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Angela Sparago

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Ilaria Baglivo; Marco Cammisa; Lucia De Cesare; Sabrina Esposito; Roberto Fattorusso; Giovanna Grimaldi; Andrea Riccio; Vincenzo Riso; Angela Sparago; Zahra Anvar; Paolo V Pedone
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1.
Isabel Iglesias-Platas; Alex Martin-Trujillo; Cristina Camprubi; Franck Court; Amy Guillaumet-Adkins; Gudrun E Moore; Andrea Riccio; Angela Sparago; David Monk
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop.
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.

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All Publications

2013: Ilaria Baglivo; Marco Cammisa; Lucia De Cesare; Sabrina Esposito; Roberto Fattorusso; Giovanna Grimaldi; Andrea Riccio; Vincenzo Riso; Angela Sparago; Zahra Anvar; Paolo V Pedone
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1.
FEBS letters 2013;587(10):1474-81.
2013: Isabel Iglesias-Platas; Alex Martin-Trujillo; Cristina Camprubi; Franck Court; Amy Guillaumet-Adkins; Gudrun E Moore; Andrea Riccio; Angela Sparago; David Monk
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop.
Nucleic acids research 2013;41(4):2171-9.
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: Raffaella Nativio; Angela Sparago; Yoko Ito; Rosanna Weksberg; Andrea Riccio; Adele Murrell
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
Human molecular genetics 2011;20(7):1363-74.
2010: Laura Cardarelli; Angela Sparago; Agostina De Crescenzo; Elisa Nalesso; Barbara Zavan; Maria Vittoria Cubellis; Angelo Selicorni; Paola Cavicchioli; Giovanni Battista Pozzan; Marilena Petrella; Andrea Riccio
Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2010;13(4):326-30.
2009: Jet Bliek; Gaetano Verde; Jonathan Callaway; Saskia M Maas; Agostina De Crescenzo; Angela Sparago; Flavia Cerrato; Silvia Russo; Serena Ferraiuolo; Maria Michela Rinaldi; Rita Fischetto; Faustina Lalatta; Lucio Giordano; Paola Ferrari; Maria Vittoria Cubellis; Lidia Larizza; I Karen Temple; marcel mannens; Deborah J G Mackay; Andrea Riccio
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.
European journal of human genetics : EJHG 2009;17(5):611-9.
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.
2008: Manuela Priolo; Angela Sparago; Corrado Mammì; Flavia Cerrato; Carmelo Laganà; Andrea Riccio
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.
European journal of human genetics : EJHG 2008;16(5):565-71.
2008: Adele Murrell; Yoko Ito; Gaetano Verde; Joanna Huddleston; Kathryn Woodfine; Margherita Silengo; Filippo Spreafico; D Perotti; Agostina De Crescenzo; Angela Sparago; Flavia Cerrato; Andrea Riccio
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.
PloS one 2008;3(3):e1849.
2007: Andrea Guala; Roberta Guarino; Angela Sparago; Andrea Riccio; Piergiorgio Franceschini
Familial posterior helical ear pits.
American journal of medical genetics. Part A 2007;143A(23):2832-4.
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.
2003: Tiziana Bardaro; Geppino Falco; Angela Sparago; Vincenzo Mercadante; Esther Gean Molins; Enrico Tarantino; Matilde Valeria Ursini; Michele D'Urso
Two cases of misinterpretation of molecular results in incontinentia pigmenti, and a PCR-based method to discriminate NEMO/IKKgamma dene deletion.
Human mutation 2003;21(1):8-11.