Author

Zachary T. Yoneda

Vanderbilt University Medical CenterORCID 0000-0002-2055-732XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant effect prediction· 2 Assay:bulk RNA-seq· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Dan M. RodeniD· 3 shared Moore Benjamin ShoemakeriD· 3 shared Alanna C. MorrisoniD· 2 shared Barry I. FreedmaniD· 2 shared Bertha HidalgoiD· 2 shared Braxton D. MitchelliD· 2 shared Daniel E. WeeksiD· 2 shared Dawood DarbariD· 2 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Dan M. RodenORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineScience AdvancesPeer-reviewedApr 6, 2022

Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

Tetsushi Nakao, Alexander G. Bick, Margaret A. Taub…·Brian Custer

The paper uses bidirectional Mendelian randomization to show LTL lengthening increases CHIP risk, while CHIP accelerates LTL shortening, with modest mediation between CHIP and CAD via LTL.

94 citationstop 1%

humanbulk RNA-seq

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Genetic & Genomic MedicineCirculationPeer-reviewedDec 21, 2021

Arrhythmia variant associations and reclassifications in the eMERGE-III sequencing study

Andrew Michael Glazer, Giovanni Davogustto, Christian M. Shaffer…·Dan M. Roden

The paper identifies pathogenic variants in arrhythmia genes in eMERGE-III participants and reclassifies variants of uncertain significance using functional studies.

44 citationstop 2%

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintNov 13, 2020

Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program

Jennifer Wessel, Timothy D. Majarian, Heather M. Highland…·José C. Florez

The paper identifies rare non-coding variants from whole genome sequencing in the TOPMed program, showing they contribute significantly to type 2 diabetes heritability.

12 citations

humanwhole-genome sequencing

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