Myriad Genetics

654 papers and 40.2k indexed citations i.

About

In recent decades, authors affiliated with Myriad Genetics have published 654 papers, which have received a total of 40.2k indexed citations. Scholars at this organization have produced 255 papers in Genetics, 243 papers in Molecular Biology and 169 papers in Oncology on the topics of BRCA gene mutations in cancer (185 papers), Cancer Genomics and Diagnostics (89 papers) and DNA Repair Mechanisms (81 papers). Their work is cited by papers focused on Molecular Biology (18.5k citations), Oncology (11.9k citations) and Genetics (11.7k citations). Authors at Myriad Genetics collaborate with scholars in United States, United Kingdom and Canada and have published in prestigious journals including Science, Cell and New England Journal of Medicine. Some of Myriad Genetics's most productive authors include Sean V. Tavtigian, Richard Wenstrup, Alexander Kamb, Scott G. Morham, Jennifer Saam, Kelsey Moyes, Mark H. Skolnick, Krystal Brown, Steven Stone and Alexander Gutin.

In The Last Decade

Fields of papers published by authors at Myriad Genetics

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers affiliated with Myriad Genetics at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with Myriad Genetics at the time of their publication.

Countries citing scholars working at Myriad Genetics

Since Specialization
Citations

This map shows the geographic impact of research produced by authors working at Myriad Genetics. 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 papers produced at Myriad Genetics with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Myriad Genetics more than expected).

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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2025