Not logged in Clinician-Reported Management Recommendations in Response to Universal Germline Genetic Testing in Patients With Prostate Cancer Shore, Neal; Pieczonka, Christopher; Heron, Sean; Gazi, Mukaram; Cahn, David; Belkoff, Laurence H.; Berger, Aaron; Mazzarella, Brian; Veys, Joseph; Idom, Charles; Morris, David; Jayram, Gautam; Engelman, Alexander; Dato, Paul; Bevan-Thomas, Richard; Wise, David R.; Hardwick, Mary Kay; Rojahn, Susan; Layman, Paige; Heald, Brandie; Ellsworth, Rachel E.; Hatchell, Kathryn E.; Nussbaum, Robert L.; Nielsen, Sarah M.; Esplin, Edward D. Share Save
Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy Morales, Ana; Moretz, Chad; Ren, Sheng; Smith, Elizabeth; Callis, Thomas E.; Hall, Taryn; Hatchell, Kathryn E.; Nussbaum, Robert L.; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Esplin, Edward D.; Murillo, Jaime Share Save
Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing Chen, Elaine; Facio, Flavia M.; Aradhya, Kerry W.; Rojahn, Susan; Hatchell, Kathryn E.; Aguilar, Sienna; Ouyang, Karen; Saitta, Sulagna; Hanson-Kwan, Andrea K.; Capurro, Nicole Nakousi; Takamine, Eriko; Jamuar, Saumya Shekhar; McKnight, Dianalee; Johnson, Britt; Aradhya, Swaroop Share Save
Efficacy of National Comprehensive Cancer Network Guidelines in Identifying Pathogenic Germline Variants Among Unselected Patients with Prostate Cancer: The PROCLAIM Trial Shore, Neal; Gazi, Mukaram; Pieczonka, Christopher; Heron, Sean; Modh, Rishi; Cahn, David; Belkoff, Laurence H.; Berger, Aaron; Mazzarella, Brian; Veys, Joseph; Idom, Charles; Morris, David; Jayram, Gautam; Engelman, Alexander; Bukkapatnam, Raviender; Dato, Paul; Bevan-Thomas, Richard; Cornell, Robert; Wise, David R.; Hardwick, Mary Kay; Hernandez, Ryan D.; Rojahn, Susan; Layman, Paige; Hatchell, Kathryn E.; Heald, Brandie; Nussbaum, Robert L.; Nielsen, Sarah M.; Esplin, Edward D. Share Save
Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals Truty, Rebecca; Rojahn, Susan; Ouyang, Karen; Kautzer, Curtis; Kennemer, Michael; Pineda-Alvarez, Daniel; Johnson, Britt; Stafford, Amanda; Basel-Salmon, Lina; Saitta, Sulagna; Slavotinek, Anne; Chandrasekharappa, Settara C.; Suarez, Carlos Jose; Burnett, Leslie; Nussbaum, Robert L.; Aradhya, Swaroop Share Save
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing Dellefave-Castillo, Lisa M.; Cirino, Allison L.; Callis, Thomas E.; Esplin, Edward D.; Garcia, John; Hatchell, Kathryn E.; Johnson, Britt; Morales, Ana; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Nussbaum, Robert L.; McNally, Elizabeth M. Share Save
Unmanaged Pharmacogenomic and Drug Interaction Risk Associations with Hospital Length of Stay among Medicare Advantage Members with COVID-19: A Retrospective Cohort Study Ashcraft, Kristine; Moretz, Chad; Schenning, Chantelle; Rojahn, Susan; Vines Tanudtanud, Kae; Magoncia, Gwyn Omar; Reyes, Justine; Marquez, Bernardo; Guo, Yinglong; Erdemir, Elif Tokar; Hall, Taryn O. Share Save
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Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis Sturm, Amy C.; Truty, Rebecca; Callis, Thomas E.; Aguilar, Sienna; Esplin, Edward D.; Garcia, Sarah; Haverfield, Eden, V; Morales, Ana; Nussbaum, Robert L.; Rojahn, Susan; Vatta, Matteo; Rader, Daniel J. Share Save
Spectrum of splicing variants in disease genes and the ability of RNA analysis to reduce uncertainty in clinical interpretation Truty, Rebecca; Ouyang, Karen; Rojahn, Susan; Garcia, Sarah; Colavin, Alexandre; Hamlington, Barbara; Freivogel, Mary; Nussbaum, Robert L.; Nykamp, Keith; Aradhya, Swaroop Share Save
Common Variants in KCNE1, KCNH2, and SCN5A May Impact Cardiac Arrhythmia Risk Vatta, Matteo; Truty, Rebecca; Garcia, John; Callis, Thomas E.; Hatchell, Kathryn; Rojahn, Susan; Morales, Ana; Aradhya, Swaroop; Nussbaum, Robert Share Save
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