Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Christine Moung"'
Autor:
A. Rose Brannon, Gowtham Jayakumaran, Monica Diosdado, Juber Patel, Anna Razumova, Yu Hu, Fanli Meng, Mohammad Haque, Justyna Sadowska, Brian J. Murphy, Tessara Baldi, Ian Johnson, Ryan Ptashkin, Maysun Hasan, Preethi Srinivasan, Anoop Balakrishnan Rema, Ivelise Rijo, Aaron Agarunov, Helen Won, Dilmi Perera, David N. Brown, Aliaksandra Samoila, Xiaohong Jing, Erika Gedvilaite, Julie L. Yang, Dennis P. Stephens, Jenna-Marie Dix, Nicole DeGroat, Khedoudja Nafa, Aijazuddin Syed, Alan Li, Emily S. Lebow, Anita S. Bowman, Donna C. Ferguson, Ying Liu, Douglas A. Mata, Rohit Sharma, Soo-Ryum Yang, Tejus Bale, Jamal K. Benhamida, Jason C. Chang, Snjezana Dogan, Meera R. Hameed, Jaclyn F. Hechtman, Christine Moung, Dara S. Ross, Efsevia Vakiani, Chad M. Vanderbilt, JinJuan Yao, Pedram Razavi, Lillian M. Smyth, Sarat Chandarlapaty, Gopa Iyer, Wassim Abida, James J. Harding, Benjamin Krantz, Eileen O’Reilly, Helena A. Yu, Bob T. Li, Charles M. Rudin, Luis Diaz, David B. Solit, Maria E. Arcila, Marc Ladanyi, Brian Loomis, Dana Tsui, Michael F. Berger, Ahmet Zehir, Ryma Benayed
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Liquid biopsies allow the non-invasive detection of somatic mutations from tumours. Here, the authors develop and test MSK-ACCESS, an NGS-based clinical assay for identifying low frequency mutations in 129 genes and describe how it benefits patients
Externí odkaz:
https://doaj.org/article/ca7c61a9651341a5819f1ee6a4c47bfa
Autor:
Kseniya Petrova-Drus, Mustafa Syed, Wayne Yu, Kasey Hutt, Alyssa M. Zlotnicki, Ying Huang, Monika Kamalska-Cyganik, Lidia Maciag, Meiyi Wang, Yuanyuan G. Ma, Caleb Ho, Christine Moung, Jinjuan Yao, Khedoudja Nafa, Jeeyeon Baik, Chad M. Vanderbilt, Jamal K. Benhamida, Ying Liu, Menglei Zhu, Benjamin Durham, Mark D. Ewalt, Paulo Salazar, Ivelise Rijo, Tessara Baldi, Anthony Mato, Lindsey E. Roeker, Mikhail Roshal, Ahmet Dogan, Maria E. Arcila
Publikováno v:
The Journal of Molecular Diagnostics. 25:352-366
Autor:
Ahmet Dogan, Kseniya Petrova-Drus, Maria E. Arcila, Anita S. Bowman, Ryan Ptashkin, Chad M. Vanderbilt, Christine Moung, Ryma Benayed, Andrés E. Quesada, Caleb Ho, Pallavi Galera, Jinjuan Yao, Jamal Benhamida, Jennifer Regalado
Publikováno v:
J Mol Diagn
Epstein-Barr virus (EBV) is associated with hematologic and solid tumors. In this study, we utilized a hybridization capture-based next generation sequencing (NGS) platform that targets 400 genes associated with hematological malignancies to detect a
Autor:
Marc Ladanyi, JinYuan Yao, Snjezana Dogan, Amir Momeni-Boroujeni, Maria E. Arcila, Natasha Rekhtman, William D. Travis, Jamal Benhamida, Khedoudja Nafa, Paulo Salazar, Jason C. Chang, Tao Zheng, Chad M. Vanderbilt, Christine Moung, Nana Mensah, Ivelise Rijo
Publikováno v:
The Journal of Molecular Diagnostics. 23:310-322
Mutations in the epidermal growth factor receptor (EGFR) are the most common targetable alterations in lung adenocarcinoma. To facilitate rapid testing, the Idylla EGFR assay was incorporated as a screening method before next-generation sequencing (N
Autor:
Malin Hultcrantz, Ola Landgren, Chad M. Vanderbilt, Christine Moung, Caleb Ho, Benjamin Diamond, Meiyi Wang, Ying Liu, Ahmet Dogan, Yuanyuan Ma, Kseniya Petrova-Drus, Jinjuan Yao, Jamal Benhamida, Lidia Maciag, Kasey Hutt, Andrés E. Quesada, Binbin Zheng-Lin, Wayne Yu, Jeffrey E. Miller, Menglei Zhu, Maria E. Arcila, Khedoudja Nafa, Mustafa H Syed, Even H Rustad, Mikhail Roshal, Ying Huang, Qi Gao
Publikováno v:
The Journal of Molecular Diagnostics : JMD
The 2016 International Myeloma Working Group consensus recommendations emphasize high-sensitivity methods for minimal residual disease (MRD) detection, treatment response assessment, and prognostication. Next-generation sequencing (NGS) of IGH gene r
Autor:
Yanming Zhang, Khedoudja Nafa, Ahmet Dogan, Priyadarshini Kumar, Umut Aypar, Wenbin Xiao, Caleb Ho, Wayne Yu, Mustafa H Syed, Christine Moung, Maria E. Arcila, Qi Gao, Jae H. Park, Mikhail Roshal, Anita Kumar, Manik Uppal, Jinjuan Yao
Publikováno v:
Leukemia & lymphoma
Approximately 15% of chronic lymphocytic leukemia/small lymphocytic lymphomas (CLL/SLL) transform into aggressive lymphomas, often diffuse large B cell lymphomas (DLBCL), known as Richter Syndrome ...
