Sandro Morganella
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Oncology top 1%
- PARP inhibition in cancer therapy
Papers in
-
- Cancer Genomics and Diagnostics 25
- Genetics 16
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Co-authors
- Serena Nik-Zainal (6 shared papers)Michele Ceccarelli (8 shared papers)Pietro Zoppoli (4 shared papers)Xueqing Zou (4 shared papers)Jill E. Kucab (2 shared papers)Volker Manfred Arlt (2 shared papers)David H. Phillips (2 shared papers)Andrea Degasperi (2 shared papers)
- Journals
- Nature Communications (13 papers)Nature Genetics (7 papers)Nature (7 papers)Bioinformatics (3 papers)BMC Bioinformatics (3 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Sandro Morganella
48 papers receiving 13.2k citations
Sandro Morganella's Hit Papers
Peers
Comparison fields: 5 of 160
- Cancer Research 6.1k
- Oncology 3.1k
- Molecular Biology 7.3k
- Pathology and Forensic Medicine 1.5k
- Genetics 2.2k
Countries citing papers authored by Sandro Morganella
This map shows the geographic impact of Sandro Morganella'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 Sandro Morganella with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandro Morganella more than expected).
Fields of papers citing papers by Sandro Morganella
This network shows the impact of papers produced by Sandro Morganella. 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 Sandro Morganella. The network helps show where Sandro Morganella may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandro Morganella, 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 48 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 → | 2020 | 2339 |
| 2 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 3 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences Hit paper breakdown → | 2016 | 1649 |
| 4 | HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures Hit paper breakdown → | 2017 | 780 |
| 5 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 6 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 7 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 8 | A Compendium of Mutational Signatures of Environmental Agents Hit paper breakdown → | 2019 | 464 |
| 9 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 10 | 2020 | 317 | |
| 11 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 309 |
| 12 | 2020 | 301 | |
| 13 | 2020 | 293 | |
| 14 | 2016 | 202 | |
| 15 | 2020 | 184 | |
| 16 | 2020 | 180 | |
| 17 | 2010 | 178 | |
| 18 | 2015 | 160 | |
| 19 | 2020 | 160 | |
| 20 | 2020 | 159 |
About Sandro Morganella
Sandro Morganella is a scholar working on Cancer Research, Genetics, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 48 papers that have together received 13.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (25 papers), Genomics and Chromatin Dynamics (11 papers), Genetic factors in colorectal cancer (11 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), RNA modifications and cancer (5 papers), DNA Repair Mechanisms (5 papers) and Bioinformatics and Genomic Networks (5 papers). The work is most often cited by research in Cancer Research (6.1k citations), Oncology (3.1k citations), Molecular Biology (7.3k citations), Pathology and Forensic Medicine (1.5k citations) and Genetics (2.2k citations). Sandro Morganella has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Serena Nik-Zainal, Michele Ceccarelli, Pietro Zoppoli, Xueqing Zou, Jill E. Kucab, Volker Manfred Arlt, David H. Phillips, Andrea Degasperi, Arjun Scott Nanda and Stephen Philip Jackson. Their work appears in journals such as Nature Communications, Nature Genetics, Nature, Bioinformatics and BMC Bioinformatics.
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.