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Maria Antonella Bardi

University of Ferrara · IT
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Area of research
Genetics · Pathology and Forensic Medicine
Research interest
Research interests include Chronic lymphocytic leukemia, Karyotype, Internal medicine, IGHV@, Medicine, and Biology.
h-index
citations
346
works
13
NIH funding
primary concept
email

Recent publications

The complex karyotype landscape in chronic lymphocytic leukemia allows the refinement of the risk of Richter syndrome transformation
Haematologica 2021cited by 57position: middledoi
In chronic lymphocytic leukaemia, <i>SLAMF1</i> deregulation is associated with genomic complexity and independently predicts a worse outcome
British Journal of Haematology 2020cited by 9position: middledoi
Complex Karyotype Subtypes at Chronic Lymphocytic Leukemia Diagnosis Refine the Risk of Developing a Richter Syndrome. the Richter Syndrome Scoring System
Blood 2020cited by 1position: middledoi
The combination of complex karyotype subtypes and IGHV mutational status identifies new prognostic and predictive groups in chronic lymphocytic leukaemia
British Journal of Cancer 2019cited by 44position: middledoi
In chronic lymphocytic leukaemia with complex karyotype, major structural abnormalities identify a subset of patients with inferior outcome and distinct biological characteristics
British Journal of Haematology 2018cited by 45position: middledoi
In CLL, comorbidities and the complex karyotype are associated with an inferior outcome independently of CLL-IPI
Blood 2017cited by 99position: middledoi
An extensive molecular cytogenetic characterization in high-risk chronic lymphocytic leukemia identifies karyotype aberrations and <i>TP53</i> disruption as predictors of outcome and chemorefractoriness
Oncotarget 2017cited by 14position: middledoi
AN EXTENSIVE MOLECULAR CYTOGENETIC CHARACTERIZATION IN HIGH-RISK CHRONIC LYMPHOCYTIC LEUKEMIA IDENTIFIES KARYOTYPE ABERRATIONS AND TP53 DISRUPTION AS PREDICTORS OF OUTCOME AND CHEMOREFRACTORINESS
Institutional Research Information System University of Ferrara (University of Ferrara) 2017cited by 1position: middle
Extensive next-generation sequencing analysis in chronic lymphocytic leukemia at diagnosis: clinical and biological correlations
Journal of Hematology & Oncology 2016cited by 39position: middledoi
Complex chromosomal rearrangements leading to <scp><i>MECOM</i></scp> overexpression are recurrent in myeloid malignancies with various 3q abnormalities
Genes Chromosomes and Cancer 2016cited by 14position: middledoi
Erratum to: Extensive next-generation sequencing analysis in chronic lymphocytic leukemia at diagnosis: clinical and biological correlations
Journal of Hematology & Oncology 2016cited by 1position: middledoi
Expression of the immunoglobulin superfamily cell membrane adhesion molecule Cd146 in acute leukemia
Cytometry Part B Clinical Cytometry 2015cited by 9position: middledoi
Cytogenetic and molecular cytogenetic profile of bone marrow-derived mesenchymal stromal cells in chronic and acute lymphoproliferative disorders
Annals of Hematology 2012cited by 13position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Antonio Cuneo · University of Ferrara12 papers (2012–2021)Francesco Cavazzini · University of Padua10 papers (2012–2021)Gian Matteo Rigolin · University of Ferrara10 papers (2016–2021)Maurizio Cavallari · University of Ferrara8 papers (2016–2021)Eleonora Volta · University of Ferrara8 papers (2012–2021)Elisa Tammiso · University of Ferrara7 papers (2012–2020)Elena Saccenti · University of Ferrara6 papers (2016–2020)Aurora Melandri · University of Ferrara6 papers (2016–2020)Antonio Urso · University of Ferrara6 papers (2016–2020)Massimo Negrini · The Ohio State University6 papers (2016–2020)Laura Lupini · University of Ferrara5 papers (2016–2017)Enrico Lista · University of Ferrara5 papers (2016–2017)Francesca Maria Quaglia · University of Ferrara5 papers (2016–2017)Cristian Bassi · University of Ferrara5 papers (2016–2017)Luca Formigaro · University of Ferrara5 papers (2016–2017) · 4 papers (2016–2021)Sara Martinelli · University of Ferrara4 papers (2016–2017)Robin Foà · Policlinico Umberto I3 papers (2019–2021)Livio Trentin · Veneto Institute of Molecular Medicine3 papers (2019–2021) · 3 papers (2019–2021)
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