Autor:
Jason C. Chang, Alan Li, Ian Johnson, Charles M. Rudin, David N Brown, Snjezana Dogan, Preethi Srinivasan, Julie L. Yang, Aijazuddin Syed, Meera Hameed, JinJuan Yao, Aaron Agarunov, Emily S. Lebow, Chad M. Vanderbilt, Christine Moung, Rohit Sharma, David B. Solit, Efsevia Vakiani, Anna Razumova, Bob T. Li, Monica Diosdado, James J. Harding, Mohammad Haque, Wassim Abida, Marc Ladanyi, Michael F. Berger, Anita S. Bowman, Dilmi Perera, Dennis Stephens, Luis A. Diaz, Brian J. Murphy, Benjamin A. Krantz, Maria E. Arcila, Tejus Bale, Ryan Ptashkin, Gopa Iyer, Helena A. Yu, Eileen M. O'Reilly, Angela Rose Brannon, Aliaksandra Samoila, Khedoudja Nafa, Dana Tsui, Maysun Hasan, Erika Gedvilaite, Sarat Chandarlapaty, Tessara Baldi, Lillian M. Smyth, Brian Houck-Loomis, Juber Patel, Yu Hu, Ryma Benayed, Helen Won, Ivelise Rijo, Nicole DeGroat, Jaclyn F. Hechtman, Douglas A. Mata, Justyna Sadowska, Dara S. Ross, Jamal Benhamida, Gowtham Jayakumaran, Ying Liu, Fanli Meng, Donna C. Ferguson, Pedram Razavi, Anoop Balakrishnan Rema, Ahmet Zehir, Soo-Ryum Yang, Xiaohong Jing, Jenna-Marie Dix
Circulating cell-free DNA (cfDNA) from blood plasma of cancer patients can be used to interrogate somatic tumor alterations non-invasively or when adequate tissue is unavailable. We have developed and clinically implemented MSK-ACCESS (Analysis of Ci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::678ac8daac5ab721d94a6f9a62c5eab1
https://doi.org/10.1101/2020.06.27.175471
https://doi.org/10.1101/2020.06.27.175471
Autor:
Ahmet Dogan, Ivelise Rijo, Maria E. Arcila, Lidia Maciag, Christine Moung, Hannah Kim, Kseniya Petrova, Wayne Yu, Paulo Salazar, Ola Landgren, Khedoudja Nafa, Jae H. Park, Mikhail Roshal, Tessara Baldi, Caleb Ho, Ahmet Zehir, Mustafa H Syed, Jinjuan Yao
Immunoglobulin heavy chain (IGH) clonality testing by next-generation sequencing (NGS) offers unique advantages over current low-throughput methods in the assessment of B-cell lineage neoplasms. Clinical use remains limited because assays are not sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489f9d2a3e34c22dad66596adf935271
https://europepmc.org/articles/PMC6436112/
https://europepmc.org/articles/PMC6436112/
Autor:
Chad M. Vanderbilt, Christine Moung, Yuanyuan Ma, Jason C. Chang, Ola Landgren, Lidia Maciag, Jeffrey E. Miller, Jin Juan Yao, Caleb Ho, Kseniya Petrova-Drus, Kasey Hutt, Ying Huang, Jamal Benhamida, Khedoudja Nafa, Meiyi Wang, Maria E. Arcila, Mustafa H Syed, Qi Gao, Mikhail Roshal, Wayne Yu, Even H Rustad
Publikováno v:
Blood. 134:3380-3380
Introduction: Next-generation sequencing (NGS)-based IGH clonal rearrangement assays can characterize and subsequently track disease-associated clonal sequences for lymphoid and plasma cell neoplasms, even at very low levels. As IGH PCR primers are u
Autor:
Jo-ann Tonon, Tyler D. Leiva, Steven Marionneaux, Christine Moung, Peter Maslak, Virgil Chan, Scott T. Avecilla, Richard Meagher
Publikováno v:
Transfusion. 56:528-532
BACKGROUND Allogeneic hematopoietic stem cell donor selection is based primarily on human leukocyte antigen degree of match and it often occurs without regard to the red blood cell (RBC) compatibility between donor and recipient. When major ABO-misma