Author

Bart S. Ferket

Icahn School of Medicine at Mount SinaiORCID 0000-0003-2754-545XUnclaimed 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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Research Focus:benchmarking· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Assay:proteomics· 1

Frequent Co-Authors

Bruce D. GelbiD· 2 shared Aaron BaumiD· 1 shared Anne Michele SlavotinekiD· 1 shared Arye Rubinstein· 1 shared Avinash AbhyankariD· 1 shared Carol R. HorowitziD· 1 shared Charlotte Cunningham‐RundlesiD· 1 shared Christian StolteiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Bruce D. GelbORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 10, 2022

Cost and Clinical Utility of WES and WGS in pediatric patients with suspected genetic disease

Michael P. Douglas, Patricia A. Deverka, Bruce D. Gelb…·Kathryn A. Phillips

This study reviews the cost and clinical utility of whole exome sequencing (WES) and whole genome sequencing (WGS) in pediatric genetic disease diagnosis, finding limited evidence of WGS superiority over WES in changing clinical management.

2 citations

humanwhole-exome sequencing

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Genetic & Genomic MedicineTrialsPeer-reviewedJan 14, 2021

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Jacqueline A. Odgis, Katie M. Gallagher, Sabrina A. Suckiel…·Eimear E. Kenny

The NYCKidSeq project evaluates the clinical utility and communication of genomic testing in diverse children through a randomized controlled trial.

32 citationstop 5%

humanwhole-genome sequencing

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