Similar articles for PMID: 27301862

Year	Number of Results
1872	1
1885	1
2006	1
2007	1
2008	2
2009	1
2010	1
2012	3
2013	12
2014	18
2015	14
2016	23
2017	21
2018	16
2019	13
2020	19
2021	25
2022	11
2023	7
2024	0

1

Transcriptome sequencing reveals a profile that corresponds to genomic variants in Waldenström macroglobulinemia.

Hunter ZR, Xu L, Yang G, Tsakmaklis N, Vos JM, Liu X, Chen J, Manning RJ, Chen JG, Brodsky P, Patterson CJ, Gustine J, Dubeau T, Castillo JJ, Anderson KC, Munshi NM, Treon SP. Hunter ZR, et al. Blood. 2016 Aug 11;128(6):827-38. doi: 10.1182/blood-2016-03-708263. Epub 2016 Jun 14. Blood. 2016. PMID: 27301862 Free PMC article.

2

Genomics, Signaling, and Treatment of Waldenström Macroglobulinemia.

Hunter ZR, Yang G, Xu L, Liu X, Castillo JJ, Treon SP. Hunter ZR, et al. J Clin Oncol. 2017 Mar 20;35(9):994-1001. doi: 10.1200/JCO.2016.71.0814. Epub 2017 Feb 13. J Clin Oncol. 2017. PMID: 28294689 Review.

3

Genomic Landscape of Waldenström Macroglobulinemia and Its Impact on Treatment Strategies.

Treon SP, Xu L, Guerrera ML, Jimenez C, Hunter ZR, Liu X, Demos M, Gustine J, Chan G, Munshi M, Tsakmaklis N, Chen JG, Kofides A, Sklavenitis-Pistofidis R, Bustoros M, Keezer A, Meid K, Patterson CJ, Sacco A, Roccaro A, Branagan AR, Yang G, Ghobrial IM, Castillo JJ. Treon SP, et al. J Clin Oncol. 2020 Apr 10;38(11):1198-1208. doi: 10.1200/JCO.19.02314. Epub 2020 Feb 21. J Clin Oncol. 2020. PMID: 32083995 Free PMC article. Review.

4

The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis.

Hunter ZR, Xu L, Yang G, Zhou Y, Liu X, Cao Y, Manning RJ, Tripsas C, Patterson CJ, Sheehy P, Treon SP. Hunter ZR, et al. Blood. 2014 Mar 13;123(11):1637-46. doi: 10.1182/blood-2013-09-525808. Epub 2013 Dec 23. Blood. 2014. PMID: 24366360 Free article.

5

Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia.

Treon SP, Cao Y, Xu L, Yang G, Liu X, Hunter ZR. Treon SP, et al. Blood. 2014 May 1;123(18):2791-6. doi: 10.1182/blood-2014-01-550905. Epub 2014 Feb 19. Blood. 2014. PMID: 24553177 Free article.

6

Waldenström macroglobulinemia.

Treon SP, Hunter ZR, Castillo JJ, Merlini G. Treon SP, et al. Hematol Oncol Clin North Am. 2014 Oct;28(5):945-70. doi: 10.1016/j.hoc.2014.06.003. Epub 2014 Aug 5. Hematol Oncol Clin North Am. 2014. PMID: 25212891 Review.

7

Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance.

Varettoni M, Zibellini S, Defrancesco I, Ferretti VV, Rizzo E, Malcovati L, Gallì A, Porta MGD, Boveri E, Arcaini L, Candido C, Paulli M, Cazzola M. Varettoni M, et al. Haematologica. 2017 Dec;102(12):2077-2085. doi: 10.3324/haematol.2017.172718. Epub 2017 Oct 5. Haematologica. 2017. PMID: 28983055 Free PMC article.

8

Characteristics of Waldenström Macroglobulinemia in Korean Patients According to Mutational Status of MYD88 and CXCR4: Analysis Using Ultra-Deep Sequencing.

Shin DW, Kim SM, Kim JA, Park HS, Hwang SM, Im K, Kim S, Kim J, Kwon S, Yoon SS, Lee DS. Shin DW, et al. Clin Lymphoma Myeloma Leuk. 2019 Aug;19(8):e496-e505. doi: 10.1016/j.clml.2019.03.009. Epub 2019 Mar 15. Clin Lymphoma Myeloma Leuk. 2019. PMID: 31221512 Free article.

9

Detection of the MYD88^L265P and CXCR4^S338X mutations by cell-free DNA in Waldenström macroglobulinemia.

Wu YY, Jia MN, Cai H, Qiu Y, Zhou DB, Li J, Cao XX. Wu YY, et al. Ann Hematol. 2020 Aug;99(8):1763-1769. doi: 10.1007/s00277-020-04139-7. Epub 2020 Jun 23. Ann Hematol. 2020. PMID: 32577844 Clinical Trial.

10

Detection of MYD88 L265P and WHIM-like CXCR4 mutation in patients with IgM monoclonal gammopathy related disease.

Cao XX, Meng Q, Cai H, He TH, Zhang CL, Su W, Sun J, Li Y, Xu W, Zhou DB, Li J. Cao XX, et al. Ann Hematol. 2017 Jun;96(6):971-976. doi: 10.1007/s00277-017-2968-z. Epub 2017 Mar 9. Ann Hematol. 2017. PMID: 28280994

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