Consortium Member of the Month
Our consortium member of the month for the month of February goes to Briant Fruth from Mayo Clinic!
Briant Fruth
Principal Statistical Programmer
Briant has been an invaluable member of our statistical team at Mayo Clinic. His contributions have been pivotal in the statistical analysis efforts of the MPN-RC 106 specimen bank. He has expertly addressed various queries, seamlessly integrated biomarker data, and conducted comprehensive cytokine statistical analyses.
Written by: Amylou C. Dueck, PhD
Nominated by: Victoria Rivera
Briant, thank you so much for all of the phenomenal work you have done for the consortium.
Keep up the great work!
MPN-RC Monthly Publication
Title: Sequential treatment with ruxolitinib and imetelstat effectively depletes myelofibrosis hematopoietic stem and progenitor cells
Author(s): Xiaoli Wang, Andrew Davis, Cing Siang Hu, Fei Huang, Sophia Jiang, John Mascarenhas, and Ronald Hoffman
We are HIRING!
Mount Sinai Health System is looking to hire three Senior Scientists. Use the links below for more information and to apply for the position(s).
ASH Conference 2025
ASH Abstracts
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Marina Kremyanskaya, MD,PhD
Phase II study of reparixin in patients with myelofibrosis. myeloproliferative neoplasms research consortium (MPN-RC) 120 trial

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John Crispino, PhD,MBA
Menin inhibition as a new therapeutic option for the myeloproliferative neoplasms

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John Mascarenhas, MD
Bone marrow adipocytes (BMA) as a novel biomarker of molecular response in patients with essential thrombocythemia (ET) and polycythemia vera (PV) treated with pegylated interferon alfa-2A

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Andrew Kuykendall, MD
A phase 2 study of canakinumab in patient with myelofibrosis: Results from part 1

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Min Lu, MD,PhD
Myelofibrosis stem cell fitness requires microenvironmental cell interactions

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Xiaoli Wang, MD,PhD
Therapy resistance and disease relapse in patients with MPN-blast phase are associated with clonal evolution and transcriptomic changes in MPN- blast phase stem cells

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MD Babu Mia, PhD
Single cell transcriptional profiling reveals distinct subsets of human megakaryocytes in myelofibrosis

