Author

Matthew E. Levy

Helix (United States)ORCID 0000-0002-2164-1726Unclaimed 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:GWAS / association mapping· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alexandre BolzeiD· 2 shared Ashley Arana Waring· 2 shared Basil KhuderiD· 2 shared C. Anwar A. ChahaliD· 2 shared Christopher N. Chapman· 2 shared David Kann· 2 shared Douglas A. Olson· 2 shared Douglas A. StolleriD· 2 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alexandre BolzeORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineCirculation Genomic and Precision MedicinePeer-reviewedNov 5, 2025

Population genomic screening leads to improved lipid management in patients with familial hypercholesterolemia

Matthew E. Levy, Kelly M. Schiabor Barrett, Megan N. Betts…·Catherine A. Hajek

Population genomic screening identified familial hypercholesterolemia patients, leading to improved lipid-lowering therapies and LDL-C reductions.

1 citation

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintNov 1, 2024

A novel method for predicting Lp(a) levels from routine outpatient genomic testing identifies those at risk of cardiovascular disease across a diverse cohort

Natalie Telis, Hang Dai, Ashley Arana Waring…·Kelly M. Schiabor Barrett

This paper develops a method to predict Lp(a) levels from genomic data, combining SNV risk scores and KIV-2 repeat counts, and shows it improves risk prediction for cardiovascular disease in diverse populations.

DOI 10.1101/2024.11.01.24316526

humanwhole-exome sequencing

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