Anja Füllgrabe

18.1k citations
38 papers · 11.3k · 7 hit papers · h-index 31

Impact in

    • Cancer Genomics and Diagnostics
    • RNA modifications and cancer
    • Epigenetics and DNA Methylation
    • Genomics and Chromatin Dynamics
    • Bioinformatics and Genomic Networks
    • DNA Repair Mechanisms
    • Single-cell and spatial transcriptomics

Papers in

    • Cancer Genomics and Diagnostics 18
    • Genomics and Phylogenetic Studies 7
    • Molecular Biology Techniques and Applications 6
    • RNA Research and Splicing 6
    • Genomics and Chromatin Dynamics 5
    • RNA modifications and cancer 5
    • Gene expression and cancer classification 5

Anja Füllgrabe

38 papers receiving 11.2k citations

Anja Füllgrabe'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

Anja Füllgrabe
Comparison fields: 5 of 153
  • Cancer Research 4.4k
  • Molecular Biology 6.5k
  • Oncology 2.0k
  • Pathology and Forensic Medicine 1.0k
  • Genetics 1.6k
Replace Maria Keays with:
Maria Keays United Kingdom
Lina Wadi Canada
Natalie Saini United States
Hardeep K. Nahal-Bose Canada
Aurélien Chateigner Canada
Shriram G. Bhosle United Kingdom
Xiaotong Li China
Elisabet Barrera Canada
Ruben M. Drews Canada
Kin Chan United States
Anja Füllgrabe relative to Maria Keays United Kingdom Maria Keays's profile →
Citations per field
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Maria Keays · 1×
Citations per year

Countries citing papers authored by Anja Füllgrabe

Since Specialization
Citations

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

Fields of papers citing papers by Anja Füllgrabe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Anja Füllgrabe, 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 Anja Füllgrabe Line = papers co-authored together Anja Füllgrabe links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 38 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 2018433
7 2015432
8
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Hit paper breakdown →
2020419
9 2019374
10 2020317
11
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020309
12 2017303
13 2020301
14 2020293
15 2017239
16 2020184
17 2020160
18 2020159
19 2020152
20 2021150

About Anja Füllgrabe

Anja Füllgrabe is a scholar working on Cancer Research, Molecular Biology, Pathology and Forensic Medicine, Genetics and Urology, having authored 38 papers that have together received 11.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (18 papers), Genetic factors in colorectal cancer (8 papers), Genomics and Phylogenetic Studies (7 papers), Molecular Biology Techniques and Applications (6 papers), RNA Research and Splicing (6 papers), Genomics and Chromatin Dynamics (5 papers), RNA modifications and cancer (5 papers) and Gene expression and cancer classification (5 papers). The work is most often cited by research in Cancer Research (4.4k citations), Molecular Biology (6.5k citations), Oncology (2.0k citations), Pathology and Forensic Medicine (1.0k citations) and Genetics (1.6k citations). Anja Füllgrabe has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Alvis Brāzma, Haider Iqbal, Awais Athar, Nancy George, Irene Papatheodorou, Ahmed Yousif Ali, Uğis Sarkans, Laura Huerta, Robert Petryszak and Nuno A. Fonseca. Their work appears in journals such as Nature Communications, Nucleic Acids Research, Nature, Nature Genetics and eLife.

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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