Ann‐Marie Patch
Impact in
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
- Oncology top 0.1%
- Pancreatic and Hepatic Oncology Research
- Cancer Immunotherapy and Biomarkers
Papers in
-
- Cancer Genomics and Diagnostics 35
- Oncology 25
- Pancreatic and Hepatic Oncology Research 10
- Cutaneous Melanoma Detection and Management 8
- Co-authors
- Sian Ellard (16 shared papers)Sarah Elizabeth Flanagan (14 shared papers)Andrew Tym Hattersley (13 shared papers)Emma L. Edghill (7 shared papers)Khalid Hussain (5 shared papers)Julie Støy (2 shared papers)Louis H. Philipson (2 shared papers)Donald F. Steiner (2 shared papers)
- Journals
- Nature Communications (15 papers)Nature (13 papers)Nature Genetics (6 papers)Cancers (5 papers)Genome Medicine (4 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Ann‐Marie Patch
103 papers receiving 27.9k citations
Ann‐Marie Patch's Hit Papers
Peers
Comparison fields: 5 of 173
- Cancer Research 8.3k
- Oncology 9.1k
- Genetics 4.8k
- Molecular Biology 12.0k
- Pathology and Forensic Medicine 1.9k
Countries citing papers authored by Ann‐Marie Patch
This map shows the geographic impact of Ann‐Marie Patch'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 Ann‐Marie Patch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ann‐Marie Patch more than expected).
Fields of papers citing papers by Ann‐Marie Patch
This network shows the impact of papers produced by Ann‐Marie Patch. 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 Ann‐Marie Patch. The network helps show where Ann‐Marie Patch may publish in the future.
Co-authors
The 25 scholars most cited alongside Ann‐Marie Patch, 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 103 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity Hit paper breakdown → | 2007 | 3653 |
| 2 | Genomic analyses identify molecular subtypes of pancreatic cancer Hit paper breakdown → | 2016 | 2794 |
| 3 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 4 | Whole genomes redefine the mutational landscape of pancreatic cancer Hit paper breakdown → | 2015 | 2115 |
| 5 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 6 | Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes Hit paper breakdown → | 2012 | 1704 |
| 7 | Whole–genome characterization of chemoresistant ovarian cancer Hit paper breakdown → | 2015 | 1233 |
| 8 | Whole-genome landscapes of major melanoma subtypes Hit paper breakdown → | 2017 | 1099 |
| 9 | Whole-genome landscape of pancreatic neuroendocrine tumours Hit paper breakdown → | 2017 | 774 |
| 10 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 11 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 12 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 13 | 2007 | 469 | |
| 14 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 15 | 2017 | 331 | |
| 16 | 2007 | 320 | |
| 17 | 2010 | 318 | |
| 18 | 2020 | 317 | |
| 19 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 309 |
| 20 | 2020 | 301 |
About Ann‐Marie Patch
Ann‐Marie Patch is a scholar working on Cancer Research, Oncology, Pathology and Forensic Medicine, Molecular Biology and Genetics, having authored 103 papers that have together received 28.4k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (35 papers), Pancreatic function and diabetes (15 papers), Genetic factors in colorectal cancer (14 papers), Pancreatic and Hepatic Oncology Research (10 papers), Epigenetics and DNA Methylation (9 papers), Cutaneous Melanoma Detection and Management (8 papers), RNA modifications and cancer (8 papers) and Diabetes and associated disorders (6 papers). The work is most often cited by research in Cancer Research (8.3k citations), Oncology (9.1k citations), Genetics (4.8k citations), Molecular Biology (12.0k citations) and Pathology and Forensic Medicine (1.9k citations). Ann‐Marie Patch has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Sian Ellard, Sarah Elizabeth Flanagan, Andrew Tym Hattersley, Emma L. Edghill, Khalid Hussain, Julie Støy, Louis H. Philipson, Donald F. Steiner, Graeme I. Bell and Julian P. Hamilton-Shield. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Cancers and Genome Medicine.
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.