Anna Ehinger

19.0k citations
77 papers · 11.7k · 7 hit papers · h-index 42

Impact in

Papers in

    • Cancer Genomics and Diagnostics 32
    • Breast Cancer Treatment Studies 18
    • Cancer Immunotherapy and Biomarkers 10
    • HER2/EGFR in Cancer Research 5

Anna Ehinger

74 papers receiving 11.5k citations

Anna Ehinger's Hit Papers

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes 2020 · 419 citations
4190+2+4Years since publication50010001.5k2.0k

Peers

Anna Ehinger
Comparison fields: 5 of 152
  • Cancer Research 5.0k
  • Oncology 2.8k
  • Molecular Biology 5.8k
  • Pathology and Forensic Medicine 1.1k
  • Genetics 1.6k
Replace Ignacio Vázquez-García with:
Ignacio Vázquez-García United States
Yoke-Eng Chiew United States
Sarah‐Jane Schramm Canada
Hazel Burke United States
Prue A. Cowin Canada
Dale W. Garsed Australia
Jillian A. Hung United States
Ilinca M. Lungu Canada
Geoff Macintyre United Kingdom
Gerrit K. J. Hooijer Netherlands
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Citations per field
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Citations per year

Countries citing papers authored by Anna Ehinger

Since Specialization
Citations

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

Fields of papers citing papers by Anna Ehinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Anna Ehinger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Ehinger Line = papers co-authored together Anna Ehinger links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 77 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The repertoire of mutational signatures in human cancer
Hit paper breakdown →
20202339
2
Pan-cancer analysis of whole genomes
Hit paper breakdown →
20202109
3
The evolutionary history of 2,658 cancers
Hit paper breakdown →
2020705
4
Patterns of somatic structural variation in human cancer genomes
Hit paper breakdown →
2020550
5
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Hit paper breakdown →
2020476
6
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Hit paper breakdown →
2020419
7 2020317
8
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020309
9 2020301
10 2020293
11 2021255
12 2019213
13 2021193
14 2020184
15 2015167
16 2020164
17 2020160
18 2020159
19 2020156
20 2020152

About Anna Ehinger

Anna Ehinger is a scholar working on Cancer Research, Oncology, Pathology and Forensic Medicine, Genetics and Molecular Biology, having authored 77 papers that have together received 11.7k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (32 papers), Breast Cancer Treatment Studies (18 papers), Cancer Immunotherapy and Biomarkers (10 papers), Genetic factors in colorectal cancer (9 papers), HER2/EGFR in Cancer Research (5 papers), RNA modifications and cancer (5 papers), RNA Research and Splicing (5 papers) and Radiomics and Machine Learning in Medical Imaging (5 papers). The work is most often cited by research in Cancer Research (5.0k citations), Oncology (2.8k citations), Molecular Biology (5.8k citations), Pathology and Forensic Medicine (1.1k citations) and Genetics (1.6k citations). Anna Ehinger has collaborated with scholars based in Sweden, United States and Canada. Frequent co-authors include Åke Borg, Lisa Rydén, Johan Vallon‐Christersson, Lao H. Saal, Martin Malmberg, Cecilia Hegardt, Niklas Loman, Jari Häkkinen, Christer Larsson and Christian Brueffer. Their work appears in journals such as Nature Communications, npj Breast Cancer, Nature, Nature Genetics and Breast Cancer Research.

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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