Andrea Wittmann

7.3k total citations
10 papers, 822 citations indexed

About

Andrea Wittmann is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Andrea Wittmann has authored 10 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Genetics. Recurrent topics in Andrea Wittmann's work include Genomic variations and chromosomal abnormalities (5 papers), Hedgehog Signaling Pathway Studies (4 papers) and Chromatin Remodeling and Cancer (4 papers). Andrea Wittmann is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Hedgehog Signaling Pathway Studies (4 papers) and Chromatin Remodeling and Cancer (4 papers). Andrea Wittmann collaborates with scholars based in Germany, United Kingdom and United States. Andrea Wittmann's co-authors include Andreas E. Kulozik, Peter Lichter, Stefan M. Pfister, Axel Benner, Marc Remke, Andrey Korshunov, Wolfram Scheurlen, Hendrik Witt, Andreas von Deimling and Marina Ryzhova and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Blood.

In The Last Decade

Andrea Wittmann

10 papers receiving 809 citations

Peers

Andrea Wittmann

GENET

NEURO

ONCOL

Suzanne E. Little United Kingdom

Ruth Tatevossian United States

D Jadayel United Kingdom

M. Eva Alonso Spain

Patricia Rakopoulos Canada

Alexa Jury United Kingdom

David Shih United States

Rebekah Kennedy United States

Jacques Vargaftig France

Małgorzata Szybka Poland

Suzanne E. Little United Kingdom

Andrea Wittmann

538 ×1.0

347 ×0.6

GENET

229 ×1.3

153 ×1.0

NEURO

138 ×1.4

ONCOL

Citations per year, relative to Andrea Wittmann Andrea Wittmann (= 1×) peers Suzanne E. Little

Countries citing papers authored by Andrea Wittmann

Since Specialization

Citations

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

Fields of papers citing papers by Andrea Wittmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Wittmann

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

All Works

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10 of 10 papers shown

Wittmann, Andrea, et al.. (2023). Chronic inflammatory effects of in vivo irradiation of the murine heart on endothelial cells mimic mechanisms involved in atherosclerosis. Strahlentherapie und Onkologie. 199(12). 1214–1224. 2 indexed citations

Tzaridis, Theophilos, Till Milde, Kristian W. Pajtler, et al.. (2016). Low-dose Actinomycin-D treatment re-establishes the tumoursuppressive function of P53 in RELA-positive ependymoma. Oncotarget. 7(38). 61860–61873. 22 indexed citations

Remke, Marc, Thomas Hielscher, Paul A. Northcott, et al.. (2011). Adult Medulloblastoma Comprises Three Major Molecular Variants. Journal of Clinical Oncology. 29(19). 2717–2723. 160 indexed citations

Korshunov, Andrey, Marc Remke, Wiebke Werft, et al.. (2010). Adult and Pediatric Medulloblastomas Are Genetically Distinct and Require Different Algorithms for Molecular Risk Stratification. Journal of Clinical Oncology. 28(18). 3054–3060. 102 indexed citations

Korshunov, Andrey, Hendrik Witt, Thomas Hielscher, et al.. (2010). Molecular Staging of Intracranial Ependymoma in Children and Adults. Journal of Clinical Oncology. 28(19). 3182–3190. 147 indexed citations

Pfister, Stefan M., Marc Remke, Axel Benner, et al.. (2009). Outcome Prediction in Pediatric Medulloblastoma Based on DNA Copy-Number Aberrations of Chromosomes 6q and 17q and the MYC and MYCN Loci. Journal of Clinical Oncology. 27(10). 1627–1636. 198 indexed citations

Remke, Marc, Stefan M. Pfister, Corinne Kox, et al.. (2009). High-resolution genomic profiling of childhood T-ALL reveals frequent copy-number alterations affecting the TGF-β and PI3K-AKT pathways and deletions at 6q15-16.1 as a genomic marker for unfavorable early treatment response. Blood. 114(5). 1053–1062. 85 indexed citations

Rieber, Juliane, Marc Remke, Christian Hartmann, et al.. (2009). Novel oncogene amplifications in tumors from a family with Li–Fraumeni syndrome. Genes Chromosomes and Cancer. 48(7). 558–568. 5 indexed citations

Pfister, Stefan M., Frank Mendrzyk, Andrea Wittmann, et al.. (2007). Array-based profiling of reference-independent methylation status (aPRIMES) identifies frequent promoter methylation and consecutive downregulation of ZIC2 in pediatric medulloblastoma. Nucleic Acids Research. 35(7). e51–e51. 48 indexed citations

10.

Pfister, Stefan M., Marc Remke, Grischa Toedt, et al.. (2007). Supratentorial primitive neuroectodermal tumors of the central nervous system frequently harbor deletions of the CDKN2A locus and other genomic aberrations distinct from medulloblastomas. Genes Chromosomes and Cancer. 46(9). 839–851. 53 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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