Patrick Tarpey
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Oral Surgery top 5%
- Oral and Maxillofacial Pathology
Papers in
-
- Genomics and Phylogenetic Studies 4
- Genetics 19
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
- Co-authors
- Sam Behjati (6 shared papers)Jon W. Teague (7 shared papers)F. Lucy Raymond (3 shared papers)Michael R. Stratton (15 shared papers)Peter J. Campbell (7 shared papers)Adam P. Butler (5 shared papers)Serena Nik‐Zainal (4 shared papers)Keiran Raine (5 shared papers)
- Journals
- Current Protocols in Bioinformatics (4 papers)Journal of Clinical Pathology (3 papers)Genes Chromosomes and Cancer (3 papers)Biochemical Society Transactions (3 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Patrick Tarpey
53 papers receiving 1.9k citations
Patrick Tarpey's Hit Papers
Peers
Comparison fields: 5 of 115
- Cancer Research 336
- Oral Surgery 143
- Genetics 496
- Molecular Biology 1.0k
- Rheumatology 217
Countries citing papers authored by Patrick Tarpey
This map shows the geographic impact of Patrick Tarpey'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 Patrick Tarpey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Tarpey more than expected).
Fields of papers citing papers by Patrick Tarpey
This network shows the impact of papers produced by Patrick Tarpey. 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 Patrick Tarpey. The network helps show where Patrick Tarpey may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Tarpey, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | What is next generation sequencing? Hit paper breakdown → | 2013 | 480 |
| 2 | 2015 | 124 | |
| 3 | 2008 | 110 | |
| 4 | 2012 | 92 | |
| 5 | 2016 | 82 | |
| 6 | 2012 | 76 | |
| 7 | 2008 | 72 | |
| 8 | 2009 | 59 | |
| 9 | 2016 | 57 | |
| 10 | 2010 | 55 | |
| 11 | 2006 | 51 | |
| 12 | 2009 | 50 | |
| 13 | 2014 | 50 | |
| 14 | 1980 | 44 | |
| 15 | 2015 | 44 | |
| 16 | 2011 | 42 | |
| 17 | 2007 | 42 | |
| 18 | 2015 | 40 | |
| 19 | 2018 | 38 | |
| 20 | 2012 | 36 |
About Patrick Tarpey
Patrick Tarpey is a scholar working on Molecular Biology, Genetics, Cancer Research, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine, having authored 55 papers that have together received 2.0k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (12 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genetic factors in colorectal cancer (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Sarcoma Diagnosis and Treatment (5 papers), Genomics and Phylogenetic Studies (4 papers) and Renal Diseases and Glomerulopathies (3 papers). The work is most often cited by research in Cancer Research (336 citations), Oral Surgery (143 citations), Genetics (496 citations), Molecular Biology (1.0k citations) and Rheumatology (217 citations). Patrick Tarpey has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Sam Behjati, Jon W. Teague, F. Lucy Raymond, Michael R. Stratton, Peter J. Campbell, Adam P. Butler, Serena Nik‐Zainal, Keiran Raine, Jozef Gécz and Charles E. Schwartz. Their work appears in journals such as Current Protocols in Bioinformatics, Journal of Clinical Pathology, Genes Chromosomes and Cancer, Biochemical Society Transactions and Human Molecular 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.