Nicholas Pachter
- Co-authors
- Ingrid WinshipAnthony J. GillPeter EarlsAdele ClarksonRoderick Clifton‐BlighStewart FlemingDiana E. BennBarbara Young
- Topics
- BRCA gene mutations in cancer (10 papers)Genomics and Rare Diseases (7 papers)Genetic factors in colorectal cancer (6 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Nicholas Pachter
29 papers receiving 567 citations
Peers
Comparison fields: 5 of 81
- Molecular Biology 233
- Genetics 210
- Pulmonary and Respiratory Medicine 123
- Cancer Research 121
- Surgery 86
Countries citing papers authored by Nicholas Pachter
This map shows the geographic impact of Nicholas Pachter'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 Nicholas Pachter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicholas Pachter more than expected).
Fields of papers citing papers by Nicholas Pachter
This network shows the impact of papers produced by Nicholas Pachter. 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 Nicholas Pachter. The network helps show where Nicholas Pachter may publish in the future.
Co-authorship network of co-authors of Nicholas Pachter
This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas Pachter. A scholar is included among the top collaborators of Nicholas Pachter based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nicholas Pachter. Nicholas Pachter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 1 | |
| 4 | 1 | |
| 5 | 8 | |
| 6 | 24 | |
| 7 | 5 | |
| 8 | 13 | |
| 9 | 12 | |
| 10 | 16 | |
| 11 | 45 | |
| 12 | 1 | |
| 13 | 37 | |
| 14 | 7 | |
| 15 | 9 | |
| 16 | 9 | |
| 17 | 18 | |
| 18 | 20 | |
| 19 | 0 | |
| 20 | 138 |
About Nicholas Pachter
Nicholas Pachter is a scholar working on Genetics, Reproductive Medicine and Pathology and Forensic Medicine, having authored 30 papers that have together received 578 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (7 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Cancer Research (121 citations), Genetics (210 citations) and Pulmonary and Respiratory Medicine (123 citations). Nicholas Pachter has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Ingrid Winship, Anthony J. Gill, Peter Earls, Adele Clarkson, Roderick Clifton‐Bligh, Stewart Fleming, Diana E. Benn, Barbara Young, Angela Chou and Bruce G. Robinson. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and International Journal of Cancer.
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.