Jennifer Hammes

663 total citations
12 papers, 457 citations indexed

About

Jennifer Hammes is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Jennifer Hammes has authored 12 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Jennifer Hammes's work include Glioma Diagnosis and Treatment (7 papers), Epigenetics and DNA Methylation (3 papers) and RNA modifications and cancer (2 papers). Jennifer Hammes is often cited by papers focused on Glioma Diagnosis and Treatment (7 papers), Epigenetics and DNA Methylation (3 papers) and RNA modifications and cancer (2 papers). Jennifer Hammes collaborates with scholars based in Germany, United States and Italy. Jennifer Hammes's co-authors include Andreas Waha, Torsten Pietsch, Marco Gessi, Gerrit H. Gielen, Christof M. Kramm, Dorota Denkhaus, Anja zur Mühlen, Anke Waha, Matthias Simon and Evelyn Dörner and has published in prestigious journals such as American Journal Of Pathology, International Journal of Cancer and Acta Neuropathologica.

In The Last Decade

Jennifer Hammes

12 papers receiving 450 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jennifer Hammes Germany 9 280 268 118 115 68 12 457
Mariko DeWire United States 14 266 0.9× 194 0.7× 125 1.1× 57 0.5× 90 1.3× 23 416
Anja zur Mühlen Germany 10 226 0.8× 229 0.9× 86 0.7× 72 0.6× 51 0.8× 19 361
Simon Loeser Germany 3 333 1.2× 198 0.7× 59 0.5× 125 1.1× 101 1.5× 3 403
Claire Faulkner United Kingdom 10 204 0.7× 145 0.5× 81 0.7× 72 0.6× 63 0.9× 13 324
Nathalène Truffaux France 5 437 1.6× 300 1.1× 191 1.6× 102 0.9× 93 1.4× 9 582
Donatella Bianchessi Italy 9 176 0.6× 122 0.5× 68 0.6× 88 0.8× 77 1.1× 11 306
Yuhei Sangatsuda Japan 14 320 1.1× 170 0.6× 103 0.9× 132 1.1× 84 1.2× 48 463
Isabelle Nanni‐Metellus France 10 223 0.8× 188 0.7× 64 0.5× 144 1.3× 67 1.0× 22 404
Annett Hölsken Germany 16 391 1.4× 334 1.2× 181 1.5× 105 0.9× 24 0.4× 25 875
Michal Zápotocký Czechia 12 397 1.4× 168 0.6× 199 1.7× 53 0.5× 104 1.5× 47 508

Countries citing papers authored by Jennifer Hammes

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Hammes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Hammes

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

All Works

12 of 12 papers shown
1.
Gielen, Gerrit H., Anke Waha, Tim Müller, et al.. (2016). MTSS1 is epigenetically regulated in glioma cells and inhibits glioma cell motility. Translational Oncology. 10(1). 70–79. 6 indexed citations
2.
Gessi, Marco, et al.. (2014). FGFR1 N546K mutation in a case of papillary glioneuronal tumor (PGNT). Acta Neuropathologica. 127(6). 935–936. 12 indexed citations
3.
Gessi, Marco, Jennifer Hammes, Tobias Goschzik, et al.. (2014). FGFR1Mutations in Rosette-Forming Glioneuronal Tumors of the Fourth Ventricle. Journal of Neuropathology & Experimental Neurology. 73(6). 580–584. 56 indexed citations
4.
Gielen, Gerrit H., Marco Gessi, Francesca Romana Buttarelli, et al.. (2014). Genetic Analysis of Diffuse High‐Grade Astrocytomas in Infancy Defines a Novel Molecular Entity. Brain Pathology. 25(4). 409–417. 30 indexed citations
5.
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
6.
Gessi, Marco, Anja zur Mühlen, Jennifer Hammes, et al.. (2013). Genome-Wide DNA Copy Number Analysis of Desmoplastic Infantile Astrocytomas and Desmoplastic Infantile Gangliogliomas. Journal of Neuropathology & Experimental Neurology. 72(9). 807–815. 27 indexed citations
7.
Gielen, Gerrit H., Marco Gessi, Jennifer Hammes, et al.. (2013). H3F3A K27M Mutation in Pediatric CNS Tumors. American Journal of Clinical Pathology. 139(3). 345–349. 90 indexed citations
8.
Felsberg, Jörg, Anke Waha, Wolfgang Hartmann, et al.. (2012). RANK (TNFRSF11A) Is Epigenetically Inactivated and Induces Apoptosis in Gliomas. Neoplasia. 14(6). 526–IN12. 22 indexed citations
9.
Müller, Tim, Marco Gessi, Anke Waha, et al.. (2012). Nuclear Exclusion of TET1 Is Associated with Loss of 5-Hydroxymethylcytosine in IDH1 Wild-Type Gliomas. American Journal Of Pathology. 181(2). 675–683. 93 indexed citations
10.
Gessi, Marco, Anke Waha, Jennifer Hammes, et al.. (2011). Sensitive Determination of BRAF Copy Number in Clinical Samples by Pyrosequencing. Diagnostic Molecular Pathology. 20(3). 148–157. 8 indexed citations
11.
Waha, Anke, Jörg Felsberg, Wolfgang Hartmann, et al.. (2011). Frequent epigenetic inactivation of the chaperone SGNE1/7B2 in human gliomas. International Journal of Cancer. 131(3). 612–622. 7 indexed citations
12.
Hammes, Jennifer, et al.. (2010). A Pyrosequencing-Based Assay for the Rapid Detection of IDH1 Mutations in Clinical Samples. Journal of Molecular Diagnostics. 12(6). 750–756. 52 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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