Out of the F-box: Reawakening the Pancreas

par Seifert, Bryce A., Xiong, Yue
Publié 2014

Ronin influences the DNA damage response in pluripotent stem cells

par Seifert, Bryce A., Dejosez, Marion, Zwaka, Thomas P.
Publié dans Stem Cell Res (2017)

An Unusual Association: Total Anomalous Pulmonary Venous Return and Aortic Arch Obstruction in Patients with Cat Eye Syndrome

par Williams, Jason L., McDonald, Marie T., Seifert, Bryce A., Deak, Kristen L., Rehder, Catherine W., Campbell, Michael J.
Publié dans J Pediatr Genet (2021)

Clinical Validity Assessment of Genes Frequently Tested on Hereditary Breast and Ovarian Cancer Susceptibility Sequencing Panels

par Lee, Kristy, Seifert, Bryce A., Shimelis, Hermela, Ghosh, Rajarshi, Crowley, Stephanie B., Carter, Natalie J., Doonanco, Kurston, Foreman, A. Katherine, Ritter, Deborah I., Jimenez, Sharisse, Trapp, Mackenzie, Offit, Kenneth, Plon, Sharon E., Couch, Fergus J.
Publié dans Genet Med (2018)

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

par Seifert, Bryce A., McGlaughon, Jennifer L., Jackson, Sarah A., Ritter, Deborah I, Roberts, Maegan E., Schmidt, Ryan J., Thompson, Bryony A., Jimenez, Sharisse, Trapp, Mackenzie, Lee, Kristy, Plon, Sharon E., Offit, Kenneth, Stadler, Zsofia K., Zhang, Liying, Greenblatt, Marc S., Ferber, Matthew J.
Publié dans Genet Med (2018)

Germline Analysis from Tumor-Germline Sequencing Dyads to identify clinically actionable secondary findings

par Seifert, Bryce A., O'Daniel, Julianne M., Amin, Krunal, Marchuk, Daniel S., Patel, Nirali M., Parker, Joel S., Hoyle, Alan P., Mose, Lisle E., Marron, Andrew, Hayward, Michele C., Bizon, Christopher, Wilhelmsen, Kirk C., Evans, James P., Earp, H. Shelton, Sharpless, Norman E., Hayes, D. Neil, Berg, Jonathan S.
Publié dans Clin Cancer Res (2016)

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

par Ingles, Jodie, Goldstein, Jennifer, Thaxton, Courtney, Caleshu, Colleen, Corty, Edward W., Crowley, Stephanie B., Dougherty, Kristen, Harrison, Steven M., McGlaughon, Jennifer, Milko, Laura V., Morales, Ana, Seifert, Bryce A., Strande, Natasha, Thomson, Kate, Peter van Tintelen, J., Wallace, Kathleen, Walsh, Roddy, Wells, Quinn, Whiffin, Nicola, Witkowski, Leora, Semsarian, Christopher, Ware, James S., Hershberger, Ray E., Funke, Birgit
Publié dans Circ Genom Precis Med (2019)

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

par Strande, Natasha T., Riggs, Erin Rooney, Buchanan, Adam H., Ceyhan-Birsoy, Ozge, DiStefano, Marina, Dwight, Selina S., Goldstein, Jenny, Ghosh, Rajarshi, Seifert, Bryce A., Sneddon, Tam P., Wright, Matt W., Milko, Laura V., Cherry, J. Michael, Giovanni, Monica A., Murray, Michael F., O’Daniel, Julianne M., Ramos, Erin M., Santani, Avni B., Scott, Alan F., Plon, Sharon E., Rehm, Heidi L., Martin, Christa L., Berg, Jonathan S.
Publié dans Am J Hum Genet (2017)

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

par Roman, Tamara S., Crowley, Stephanie B., Roche, Myra I., Foreman, Ann Katherine M., O’Daniel, Julianne M., Seifert, Bryce A., Lee, Kristy, Brandt, Alicia, Gustafson, Chelsea, DeCristo, Daniela M., Strande, Natasha T., Ramkissoon, Lori, Milko, Laura V., Owen, Phillips, Roy, Sayanty, Xiong, Mai, Paquin, Ryan S., Butterfield, Rita M., Lewis, Megan A., Souris, Katherine J., Bailey, Donald B., Rini, Christine, Booker, Jessica K., Powell, Bradford C., Weck, Karen E., Powell, Cynthia M., Berg, Jonathan S.
Publié dans Am J Hum Genet (2020)