Author

Roni Winkler

Rockefeller University

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

Biology Disciplines

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Immunology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

Alexander S. BrandisiD· 1 shared Alison W. AshbrookiD· 1 shared Ana PinharandaiD· 1 shared Ansgar F. StenzeliD· 1 shared Aurélie CobatiD· 1 shared Avery PeaceiD· 1 shared Brandon S. RazookyiD· 1 shared Carltin SchmidtiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperMolecular Biology

Alexander S. BrandisORCID

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2 papers

Recent·Most cited

A genome-wide arrayed CRISPR screen identifies PLSCR1 as an intrinsic barrier to SARS-CoV-2 entry that recent virus variants have evolved to resist

Jérémie Le Pen, Gabrielle Paniccia, Volker Kinast, Marcela Moncada‐Vélez, Alison W. Ashbrook, Michael Bauer, H.-Heinrich Hoffmann, Ana Pinharanda, Inna Ricardo-Lax, Ansgar F. Stenzel, Edwin A. Rosado-Olivieri, Kenneth H. Dinnon, William C. Doyle, Catherine A. Freije, Seon-Hui Hong, , Charles M. Rice

The paper identifies PLSCR1 as a host factor restricting SARS-CoV-2 entry, which recent variants have evolved to bypass, through a CRISPR screen and integration of genetic studies.

PLoS Biology · Sep 24, 2024Peer-reviewedImmunology

Deciphering the ‘m6A code’ via quantitative profiling of m6A at single-nucleotide resolution

Miguel Angel García-Campos, Sarit Edelheit, Ursula Toth, Modi Safra, Ran Shachar, Sergey V. Viukov, Roni Winkler, Ronit Nir, Lior Lasman, Alexander S. Brandis, Jacob H. Hanna, Walter Rossmanith, Schraga Schwartz

This paper introduces MASTER-seq, a method to quantitatively profile m6A sites at single-nucleotide resolution, revealing a predictable code that determines m6A stoichiometry and dynamics.

Cell · Jun 27, 2019Peer-reviewedMolecular Biology