Ryan J. Schmidt

Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing

Diana Mandelker, Ryan J. Schmidt, Arunkanth Ankala et al. · Genetics in Medicine · 2016 · 237 citations · Full text

Engineering, Genetics, Molecular Biology +16

Expanding the spectrum of dicer1-associated sarcomas

Mikako Warren, Matthew Hiemenz, Ryan J. Schmidt et al. · Modern Pathology · 2019 · 81 citations · Full text

Dicer1-associated Sarcomas, Pathology, Molecular Pathology +3

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

Ryan J. Schmidt, Marcie Steeves, Pınar Bayrak‐Toydemir et al. · Genetics in Medicine · 2023 · 55 citations · Full text

Health Policy, Disease Risk Assessment, Patient Safety +5

Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease risk

Ozlem Senol-Cosar, Ryan J. Schmidt, Emily Qian et al. · Genetics in Medicine · 2019 · 33 citations · Full text

Clinical Curation, Disease Risk, Disease Risk Assessment +11

Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework

Bryce A. Seifert, Jennifer McGlaughon, Sarah A. Jackson et al. · Genetics in Medicine · 2018 · 27 citations · Full text