Melissa Pronold

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients

Holly LaDuca, Eric C. Polley, Amal Yussuf et al. · Genetics in Medicine · 2019 · 212 citations · Full text

Detection of structural variation using target captured next-generation sequencing data for genetic diagnostic testing

Wenbo Mu, Bing Li, Sitao Wu et al. · Genetics in Medicine · 2018 · 44 citations · Full text

Advanced bone age in a girl with Wiedemann–Steiner syndrome and an exonic deletion in <i>KMT2A</i> (<i>MLL</i>)

Bryce A. Mendelsohn, Melissa Pronold, Roger Long et al. · American Journal of Medical Genetics Part A · 2014 · 40 citations

Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic Process

Monalyn Umali Salvador, Melissa R.F. Truelson, Carla L. Mason et al. · Journal of Clinical Oncology · 2019 · 32 citations

Incidental detection of acquired variants in germline genetic and genomic testing: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

Elizabeth Chao, Caroline Astbury, Joshua L. Deignan et al. · Genetics in Medicine · 2021 · 22 citations · Full text

Genetic Analysis, Genetic Testing, Incidental Detection +11