Francesca Amati
Francesca Amati
Ricercatore confermato Genetica Medica, Universitą Tor Vergata Roma
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Practical guidelines for managing patients with 22q11. 2 deletion syndrome
AS Bassett, DM McDonald-McGinn, K Devriendt, MC Digilio, ...
The Journal of pediatrics 159 (2), 332-339. e1, 2011
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1
R Menghini, V Casagrande, M Cardellini, E Martelli, A Terrinoni, F Amati, ...
Circulation 120 (15), 1524-1532, 2009
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
A Pizzuti, A Sarkozy, AL Newton, E Conti, E Flex, M Cristina Digilio, ...
Human mutation 22 (5), 372-377, 2003
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
F Amati, A Mari, MC Digilio, R Mingarelli, B Marino, A Giannotti, G Novelli, ...
Human genetics 95, 479-482, 1995
In Vivo and In Vitro Studies Support That a New Splicing Isoform of OLR1 Gene Is Protective Against Acute Myocardial Infarction
R Mango, S Biocca, F del Vecchio, F Clementi, F Sangiuolo, F Amati, ...
Circulation Research 97 (2), 152-158, 2005
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
A Pizzuti, G Novelli, A Ratti, F Amati, A Mari, G Calabrese, S Nicolis, ...
Human molecular genetics 6 (2), 259-265, 1997
Atypical deletions suggest five 22q11. 2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
F Amati, E Conti, A Novelli, M Bengala, MC Digilio, B Marino, A Giannotti, ...
European Journal of Human Genetics 7 (8), 903-909, 1999
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene
A Pizzuti, F Amati, G Calabrese, A Mari, A Colosimo, V Silani, L Giardino, ...
Human molecular genetics 5 (7), 953-958, 1996
Biased T-cell receptor repertoires in patients with chromosome 22q11. 2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
M Pierdominici, F Mazzetta, E Caprini, M Marziali, MC Digilio, B Marino, ...
Clinical & Experimental Immunology 132 (2), 323-331, 2003
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome
A Mari, F Amati, R Mingarelli, A Giannotti, G Sebastio, V Colloridi, ...
Human genetics 96, 444-448, 1995
Epigenetic Modification in Coronary Atherosclerosis: JACC Review Topic of the Week
B Rizzacasa, F Amati, F Romeo, G Novelli, JL Mehta
Journal of the American College of Cardiology 74 (10), 1352-1365, 2019
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways
M Massimiani, L Vecchione, D Piccirilli, P Spitalieri, F Amati, S Salvi, ...
MHR: Basic science of reproductive medicine 21 (5), 435-451, 2015
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.
A Pizzuti, G Novelli, A Mari, A Ratti, A Colosimo, F Amati, D Penso, ...
American journal of human genetics 58 (4), 722, 1996
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2
A Botta, L Vallo, F Rinaldi, E Bonifazi, F Amati, M Biancolella, ...
Gene expression 13 (6), 339, 2007
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit
L Berti, G Mittler, GKH Przemeck, G Stelzer, B Günzler, F Amati, E Conti, ...
Genomics 74 (3), 320-332, 2001
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line
A Valentini, M Biancolella, F Amati, P Gravina, R Miano, G Chillemi, ...
Drug metabolism and disposition 35 (6), 968-972, 2007
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death
E Morini, F Sangiuolo, D Caporossi, G Novelli, F Amati
Frontiers in genetics 6, 127339, 2015
Association study of a promoter polymorphism of UFD1L gene with schizophrenia
A De Luca, A Pasini, F Amati, A Botta, G Spalletta, S Alimenti, F Caccamo, ...
American journal of medical genetics 105 (6), 529-533, 2001
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation
B Bucci, S Misiti, A Cannizzaro, R Marchese, GH Raza, R Miceli, ...
Anticancer research 26 (6B), 4549-4557, 2006
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study
B Rizzacasa, E Morini, R Mango, C Vancheri, S Budassi, G Massaro, ...
PLoS One 14 (5), e0216363, 2019
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