Francesco Pasquali - Concepedia

Author

Francesco Pasquali

Also Known As

F Pasquali, F. PASQUALI, F. Pasquali, FRANCESCO PASQUALI, Francesco Pasquali, PASQUALI, FRANCESCO, Pasquali, Francesco, Rita De Vito

170

Publications

2.8K

Citations

H-Index

101

Concepts

All Affiliations

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

About

Francesco Pasquali is an author at University of Pavia specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	35	1.2K
2	Health Sciences	10	11	395
3	Natural Sciences	2	2	91
4	Public Health	2	2	141
5	Engineering	1	1	54

Francesco Pasquali

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
The 11q;22q translocation: A European collaborative analysis of 43 cases M. Fraccaro, J. Lindsten, C. E. Ford, Human Genetics European Collaborative Analysis	1980	201
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages G. R. Burgio, Alberto G. Ugazio, Luigi Nespoli, European Journal of Immunology HistocompatibilityImmunohematologyImmunodeficienciesImmunologyPathology	1975	133
High variability of genomic instability and gene expression profiling in different HeLa clones Annalisa Frattini, Marco Fabbri, Roberto Valli, Scientific Reports	2015	107
Women heterozygous for deficiency of the (p21 ? pter) region of the X chromosome are fertile M. Fraccaro, P Maraschio, Francesco Pasquali, Human Genetics InfertilityMendelian DisorderFertilityCytogeneticsX Chromosome	1977	87
Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies Giuliana Alimena, Rolf Billström, Rosario Casalone, Cancer Genetics and Cytogenetics Hematological MalignancyChromatinCytogenetic PatternCytogeneticsMixed-phenotype Acute Leukemia	1985	81
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

Page 1