Pardeep Kaurah
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 15
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- Wnt/β-catenin signaling in development and cancer 13
- Cancer-related gene regulation 4
- RNA modifications and cancer 2
- Co-authors
- David George Huntsman (13 shared papers)Janine Senz (6 shared papers)Niki Boyd (3 shared papers)Fátima Carneiro (4 shared papers)Geoffrey Liu (1 shared paper)Steven A. Narod (1 shared paper)Geeta Lal (1 shared paper)Mark S. Redston (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)Familial Cancer (3 papers)The American Journal of Human Genetics (2 papers)Gut (2 papers)European Journal of Human Genetics (1 paper)
- Partner nations
- CanadaUnited StatesPortugal
In The Last Decade
Pardeep Kaurah
36 papers receiving 3.8k citations
Pardeep Kaurah's Hit Papers
Peers
Comparison fields: 5 of 83
- Pathology and Forensic Medicine 1.5k
- Cancer Research 556
- Genetics 987
- Oncology 715
- Gastroenterology 131
Countries citing papers authored by Pardeep Kaurah
This map shows the geographic impact of Pardeep Kaurah'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 Pardeep Kaurah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pardeep Kaurah more than expected).
Fields of papers citing papers by Pardeep Kaurah
This network shows the impact of papers produced by Pardeep Kaurah. 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 Pardeep Kaurah. The network helps show where Pardeep Kaurah may publish in the future.
Co-authors
The 25 scholars most cited alongside Pardeep Kaurah, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Hereditary Diffuse Gastric Cancer Syndrome Hit paper breakdown → | 2015 | 536 |
| 2 | Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers Hit paper breakdown → | 2015 | 424 |
| 3 | 2007 | 360 | |
| 4 | Hereditary diffuse gastric cancer: updated clinical practice guidelines Hit paper breakdown → | 2020 | 314 |
| 5 | 2008 | 239 | |
| 6 | 2011 | 212 | |
| 7 | Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations. | 2000 | 202 |
| 8 | 2016 | 193 | |
| 9 | 2009 | 171 | |
| 10 | 2007 | 150 | |
| 11 | 2009 | 140 | |
| 12 | 2005 | 139 | |
| 13 | 2018 | 129 | |
| 14 | 2007 | 99 | |
| 15 | 2008 | 92 | |
| 16 | 2009 | 91 | |
| 17 | 2010 | 70 | |
| 18 | 2014 | 56 | |
| 19 | 2010 | 49 | |
| 20 | 1994 | 32 |
About Pardeep Kaurah
Pardeep Kaurah is a scholar working on Pathology and Forensic Medicine, Molecular Biology, Genetics, Cancer Research and Surgery, having authored 37 papers that have together received 3.9k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (15 papers), Wnt/β-catenin signaling in development and cancer (13 papers), BRCA gene mutations in cancer (6 papers), Helicobacter pylori-related gastroenterology studies (5 papers), Cancer-related gene regulation (4 papers), Cancer Genomics and Diagnostics (3 papers), Digestive system and related health (3 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.5k citations), Cancer Research (556 citations), Genetics (987 citations), Oncology (715 citations) and Gastroenterology (131 citations). Pardeep Kaurah has collaborated with scholars based in Canada, United States and Portugal. Frequent co-authors include David George Huntsman, Janine Senz, Niki Boyd, Fátima Carneiro, Geoffrey Liu, Steven A. Narod, Geeta Lal, Mark S. Redston, Steven Gallinger and Hilmi Özçelik. Their work appears in journals such as Journal of Medical Genetics, Familial Cancer, The American Journal of Human Genetics, Gut and European Journal of Human 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.