Emanuela Maserati - Concepedia

Author

Emanuela Maserati

University of Pavia ORCID

Also Known As

E Maserati, E. MASERATI, E. Maserati, EMANUELA MASERATI, Emanuela Maserati, MASERATI, EMANUELA, Seghezzi L.

132

Publications

Citations

H-Index

Concepts

All Affiliations

University of Pavia University of Insubria Istituti di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo Fondazione University of Padua

About

Emanuela Maserati is an author at University of Pavia specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	444
2	Health Sciences	5	5	114
3	Cell Biology	2	2	67
4	Natural Sciences	1	1	20
5	Biostatistics	1	1	33

Emanuela Maserati

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome María Clara Bonaglia, Roberto Giorda, Silvana Beri, PLoS Genetics	2011	223
High variability of genomic instability and gene expression profiling in different HeLa clones Annalisa Frattini, Marco Fabbri, Roberto Valli, Scientific Reports	2015	107
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome Antonella Minelli, Emanuela Maserati, Elena Nicolis, Leukemia Hematological MalignancyChromatinSbds GeneChromatin StructureGenetic Disorder	2009	68
HCMOGT-1 Is a Novel Fusion Partner to <b> <i>PDGFRB</i> </b> in Juvenile Myelomonocytic Leukemia with t(5;17)(q33;p11.2) Cristina Morerio, Maura Acquila, Cristina Rosanda, Cancer Research	2004	66
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells Roberto Valli, Cristina Marletta, Barbara Pressato, Molecular Cytogenetics	2011	65
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman‐Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies Emanuela Maserati, Barbara Pressato, Roberto Valli, British Journal of Haematology	2009	61
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: Clinical, cytogenetic, and molecular data on three cases Laura Seghezzi, Emanuela Maserati, Antonella Minelli, Genes Chromosomes and Cancer	1996	60
Restricted TCR repertoire and long-term persistence of donor-derived antigen-experienced CD4+ T cells in allogeneic bone marrow transplantation recipients M Vavassori, Rita Maccario, Antonia Moretta, The Journal of Immunology	1996	59
Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromes. Franco Locatelli, Andrea Pession, F Bonetti, PubMed	1994	59
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies Emanuela Maserati, Antonella Minelli, Barbara Pressato, Genes Chromosomes and Cancer	2005	48

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