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Francesca Amati

MicroRNA 217 Modulates Endothelial Cell Senescence via Silent Information Regulator 1
2009 · Rossella Menghini, Viviana Casagrande, et al. · Circulation · 482
Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
2003 · Antonio Pizzuti, Anna Sarkozy, et al. · Human Mutation · 141
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
1999 · Francesca Amati, Emanuela Conti, et al. · European Journal of Human Genetics · 133
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22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
1995 · Francesca Amati, Aldo Mari, et al. · Human Genetics · 124
In Vivo and In Vitro Studies Support That a New Splicing Isoform of OLR1 Gene Is Protective Against Acute Myocardial Infarction
2005 · Ruggiero Mango, Silvia Biocca, et al. · Circulation Research · 120
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In Vitro Acute Exposure to DEHP Affects Oocyte Meiotic Maturation, Energy and Oxidative Stress Parameters in a Large Animal Model
2011 · Barbara Ambruosi, Manuel Filioli Uranio, et al. · PLoS ONE · 88
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Epigenetic Modification in Coronary Atherosclerosis
2019 · Barbara Rizzacasa, Francesca Amati, et al. · Journal of the American College of Cardiology · 87
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UFD1L, a Developmentally Expressed Ubiquitination Gene, is Deleted in CATCH 22 Syndrome
1997 · A. Pizzuti, G. Novelli, et al. · Human Molecular Genetics · 87
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
2003 · M PIERDOMINICI, F MAZZETTA, et al. · Clinical & Experimental Immunology · 65
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome
1995 · A. Mari, F. Amati, et al. · Human Genetics · 57
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study
2019 · Barbara Rizzacasa, Elena Morini, et al. · PLoS ONE · 54
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Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways
2015 · M. Massimiani, L. Vecchione, et al. · Molecular Human Reproduction · 52
Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2
2006 · ANNALISA BOTTA, LAURA VALLO, et al. · Gene Expression · 51
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.
1996 · A Pizzuti, G Novelli, et al. · PubMed · 47
Valproic Acid Induces Neuroendocrine Differentiation and UGT2B7 Up-Regulation in Human Prostate Carcinoma Cell Line
2007 · Alessandra Valentini, Michela Biancolella, et al. · Drug Metabolism and Disposition · 45
LOX-1 and Its Splice Variants: A New Challenge for Atherosclerosis and Cancer-Targeted Therapies
2017 · Barbara Rizzacasa, Elena Morini, et al. · International Journal of Molecular Sciences · 44
Association study of a promoter polymorphism of UFD1L gene with schizophrenia
2001 · Alessandro De Luca, Augusto Pasini, et al. · American Journal of Medical Genetics · 40
Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit
2001 · Lucia Berti, Gerhard Mittler, et al. · Genomics · 40
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice
2006 · Daria Cipollone, Francesca Amati, et al. · Cardiovascular Pathology · 38
Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11
1999 · Roy Wadey, Judith McKie, et al. · The American Journal of Human Genetics · 37
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Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes
2019 · Sabina Pucci, Chiara Polidoro, et al. · Cell Death and Disease · 32
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Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients
2020 · Francesca Amati, Chiara Vancheri, et al. · Heliyon · 30
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Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation.
2007 · Barbara Bucci, Silvia Misiti, et al. · PubMed · 30
Structure and expression of the human ubiquitin fusion–degradation gene (UFD1L)
1998 · Giuseppe Novelli, Aldo Mari, et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 28
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death
2015 · Elena Morini, Federica Sangiuolo, et al. · Frontiers in Genetics · 27
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Works count: 90
Citation count: 2,419
H-index: 25
I10-index: 43
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