Author

Hanna Rennert

NewYork–Presbyterian HospitalORCID 0000-0002-1759-2562Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:variant calling· 3 Approach:experimental assay· 2 Organism:human· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Andrea SboneriD· 2 shared Jenny XiangiD· 2 shared Olivier ElementoiD· 2 shared Adrian Y. TaniD· 1 shared Alain BorczukiD· 1 shared Alessandro RomaneliD· 1 shared Alon ShaiberiD· 1 shared Amos J. ShemeshiD· 1 shared

Activity by Year

2016-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenomics

Andrea SbonerORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Molecular BiologyNature CommunicationsPeer-reviewedMar 12, 2021

Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions

Daniel Butler, Christopher Mozsary, Cem Meydan…·Christopher E. Mason

This study uses rapid diagnostics and metatranscriptomics to analyze SARS-CoV-2 infection, revealing viral evolution, host responses, and drug interactions in NYC samples.

201 citationstop 1%

humanbulk RNA-seq

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GenomicsbioRxivPreprintMar 1, 2017

Discovery and reporting of clinically-relevant germline variants in advanced cancer patients assessed using whole-exome sequencing

Tuo Zhang, Alessandro Romanel, Kenneth Eng…·Olivier Elemento

This study reports that 17% of advanced cancer patients have clinically relevant germline variants, with higher rates of cancer-associated variants compared to control cohorts.

2 citations

humanwhole-exome sequencing

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GenomicsJournal of the American Medical Informatics AssociationPeer-reviewedOct 27, 2016

The Precision Medicine Knowledge Base: an online application for collaborative editing, maintenance and sharing of structured clinical-grade cancer mutations interpretations

Linda Huang, Helen Fernandes, Hamid Zia…·Olivier Elemento

The paper introduces PMKB, a platform for collaborative editing and sharing of clinical-grade cancer mutation interpretations, and reports its usage in genomic testing.

DOI 10.1093/jamia/ocw148

whole-exome sequencingexperimental assay

𝕏 PostBluesky