Evelyn Dörner

720 total citations
11 papers, 210 citations indexed

About

Evelyn Dörner is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Evelyn Dörner has authored 11 papers receiving a total of 210 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Evelyn Dörner's work include Glioma Diagnosis and Treatment (9 papers), Chromatin Remodeling and Cancer (3 papers) and Sarcoma Diagnosis and Treatment (2 papers). Evelyn Dörner is often cited by papers focused on Glioma Diagnosis and Treatment (9 papers), Chromatin Remodeling and Cancer (3 papers) and Sarcoma Diagnosis and Treatment (2 papers). Evelyn Dörner collaborates with scholars based in Germany, Switzerland and Italy. Evelyn Dörner's co-authors include Torsten Pietsch, Andreas Waha, Anja zur Mühlen, Marco Gessi, Gerrit H. Gielen, Jennifer Hammes, Verena Dreschmann, Stephanie T. Jünger, Ivo Leuschner and Gabriele Calaminus and has published in prestigious journals such as The American Journal of Surgical Pathology, Acta Neuropathologica and Journal of Neuropathology & Experimental Neurology.

In The Last Decade

Evelyn Dörner

11 papers receiving 210 citations

Peers

Evelyn Dörner
Evelyn Dörner
Citations per year, relative to Evelyn Dörner Evelyn Dörner (= 1×) peers Э. В. Кумирова

Countries citing papers authored by Evelyn Dörner

Since Specialization
Citations

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

Fields of papers citing papers by Evelyn Dörner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Evelyn Dörner

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

All Works

11 of 11 papers shown
1.
Andreiuolo, Felipe, et al.. (2023). p16 Immunohistochemistry as a Screening Tool for Homozygous CDKN2A Deletions in CNS Tumors. The American Journal of Surgical Pathology. 48(1). 46–53. 8 indexed citations
2.
Jünger, Stephanie T., Felipe Andreiuolo, Martin Mynarek, et al.. (2020). CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort. Acta Neuropathologica. 140(3). 405–407. 31 indexed citations
3.
Jünger, Stephanie T., Felipe Andreiuolo, Martin Mynarek, et al.. (2020). Ependymomas in infancy: underlying genetic alterations, histological features, and clinical outcome. Child s Nervous System. 36(11). 2693–2700. 16 indexed citations
4.
Jünger, Stephanie T., Martin Mynarek, Inken Wohlers, et al.. (2019). Improved risk-stratification for posterior fossa ependymoma of childhood considering clinical, histological and genetic features – a retrospective analysis of the HIT ependymoma trial cohort. Acta Neuropathologica Communications. 7(1). 181–181. 18 indexed citations
5.
Jünger, Stephanie T., Martin Mynarek, Evelyn Dörner, et al.. (2019). EPEN-07. EPENDYMOMAS IN INFANCY: UNDERLYING GENETIC ALTERATIONS, HISTOLOGICAL FEATURES AND CLINICAL OUTCOME. Neuro-Oncology. 21(Supplement_2). ii78–ii78. 1 indexed citations
6.
Dörner, Evelyn, Verena Dreschmann, Glen Kristiansen, et al.. (2017). Type, Frequency, and Spatial Distribution of Immune Cell Infiltrates in CNS Germinomas: Evidence for Inflammatory and Immunosuppressive Mechanisms. Journal of Neuropathology & Experimental Neurology. 77(2). 119–127. 20 indexed citations
7.
Gessi, Marco, Elke Hattingen, Evelyn Dörner, et al.. (2016). Dysembryoplastic Neuroepithelial Tumor of the Septum Pellucidum and the Supratentorial Midline. The American Journal of Surgical Pathology. 40(6). 806–811. 7 indexed citations
8.
Waha, Andreas, Dorota Denkhaus, Evelyn Dörner, et al.. (2016). CNS germinomas are characterized by global demethylation, chromosomal instability and mutational activation of the Kit-, Ras/Raf/Erk- and Akt-pathways. Oncotarget. 7(34). 55026–55042. 27 indexed citations
9.
Gessi, Marco, Verena Dreschmann, Anja zur Mühlen, et al.. (2015). High-Resolution Genomic Analysis of Cribriform Neuroepithelial Tumors of the Central Nervous System. Journal of Neuropathology & Experimental Neurology. 74(10). 970–974. 7 indexed citations
10.
Gessi, Marco, Evelyn Dörner, Verena Dreschmann, et al.. (2015). Intramedullary gangliogliomas: histopathologic and molecular features of 25 cases. Human Pathology. 49. 107–113. 21 indexed citations
11.
Gessi, Marco, Gerrit H. Gielen, Jennifer Hammes, et al.. (2013). H3.3 G34R mutations in pediatric primitive neuroectodermal tumors of central nervous system (CNS-PNET) and pediatric glioblastomas: possible diagnostic and therapeutic implications?. Journal of Neuro-Oncology. 112(1). 67–72. 54 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026