Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis

Paola Guglielmelli; Chiara Maccari; Benedetta Sordi; Manjola Balliu; Alessandro Atanasio; Carmela Mannarelli; Giulio Capecchi; Ilaria Sestini; Giacomo Coltro; Giuseppe Gaetano Loscocco; Giada Rotunno; Eva Angori; Filippo C. Borri; Ayalew Tefferi; Alessandro M. Vannucchi

doi:10.1038/s41408-023-00786-x

Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis

Paola Guglielmelli, Chiara Maccari, Benedetta Sordi, Manjola Balliu, Alessandro Atanasio, Carmela Mannarelli, Giulio Capecchi, Ilaria Sestini, Giacomo Coltro, Giuseppe Gaetano Loscocco, Giada Rotunno, Eva Angori, Filippo C. Borri, Ayalew Tefferi, Alessandro M. Vannucchi

Hematology

Research output: Contribution to journal › Letter › peer-review

Original language	English (US)
Article number	21
Journal	Blood cancer journal
Volume	13
Issue number	1
DOIs	https://doi.org/10.1038/s41408-023-00786-x
State	Published - Dec 2023

ASJC Scopus subject areas

Hematology
Oncology

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Guglielmelli, P., Maccari, C., Sordi, B., Balliu, M., Atanasio, A., Mannarelli, C., Capecchi, G., Sestini, I., Coltro, G., Loscocco, G. G., Rotunno, G., Angori, E., Borri, F. C., Tefferi, A., & Vannucchi, A. M. (2023). Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis. Blood cancer journal, 13(1), Article 21. https://doi.org/10.1038/s41408-023-00786-x

Guglielmelli, P, Maccari, C, Sordi, B, Balliu, M, Atanasio, A, Mannarelli, C, Capecchi, G, Sestini, I, Coltro, G, Loscocco, GG, Rotunno, G, Angori, E, Borri, FC, Tefferi, A & Vannucchi, AM 2023, 'Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis', Blood cancer journal, vol. 13, no. 1, 21. https://doi.org/10.1038/s41408-023-00786-x

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title = "Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis",

author = "Paola Guglielmelli and Chiara Maccari and Benedetta Sordi and Manjola Balliu and Alessandro Atanasio and Carmela Mannarelli and Giulio Capecchi and Ilaria Sestini and Giacomo Coltro and Loscocco, {Giuseppe Gaetano} and Giada Rotunno and Eva Angori and Borri, {Filippo C.} and Ayalew Tefferi and Vannucchi, {Alessandro M.}",

note = "Funding Information: This work was supported by AIRC 5 × 1000 call “Metastatic disease: the key unmet need in oncology” to MYNERVA project, #21267 (MYeloid NEoplasms Research Venture AIRC). A detailed description of the MYNERVA project is available at http://www.progettoagimm.it . Also supported by the “EDITOR”, Accelerator Award project funded through a partnership between Cancer Research UK, Fondazione AIRC and Fundaci{\'o}n Cient{\'i}fica de la Asociacion Espa{\~n}ola Contra el C{\'a}ncer. PG and CM were also supported by Ministero della Salute, Rome, Italy [Finalizzata 2018, NET-2018–12365935, Personalized medicine program on myeloid neoplasms: characterization of the patient{\textquoteright}s genome for clinical decision making and systematic collection of real world data to improve quality of health care]. A special thanks for the generous support by Famiglia Olmetti/Minguzzi and Famiglia Cuomo. Funding Information: This work was supported by AIRC 5 × 1000 call “Metastatic disease: the key unmet need in oncology” to MYNERVA project, #21267 (MYeloid NEoplasms Research Venture AIRC). A detailed description of the MYNERVA project is available at http://www.progettoagimm.it. Also supported by the “EDITOR”, Accelerator Award project funded through a partnership between Cancer Research UK, Fondazione AIRC and Fundaci{\'o}n Cient{\'i}fica de la Asociacion Espa{\~n}ola Contra el C{\'a}ncer. PG and CM were also supported by Ministero della Salute, Rome, Italy [Finalizzata 2018, NET-2018–12365935, Personalized medicine program on myeloid neoplasms: characterization of the patient{\textquoteright}s genome for clinical decision making and systematic collection of real world data to improve quality of health care]. A special thanks for the generous support by Famiglia Olmetti/Minguzzi and Famiglia Cuomo.",

year = "2023",

month = dec,

doi = "10.1038/s41408-023-00786-x",

language = "English (US)",

volume = "13",

journal = "Blood cancer journal",

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T1 - Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis

AU - Guglielmelli, Paola

AU - Maccari, Chiara

AU - Sordi, Benedetta

AU - Balliu, Manjola

AU - Atanasio, Alessandro

AU - Mannarelli, Carmela

AU - Capecchi, Giulio

AU - Sestini, Ilaria

AU - Coltro, Giacomo

AU - Loscocco, Giuseppe Gaetano

AU - Rotunno, Giada

AU - Angori, Eva

AU - Borri, Filippo C.

AU - Tefferi, Ayalew

AU - Vannucchi, Alessandro M.

N1 - Funding Information: This work was supported by AIRC 5 × 1000 call “Metastatic disease: the key unmet need in oncology” to MYNERVA project, #21267 (MYeloid NEoplasms Research Venture AIRC). A detailed description of the MYNERVA project is available at http://www.progettoagimm.it . Also supported by the “EDITOR”, Accelerator Award project funded through a partnership between Cancer Research UK, Fondazione AIRC and Fundación Científica de la Asociacion Española Contra el Cáncer. PG and CM were also supported by Ministero della Salute, Rome, Italy [Finalizzata 2018, NET-2018–12365935, Personalized medicine program on myeloid neoplasms: characterization of the patient’s genome for clinical decision making and systematic collection of real world data to improve quality of health care]. A special thanks for the generous support by Famiglia Olmetti/Minguzzi and Famiglia Cuomo. Funding Information: This work was supported by AIRC 5 × 1000 call “Metastatic disease: the key unmet need in oncology” to MYNERVA project, #21267 (MYeloid NEoplasms Research Venture AIRC). A detailed description of the MYNERVA project is available at http://www.progettoagimm.it. Also supported by the “EDITOR”, Accelerator Award project funded through a partnership between Cancer Research UK, Fondazione AIRC and Fundación Científica de la Asociacion Española Contra el Cáncer. PG and CM were also supported by Ministero della Salute, Rome, Italy [Finalizzata 2018, NET-2018–12365935, Personalized medicine program on myeloid neoplasms: characterization of the patient’s genome for clinical decision making and systematic collection of real world data to improve quality of health care]. A special thanks for the generous support by Famiglia Olmetti/Minguzzi and Famiglia Cuomo.

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Phenotypic correlations of CALR mutation variant allele frequency in patients with myelofibrosis

ASJC Scopus subject areas

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