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 · 248 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Expanding the spectrum of dicer1-associated sarcomas

Mikako Warren, Matthew Hiemenz, Ryan J. Schmidt et al. · Modern Pathology · 2019 · 83 citations · Full text

Medicine, Cancer Biology, Oncology +12

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 · 69 citations · Full text

Health Professions, Health Sciences, Epidemiology +8

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 · 34 citations · Full text

Life Sciences, Biostatistics, Genetics +16

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 · 28 citations · Full text

Life Sciences, Genetics, Oncology +17