Author

Jodell E. Linder

Vanderbilt University Medical CenterORCID 0000-0002-0081-4712Unclaimed 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 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:polygenic risk· 1

Frequent Co-Authors

Chunhua WengiD· 2 shared Cynthia A. ProwsiD· 2 shared Dan M. RodeniD· 2 shared Eimear E. KennyiD· 2 shared Gail Pairitz JarvikiD· 2 shared Georgia L. WiesneriD· 2 shared Hakon H. HakonarsoniD· 2 shared Jordan W. SmolleriD· 2 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chunhua WengORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 12, 2026

Systematic common and rare variant association testing in 392,030 whole genomes in All of Us

Wenhan Lu, Robert J. Carroll, Matthew Solomonson…·Konrad J. Karczewski

The paper performs large-scale GWAS and RVAS on 392,030 whole genomes from All of Us, identifying 49,863 associations and 193 novel pLoF gene-phenotype links through meta-analysis with UK Biobank.

4 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMay 22, 2025

Implementing Integrated Genomic Risk Assessments for Breast Cancer: Lessons Learned from the eMERGE Study

Cong Liu, Katherine D. Crew, Jennifer Morse…·Georgia L. Wiesner

The paper develops a pipeline for integrated breast cancer risk assessment using polygenic risk scores and other factors in the eMERGE study, showing high concordance between API and UI results.

3 citations

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintMay 25, 2023

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

Niall J. Lennon, Leah Claire Kottyan, C. Kachulis…·Eimear E. Kenny

The paper selects and validates ten polygenic risk scores for clinical use in diverse populations, focusing on chronic diseases and addressing disparities in predictive performance.

7 citations

humanwhole-genome sequencing

𝕏 PostBluesky