YAP-associated chromosomal instability and cholangiocarcinoma in mice

por Rizvi, Sumera, Fischbach, Samantha R., Bronk, Steven F., Hirsova, Petra, Krishnan, Anuradha, Dhanasekaran, Renumathy, Smadbeck, James B., Smoot, Rory L., Vasmatzis, George, Gores, Gregory J.
Publicado 2017

Elucidating a false-negative MYC break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with IGH/MYC...

por Peterson, Jess F., Pitel, Beth A., Smoley, Stephanie A., Vasmatzis, George, Smadbeck, James B., Greipp, Patricia T., Ketterling, Rhett P., Macon, William R., Baughn, Linda B.
Publicado 2019

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

Mate-pair sequencing identifies a cryptic BMPR2 mutation in hereditary pulmonary arterial hypertension

por Chalmers, Sarah J., Murphy, Stephen J., Thompson, Laura L., Hoppman, Nicole L., Smadbeck, James B., Balcom, Jessica R., Harris, Faye R., Frantz, Robert P., Vasmatzis, George, E. Wylam, Mark
Publicado 2021

Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TE...

por Rowsey, Ross A., Smoley, Stephanie A., Williamson, Cynthia M., Vasmatzis, George, Smadbeck, James B., Ning, Yi, Greipp, Patricia T., Hoppman, Nicole L., Baughn, Linda B., Ketterling, Rhett P., Peterson, Jess F.
Publicado 2019

Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma

por Dalland, Joanna C., Smadbeck, James B., Sharma, Neeraj, Meyer, Reid G., Pearce, Kathryn E., Greipp, Patricia T., Peterson, Jess F., Kumar, Shaji, Ketterling, Rhett P., King, Rebecca L., Baughn, Linda B.
Publicado 2021

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

The Prognostic Role of MYC Structural Variants Identified by NGS and FISH in Multiple Myeloma

por Sharma, Neeraj, Smadbeck, James B., Abdallah, Nadine, Zepeda-Mendoza, Cinthya, Binder, Moritz, Pearce, Kathryn E., Asmann, Yan W., Peterson, Jess F., Ketterling, Rhett P., Greipp, Patricia T., Bergsagel, P. Leif, Rajkumar, S. Vincent, Kumar, Shaji K., Baughn, Linda B.
Publicado 2021

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

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

Personalized tumor-specific DNA junctions to detect circulating tumor in patients with endometrial cancer

por Grassi, Tommaso, Harris, Faye R., Smadbeck, James B., Murphy, Stephen J., Block, Matthew S., Multinu, Francesco, Schaefer Klein, Janet L., Zhang, Piyan, Karagouga, Giannoula, Liu, Minetta C., Larish, Alyssa, Lemens, Maureen A., Sommerfield, Marla Kay S., Cappuccio, Serena, Cheville, John C., Vasmatzis, George, Mariani, Andrea
Publicado 2021

Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma

por Baughn, Linda B., Jessen, Erik, Sharma, Neeraj, Tang, Hongwei, Smadbeck, James B., Long, Mark D., Pearce, Kathryn, Smith, Matthew, Dasari, Surendra, Sachs, Zohar, Linden, Michael A., Cook, Joselle, Keith Stewart, A., Chesi, Marta, Mitra, Amit, Leif Bergsagel, P., Van Ness, Brian, Kumar, Shaji K.
Publicado 2023

Biliary tract cancer patient-derived xenografts: Surgeon impact on individualized medicine

por Leiting, Jennifer L., Murphy, Stephen J., Bergquist, John R., Hernandez, Matthew C., Ivanics, Tommy, Abdelrahman, Amro M., Yang, Lin, Lynch, Isaac, Smadbeck, James B., Cleary, Sean P., Nagorney, David M., Torbenson, Michael S., Graham, Rondell P., Roberts, Lewis R., Gores, Gregory J., Smoot, Rory L., Truty, Mark J.
Publicado 2020

Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis

por Pitel, Beth A., Sharma, Neeraj, Zepeda-Mendoza, Cinthya, Smadbeck, James B., Pearce, Kathryn E., Cook, Joselle M., Vasmatzis, George, Sachs, Zohar, Kanagal-Shamanna, Rashmi, Viswanatha, David, Xiao, Sheng, Jenkins, Robert B., Xu, Xinjie, Hoppman, Nicole L., Ketterling, Rhett P., Peterson, Jess F., Greipp, Patricia T., Baughn, Linda B.
Publicado 2021

Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group

por Koleilat, Alaa, Smadbeck, James B., Zepeda‐Mendoza, Cinthya J., Williamson, Cynthia M., Pitel, Beth A., Golden, Crystal L., Xu, Xinjie, Greipp, Patricia T., Ketterling, Rhett P., Hoppman, Nicole L., Peterson, Jess F., Harrison, Christine J., Akkari, Yassmine M. N., Tsuchiya, Karen D., Shago, Mary, Baughn, Linda B.
Publicado 2022

Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia

por Pitel, Beth A., Zepeda-Mendoza, Cinthya, Sachs, Zohar, Tang, Hongwei, Shivaram, Suganti, Sharma, Neeraj, Smadbeck, James B., Smoley, Stephanie A., Pearce, Kathryn E., Luoma, Ivy M., Cook, Joselle, Litzow, Mark R., Hoppman, Nicole L., Viswanatha, David, Xu, Xinjie, Ketterling, Rhett P., Greipp, Patricia T., Peterson, Jess F., Baughn, Linda B.
Publicado 2023

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