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European Journal of Human Genetics : EJHG|April 14, 2016
Nucleoporin genes in human diseasesValeria Nofrini, Danika Di Giacomo, Cristina MecucciPediatric Blood & Cancer|July 17, 2015
Molecular Cytogenetics Detect an Unbalanced t(2;13)(q36;q14) and PAX3-FOXO1 Fusion in Rhabdomyosarcoma With Mixed Embryonal/Alveolar FeaturesRoberta La Starza, Valeria Nofrini, Tiziana Pierini, et al.British Journal of Haematology|November 20, 2008
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndromeBarbara Crescenzi, Roberta La Starza, Constantina Sambani, et al.International Journal of Cancer|October 27, 2021
Accuracy of different triage strategies for human papillomavirus positivity in an Italian screening populationDaniela Gustinucci, Maria Benevolo, Elena Cesarini, et al.Leukemia Research|May 26, 2015
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemiasBarbara Crescenzi, Valeria Nofrini, Gianluca Barba, et al.Cancer Genetics|March 26, 2013
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemiaPaolo Gorello, Valeria Nofrini, Lucia Brandimarte, et al.Cancer Genetics|December 6, 2011
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemiaValentina Pierini, Valeria Nofrini, Roberta La Starza, et al.Plos One|October 22, 2020
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot studyYlenia Barbanera, Francesco Arcioni, Hovirag Lancioni, et al.Cancer Genetics and Cytogenetics|August 12, 2009
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvementRoberta La Starza, Lucia Brandimarte, Valentina Pierini, et al.Cancer Genetics|January 7, 2014
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumorRoberta La Starza, Gianluca Barba, Valeria Nofrini, et al.Pageof 2