Rabea Wagener

15.7k total citations
26 papers, 236 citations indexed

About

Rabea Wagener is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Rabea Wagener has authored 26 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Pathology and Forensic Medicine and 7 papers in Genetics. Recurrent topics in Rabea Wagener's work include Lymphoma Diagnosis and Treatment (7 papers), Acute Lymphoblastic Leukemia research (5 papers) and Genomics and Rare Diseases (3 papers). Rabea Wagener is often cited by papers focused on Lymphoma Diagnosis and Treatment (7 papers), Acute Lymphoblastic Leukemia research (5 papers) and Genomics and Rare Diseases (3 papers). Rabea Wagener collaborates with scholars based in Germany, United States and Austria. Rabea Wagener's co-authors include Susanne Bens, Reiner Siebert, Triantafyllia Brozou, Arndt Borkhardt, Mark W. Linder, R Valdes, William D. Foulkes, Nelly Sabbaghian, John R. Priest and Dorothée Bouron‐Dal Soglio and has published in prestigious journals such as New England Journal of Medicine, Blood and Bioinformatics.

In The Last Decade

Rabea Wagener

26 papers receiving 228 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rabea Wagener Germany 8 66 64 57 46 42 26 236
Triantafyllia Brozou Germany 9 52 0.8× 69 1.1× 91 1.6× 24 0.5× 56 1.3× 24 237
Nisreen Amayiri Jordan 11 48 0.7× 51 0.8× 21 0.4× 22 0.5× 40 1.0× 28 259
D R Betts Switzerland 9 38 0.6× 111 1.7× 110 1.9× 16 0.3× 20 0.5× 15 300
Michelle F. Jacobs United States 8 55 0.8× 60 0.9× 60 1.1× 42 0.9× 45 1.1× 35 235
Eleonora Zanetti Italy 10 48 0.7× 77 1.2× 25 0.4× 23 0.5× 31 0.7× 29 253
Asad Haider United States 6 49 0.7× 75 1.2× 26 0.5× 33 0.7× 33 0.8× 13 287
Wanling Sun China 8 28 0.4× 80 1.3× 18 0.3× 24 0.5× 21 0.5× 41 297
Ljiljana Milojevic United States 4 23 0.3× 66 1.0× 17 0.3× 79 1.7× 26 0.6× 4 313
Edgardo R. Parrilla Castellar United States 6 110 1.7× 38 0.6× 19 0.3× 36 0.8× 29 0.7× 9 257
E. Piazzola Italy 9 57 0.9× 67 1.0× 101 1.8× 24 0.5× 47 1.1× 12 364

Countries citing papers authored by Rabea Wagener

Since Specialization
Citations

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

Fields of papers citing papers by Rabea Wagener

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rabea Wagener

This figure shows the co-authorship network connecting the top 25 collaborators of Rabea Wagener. A scholar is included among the top collaborators of Rabea Wagener 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 Rabea Wagener. Rabea Wagener 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.
Wagener, Rabea, Ute Fischer, Anna Hoffmann, et al.. (2024). Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants. HemaSphere. 8(1). e26–e26. 2 indexed citations
2.
Friedrich, Ulrike, Arne Jahn, Carolin Walter, et al.. (2023). A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children. Genetics in Medicine. 25(8). 100875–100875. 2 indexed citations
3.
Wagener, Rabea, Sarah Elitzur, Triantafyllia Brozou, & Arndt Borkhardt. (2023). Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia. European Journal of Medical Genetics. 66(4). 104725–104725. 5 indexed citations
4.
Wagener, Rabea, Anke K. Bergmann, Stephanie Panier, et al.. (2023). Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients. International Journal of Cancer. 154(4). 607–614. 3 indexed citations
5.
Nebral, Karin, Jana Ebler, Daniel Picard, et al.. (2023). Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia. HemaSphere. 7(8). e925–e925. 15 indexed citations
6.
Picard, Daniel, Tobias Lautwein, Rabea Wagener, et al.. (2022). A Human iPSC Model Reveals Specific Upregulation of Linker Histone H1-0 in ETV6::RUNX1+ Preleukemia and B Cell Precursor Acute Lymphoblastic Leukemia. Blood. 140(Supplement 1). 3469–3470. 1 indexed citations
7.
Wagener, Rabea, Carolin Walter, Franziska Auer, et al.. (2022). The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients. International Journal of Cancer. 152(7). 1388–1398. 5 indexed citations
8.
Wagener, Rabea, Carolin Walter, Harald Surowy, et al.. (2022). Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents. Journal of Pediatric Hematology/Oncology. 45(2). e244–e248. 2 indexed citations
9.
Wagener, Rabea, et al.. (2021). Genome‐wide DNA methylation analysis along the progression of gastric marginal zone B‐cell lymphoma of mucosa‐associated lymphoid tissue (MALT) type. British Journal of Haematology. 193(2). 369–374. 2 indexed citations
10.
Wagener, Rabea, Carolin Walter, Christoph Bartenhagen, et al.. (2021). Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer. European Journal of Human Genetics. 29(8). 1301–1311. 30 indexed citations
11.
Friedrich, Ulrike, Rabea Wagener, Juha Mehtonen, et al.. (2021). Germline POT1 Deregulation Can Predispose to Myeloid Malignancies in Childhood. International Journal of Molecular Sciences. 22(21). 11572–11572. 6 indexed citations
12.
Nagel, Inga, Cristina López, Susanne Bens, et al.. (2020). Double-hit lymphoma of the male breast: a case report. Journal of Medical Case Reports. 14(1). 245–245. 5 indexed citations
13.
López, Cristina, Rabea Wagener, Katja Dettmer, et al.. (2020). Acquired resistance to DZNep-mediated apoptosis is associated with copy number gains of AHCY in a B-cell lymphoma model. BMC Cancer. 20(1). 427–427. 4 indexed citations
14.
Horn, Heike, Rabea Wagener, Annette M. Staiger, et al.. (2020). A Diagnostic Approach to the Identification of Burkitt-like Lymphoma With 11q Aberration in Aggressive B-Cell Lymphomas. The American Journal of Surgical Pathology. 45(3). 356–364. 29 indexed citations
15.
Kock, Leanne de, Bárbara Rivera, Rabea Wagener, et al.. (2018). Multiple DICER1‐related tumors in a child with a large interstitial 14q32 deletion. Genes Chromosomes and Cancer. 57(5). 223–230. 32 indexed citations
16.
Vogt, J., Rabea Wagener, Manuel Montesinos‐Rongen, et al.. (2018). Array‐based profiling of the lymphoma cell DNA methylome does not unequivocally distinguish primary lymphomas of the central nervous system from non‐CNS diffuse large B‐cell lymphomas. Genes Chromosomes and Cancer. 58(1). 66–69. 7 indexed citations
17.
Doose, Gero, Stephan Wolf, Rabea Wagener, & Steve Hoffman. (2017). DIEGO: detection of differential alternative splicing using Aitchison’s geometry. Bioinformatics. 34(6). 1066–1068. 5 indexed citations
18.
Bens, Susanne, Thomas Zichner, Adrian M. Stütz, et al.. (2014). SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome. Genes and Immunity. 15(3). 190–194. 17 indexed citations
19.
Wagener, Rabea, et al.. (1999). [Feeding of patients with Alzheimer's disease].. PubMed. 53(6). 357–60. 2 indexed citations
20.
Wagener, Rabea, et al.. (1998). [Eating and drinking in patients with Alzheimer dementia. A study of interactions].. PubMed. 11(2). 89–95. 2 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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