Inga Vater
Impact in
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- Lymphoma Diagnosis and Treatment
- Cancer Mechanisms and Therapy
- Genetics top 5%
- Chronic Lymphocytic Leukemia Research
Papers in
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- RNA modifications and cancer 5
- Epigenetics and DNA Methylation 3
-
- Lymphoma Diagnosis and Treatment 13
- Co-authors
- Reiner Siebert (24 shared papers)Stefan Gesk (9 shared papers)Ralf Küppers (8 shared papers)José I. Martı́n-Subero (7 shared papers)Wolfram Klapper (7 shared papers)Maciej Giefing (5 shared papers)Martin‐Leo Hansmann (5 shared papers)Julia Richter (6 shared papers)
- Journals
- Blood (4 papers)British Journal of Haematology (3 papers)Genes Chromosomes and Cancer (3 papers)European Journal of Human Genetics (2 papers)Leukemia (2 papers)
- Partner nations
- GermanyUnited KingdomPoland
In The Last Decade
Inga Vater
35 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 70
- Pathology and Forensic Medicine 701
- Genetics 315
- Cancer Research 304
- Hematology 181
- Neurology 243
Countries citing papers authored by Inga Vater
This map shows the geographic impact of Inga Vater'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 Inga Vater with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Vater more than expected).
Fields of papers citing papers by Inga Vater
This network shows the impact of papers produced by Inga Vater. 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 Inga Vater. The network helps show where Inga Vater may publish in the future.
Co-authors
The 25 scholars most cited alongside Inga Vater, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 344 | |
| 2 | 2010 | 222 | |
| 3 | 2010 | 150 | |
| 4 | 2014 | 105 | |
| 5 | 2012 | 75 | |
| 6 | 2014 | 66 | |
| 7 | 2009 | 58 | |
| 8 | 2013 | 56 | |
| 9 | 2009 | 54 | |
| 10 | 2015 | 52 | |
| 11 | 2010 | 41 | |
| 12 | 2009 | 40 | |
| 13 | 2011 | 39 | |
| 14 | 2010 | 36 | |
| 15 | 2016 | 27 | |
| 16 | 2011 | 25 | |
| 17 | 2009 | 24 | |
| 18 | 2016 | 23 | |
| 19 | 2008 | 22 | |
| 20 | 2011 | 22 |
About Inga Vater
Inga Vater is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Cancer Research, Genetics and Genetics, having authored 35 papers that have together received 1.6k indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (13 papers), Chronic Lymphocytic Leukemia Research (6 papers), Chronic Myeloid Leukemia Treatments (5 papers), RNA modifications and cancer (5 papers), NF-κB Signaling Pathways (5 papers), Acute Lymphoblastic Leukemia research (4 papers), Epigenetics and DNA Methylation (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (701 citations), Genetics (315 citations), Cancer Research (304 citations), Hematology (181 citations) and Neurology (243 citations). Inga Vater has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Reiner Siebert, Stefan Gesk, Ralf Küppers, José I. Martı́n-Subero, Wolfram Klapper, Maciej Giefing, Martin‐Leo Hansmann, Julia Richter, Roland Schmitz and Markus Kreuz. Their work appears in journals such as Blood, British Journal of Haematology, Genes Chromosomes and Cancer, European Journal of Human Genetics and Leukemia.
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.