Michelle Landon

2.0k total citations · 1 hit paper
4 papers, 1.4k citations indexed

About

Michelle Landon is a scholar working on Pathology and Forensic Medicine, Surgery and Oncology. According to data from OpenAlex, Michelle Landon has authored 4 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pathology and Forensic Medicine, 2 papers in Surgery and 2 papers in Oncology. Recurrent topics in Michelle Landon's work include Genetic factors in colorectal cancer (4 papers), Colorectal Cancer Screening and Detection (2 papers) and Cancer Genomics and Diagnostics (2 papers). Michelle Landon is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), Colorectal Cancer Screening and Detection (2 papers) and Cancer Genomics and Diagnostics (2 papers). Michelle Landon collaborates with scholars based in United States and Switzerland. Michelle Landon's co-authors include Richard Wenstrup, Kelsey Moyes, Jennifer Saam, Krystal Brown, Brent Evans, Christopher Arnell, Rajesh Kaldate, Lynn Anne Burbidge, Erin Mundt and Bradford Coffee and has published in prestigious journals such as Frontiers in Oncology, Clinical Genetics and Oncology.

In The Last Decade

Michelle Landon

4 papers receiving 1.4k citations

Hit Papers

Lynch Syndrome Patients with Limited Family History Ident... 2015 2026 2018 2022 2015 400 800 1.2k

Peers

Michelle Landon
Rachel Pearlman United States
Ilene Comeras United States
Ingrid Marino United States
Janet Lockman United States
Dan Fix United States
Christopher Arnell United States
Erin Salo‐Mullen United States
Kaisa Sotamaa United States
Rachel Pearlman United States
Michelle Landon
Citations per year, relative to Michelle Landon Michelle Landon (= 1×) peers Rachel Pearlman

Countries citing papers authored by Michelle Landon

Since Specialization
Citations

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

Fields of papers citing papers by Michelle Landon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michelle Landon

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

All Works

4 of 4 papers shown
1.
Pan, Shujuan, Hannah C. Cox, Erin Mundt, et al.. (2023). Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome. Frontiers in Oncology. 13. 1069467–1069467. 5 indexed citations
2.
Landon, Michelle, Jennifer Saam, Krystal Brown, et al.. (2015). Lynch Syndrome Patients with Limited Family History Identified in a Laboratory Setting: A Descriptive Study. Oncology. 89(4). 221–226. 1380 indexed citations breakdown →
3.
4.
Landon, Michelle, Christopher Arnell, Lynn Anne Burbidge, et al.. (2014). Analysis of current testing practices for biallelic MUTYH mutations in MUTYH‐associated polyposis. Clinical Genetics. 87(4). 368–372. 10 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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