Yvonne Engwall

705 total citations
9 papers, 508 citations indexed

About

Yvonne Engwall is a scholar working on Pathology and Forensic Medicine, Cancer Research and Genetics. According to data from OpenAlex, Yvonne Engwall has authored 9 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 4 papers in Cancer Research and 3 papers in Genetics. Recurrent topics in Yvonne Engwall's work include Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (3 papers) and Colorectal Cancer Treatments and Studies (2 papers). Yvonne Engwall is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (3 papers) and Colorectal Cancer Treatments and Studies (2 papers). Yvonne Engwall collaborates with scholars based in Sweden, United Kingdom and Denmark. Yvonne Engwall's co-authors include Margareta Nordling, Jan Björk, Tommy Martinsson, Jan Wahlström, Anna Rohlin, Annika Bergman, Leif Wiklund, Per Karlsson, Lennart Iselius and Rolf Hultcrantz and has published in prestigious journals such as Gastroenterology, Oncogene and Clinical Gastroenterology and Hepatology.

In The Last Decade

Yvonne Engwall

9 papers receiving 500 citations

Peers

Yvonne Engwall
Dietlinde Stienen Germany
I. Tomlinson United Kingdom
Longina M. Gibas United States
Pardeep Kaurah Canada
Henry T. Lynch United States
Ian Chandler United Kingdom
M.G. Tibiletti Italy
Hamid Mehenni Switzerland
Rumen Kostadinov United States
Pardeep Kaurah Canada
Dietlinde Stienen Germany
Yvonne Engwall
Citations per year, relative to Yvonne Engwall Yvonne Engwall (= 1×) peers Dietlinde Stienen

Countries citing papers authored by Yvonne Engwall

Since Specialization
Citations

This map shows the geographic impact of Yvonne Engwall'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 Yvonne Engwall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yvonne Engwall more than expected).

Fields of papers citing papers by Yvonne Engwall

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yvonne Engwall. 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 Yvonne Engwall. The network helps show where Yvonne Engwall may publish in the future.

Co-authorship network of co-authors of Yvonne Engwall

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

All Works

9 of 9 papers shown
1.
Rohlin, Anna, Yvonne Engwall, Katarina E. Göransson, et al.. (2011). Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis. Oncogene. 30(50). 4977–4989. 44 indexed citations
2.
Rohlin, Anna, et al.. (2009). Parallel sequencing used in detection of mosaic mutations: Comparison with four diagnostic DNA screening techniques. Human Mutation. 30(6). 1012–1020. 138 indexed citations
3.
Kanter-Smoler, Gunilla, Anna Rohlin, Yvonne Engwall, et al.. (2008). Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families. BMC Medicine. 6(1). 10–10. 36 indexed citations
4.
Kanter-Smoler, Gunilla, Jan Björk, Yvonne Engwall, et al.. (2006). Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization. Clinical Gastroenterology and Hepatology. 4(4). 499–506. 22 indexed citations
5.
Bergman, Annika, Yvonne Engwall, Eva Lagberg Arkblad, et al.. (2005). A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques. Familial Cancer. 4(2). 89–96. 25 indexed citations
6.
Björk, Jan, Lennart Iselius, Annika Bergman, et al.. (2001). Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: Cumulative risks and APC gene mutations. Gastroenterology. 121(5). 1127–1135. 174 indexed citations
7.
Nordling, Margareta, Yvonne Engwall, Justin T. Wahlstrom, et al.. (1998). Novel mutations in the APC gene and clinical features in Swedish patients with polyposis coli.. PubMed. 17(6D). 4275–80. 5 indexed citations
8.
Nordling, Margareta, Per Karlsson, Jan Wahlström, et al.. (1998). A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.. PubMed. 58(7). 1372–5. 62 indexed citations
9.
Wiklund, L, Margareta Nordling, J. Wahlström, Yvonne Engwall, & Tommy Martinsson. (1997). Novel germline mutations in Swedish von Hippel-Lindau disease patients. International Journal of Oncology. 11(3). 509–12. 2 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.

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