Shawn Yost

2.0k total citations
15 papers, 1.0k citations indexed

About

Shawn Yost is a scholar working on Cancer Research, Molecular Biology and Genetics. According to data from OpenAlex, Shawn Yost has authored 15 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cancer Research, 9 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Shawn Yost's work include Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (4 papers) and BRCA gene mutations in cancer (3 papers). Shawn Yost is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (4 papers) and BRCA gene mutations in cancer (3 papers). Shawn Yost collaborates with scholars based in United States, United Kingdom and Germany. Shawn Yost's co-authors include Kelly A. Frazer, Olivier Harismendy, Kristen Jepsen, Sheila Seal, Hisanobu Ogata, Debanjan Dhar, Kazuhiko Koike, Hayato Nakagawa, Ryosuke Tateishi and Dimitrios Iliopoulos and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Communications.

In The Last Decade

Shawn Yost

15 papers receiving 1.0k citations

Peers

Shawn Yost
Michela Visani Italy
Anna Sankila Finland
Reiko Ogawa Japan
Ritsuto Fujiwaki Japan
Keisuke Matsusaki Japan
Matthew A. Nehs United States
Stephanie Petrillo Canada
Caroline Chapusot France
Takaomi Suzuma Japan
Claire Palles United Kingdom
Michela Visani Italy
Shawn Yost
Citations per year, relative to Shawn Yost Shawn Yost (= 1×) peers Michela Visani

Countries citing papers authored by Shawn Yost

Since Specialization
Citations

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

Fields of papers citing papers by Shawn Yost

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shawn Yost

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

All Works

15 of 15 papers shown
1.
Oghabian, Ali, Maureen V. Akinyi, Sandra Hanks, et al.. (2021). Chromosomal instability by mutations in the novel minor spliceosome component CENATAC. The EMBO Journal. 40(14). e106536–e106536. 27 indexed citations
2.
Kemp, Zoe, Shawn Yost, Sheila Seal, et al.. (2019). Evaluation of Cancer-Based Criteria for Use in MainstreamBRCA1andBRCA2Genetic Testing in Patients With Breast Cancer. JAMA Network Open. 2(5). e194428–e194428. 78 indexed citations
3.
Yost, Shawn, Elise Ruark, Ludmil B. Alexandrov, & Nazneen Rahman. (2019). Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers. JNCI Cancer Spectrum. 3(2). pkz028–pkz028. 4 indexed citations
4.
Tatton‐Brown, Katrina, Chey Loveday, Shawn Yost, et al.. (2017). Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. The American Journal of Human Genetics. 100(5). 725–736. 128 indexed citations
5.
Alakus, Hakan, Shawn Yost, Brian Woo, et al.. (2015). BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma. Journal of Translational Medicine. 13(1). 122–122. 51 indexed citations
6.
Bao, Lei, Karen Messer, Richard B. Schwab, et al.. (2015). Mutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors. PLoS ONE. 10(11). e0142487–e0142487. 14 indexed citations
7.
Harismendy, Olivier, Hakan Alakus, Shawn Yost, et al.. (2015). Abstract 4803: BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma. Cancer Research. 75(15_Supplement). 4803–4803. 1 indexed citations
8.
Litchfield, Kevin, Brenda Summersgill, Shawn Yost, et al.. (2015). Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours. Nature Communications. 6(1). 5973–5973. 132 indexed citations
9.
Alakus, Hakan, Michele Babicky, Pradipta Ghosh, et al.. (2014). Genome-wide mutational landscape of mucinous carcinomatosis peritonei of appendiceal origin. Genome Medicine. 6(5). 43–43. 96 indexed citations
10.
Yost, Shawn, Sandra Pastorino, Sophie Rozenzhak, et al.. (2013). High-Resolution Mutational Profiling Suggests the Genetic Validity of Glioblastoma Patient-Derived Pre-Clinical Models. PLoS ONE. 8(2). e56185–e56185. 21 indexed citations
11.
He, Guobin, Debanjan Dhar, Hayato Nakagawa, et al.. (2013). Identification of Liver Cancer Progenitors Whose Malignant Progression Depends on Autocrine IL-6 Signaling. Cell. 155(2). 384–396. 358 indexed citations
12.
Harismendy, Olivier, Richard B. Schwab, Hakan Alakus, et al.. (2013). Evaluation of ultra-deep targeted sequencing for personalized breast cancer care. Breast Cancer Research. 15(6). R115–R115. 15 indexed citations
13.
Yost, Shawn, Hakan Alakus, Hiroko Matsui, et al.. (2013). Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing. Bioinformatics. 29(15). 1908–1909. 20 indexed citations
14.
Yost, Shawn, Erin N. Smith, Richard B. Schwab, et al.. (2012). Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens. Nucleic Acids Research. 40(14). e107–e107. 66 indexed citations
15.
Yost, Shawn, Hakan Alakus, Hiroko Matsui, et al.. (2012). MutaScope: a high-sensitivity variant caller dedicated to high-throughput PCR amplicons sequencing. BMC Proceedings. 6(S6). 1 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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