Frangella, Silvia
Frangella, Silvia
ROMA - Dipartimento di Scienze della vita e sanità pubblica
CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories
2023 Amenta, Simona; Marangi, Giuseppe; Orteschi, D.; Frangella, Silvia; Gurrieri, Fiorella; Paccagnella, E.; Torella, A.; Cappuccio, G.; Musacchia, F.; Mutarelli, Massimiano; Carrella, D.; Vitiello, G.; Parenti, Gian Paolo; Leuzzi, V.; Selicorni, A.; Maitz, S.; Brunetti-Pierri, N.; Banfi, S.; Montomoli, M.; Milani, Daniela; Romano, Maria Concetta; Tummolo, Aida Angela; De Brasi, D.; Coppola, A.; Santoro, C.; Scala, M.; Romano, Federica; Capra, V.; Nigro, V.; Zollino, Marcella
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome
2020 Amenta, S.; Frangella, S.; Marangi, G.; Lattante, S.; Ricciardi, S.; Doronzio, P. N.; Orteschi, D.; Veredice, C.; Contaldo, I.; Zampino, G.; Gentile, M.; Scarano, E.; Graziano, C.; Zollino, M.
Clinical genetics can solve the pitfalls of genome-wide investigations: Lesson from mismapping a loss-of-function variant in KANSL1
2020 Bigoni, S.; Marangi, G.; Frangella, S.; Panfili, A.; Ognibene, D.; Squeo, G. M.; Merla, G.; Zollino, M.
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers
2020 Marangi, G.; Garcovich, S.; Di Sante, G.; Orteschi, D.; Frangella, S.; Scaldaferri, F.; Genuardi, M.; Peris, K.; Gurrieri, F.; Zollino, M.
A novel truncating variant within exon 7 of KAT6B associated with features of both SayâBarberâBiesekerâYoungâSimpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders
2018 Marangi, Giuseppe; Di Giacomo, Marilena Carmela; Lattante, Serena; Orteschi, Daniela; Patrizi, Sara; Doronzio, Paolo N.; Riviello, Francesco Nicola; Vaisfeld, Alessandro; Frangella, Silvia; Zollino, Marcella
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4
2017 Bedeschi, Maria Francesca; Marangi, Giuseppe; Calvello, Maria Rosaria; Ricciardi, Stefania; Leone, Francesca Pia Chiara; Baccarin, Marco; Guerneri, Silvana; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Frangella, Silvia; Keena, Beth; Harr, Margaret H.; Zackai, Elaine; Zollino, Marcella
Syndromic craniosynostosis can define new candidate genes for suture development or result from the non-specifc effects of pleiotropic genes: Rasopathies and chromatinopathies as examples
2017 Zollino, Marcella; Lattante, Serena; Orteschi, Daniela; Frangella, Silvia; Doronzio, Paolo Niccolo'; Contaldo, Ilaria; Mercuri, Eugenio Maria; Marangi, Giuseppe
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2023 | CHAMP1-related disorders: pathomechanisms triggered by different genomic alterations define distinct nosological categories | Amenta, Simona; Marangi, Giuseppe; Orteschi, D.; Frangella, Silvia; Gurrieri, Fiorella; Paccagnella, E.; Torella, A.; Cappuccio, G.; Musacchia, F.; Mutarelli, Massimiano; Carrella, D.; Vitiello, G.; Parenti, Gian Paolo; Leuzzi, V.; Selicorni, A.; Maitz, S.; Brunetti-Pierri, N.; Banfi, S.; Montomoli, M.; Milani, Daniela; Romano, Maria Concetta; Tummolo, Aida Angela; De Brasi, D.; Coppola, A.; Santoro, C.; Scala, M.; Romano, Federica; Capra, V.; Nigro, V.; Zollino, Marcella | |
| 1-gen-2020 | Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome | Amenta, S.; Frangella, S.; Marangi, G.; Lattante, S.; Ricciardi, S.; Doronzio, P. N.; Orteschi, D.; Veredice, C.; Contaldo, I.; Zampino, G.; Gentile, M.; Scarano, E.; Graziano, C.; Zollino, M. | |
| 1-gen-2020 | Clinical genetics can solve the pitfalls of genome-wide investigations: Lesson from mismapping a loss-of-function variant in KANSL1 | Bigoni, S.; Marangi, G.; Frangella, S.; Panfili, A.; Ognibene, D.; Squeo, G. M.; Merla, G.; Zollino, M. | |
| 1-gen-2020 | Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers | Marangi, G.; Garcovich, S.; Di Sante, G.; Orteschi, D.; Frangella, S.; Scaldaferri, F.; Genuardi, M.; Peris, K.; Gurrieri, F.; Zollino, M. | |
| 1-gen-2018 | A novel truncating variant within exon 7 of KAT6B associated with features of both SayâBarberâBiesekerâYoungâSimpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders | Marangi, Giuseppe; Di Giacomo, Marilena Carmela; Lattante, Serena; Orteschi, Daniela; Patrizi, Sara; Doronzio, Paolo N.; Riviello, Francesco Nicola; Vaisfeld, Alessandro; Frangella, Silvia; Zollino, Marcella | |
| 1-gen-2017 | Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4 | Bedeschi, Maria Francesca; Marangi, Giuseppe; Calvello, Maria Rosaria; Ricciardi, Stefania; Leone, Francesca Pia Chiara; Baccarin, Marco; Guerneri, Silvana; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Frangella, Silvia; Keena, Beth; Harr, Margaret H.; Zackai, Elaine; Zollino, Marcella | |
| 1-gen-2017 | Syndromic craniosynostosis can define new candidate genes for suture development or result from the non-specifc effects of pleiotropic genes: Rasopathies and chromatinopathies as examples | Zollino, Marcella; Lattante, Serena; Orteschi, Daniela; Frangella, Silvia; Doronzio, Paolo Niccolo'; Contaldo, Ilaria; Mercuri, Eugenio Maria; Marangi, Giuseppe |