Carina Lorenz

453 total citations
5 papers, 35 citations indexed

About

Carina Lorenz is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Carina Lorenz has authored 5 papers receiving a total of 35 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cancer Research and 2 papers in Genetics. Recurrent topics in Carina Lorenz's work include Cancer Genomics and Diagnostics (3 papers), Gene expression and cancer classification (1 paper) and Nonmelanoma Skin Cancer Studies (1 paper). Carina Lorenz is often cited by papers focused on Cancer Genomics and Diagnostics (3 papers), Gene expression and cancer classification (1 paper) and Nonmelanoma Skin Cancer Studies (1 paper). Carina Lorenz collaborates with scholars based in Germany and United States. Carina Lorenz's co-authors include Christina Curtis, Jennifer L. Caswell‐Jin, Sarah Kittel‐Schneider, Andreas Reif, Roman K. Thomas, Johannes Brägelmann, Konstantin Drexler, Hannah L. Tumbrink, Johannes Berg and Dennis Plenker and has published in prestigious journals such as Cancer Research, Journal of Affective Disorders and Signal Transduction and Targeted Therapy.

In The Last Decade

Carina Lorenz

5 papers receiving 35 citations

Peers

Carina Lorenz
Cody Plasterer United States
Andrew S. Boghossian United States
Januka Khanal United States
Milena Jakimovska North Macedonia
Cody Plasterer United States
Carina Lorenz
Citations per year, relative to Carina Lorenz Carina Lorenz (= 1×) peers Cody Plasterer

Countries citing papers authored by Carina Lorenz

Since Specialization
Citations

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

Fields of papers citing papers by Carina Lorenz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carina Lorenz

This figure shows the co-authorship network connecting the top 25 collaborators of Carina Lorenz. A scholar is included among the top collaborators of Carina Lorenz 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 Carina Lorenz. Carina Lorenz 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.
Helbig, Doris, Corinna Bürger, Anne Fröhlich, et al.. (2025). Explainable, federated deep learning model predicts disease progression risk of cutaneous squamous cell carcinoma. npj Precision Oncology. 9(1). 205–205. 2 indexed citations
2.
Lorenz, Carina, Maria Cartolano, Dennis Plenker, et al.. (2023). Characterizing Evolutionary Dynamics Reveals Strategies to Exhaust the Spectrum of Subclonal Resistance in EGFR-Mutant Lung Cancer. Cancer Research. 83(15). 2471–2479. 7 indexed citations
3.
Lorenz, Carina, Axel M. Hillmer, & Johannes Brägelmann. (2023). Predicting the next move: tracking the complexity of lung cancer evolution and metastasis. Signal Transduction and Targeted Therapy. 8(1). 291–291. 1 indexed citations
4.
Caswell‐Jin, Jennifer L., Carina Lorenz, & Christina Curtis. (2020). Molecular Heterogeneity and Evolution in Breast Cancer. 5(1). 79–94. 14 indexed citations
5.
Kittel‐Schneider, Sarah, et al.. (2016). DGKH genetic risk variant influences gene expression in bipolar affective disorder. Journal of Affective Disorders. 198. 148–157. 11 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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