuan Chen 1.6k 1.5× 1.6k 1.8× 1.1k 1.4× 565 1.1× 296 0.8× 28 3.0k

Countries citing papers authored by Barbara Klink

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Klink

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Klink

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Klink. A scholar is included among the top collaborators of Barbara Klink 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 Barbara Klink. Barbara Klink 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.
Lucas, Morghan C., T. Keßler, Verena Steinke‐Lange, et al.. (2025). A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?. Familial Cancer. 24(2). 42–42. 1 indexed citations
2.
Lucas, Morghan C., T. Keßler, Thomas S. Risch, et al.. (2025). Improving genetic diagnosis of hereditary tumor syndromes: From expanded gene panels to functional genomics. International Journal of Cancer.
3.
Olinger, Christophe M., et al.. (2023). Digital PCR cluster predictor: a universal R-package and shiny app for the automated analysis of multiplex digital PCR data. Bioinformatics. 39(5). 5 indexed citations
4.
Seifert, Michael, Gabriele Schackert, Achim Temme, et al.. (2020). Molecular Characterization of Astrocytoma Progression Towards Secondary Glioblastomas Utilizing Patient-Matched Tumor Pairs. Cancers. 12(6). 1696–1696. 10 indexed citations
5.
Schuster, Anne, Eliane Klein, Virginie Neirinckx, et al.. (2020). AN1-type zinc finger protein 3 (ZFAND3) is a transcriptional regulator that drives Glioblastoma invasion. Nature Communications. 11(1). 6366–6366. 22 indexed citations
6.
Szczurek, Ewa, et al.. (2020). A mathematical model of the metastatic bottleneck predicts patient outcome and response to cancer treatment. PLoS Computational Biology. 16(10). e1008056–e1008056. 20 indexed citations
7.
Conde, Marina Clemente, Mirko Peitzsch, Susan Richter, et al.. (2019). Mutant IDH1 Differently Affects Redox State and Metabolism in Glial Cells of Normal and Tumor Origin. Cancers. 11(12). 2028–2028. 24 indexed citations
8.
Seifert, Michael, et al.. (2019). Network-based analysis of prostate cancer cell lines reveals novel marker gene candidates associated with radioresistance and patient relapse. PLoS Computational Biology. 15(11). e1007460–e1007460. 32 indexed citations
9.
Gieldon, Laura, Luisa Mackenroth, Anne‐Karin Kahlert, et al.. (2018). Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE. 13(8). e0201041–e0201041. 29 indexed citations
10.
Marrone, Lara, David C. Schöndorf, Julia C. Fitzgerald, et al.. (2018). Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease. PLoS ONE. 13(3). e0192497–e0192497. 21 indexed citations
11.
Lauber, Chris, Barbara Klink, & Michael Seifert. (2018). Comparative analysis of histologically classified oligodendrogliomas reveals characteristic molecular differences between subgroups. BMC Cancer. 18(1). 399–399. 14 indexed citations
12.
Reher, David, Barbara Klink, Andreas Deutsch, & Anja Voss–Böhme. (2017). Cell adhesion heterogeneity reinforces tumour cell dissemination: novel insights from a mathematical model. Biology Direct. 12(1). 18–18. 28 indexed citations
13.
Peitzsch, Claudia, Monica Cojoc, Ina Kurth, et al.. (2016). An Epigenetic Reprogramming Strategy to Resensitize Radioresistant Prostate Cancer Cells. Cancer Research. 76(9). 2637–2651. 57 indexed citations
14.
Klink, Barbara, Matthias Lehmann, Mirko Peitzsch, et al.. (2016). OS1.2 Effects of the IDH1R132H mutation on redox-status and metabolism are cell type dependent but independent from D-2-hydroxyglutarate accumulation. Neuro-Oncology. 18(suppl_4). iv2–iv2. 1 indexed citations
15.
Pistorius, Steffen, Barbara Klink, Jessica Pablik, et al.. (2016). An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis. Hereditary Cancer in Clinical Practice. 14(1). 11–11. 6 indexed citations
16.
Hackmann, Karl, Anne‐Karin Kahlert, Luisa Mackenroth, et al.. (2016). Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH. Breast Cancer Research and Treatment. 159(3). 585–590. 12 indexed citations
17.
Buder, Thomas, Andreas Deutsch, Barbara Klink, & Anja Voss–Böhme. (2015). Model-Based Evaluation of Spontaneous Tumor Regression in Pilocytic Astrocytoma. PLoS Computational Biology. 11(12). e1004662–e1004662. 11 indexed citations
18.
Donato, Nataliya Di, C. Le Caignec, Barbara Klink, et al.. (2014). Distinct phenotype of PHF6 deletions in females. European Journal of Medical Genetics. 57(2-3). 85–89. 15 indexed citations
19.
Donato, Nataliya Di, Barbara Klink, Gabriele Hahn, Evelin Schröck, & Karl Hackmann. (2014). Interstitial deletion 1p36.32 in two brothers with a distinct phenotype – Overgrowth, macrocephaly and nearly normal intellectual function. European Journal of Medical Genetics. 57(9). 494–497. 3 indexed citations
20.
Warnke, Clemens, Rotem S. Lanzman, Barbara Klink, et al.. (2009). Diffuse Leptomeningeal Astrocytoma in a Patient With Infantile Epilepsy. Archives of Neurology. 66(3). 408–9.

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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