Author

Holly LaDuca

Ambry Genetics (United States)ORCID 0000-0002-3745-9072Unclaimed ORCID profile · follow to get notified of new preprints

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 Jill S. DolinskyiD· 1 shared June Fujimoto· 1 shared Laura Panos Smith· 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