Mutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai–Dorfman disease von Garces, Sofia, Medeiros, L Jeffrey, Patel, Keyur P, Li, Shaoying, Pina-Oviedo, Sergio, Li, Jingyi, Garces, Juan C, Khoury, Joseph D, Yin, C Cameron

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Characteristics, clinical outcome, and prognostic significance of IDH mutations in AML von DiNardo, Courtney D., Ravandi, Farhad, Agresta, Sam, Konopleva, Marina, Takahashi, Koichi, Kadia, Tapan, Routbort, Mark, Patel, Keyur P., Mark Brandt, Pierce, Sherry, Garcia‐Manero, Guillermo, Cortes, Jorge, Kantarjian, Hagop

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Secondary mutations as mediators of resistance to targeted therapy in leukemia von Daver, Naval, Cortes, Jorge, Ravandi, Farhad, Patel, Keyur P., Burger, Jan A., Konopleva, Marina, Kantarjian, Hagop

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Clearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia von Morita, Kiyomi, Kantarjian, Hagop M, Wang, Feng, Yan, Yuanqing, Bueso-Ramos, Carlos, Sasaki, Koji, Issa, Ghayas C, Wang, Sa, Jorgensen, Jeffrey, Song, Xingzhi, Zhang, Jianhua, Tippen, Samantha, Thornton, Rebecca, Coyle, Marcus, Little, Latasha, Gumbs, Curtis, Pemmaraju, Naveen, Daver, Naval, DiNardo, Courtney D, Konopleva, Marina, Andreeff, Michael, Ravandi, Farhad, Cortes, Jorge E, Kadia, Tapan, Jabbour, Elias, Garcia-Manero, Guillermo, Patel, Keyur P, Futreal, P Andrew, Takahashi, Koichi

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Clinical utility of recently identified diagnostic, prognostic, and predictive molecular biomarkers in mature B-cell neoplasms von Onaindia, Arantza, Medeiros, L Jeffrey, Patel, Keyur P

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Prognostic and therapeutic implications of measurable residual disease in acute myeloid leukemia von Aitken, Marisa J. L, Ravandi, Farhad, Patel, Keyur P, Short, Nicholas J

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Sample-to-answer, extraction-free, real-time RT-LAMP test for SARS-CoV-2 in nasopharyngeal, nasal, and saliva samples: Implications and use for surveillance testing von Kundrod, Kathryn A, Natoli, Mary E, Chang, Megan M, Smith, Chelsey A, Paul, Sai, Ogoe, Dereq, Goh, Christopher, Santhanaraj, Akshaya, Price, Anthony, Eldin, Karen W, Patel, Keyur P, Baker, Ellen, Schmeler, Kathleen M, Richards-Kortum, Rebecca

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Concurrent fine needle aspirations and core needle biopsies: a comparative study of substrates for next-generation sequencing in solid organ malignancies von Roy-Chowdhuri, Sinchita, Chen, Hui, Singh, Rajesh R, Krishnamurthy, Savitri, Patel, Keyur P, Routbort, Mark J, Manekia, Jawad, Barkoh, Bedia A, Yao, Hui, Sabir, Sharjeel, Broaddus, Russell R, Medeiros, L Jeffrey, Staerkel, Gregg, Stewart, John, Luthra, Rajyalakshmi

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A decision support framework for genomically informed investigational cancer therapy von Meric-Bernstam, Funda, Johnson, Amber, Holla, Vijaykumar, Bailey, Ann Marie, Brusco, Lauren, Chen, Ken, Routbort, Mark, Patel, Keyur P, Zeng, Jia, Kopetz, Scott, Davies, Michael A, Piha-Paul, Sarina A, Hong, David S, Eterovic, Agda Karina, Tsimberidou, Apostolia M, Broaddus, Russell, Bernstam, Elmer V, Shaw, Kenna R, Mendelsohn, John, Mills, Gordon B

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Clinical Validation of a Next-Generation Sequencing Screen for Mutational Hotspots in 46 Cancer-Related Genes von Singh, Rajesh R, Patel, Keyur P, Routbort, Mark J, Reddy, Neelima G, Barkoh, Bedia A, Handal, Brian, Kanagal-Shamanna, Rashmi, Greaves, Wesley O, Medeiros, L. Jeffrey, Aldape, Kenneth D, Luthra, Rajyalakshmi

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Atypical chronic myeloid leukemia is clinically distinct from unclassifiable myelodysplastic/myeloproliferative neoplasms von Wang, Sa A., Hasserjian, Robert P., Fox, Patricia S., Rogers, Heesun J., Geyer, Julia T., Chabot-Richards, Devon, Weinzierl, Elizabeth, Hatem, Joseph, Jaso, Jesse, Kanagal-Shamanna, Rashmi, Stingo, Francesco C., Patel, Keyur P., Mehrotra, Meenakshi, Bueso-Ramos, Carlos, Young, Ken H., Dinardo, Courtney D., Verstovsek, Srdan, Tiu, Ramon V., Bagg, Adam, Hsi, Eric D., Arber, Daniel A., Foucar, Kathryn, Luthra, Raja, Orazi, Attilio

