RICCIO, ANDREA
RICCIO, ANDREA
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature
2023 Elefante, Pierandrea; Spedicati, Beatrice; Faletra, Flavio; Pignata, Laura; Cerrato, Flavia; Riccio, Andrea; Barbi, Egidio; Memo, Luigi; Travan, Laura
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer
2023 Cecere, Francesco; Pignata, Laura; Hay Mele, Bruno; Saadat, Abu; D'Angelo, Emilia; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Scarano, Gioacchino; Battista Rossi, Giovanni; Angelini, Claudia; Sparago, Angela; Cerrato, Flavia; Riccio, Andrea
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer
2023 Cecere, F; Pignata, L; Hay Mele, B; Saadat, A; D'Angelo, E; Palumbo, O; Palumbo, P; Carella, M; Scarano, G; Rossi, Gb; Angelini, C; Sparago, A; Cerrato, F; Riccio, A
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
2023 Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea
ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming
2023 Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; R Matarazzo, Maria; Riccio, Andrea
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
2023 Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; Matarazzo, Maria R.; Riccio, Andrea
Imprinting disorders
2023 Thomas Eggermann ; David Monk ; Guiomar Perez de Nanclares ; Masayo Kagami ; Eloïse Giabicani ; Andrea Riccio ; Zeynep Tümer ; Jennifer M Kalish ; Maithé Tauber ; Jessica Duis ; Rosanna Weksberg ; Eamonn R Maher ; Matthias Begemann ; Miriam Elbracht
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
2023 Luca M.; Carli D.; Cardaropoli S.; Milani D.; Cocchi G.; Leoni C.; Macchiaiolo M.; Bartuli A.; Tarani L.; Melis D.; Bontempo P.; D'Elia G.; Prada E.; Vitale R.; Grammegna A.; Tannorella P.; Sparago A.; Pignata L.; Riccio A.; Russo S.; Ferrero G.B.; Mussa A.
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques.
2022 Carli, Diana; Operti, Matteo; Russo, Silvia; Cocchi, Guido; Milani, Donatella; Leoni, Chiara; Prada, Elisabetta; Melis, Daniela; Falco, Mariateresa; Spina, Jennifer; Uliana, Vera; Sara, Osimani; Sirchia, Fabio; Tarani, Luigi; Macchiaiolo, Marina; Cerrato, Flavia; Sparago, Angela; Pignata, Laura; Tannorella, Pierpaola; Cardaropoli, Simona; Bartuli, Andrea; Riccio, Andrea; Battista Ferrero, Giovanni; Mussa, Alessandro
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum.
2022 Francesco Passaretti ;Laura Pignata ;Giuseppina Vitiello ;Viola Alesi ;Gemma D'Elia ;Francesco Cecere ;Fabio Acquaviva ;Daniele De Brasi ;Antonio Novelli ;Andrea Riccio ;Achille Iolascon ;Flavia Cerrato
Epigenetic Alterations in Inborn Errors of Immunity.
2022 Romano, Roberta; Cillo, Francesca; Moracas, Cristina; Pignata, Laura; Nannola, Chiara; Toriello, Elisabetta; De Rosa, Antonio; Cirillo, Emilia; Coppola, Emma; Giardino, Giuliana; Brunettipierri, Nicola; Riccio, Andrea; Pignata, Claudio
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders.
2022 Deborah Mackay ;Jet Bliek ;Masayo Kagami ;Jair TenorioCastano ;Arrate Pereda ;Frédéric Brioude ;Irène Netchine ;Dzhoy Papingi ;Elisa de Franco ;Margaret Lever ;Julie Sillibourne ;Paola Lombardi ;Véronique Gaston ;Maithé Tauber ;Gwenaelle Diene ;Eric Bieth ;Luis Fernandez ;Julian Nevado ;Zeynep Tümer ;Andrea Riccio ;Eamonn R Maher ;Jasmin Beygo ;Pierpaola Tannorella ;Silvia Russo ;Guiomar Perez de Nanclares ;I Karen Temple ;Tsutomu Ogata ;Pablo Lapunzina ;Thomas Eggermann
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances.
2022 Laura Pignata ;Francesco Cecere ;Ankit Verma ;Bruno Hay Mele ;Maria Monticelli ;Basilia Acurzio ;Carlo Giaccari ;Angela Sparago ;Jose Ramon Hernandez Mora ;Ana MonteagudoSánchez ;Manel Esteller ;Arrate Pereda ;Jair TenorioCastano ;Orazio Palumbo ;Massimo Carella ;Paolo Prontera ;Carmelo Piscopo ;Maria Accadia ;Pablo Lapunzina ;Maria Vittoria Cubellis ;Guiomar Perez de Nanclares ;David Monk ;Andrea Riccio ;Flavia Cerrato
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex
2022 Basilia Acurzio; Francesco Cecere; Carlo Giaccari; Ankit Verma; Rosita Russo; Mariangela Valletta; Bruno Hay Mele; Claudia Angelini; Angela Chambery; Andrea Riccio
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex.
