Christina Evers
Impact in
- Obstetrics and Gynecology top 5%
- Endometrial and Cervical Cancer Treatments
- Otorhinolaryngology top 5%
- Head and Neck Cancer Studies
Papers in
-
- RNA modifications and cancer 3
- Genetics 18
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 6
- BRCA gene mutations in cancer 5
- Co-authors
- John A. Blessing (1 shared paper)Linda F. Carson (1 shared paper)Philip J. DiSaia (1 shared paper)J.T. Thigpen (1 shared paper)Edgardo Yordan (1 shared paper)Katrin Hinderhofer (14 shared papers)Ute Moog (13 shared papers)Martin Granzow (8 shared papers)
- Journals
- International Journal of Radiation Oncology*Biology*Physics (3 papers)Breast Cancer Research and Treatment (3 papers)Clinical Genetics (2 papers)Orphanet Journal of Rare Diseases (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- GermanyPolandUnited States
In The Last Decade
Christina Evers
32 papers receiving 722 citations
Peers
Comparison fields: 5 of 68
- Obstetrics and Gynecology 114
- Otorhinolaryngology 58
- Reproductive Medicine 95
- Genetics 274
- Hematology 71
Countries citing papers authored by Christina Evers
This map shows the geographic impact of Christina Evers'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 Christina Evers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christina Evers more than expected).
Fields of papers citing papers by Christina Evers
This network shows the impact of papers produced by Christina Evers. 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 Christina Evers. The network helps show where Christina Evers may publish in the future.
Co-authors
The 25 scholars most cited alongside Christina Evers, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 128 | |
| 2 | 2015 | 59 | |
| 3 | 2011 | 46 | |
| 4 | 2009 | 45 | |
| 5 | 2012 | 44 | |
| 6 | 2014 | 43 | |
| 7 | 2007 | 36 | |
| 8 | 2017 | 34 | |
| 9 | 2008 | 30 | |
| 10 | 2017 | 27 | |
| 11 | 2017 | 27 | |
| 12 | 2017 | 25 | |
| 13 | 2016 | 21 | |
| 14 | 2015 | 20 | |
| 15 | 2015 | 20 | |
| 16 | 2010 | 18 | |
| 17 | 2015 | 15 | |
| 18 | 2014 | 15 | |
| 19 | 2019 | 14 | |
| 20 | 2016 | 12 |
About Christina Evers
Christina Evers is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Surgery, having authored 33 papers that have together received 743 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), BRCA gene mutations in cancer (5 papers), Cancer Genomics and Diagnostics (5 papers), RNA modifications and cancer (3 papers), Head and Neck Cancer Studies (3 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Obstetrics and Gynecology (114 citations), Otorhinolaryngology (58 citations), Reproductive Medicine (95 citations), Genetics (274 citations) and Hematology (71 citations). Christina Evers has collaborated with scholars based in Germany, Poland and United States. Frequent co-authors include John A. Blessing, Linda F. Carson, Philip J. DiSaia, J.T. Thigpen, Edgardo Yordan, Katrin Hinderhofer, Ute Moog, Martin Granzow, Nagarajan Paramasivam and Christine Fischer. Their work appears in journals such as International Journal of Radiation Oncology*Biology*Physics, Breast Cancer Research and Treatment, Clinical Genetics, Orphanet Journal of Rare Diseases and Molecular Genetics and Metabolism.
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.