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Next-generation sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: promises and challenges for routine clinical diagnostics von Kanagal-Shamanna, Rashmi, Portier, Bryce P, Singh, Rajesh R, Routbort, Mark J, Aldape, Kenneth D, Handal, Brian A, Rahimi, Hamed, Reddy, Neelima G, Barkoh, Bedia A, Mishra, Bal M, Paladugu, Abhaya V, Manekia, Jawad H, Kalhor, Neda, Chowdhuri, Sinchita Roy, Staerkel, Gregg A, Medeiros, L Jeffrey, Luthra, Rajyalakshmi, Patel, Keyur P

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Prognostic and therapeutic impacts of mutant TP53 variant allelic frequency in newly diagnosed acute myeloid leukemia von Short, Nicholas J., Montalban-Bravo, Guillermo, Hwang, Hyunsoo, Ning, Jing, Franquiz, Miguel J., Kanagal-Shamanna, Rashmi, Patel, Keyur P., DiNardo, Courtney D., Ravandi, Farhad, Garcia-Manero, Guillermo, Takahashi, Koichi, Konopleva, Marina, Daver, Naval, Issa, Ghayas C., Andreeff, Michael, Kantarjian, Hagop, Kadia, Tapan M.

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Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancer von Mehrvarz Sarshekeh, Amir, Advani, Shailesh, Overman, Michael J, Manyam, Ganiraju, Kee, Bryan K, Fogelman, David R, Dasari, Arvind, Raghav, Kanwal, Vilar, Eduardo, Manuel, Shanequa, Shureiqi, Imad, Wolff, Robert A, Patel, Keyur P, Luthra, Raja, Shaw, Kenna, Eng, Cathy, Maru, Dipen M, Routbort, Mark J, Meric-Bernstam, Funda, Kopetz, Scott

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Persistent IDH1/2 mutations in remission can predict relapse in patients with acute myeloid leukemia von Ok, Chi Young, Loghavi, Sanam, Sui, Dawen, Wei, Peng, Kanagal-Shamanna, Rashmi, Yin, C Cameron, Zuo, Zhuang, Routbort, Mark J, Tang, Guilin, Tang, Zhenya, Jorgensen, Jeffrey L, Luthra, Rajyalakshmi, Ravandi, Farhad, Kantarjian, Hagop M, DiNardo, Courtney D, Medeiros, L Jeffrey, Wang, Sa A, Patel, Keyur P

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Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring von Luthra, Rajyalakshmi, Patel, Keyur P, Reddy, Neelima G, Haghshenas, Varan, Routbort, Mark J, Harmon, Michael A, Barkoh, Bedia A, Kanagal-Shamanna, Rashmi, Ravandi, Farhad, Cortes, Jorge E, Kantarjian, Hagop M, Medeiros, L Jeffrey, Singh, Rajesh R

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Identification of Factors Affecting the Success of Next-Generation Sequencing Testing in Solid Tumors von Goswami, Rashmi S., Luthra, Rajyalakshmi, Singh, Rajesh R., Patel, Keyur P., Routbort, Mark J., Aldape, Kenneth D., Yao, Hui, Dang, Hyvan D., Barkoh, Bedia A., Manekia, Jawad, Medeiros, L. Jeffrey, Roy-Chowdhuri, Sinchita, Stewart, John, Broaddus, Russell R., Chen, Hui

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The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy von Homan, Claire C, King-Smith, Sarah L, Lawrence, David M, Arts, Peer, Feng, Jinghua, Andrews, James, Armstrong, Mark, Ha, Thuong, Dobbins, Julia, Drazer, Michael W, Yu, Kai, Bödör, Csaba, Cantor, Alan, Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D, Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Fitzgibbon, Jude, Klco, Jeffery M, Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V, Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P, Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Liu, Paul, Godley, Lucy A, Schreiber, Andreas W, Hahn, Christopher N, Scott, Hamish S, Brown, Anna L

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Pure erythroid leukemia is characterized by biallelic TP53 inactivation and abnormal p53 expression patterns in de novo and secondary cases von Fang, Hong, Wang, Sa A, Khoury, Joseph D, El Hussein, Siba, Kim, Do Hwan, Tashakori, Mehrnoosh, Tang, Zhenya, Li, Shaoying, Hu, Zhihong, Jelloul, Fatima Zahra, Patel, Keyur P, McDonnell, Timothy J, Kadia, Tapan, Medeiros, L Jeffrey, Wang, Wei

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Characteristics and outcomes of patients with chronic myeloid leukemia and T315I mutation treated in the pre- and post-ponatinib era von Haddad, Fadi G, Sasaki, Koji, Bidikian, Aram, Issa, Ghayas C, Kadia, Tapan, Jain, Nitin, Alvarado, Yesid, Short, Nicholas J, Pemmaraju, Naveen, Loghavi, Sanam, Patel, Keyur P, Kanagal-Shamanna, Rashmi, Yilmaz, Musa, Masarova, Lucia, Jabbour, Elias, Kantarjian, Hagop

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