2022 Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
2022 Thomas Eggermann ;Elzem Yapici ;Jet Bliek ;Arrate Pereda ;Matthias Begemann ;Silvia Russo ;Pierpaola Tannorella ;Luciano Calzari ;Guiomar Perez de Nanclares ;Paola Lombardi ;I Karen Temple ;Deborah Mackay ;Andrea Riccio ;Masayo Kagami ;Tsutomu Ogata ;Pablo Lapunzina ;David Monk ;Eamonn R Maher ;Zeynep Tümer
Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c
2021 Sparago, A; Cerrato, F; Pignata, L; Cammaratascalisi, F; Garavelli, L; Piscopo, C; Vancini, A; Riccio, A
ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex
2021 Russo, Rosita; Russo, Veronica; Cecere, Francesco; Valletta, Mariangela; Teresa Gentile, Maria; Lucacoluccid'Amato, ; Angelini, Claudia; Riccio, Andrea; Vincenzo Pedone, Paolo; Chambery, Angela; Baglivo, Ilaria
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs
2021 Acurzio B.; Verma A.; Polito A.; Giaccari C.; Cecere F.; Fioriniello S.; Della Ragione F.; Fico A.; Cerrato F.; Angelini C.; Feil R.; Riccio A.
A paternally inherited 1.4 kb deletion of the 11p15.5 Imprinting Center 2 is associated with a mild familial Silver-Russell syndrome phenotype
2020 Mio, C; Allegri, L; Passon, N; Bregant, E; Demori, E; Franzoni, A; Driul, D; Riccio, A; Damante, G; Baldan, F
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature | 1-gen-2023 | Elefante, Pierandrea; Spedicati, Beatrice; Faletra, Flavio; Pignata, Laura; Cerrato, Flavia; Riccio, Andrea; Barbi, Egidio; Memo, Luigi; Travan, Laura | |
| Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer | 1-gen-2023 | Cecere, Francesco; Pignata, Laura; Hay Mele, Bruno; Saadat, Abu; D'Angelo, Emilia; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Scarano, Gioacchino; Battista Rossi, Giovanni; Angelini, Claudia; Sparago, Angela; Cerrato, Flavia; Riccio, Andrea | |
| Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer | 1-gen-2023 | Cecere, F; Pignata, L; Hay Mele, B; Saadat, A; D'Angelo, E; Palumbo, O; Palumbo, P; Carella, M; Scarano, G; Rossi, Gb; Angelini, C; Sparago, A; Cerrato, F; Riccio, A | |
| Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? | 1-gen-2023 | Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea | |
| ICF1 Syndrome Associated DNMT3B Mutations Prevent de novo Methylation at a subset of Imprinted Loci During iPSC Reprogramming | 1-gen-2023 | Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; R Matarazzo, Maria; Riccio, Andrea | |
| ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming | 1-gen-2023 | Verma, Ankit; Poondi Krishnan, Varsha; Cecere, Francesco; D'Angelo, Emilia; Lullo, Vincenzo; Strazzullo, Maria; Selig, Sara; Angelini, Claudia; Matarazzo, Maria R.; Riccio, Andrea | |
| Imprinting disorders | 1-gen-2023 | Thomas Eggermann ; David Monk ; Guiomar Perez de Nanclares ; Masayo Kagami ; Eloïse Giabicani ; Andrea Riccio ; Zeynep Tümer ; Jennifer M Kalish ; Maithé Tauber ; Jessica Duis ; Rosanna Weksberg ; Eamonn R Maher ; Matthias Begemann ; Miriam Elbracht | |
| Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development | 1-gen-2023 | Luca M.; Carli D.; Cardaropoli S.; Milani D.; Cocchi G.; Leoni C.; Macchiaiolo M.; Bartuli A.; Tarani L.; Melis D.; Bontempo P.; D'Elia G.; Prada E.; Vitale R.; Grammegna A.; Tannorella P.; Sparago A.; Pignata L.; Riccio A.; Russo S.; Ferrero G.B.; Mussa A. | |
| Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques. | 1-gen-2022 | Carli, Diana; Operti, Matteo; Russo, Silvia; Cocchi, Guido; Milani, Donatella; Leoni, Chiara; Prada, Elisabetta; Melis, Daniela; Falco, Mariateresa; Spina, Jennifer; Uliana, Vera; Sara, Osimani; Sirchia, Fabio; Tarani, Luigi; Macchiaiolo, Marina; Cerrato, Flavia; Sparago, Angela; Pignata, Laura; Tannorella, Pierpaola; Cardaropoli, Simona; Bartuli, Andrea; Riccio, Andrea; Battista Ferrero, Giovanni; Mussa, Alessandro | |
| Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum. | 1-gen-2022 | Francesco Passaretti ;Laura Pignata ;Giuseppina Vitiello ;Viola Alesi ;Gemma D'Elia ;Francesco Cecere ;Fabio Acquaviva ;Daniele De Brasi ;Antonio Novelli ;Andrea Riccio ;Achille Iolascon ;Flavia Cerrato | |
| Epigenetic Alterations in Inborn Errors of Immunity. | 1-gen-2022 | Romano, Roberta; Cillo, Francesca; Moracas, Cristina; Pignata, Laura; Nannola, Chiara; Toriello, Elisabetta; De Rosa, Antonio; Cirillo, Emilia; Coppola, Emma; Giardino, Giuliana; Brunettipierri, Nicola; Riccio, Andrea; Pignata, Claudio | |
| First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders. | 1-gen-2022 | Deborah Mackay ;Jet Bliek ;Masayo Kagami ;Jair TenorioCastano ;Arrate Pereda ;Frédéric Brioude ;Irène Netchine ;Dzhoy Papingi ;Elisa de Franco ;Margaret Lever ;Julie Sillibourne ;Paola Lombardi ;Véronique Gaston ;Maithé Tauber ;Gwenaelle Diene ;Eric Bieth ;Luis Fernandez ;Julian Nevado ;Zeynep Tümer ;Andrea Riccio ;Eamonn R Maher ;Jasmin Beygo ;Pierpaola Tannorella ;Silvia Russo ;Guiomar Perez de Nanclares ;I Karen Temple ;Tsutomu Ogata ;Pablo Lapunzina ;Thomas Eggermann | |
| Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances. | 1-gen-2022 | Laura Pignata ;Francesco Cecere ;Ankit Verma ;Bruno Hay Mele ;Maria Monticelli ;Basilia Acurzio ;Carlo Giaccari ;Angela Sparago ;Jose Ramon Hernandez Mora ;Ana MonteagudoSánchez ;Manel Esteller ;Arrate Pereda ;Jair TenorioCastano ;Orazio Palumbo ;Massimo Carella ;Paolo Prontera ;Carmelo Piscopo ;Maria Accadia ;Pablo Lapunzina ;Maria Vittoria Cubellis ;Guiomar Perez de Nanclares ;David Monk ;Andrea Riccio ;Flavia Cerrato | |
| The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex | 1-gen-2022 | Basilia Acurzio; Francesco Cecere; Carlo Giaccari; Ankit Verma; Rosita Russo; Mariangela Valletta; Bruno Hay Mele; Claudia Angelini; Angela Chambery; Andrea Riccio | |
| The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex. | 1-gen-2022 | Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea | |
| Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences | 1-gen-2022 | Thomas Eggermann ;Elzem Yapici ;Jet Bliek ;Arrate Pereda ;Matthias Begemann ;Silvia Russo ;Pierpaola Tannorella ;Luciano Calzari ;Guiomar Perez de Nanclares ;Paola Lombardi ;I Karen Temple ;Deborah Mackay ;Andrea Riccio ;Masayo Kagami ;Tsutomu Ogata ;Pablo Lapunzina ;David Monk ;Eamonn R Maher ;Zeynep Tümer | |
| Variable expressivity of the beckwith-wiedemann syndrome in four pedigrees segregating loss-of-function variants of cdkn1c | 1-gen-2021 | Sparago, A; Cerrato, F; Pignata, L; Cammaratascalisi, F; Garavelli, L; Piscopo, C; Vancini, A; Riccio, A | |
| ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex | 1-gen-2021 | Russo, Rosita; Russo, Veronica; Cecere, Francesco; Valletta, Mariangela; Teresa Gentile, Maria; Lucacoluccid'Amato, ; Angelini, Claudia; Riccio, Andrea; Vincenzo Pedone, Paolo; Chambery, Angela; Baglivo, Ilaria | |
| Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs | 1-gen-2021 | Acurzio B.; Verma A.; Polito A.; Giaccari C.; Cecere F.; Fioriniello S.; Della Ragione F.; Fico A.; Cerrato F.; Angelini C.; Feil R.; Riccio A. | |
| A paternally inherited 1.4 kb deletion of the 11p15.5 Imprinting Center 2 is associated with a mild familial Silver-Russell syndrome phenotype | 1-gen-2020 | Mio, C; Allegri, L; Passon, N; Bregant, E; Demori, E; Franzoni, A; Driul, D; Riccio, A; Damante, G; Baldan, F |