Andy G. Lynch
Impact in
- Reproductive Medicine top 2%
- Ovarian cancer diagnosis and treatment
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Gene expression and cancer classification 9
- Epigenetics and DNA Methylation 7
- Genomics and Chromatin Dynamics 4
- Single-cell and spatial transcriptomics 3
- Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Simon Tavaré (17 shared papers)Mark Dunning (13 shared papers)Charles Massie (5 shared papers)Nuno L. Barbosa‐Morais (4 shared papers)Ian G. Mills (3 shared papers)Matthew E. Ritchie (5 shared papers)Carlos Caldas (3 shared papers)James D. Brenton (2 shared papers)
- Journals
- BMC Bioinformatics (4 papers)PLoS ONE (3 papers)BMC Genomics (3 papers)Proceedings of the National Academy of Sciences (2 papers)Bioinformatics (2 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Andy G. Lynch
61 papers receiving 3.0k citations
Andy G. Lynch's Hit Papers
Peers
Comparison fields: 5 of 141
- Reproductive Medicine 292
- Cancer Research 515
- Molecular Biology 1.3k
- Pulmonary and Respiratory Medicine 472
- Genetics 408
Countries citing papers authored by Andy G. Lynch
This map shows the geographic impact of Andy G. Lynch'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 Andy G. Lynch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andy G. Lynch more than expected).
Fields of papers citing papers by Andy G. Lynch
This network shows the impact of papers produced by Andy G. Lynch. 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 Andy G. Lynch. The network helps show where Andy G. Lynch may publish in the future.
Co-authors
The 25 scholars most cited alongside Andy G. Lynch, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Driver mutations in TP53 are ubiquitous in high grade serous carcinoma of the ovary Hit paper breakdown → | 2010 | 523 |
| 2 | 2012 | 225 | |
| 3 | 2007 | 203 | |
| 4 | 2010 | 189 | |
| 5 | 2009 | 170 | |
| 6 | 2004 | 144 | |
| 7 | 2016 | 113 | |
| 8 | 2006 | 109 | |
| 9 | 2007 | 101 | |
| 10 | 2009 | 92 | |
| 11 | 2008 | 89 | |
| 12 | 2013 | 85 | |
| 13 | 2021 | 80 | |
| 14 | 2009 | 76 | |
| 15 | 2015 | 60 | |
| 16 | 2017 | 59 | |
| 17 | 2008 | 56 | |
| 18 | 2006 | 48 | |
| 19 | 2008 | 46 | |
| 20 | 2006 | 46 |
About Andy G. Lynch
Andy G. Lynch is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Oncology and Cancer Research, having authored 62 papers that have together received 3.0k indexed citations. Recurring topics across this work include Gene expression and cancer classification (9 papers), Epigenetics and DNA Methylation (7 papers), Prostate Cancer Treatment and Research (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (4 papers), Genomics and Chromatin Dynamics (4 papers), Single-cell and spatial transcriptomics (3 papers) and Prostate Cancer Diagnosis and Treatment (3 papers). The work is most often cited by research in Reproductive Medicine (292 citations), Cancer Research (515 citations), Molecular Biology (1.3k citations), Pulmonary and Respiratory Medicine (472 citations) and Genetics (408 citations). Andy G. Lynch has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Simon Tavaré, Mark Dunning, Charles Massie, Nuno L. Barbosa‐Morais, Ian G. Mills, Matthew E. Ritchie, Carlos Caldas, James D. Brenton, Colin J.R. Stewart and Mohamed Riad. Their work appears in journals such as BMC Bioinformatics, PLoS ONE, BMC Genomics, Proceedings of the National Academy of Sciences and 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.