Pardeep Kaurah

4.1k total citations
11 papers, 712 citations indexed

About

Pardeep Kaurah is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Pardeep Kaurah has authored 11 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pathology and Forensic Medicine, 8 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Pardeep Kaurah's work include Genetic factors in colorectal cancer (9 papers), Cancer-related gene regulation (5 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Pardeep Kaurah is often cited by papers focused on Genetic factors in colorectal cancer (9 papers), Cancer-related gene regulation (5 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Pardeep Kaurah collaborates with scholars based in Canada, United States and United Kingdom. Pardeep Kaurah's co-authors include David G. Huntsman, Janine Senz, Geoffrey Liu, Mark Redston, Steven Gallinger, Hilmi Özçelik, Steven A. Narod, Geeta Lal, Kasmintan A. Schrader and Fátima Carneiro and has published in prestigious journals such as Gastroenterology, Cancer and Cancer Research.

In The Last Decade

Pardeep Kaurah

11 papers receiving 688 citations

Peers

Pardeep Kaurah

PFM

MB

SURGE

ONCOL

GENET

Dietlinde Stienen Germany

Vanessa Blair New Zealand

Nicola Grehan United Kingdom

Yvonne Engwall Sweden

Ingrid P. Vogelaar Netherlands

Diane McKeone Australia

Monique Goossens Netherlands

Marina E. Croitoru Canada

Mirjam Tariverdian Germany

Maria Popoli United States

Dietlinde Stienen Germany

Pardeep Kaurah

514 ×1.4

PFM

198 ×0.7

MB

166 ×0.6

SURGE

230 ×1.0

ONCOL

198 ×1.0

GENET

Citations per year, relative to Pardeep Kaurah Pardeep Kaurah (= 1×) peers Dietlinde Stienen

Countries citing papers authored by Pardeep Kaurah

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Pardeep Kaurah

This figure shows the co-authorship network connecting the top 25 collaborators of Pardeep Kaurah. A scholar is included among the top collaborators of Pardeep Kaurah 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 Pardeep Kaurah. Pardeep Kaurah is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Aronson, Melyssa, Carol J. Swallow, Anand Govindarajan, et al.. (2020). Germline Variants and Phenotypic Spectrum in a Canadian Cohort of Individuals with Diffuse Gastric Cancer. Current Oncology. 27(2). 182–190. 2 indexed citations

2.

Hansford, Samantha, Hector Li-Chang, Pardeep Kaurah, et al.. (2014). Abstract 1282: Genetic basis of hereditary gastric cancer: Beyond the CDH1 locus. Cancer Research. 74(19_Supplement). 1282–1282. 1 indexed citations

3.

Worthley, Daniel L., Kerry Phillips, Kasmintan A. Schrader, et al.. (2011). Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome. Gut. 61(5). 774–779. 171 indexed citations

4.

Kaurah, Pardeep, Rebecca C. Fitzgerald, S Dwerryhouse, & David G. Huntsman. (2010). Pregnancy after prophylactic total gastrectomy. Familial Cancer. 9(3). 331–334. 20 indexed citations

5.

Weissman, Scott M., Cecelia Bellcross, Joy Larsen Haidle, et al.. (2010). Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review. Journal of Genetic Counseling. 20(1). 5–19. 43 indexed citations

6.

Oliveíra, Carla, Sónia Sousa, Hugo Pinheiro, et al.. (2009). Quantification of Epigenetic and Genetic 2nd Hits in CDH1 During Hereditary Diffuse Gastric Cancer Syndrome Progression. Gastroenterology. 136(7). 2137–2148. 125 indexed citations

7.

Lynch, Henry T., Pardeep Kaurah, Debrah Wirtzfeld, et al.. (2008). Hereditary diffuse gastric cancer. Cancer. 112(12). 2655–2663. 77 indexed citations

8.

Schrader, Kasmintan A., Serena Masciari, Niki Boyd, et al.. (2007). Hereditary diffuse gastric cancer: association with lobular breast cancer. Familial Cancer. 7(1). 73–82. 78 indexed citations

9.

Vaccaro, Carlos, María Ana Redal, David G. Huntsman, et al.. (2007). [Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene].. PubMed. 37(3). 158–63. 6 indexed citations

10.

Lal, Geeta, Geoffrey Liu, Pardeep Kaurah, et al.. (2000). Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations.. PubMed. 60(2). 409–16. 184 indexed citations

11.

Teebi, Ahmad S. & Pardeep Kaurah. (1996). Total anonychia congenita and microcephaly with normal intelligence: A new autosomal-recessive syndrome?. American Journal of Medical Genetics. 66(3). 257–260. 5 indexed citations

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.

Explore authors with similar magnitude of impact