Author

Jessica Wheeler

Stanford Medicine

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

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Genomics· 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

Colleen M. CraigiD· 1 shared Denis N. SalinsiD· 1 shared Elizabeth Colbert· 1 shared Hannes Luc RöstiD· 1 shared Jessilyn DunniD· 1 shared Jonathan Adam BernsteiniD· 1 shared Lars Michael SteinmetziD· 1 shared M. Reza SailaniiD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Colleen M. CraigORCID

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1 paper

Recent·Most cited

High Frequency Actionable Pathogenic Exome Mutations in an Average-Risk Cohort

Shannon M. Rego, Orit Dagan‐Rosenfeld, Wenyu Zhou, M. Reza Sailani, Patricia Limcaoco, Elizabeth Colbert, Monika Avina, Jessica Wheeler, Colleen M. Craig, Denis N. Salins, Hannes Luc Röst, Jessilyn Dunn, Tracey McLaughlin, Lars Michael Steinmetz, Jonathan Adam Bernstein, Michael P. Snyder

The paper assesses exome sequencing in a healthy cohort to determine the frequency of medically actionable and non-actionable findings, finding 17% had actionable variants, including some outside standard guidelines.

bioRxiv · Jun 18, 2017 · PreprintGenomics