Author

Peter J. Mohler

The Ohio State University Wexner Medical CenterORCID 0000-0002-7977-8717Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Auinash KalsotraiD· 1 shared Chaitali MisraiD· 1 shared Daniel R. JonesiD· 1 shared Darren J. ParkeriD· 1 shared Ellen R. LubbersiD· 1 shared Emad TajkhorshidiD· 1 shared Feikai Lin· 1 shared Huolin Tu· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Auinash KalsotraORCID

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2 papers

Recent·Most cited

Distinct Patterns of Emergence of SARS-CoV-2 Spike Variants including N501Y in Clinical Samples in Columbus Ohio

Huolin Tu, Matthew R. Avenarius, Laura Salter Kubatko, Matthew Hunt, Xiaokang Pan, Peng Ru, Jason P. Garee, Keelie Thomas, Peter J. Mohler, Preeti Pancholi, Daniel R. Jones

The paper reports the emergence of two novel SARS-CoV-2 variants in Columbus, Ohio, including one with N501Y mutation, highlighting their genetic diversity and potential clinical impact.

bioRxiv · Jan 12, 2021 · PreprintGenomics

Overexpression of a non-muscle RBFOX2 isoform triggers cardiac conduction defects in myotonic dystrophy

Chaitali Misra, Sushant Bangru, Feikai Lin, Kin Lok H. Lam, Sara N. Koenig, Ellen R. Lubbers, Jamila Hedhli, Nathaniel P. Murphy, Darren J. Parker, Lawrence W. Dobrucki, Thomas A. Cooper, Emad Tajkhorshid, Peter J. Mohler, Auinash Kalsotra

This study identifies overexpression of a non-muscle RBFOX2 isoform as a cause of cardiac conduction defects in myotonic dystrophy by inducing arrhythmia and altering ion channel splicing.

Developmental Cell · Feb 27, 2020Peer-reviewedGenetics