Author

Amal Yussuf

Ambry Genetics (United States)ORCID 0000-0002-7876-2713Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Jill S. DolinskyiD· 2 shared Shuwei LiiD· 2 shared Adam C. ElNaggariD· 1 shared Anna C. Raper· 1 shared Anton Mikhailovich SafonoviD· 1 shared Bradley Stephen WubbenhorstiD· 1 shared Carly Bess ScaliseiD· 1 shared Carolyn HortoniD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jill S. DolinskyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedApr 1, 2025

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

Anton Mikhailovich Safonov, Tomoki T. Nomakuchi, Elizabeth Chao…·Theodore G. Drivas

The paper identifies a higher prevalence of NF1 pathogenic variants using a genotype-first approach, finding many cases with somatic mosaicism and increased cancer risk.

23 citationstop 1%

humanwhole-exome sequencing

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Genetic & Genomic MedicineHuman MutationPeer-reviewedMay 22, 2020

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

Steven N. Hart, Eric C. Polley, Amal Yussuf…·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.

41 citations

humanwhole-exome sequencing

𝕏 PostBluesky