Steve Hoffmann

19.3k citations
104 papers · 12.4k · 6 hit papers · h-index 41

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
    • RNA modifications and cancer
    • Genomics and Phylogenetic Studies
    • Epigenetics and DNA Methylation
    • RNA and protein synthesis mechanisms
    • RNA Research and Splicing

Papers in

    • Cancer-related molecular mechanisms research 17
    • Cancer Genomics and Diagnostics 13
    • RNA modifications and cancer 26
    • Epigenetics and DNA Methylation 15
    • Genomics and Phylogenetic Studies 14
    • RNA Research and Splicing 13

Steve Hoffmann

99 papers receiving 12.3k citations

Steve Hoffmann's Hit Papers

Patterns of somatic structural variation in human cancer genomes 2020 · 550 citations
5500+5+10Years since publication50010001.5k2.0k

Peers

Steve Hoffmann
Comparison fields: 5 of 173
  • Cancer Research 4.3k
  • Molecular Biology 7.0k
  • Oncology 1.9k
  • Pathology and Forensic Medicine 1.2k
  • Genetics 1.8k
Replace Shriram G. Bhosle with:
Shriram G. Bhosle United Kingdom
Lina Wadi Canada
Solomon I. Shorser Canada
Jonathan Göke Singapore
Helene Kretzmer Germany
Joy C. Jayaseelan United States
Robert Petryszak United Kingdom
Kathleen H. Burns United States
Morgan L. Taschuk Canada
Adrian Baez‐Ortega United Kingdom
Steve Hoffmann relative to Shriram G. Bhosle United Kingdom Shriram G. Bhosle's profile →
Citations per field
00.5×2×4×6×8×9.7×
Shriram G. Bhosle · 1×
Citations per year

Countries citing papers authored by Steve Hoffmann

Since Specialization
Citations

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

Fields of papers citing papers by Steve Hoffmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 104 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 primary transcriptome of the major human pathogen Helicobacter pylori
Hit paper breakdown →
2010967
4
The evolutionary history of 2,658 cancers
Hit paper breakdown →
2020705
5
The African coelacanth genome provides insights into tetrapod evolution
Hit paper breakdown →
2013552
6
Patterns of somatic structural variation in human cancer genomes
Hit paper breakdown →
2020550
7 2009422
8 2010335
9 2013328
10 2020317
11 2014221
12 2020184
13 2020159
14 2020152
15 2009139
16 2015117
17 2019113
18 2009107
19 2020104
20 201699

About Steve Hoffmann

Steve Hoffmann is a scholar working on Cancer Research, Molecular Biology, Pathology and Forensic Medicine, Aging and Oncology, having authored 104 papers that have together received 12.4k indexed citations. Recurring topics across this work include RNA modifications and cancer (26 papers), Cancer-related molecular mechanisms research (17 papers), Epigenetics and DNA Methylation (15 papers), Genomics and Phylogenetic Studies (14 papers), Cancer Genomics and Diagnostics (13 papers), RNA Research and Splicing (13 papers), Genetic factors in colorectal cancer (10 papers) and Lymphoma Diagnosis and Treatment (9 papers). The work is most often cited by research in Cancer Research (4.3k citations), Molecular Biology (7.0k citations), Oncology (1.9k citations), Pathology and Forensic Medicine (1.2k citations) and Genetics (1.8k citations). Steve Hoffmann has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Peter Florian Stadler, Jörg Hackermüller, Cynthia Mira Sharma, Jörg Vogel, Christian Otto, Sven Findeiß, David Langenberger, Philipp Khaitovich, Alexandra Sittka and Fabien Darfeuille. Their work appears in journals such as Nature Communications, Nucleic Acids Research, Nature, Leukemia and Nature Genetics.

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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