Chromosomal catastrophe is a frequent event in clinically insignificant prostate cancer

por Kovtun, Irina V., Murphy, Stephen J., Johnson, Sarah H., Cheville, John C., Vasmatzis, George
Publicado 2015

Topoisomerase 2 Alpha Cooperates with Androgen Receptor to Contribute to Prostate Cancer Progression

por Schaefer-Klein, J. L., Murphy, Stephen J., Johnson, Sarah H., Vasmatzis, George, Kovtun, Irina V.
Publicado 2015

Prenatal characterization of a novel inverted SMAD2 duplication by mate pair sequencing in a fetus with dextrocardia

por Zepeda‐Mendoza, Cinthya J., Essendrup, Anna, Smoley, Stephanie A., Johnson, Sarah H., Hoppman, Nicole L, Vasmatzis, George, Jackson, Daniel L., Kearney, Hutton M., Baughn, Linda B.
Publicado 2020

Mate Pair Sequencing of Whole-Genome-Amplified DNA Following Laser Capture Microdissection of Prostate Cancer

por Murphy, Stephen J., Cheville, John C., Zarei, Shabnam, Johnson, Sarah H., Sikkink, Robert A., Kosari, Farhad, Feldman, Andrew L., Eckloff, Bruce W., Karnes, R. Jeffrey, Vasmatzis, George
Publicado 2012

Novel strategy for manufacturing autologous dendritic cell/allogeneic tumor lysate vaccines for glioblastoma

por Parney, Ian F, Gustafson, Michael P, Solseth, Mary, Bulur, Peggy, Peterson, Timothy E, Smadbeck, James B, Johnson, Sarah H, Murphy, Stephen J, Vasmatzis, George, Dietz, Allan B
Publicado 2020

Quantification of Somatic Chromosomal Rearrangements in Circulating Cell-Free DNA from Ovarian Cancers

por Harris, Faye R., Kovtun, Irina V., Smadbeck, James, Multinu, Francesco, Jatoi, Aminah, Kosari, Farhad, Kalli, Kimberly R., Murphy, Stephen J., Halling, Geoffrey C., Johnson, Sarah H., Liu, Minetta C., Mariani, Andrea, Vasmatzis, George
Publicado 2016

Shared and unique genomic structural variants of different histological components within testicular germ cell tumours identified with mate pair sequencing

por Bryce, Alan H., Egan, Jan B., Smadbeck, James B., Johnson, Sarah H., Murphy, Stephen J., Harris, Faye R., Halling, Geoffrey C., Terra, Simone B. S. P., Cheville, John, Pagliaro, Lance, Leibovich, Brad, Costello, Brian A., Vasmatzis, George
Publicado 2019

Theragnostic chromosomal rearrangements in treatment‐naive pancreatic ductal adenocarcinomas obtained via endoscopic ultrasound

por Murphy, Stephen J., Levy, Michael J., Smadbeck, James B., Karagouga, Giannoula, McCune, Alexa F., Harris, Faye R., Udell, Julia B., Johnson, Sarah H., Kerr, Sarah E., Cheville, John C., Kipp, Benjamin R., Vasmatzis, George, Gleeson, Ferga C.
Publicado 2021

Dynamics and survival associations of T cell receptor clusters in patients with pleural mesothelioma treated with immunotherapy

por Desai, Aakash P, Kosari, Farhad, Disselhorst, Maria, Yin, Jun, Agahi, Alireza, Peikert, Tobias, Udell, Julia, Johnson, Sarah H, Smadbeck, James, Murphy, Stephen, Karagouga, Giannoula, McCune, Alexa, Schaefer-Klein, Janet, Borad, Mitesh J, Cheville, John, Vasmatzis, George, Baas, Paul, Mansfield, Aaron
Publicado 2023

Integration of Comprehensive Genomic Analysis and Functional Screening of Affected Molecular Pathways to Inform Cancer Therapy

por Vasmatzis, George, Liu, Minetta C., Reganti, Sowjanya, Feathers, Ryan W., Smadbeck, James, Johnson, Sarah H., Schaefer Klein, Janet L., Harris, Faye R., Yang, Lin, Kosari, Farhad, Murphy, Stephen J., Borad, Mitesh J., Thompson, E. Aubrey, Cheville, John C., Anastasiadis, Panos Z.
Publicado 2019

Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2(+) breast cancer samples

por Vasmatzis, George, Wang, Xue, Smadbeck, James B., Murphy, Stephen J., Geiersbach, Katherine B., Johnson, Sarah H., Gaitatzes, Athanasios G., Asmann, Yan W., Kosari, Farhad, Borad, Mitesh J., Serie, Daniel J., McLaughlin, Sarah A., Kachergus, Jennifer M., Necela, Brian M., Aubrey Thompson, E.
Publicado 2018

Detection of a cryptic NUP214/ABL1 gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemia

por Peterson, Jess F., Pitel, Beth A., Smoley, Stephanie A., Smadbeck, James B., Johnson, Sarah H., Vasmatzis, George, Koon, Sarah J., Webley, Matthew R., McGrath, Mary, Bayerl, Michael G., Baughn, Linda B., Rowsey, Ross A., Ketterling, Rhett P., Greipp, Patricia T., Hoppman, Nicole L.
Publicado 2019

Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia

por Aypar, Umut, Smoley, Stephanie A., Pitel, Beth A., Pearce, Kathryn E., Zenka, Roman M., Vasmatzis, George, Johnson, Sarah H., Smadbeck, James B., Peterson, Jess F., Geiersbach, Katherine B., Van Dyke, Daniel L., Thorland, Erik C., Jenkins, Robert B., Ketterling, Rhett P., Greipp, Patricia T., Kearney, Hutton M., Hoppman, Nicole L., Baughn, Linda B.
Publicado 2018