Megan Hawley

Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History

Aniruddh P. Patel, Minxian Wang, Akl C. Fahed et al. · JAMA Network Open · 2020 · 105 citations · Full text

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

Francesco Mazzarotto, Megan Hawley, Matteo Beltrami et al. · Genetics in Medicine · 2021 · 78 citations · Full text

The genetic architecture of Plakophilin 2 cardiomyopathy

Annika M. Dries, Anna Kirillova, Chloe M. Reuter et al. · Genetics in Medicine · 2021 · 34 citations · Full text

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

Hana Zouk, Wanfeng Yu, Andrea M. Oza et al. · Genetics in Medicine · 2021 · 21 citations · Full text

Translational Bioinformatics, Automated Return, Next-generation Sequencing +14

An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Megan Hawley, Naif A. M. Almontashiri, Leslie G. Biesecker et al. · Human Mutation · 2020 · 19 citations · Full text

Heart Failure, Gene Panel, Genetics +20