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Flavia Cerrato

Research Profile

Chemicals & Drugs

Disorders

Physiology

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Publications

TOP 3
Agostina De Crescenzo; Marco Miceli; Orazio Palumbo; Andrea Riccio; Angela Sparago; Moshe Bronshtein; Massimo Carella; Flavia Cerrato; Yuval Yaron
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction.
Jasmin Beygo; Karin Buiting; Flavia Cerrato; Margherita Cirillo Silengo; Valentina Citro; Maria Vittoria Cubellis; Agostina De Crescenzo; Thorsten Enklaar; Notker Graf; Andrea Guala; Melanie Heitmann; Bernhard Horsthemke; Dirk Prawitt; Katrin Rademacher; Cecilia Anichini; Angela Sparago; Andrea Riccio
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
Agostina De Crescenzo; Luigi Falco; Pietro Falco; Gaetano Ausanio; Italo Bernardo; Flavia Cerrato; Filomena Coppola; Andrea Riccio
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

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All Publications

2013: Agostina De Crescenzo; Marco Miceli; Orazio Palumbo; Andrea Riccio; Angela Sparago; Moshe Bronshtein; Massimo Carella; Flavia Cerrato; Yuval Yaron
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction.
Journal of medical genetics 2013;50(2):99-103.
2013: Jasmin Beygo; Karin Buiting; Flavia Cerrato; Margherita Cirillo Silengo; Valentina Citro; Maria Vittoria Cubellis; Agostina De Crescenzo; Thorsten Enklaar; Notker Graf; Andrea Guala; Melanie Heitmann; Bernhard Horsthemke; Dirk Prawitt; Katrin Rademacher; Cecilia Anichini; Angela Sparago; Andrea Riccio
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
Human molecular genetics 2013;22(3):544-57.
2011: Agostina De Crescenzo; Luigi Falco; Pietro Falco; Gaetano Ausanio; Italo Bernardo; Flavia Cerrato; Filomena Coppola; Andrea Riccio
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.
European journal of medical genetics 2011;54(4):e451-4.
2009: Andrea Riccio; Angela Sparago; Gaetano Verde; Agostina De Crescenzo; Valentina Citro; Maria Vittoria Cubellis; Giovanni Battista Ferrero; Margherita Silengo; Silvia Russo; Lidia Larizza; Flavia Cerrato
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
Endocrine development 2009;14():1-9.
2008: Flavia Cerrato; Angela Sparago; Gaetano Verde; Agostina De Crescenzo; Valentina Citro; Maria Vittoria Cubellis; Maria Michela Rinaldi; Luigi Boccuto; Giovanni Neri; Cinzia Magnani; Paolo D'Angelo; Paola Collini; D Perotti; Gianfranco Sebastio; Eamonn R Maher; Andrea Riccio
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
Human molecular genetics 2008;17(10):1427-35.
2007: Angela Sparago; Silvia Russo; Flavia Cerrato; Serena Ferraiuolo; Pierangela Castorina; Angelo Selicorni; Christine Schwienbacher; Massimo Negrini; Giovanni Battista Ferrero; Margherita Silengo; Cecilia Anichini; Lidia Larizza; Andrea Riccio
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
Human molecular genetics 2007;16(3):254-64.
2005: Flavia Cerrato; Angela Sparago; Ines Di Matteo; Xiangang Zou; Wendy Dean; Hiroyuki Sasaki; Paul Smith; Rita Genesio; Marianne Bruggemann; Wolf Reik; Andrea Riccio
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
Human molecular genetics 2005;14(4):503-11.
2004: Angela Sparago; Flavia Cerrato; Maria Vernucci; Giovanni Battista Ferrero; Margherita Silengo; Andrea Riccio
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
Nature genetics 2004;36(9):958-60.
2004: Maria Vernucci; Flavia Cerrato; Paolo V Pedone; Luisa Dandolo; Carmelo B Bruni; Andrea Riccio
Developmentally regulated functions of the H19 differentially methylated domain.
Human molecular genetics 2004;13(3):353-61.
2003: Flavia Cerrato; Wendy Dean; Karen Davies; Kazuhiro Kagotani; Kohzoh Mitsuya; Katsuzumi Okumura; Andrea Riccio; Wolf Reik
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.
Human molecular genetics 2003;12(23):3123-32.
2002: Flavia Cerrato; Maria Vernucci; Paolo V Pedone; Lorenzo Chiariotti; Gianfranco Sebastio; Carmelo B Bruni; Andrea Riccio
The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome.
Human genetics 2002;111(1):105-7.
2000: Maria Vernucci; Flavia Cerrato; N Besnard; Stefano Casola; Paolo V Pedone; Carmelo B Bruni; Andrea Riccio
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis.
Oncogene 2000;19(54):6376-85.
2000: Maria Pia Sperandeo; Paola Ungaro; Maria Vernucci; Paolo V Pedone; Flavia Cerrato; Lucia Perone; Stefano Casola; M V Cubellis; Carmelo B Bruni; Generoso Andria; Gianfranco Sebastio; Andrea Riccio
Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
American journal of human genetics 2000;66(3):841-7.
1999: Paolo V Pedone; M J Pikaart; Flavia Cerrato; Maria Vernucci; Paola Ungaro; Carmelo B Bruni; Andrea Riccio
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes.
FEBS letters 1999;458(1):45-50.