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Blood|April 12, 2013
Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasmsElisa Rumi, Daniela Pietra, Paola Guglielmelli, et al.
Neurobiology of Aging|March 21, 2015
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutationsMario Sabatelli, Marcella Zollino, Amelia Conte, et al.
Clinical Biochemistry|July 24, 2020
Comparison of serologic and molecular SARS-CoV 2 results in a large cohort in Southern Tuscany demonstrates a role for serologic testing to increase diagnostic sensitivityAlessandro Pancrazzi, Pasqualino Magliocca, Maria Lorubbio, et al.
Human Molecular Genetics|July 13, 2013
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosisMario Sabatelli, Alice Moncada, Amelia Conte, et al.
American Journal of Hematology|June 7, 2016
Prognostic impact of bone marrow fibrosis in primary myelofibrosis. A study of the AGIMM group on 490 patientsPaola Guglielmelli, Giada Rotunno, Annalisa Pacilli, et al.
European Journal of Human Genetics : EJHG|February 26, 2015
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndromeConcetta Cafiero, Giuseppe Marangi, Daniela Orteschi, et al.
Blood|June 4, 2008
Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemiaAlessandro M Vannucchi, Elisabetta Antonioli, Paola Guglielmelli, et al.
Molecular Cell|June 5, 2012
HIPK2 controls cytokinesis and prevents tetraploidization by phosphorylating histone H2B at the midbodyCinzia Rinaldo, Alice Moncada, Alessandra Gradi, et al.
Blood|November 7, 2012
Spleen endothelial cells from patients with myelofibrosis harbor the JAK2V617F mutationVittorio Rosti, Laura Villani, Roberta Riboni, et al.
American Journal of Hematology|April 3, 2016
Epidemiology and clinical relevance of mutations in postpolycythemia vera and postessential thrombocythemia myelofibrosis: A study on 359 patients of the AGIMM groupGiada Rotunno, Annalisa Pacilli, Valentina Artusi, et al.
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