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Year	Number of Results
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JAK2 V617F mutation status of 232 patients diagnosed with chronic myeloproliferative neoplasms.

Payzin KB, Savasoglu K, Alacacioglu I, Ozdemirkiran F, Mutlu BB, Bener S, Calli AO, Kucukzeybek BB, Aksun S. Payzin KB, et al. Clin Lymphoma Myeloma Leuk. 2014 Dec;14(6):525-33. doi: 10.1016/j.clml.2014.02.013. Epub 2014 Mar 5. Clin Lymphoma Myeloma Leuk. 2014. PMID: 24811089

JAK2 46/1 haplotype is associated with JAK2 V617F--positive myeloproliferative neoplasms in Brazilian patients.

Macedo LC, Santos BC, Pagliarini-e-Silva S, Pagnano KB, Rodrigues C, Quintero FC, Ferreira ME, Baraldi EC, Ambrosio-Albuquerque EP, Sell AM, Visentainer JE. Macedo LC, et al. Int J Lab Hematol. 2015 Oct;37(5):654-60. doi: 10.1111/ijlh.12380. Epub 2015 May 11. Int J Lab Hematol. 2015. PMID: 25959311

Rapid identification of heterozygous or homozygous JAK2(V617F) mutations in myeloproliferative neoplasms using melting curve analysis.

Ho CL, Wu YY, Hung HM, Chang PY, Kao WY, Chen YC, Chao TY. Ho CL, et al. J Formos Med Assoc. 2012 Jan;111(1):34-40. doi: 10.1016/j.jfma.2012.01.003. Epub 2012 Feb 1. J Formos Med Assoc. 2012. PMID: 22333011 Free article.

[Significance of the JAK2V617F mutation in patients with chronic myeloproliferative neoplasia].

Iványi JL, Marton E, Plander M. Iványi JL, et al. Orv Hetil. 2011 Nov 6;152(45):1795-803. doi: 10.1556/OH.2011.29226. Orv Hetil. 2011. PMID: 22011365 Hungarian.

Clinical significance of V617F mutation of the JAK2 gene in patients with chronic myeloproliferative disorders.

Basquiera AL, Soria NW, Ryser R, Salguero M, Moiraghi B, Sackmann F, Sturich AG, Borello A, Berretta A, Bonafé M, Barral JM, Palazzo ED, García JJ. Basquiera AL, et al. Hematology. 2009 Dec;14(6):323-30. doi: 10.1179/102453309X12473408860226. Hematology. 2009. PMID: 19941738

The JAK2 V617F allele burden in essential thrombocythemia, polycythemia vera and primary myelofibrosis--impact on disease phenotype.

Larsen TS, Pallisgaard N, Møller MB, Hasselbalch HC. Larsen TS, et al. Eur J Haematol. 2007 Dec;79(6):508-15. doi: 10.1111/j.1600-0609.2007.00960.x. Epub 2007 Oct 23. Eur J Haematol. 2007. PMID: 17961178

Changing concepts of diagnostic criteria of myeloproliferative disorders and the molecular etiology and classification of myeloproliferative neoplasms: from Dameshek 1950 to Vainchenker 2005 and beyond.

Michiels JJ, Berneman Z, Schroyens W, De Raeve H. Michiels JJ, et al. Acta Haematol. 2015;133(1):36-51. doi: 10.1159/000358580. Epub 2014 Aug 7. Acta Haematol. 2015. PMID: 25116092 Review.

JAK2-v617F mutation is associated with clinical and laboratory features of myeloproliferative neoplasms.

Duletić AN, Dekanić A, Hadzisejdić I, Kusen I, Matusan-Ilijas K, Grohovac D, Grahovac B, Jonjić N. Duletić AN, et al. Coll Antropol. 2012 Sep;36(3):859-65. Coll Antropol. 2012. PMID: 23213945

The role of JAK2 V617F mutation, spontaneous erythropoiesis and megakaryocytopoiesis, hypersensitive platelets, activated leukocytes, and endothelial cells in the etiology of thrombotic manifestations in polycythemia vera and essential thrombocythemia.

Bellucci S, Michiels JJ. Bellucci S, et al. Semin Thromb Hemost. 2006 Jun;32(4 Pt 2):381-98. doi: 10.1055/s-2006-942759. Semin Thromb Hemost. 2006. PMID: 16810614 Review.

The 2001 World Health Organization and updated European clinical and pathological criteria for the diagnosis, classification, and staging of the Philadelphia chromosome-negative chronic myeloproliferative disorders.

Michiels JJ, De Raeve H, Berneman Z, Van Bockstaele D, Hebeda K, Lam K, Schroyens W. Michiels JJ, et al. Semin Thromb Hemost. 2006 Jun;32(4 Pt 2):307-40. doi: 10.1055/s-2006-942754. Semin Thromb Hemost. 2006. PMID: 16810609 Review.

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