Author

Megan T. Lynch

University of Maryland, BaltimoreORCID 0000-0003-4805-9610Unclaimed 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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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Brady J. GaynoriD· 2 shared Braxton D. MitchelliD· 2 shared Charles C. HongiD· 2 shared Aloke Virmani FinniD· 1 shared Anne CornelisseniD· 1 shared Anuj Kumar GuptaiD· 1 shared Atsushi SakamotoiD· 1 shared Bakr B. Ali· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Brady J. GaynorORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenesPeer-reviewedDec 24, 2022

Exome Array Analysis of 9,721 ischemic stroke cases from the SiGN Consortium

Huichun Xu, Kevin Nguyen, Brady J. Gaynor…·Braxton D. Mitchell

The paper analyzes exome array data from 9,721 ischemic stroke cases to identify coding variants associated with stroke, finding 15 significant variants, including 13 novel associations.

4 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineJAMA CardiologyPeer-reviewedJun 2, 2021

Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland

Liang Guo, Sho Torii, Raquel Fernandez…·Aloke Virmani Finn

This study examines the association between pathogenic or likely pathogenic genetic variants in cardiomyopathy and arrhythmia genes and unexplained sudden cardiac death in adults with no gross pathological findings.

41 citations

humanwhole-exome sequencing

𝕏 PostBluesky