Myriad Genetics

44.5k citations
717 papers ·

Impact in

Papers in

    • BRCA gene mutations in cancer 177
    • Genomic variations and chromosomal abnormalities 33
    • Genomics and Rare Diseases 27
    • Cancer Genomics and Diagnostics 62

Myriad Genetics

624 papers receiving 38.6k citations

Peers

Myriad Genetics
Comparison fields: 5 of 204
  • Cancer Research 7.2k
  • Genetics 11.5k
  • Oncology 10.4k
  • Pathology and Forensic Medicine 5.3k
  • Molecular Biology 17.6k
Replace Cancer Research Foundation with:
Cancer Research Foundation United States
BioScience Laboratories (United States) United States
ARUP Institute for Clinical and Experimental Pathology United States
PDL BioPharma (United States) United States
Genomics Institute of the Novartis Research Foundation United States
La Jolla Institute For Molecular Medicine United States
UNM Comprehensive Cancer Center United States
California Institute for Biomedical Research United States
Ligand Pharmaceuticals (United States) United States
Io Therapeutics (United States) United States
Myriad Genetics relative to Cancer Research Foundation United States Cancer Research Foundation's profile →
Citations per field
00.5×3.0×
Cancer Research Foundation · 1×
Citations per year

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).

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.

About Myriad Genetics

In recent decades, authors affiliated with Myriad Genetics have published 717 papers, which have received a total of 44.5k indexed citations . Scholars at this organization have produced 240 papers in Genetics, 103 papers in Cancer Research, 156 papers in Oncology, 65 papers in Pathology and Forensic Medicine and 30 papers in Reproductive Medicine on the topics of BRCA gene mutations in cancer (177 papers), Cancer Genomics and Diagnostics (62 papers), DNA Repair Mechanisms (59 papers), PARP inhibition in cancer therapy (57 papers), Genetic factors in colorectal cancer (53 papers), Genomic variations and chromosomal abnormalities (33 papers), CRISPR and Genetic Engineering (31 papers) and Genomics and Rare Diseases (27 papers). Their work is cited by papers focused on Cancer Research (7.2k citations), Genetics (11.5k citations), Oncology (10.4k citations), Pathology and Forensic Medicine (5.3k citations) and Molecular Biology (17.6k citations). Authors at Myriad Genetics collaborate with scholars in United States, Germany and United Kingdom and have published in prestigious journals including Journal of Clinical Oncology, Cancer Research, Cancer, JCO Precision Oncology and Gynecologic Oncology. Some of Myriad Genetics's most productive authors include Sean V. Tavtigian, Alexander Kamb, Thomas Frank, Richard Wenstrup, Scott G. Morham, Jennifer Saam, Mark H. Skolnick, Kelsey Moyes, Krystal Brown and Steven Stone.

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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