Author

Laura Panos Smith

Ambry Genetics (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amal YussufiD· 1 shared Chunling HuiD· 1 shared David E. GoldgariD· 1 shared Eric C. PolleyiD· 1 shared Fergus J. CouchiD· 1 shared Holly LaDucaiD· 1 shared Jill S. DolinskyiD· 1 shared June Fujimoto· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amal YussufORCID

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1 paper

Recent·Most cited

Mutation prevalence tables for hereditary cancer derived from multi-gene panel testing

Steven N. Hart, Eric C. Polley, Amal Yussuf, Siddhartha Yadav, David E. Goldgar, Chunling Hu, Holly LaDuca, Laura Panos Smith, June Fujimoto, Shuwei Li, Fergus J. Couch, Jill S. Dolinsky

The paper develops a tool to estimate mutation prevalence in hereditary cancer genes based on clinical and demographic factors using data from 150,000 multi-gene panel tests.

Human Mutation · May 22, 2020Peer-reviewedGenetic & Genomic Medicine