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E. Joanna Baxter

University of Cambridge

19

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5113

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Personalized Prognostic Predictions for Patients with Myeloproliferative Neoplasms through Integration of Comprehensive Genomic and Clinical Information

2017 Blood
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Effect of Mutation Order on Myeloproliferative Neoplasms

2015 The New England Journal of Medicine
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Genetic variation at MECOM , TERT , JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms

2015 Nature Communications
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Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions

2013 Clinical Epigenetics
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Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions

2013 Journal of Clinical Investigation
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Citations (33)
Methods for Detecting Mutations in the Human JAK2 Gene

2013 Methods of Molecular Biology
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Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation.

2006 Blood
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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

2005 The Lancet
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L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting.

2005 Genomics
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NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder

2004 Cancer Research
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Citations (60)