Angelo Selicorni (A Selicorni)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 22

Top Topics

Dna Methylation

Ejection Fraction

Chronic Kidney Disease

Top Venues

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Journal of endocrinological investigation

Italian journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Marcello Niceta, Andrea Ciolfi, Marco Ferilli, Lucia Pedace, Camilla Cappelletti, Claudia Nardini, Mathis Hildonen, Luigi Chiriatti, Evelina Miele, Maria Lisa Dentici, Maria Gnazzo, Claudia Cesario, Elisa Pisaneschi, Anwar Baban, Antonio Novelli, Silvia Maitz, Angelo Selicorni, Gabriella Maria Squeo, Giuseppe Merla, Bruno Dallapiccola, Zeynep Tümer, Maria Cristina Digilio, Manuela Priolo, Tartaglia Marco
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism. European journal of human genetics : EJHG 32 (7) (2024)
Marcello Niceta, Andrea Ciolfi, Marco Ferilli, Lucia Pedace, Camilla Cappelletti, Claudia Nardini, Mathis Hildonen, Luigi Chiriatti, Evelina Miele, Maria Lisa Dentici, Maria Gnazzo, Claudia Cesario, Elisa Pisaneschi, Anwar Baban, Antonio Novelli, Silvia Maitz, Angelo Selicorni, Gabriella Maria Squeo, Giuseppe Merla, Bruno Dallapiccola, Zeynep Tümer, Maria Cristina Digilio, Manuela Priolo, Tartaglia Marco
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism. European journal of human genetics : EJHG 32 (7) (2024)
Marcello Niceta, Andrea Ciolfi, Marco Ferilli, Lucia Pedace, Camilla Cappelletti, Claudia Nardini, Mathis Hildonen, Luigi Chiriatti, Evelina Miele, Maria Lisa Dentici, Maria Gnazzo, Claudia Cesario, Elisa Pisaneschi, Anwar Baban, Antonio Novelli, Silvia Maitz, Angelo Selicorni, Gabriella Maria Squeo, Giuseppe Merla, Bruno Dallapiccola, Zeynep Tümer, Maria Cristina Digilio, Manuela Priolo, Tartaglia Marco
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism. European journal of human genetics : EJHG 32 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A 194 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A 194 (7) (2024)
Marcello Niceta, Andrea Ciolfi, Marco Ferilli, Lucia Pedace, Camilla Cappelletti, Claudia Nardini, Mathis Hildonen, Luigi Chiriatti, Evelina Miele, Maria Lisa Dentici, Maria Gnazzo, Claudia Cesario, Elisa Pisaneschi, Anwar Baban, Antonio Novelli, Silvia Maitz, Angelo Selicorni, Gabriella Maria Squeo, Giuseppe Merla, Bruno Dallapiccola, Zeynep Tümer, Maria Cristina Digilio, Manuela Priolo, Tartaglia Marco
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism. European journal of human genetics : EJHG 32 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A (2024)
Marcello Niceta, Andrea Ciolfi, Marco Ferilli, Lucia Pedace, Camilla Cappelletti, Claudia Nardini, Mathis Hildonen, Luigi Chiriatti, Evelina Miele, Maria Lisa Dentici, Maria Gnazzo, Claudia Cesario, Elisa Pisaneschi, Anwar Baban, Antonio Novelli, Silvia Maitz, Angelo Selicorni, Gabriella Maria Squeo, Giuseppe Merla, Bruno Dallapiccola, Zeynep Tümer, Maria Cristina Digilio, Manuela Priolo, Tartaglia Marco
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism. European journal of human genetics : EJHG (2024)
Alessia Carrer, Maria Giovanna Romaniello, Maria Letizia Calderara, Milena Mariani, Andrea Biondi, Angelo Selicorni
Application of the Face2Gene tool in an Italian dysmorphological pediatric clinic: Retrospective validation and future perspectives. American journal of medical genetics. Part A (2023)
Riccardo G Borroni, Francesco Piscazzi, Mario Valenti, Valeria Rimoldi, Monica Barile, Paolo Pietro Bianchi, Rebecca Favaro, Alessandra Formai, Angelo Selicorni, Sofia Manara, Valeriano Vinci, Andrea Gerardo Lania, Antonio Costanzo
Multiple facial angiofibromas: A manifestation of Frank-ter Haar syndrome? American journal of medical genetics. Part A (2023)
Maria Francesca Bedeschi, Stefano Mora, Franco Antoniazzi, Silvio Boero, Roberto Ravasio, Gioacchino Scarano, Angelo Selicorni, M Sessa, F Verdoni, Giuseppe Zampino, Mohamad Maghnie, null null
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveys. Journal of endocrinological investigation (2023)
Paola Francesca Ajmone, Ludovica Giani, Beatrice Allegri, Giovanni Michelini, Francesca Dall'Ara, Claudia Rigamonti, Federico Monti, Paola Giovanna Vizziello, Angelo Selicorni, Donatella Milani, Simona Scaini, Antonella Costantino
The developmental trajectories of the behavioral phenotype and neuropsychiatric functioning in Cornelia de Lange and Rubinstein Taybi syndromes: A longitudinal study. American journal of medical genetics. Part A (2022)
Roberto Franceschi, Maria Iascone, Silvia Maitz, Daniela Marchetti, Milena Mariani, Angelo Selicorni, Massimo Soffiati, Evelina Maines
A missense mutation in DDRGK1 gene associated to Shohat-type spondyloepimetaphyseal dysplasia: Two case reports and a review of literature. American journal of medical genetics. Part A 188 (8) (2022)
Erika Solansh Apuril Velgara, Milena Mariani, Annalaura Torella, Francesco Musacchia, null null, Vincenzo Nigro, Angelo Selicorni
Cantù syndrome: Report of a patient with a novel variant in KCNJ8 and revision of literature. American journal of medical genetics. Part A 188 (6) (2022)
Lidia Pezzani, Lucia Mauri, Angelo Selicorni, Angela Peron, Marina Grasso, Alessia C Codazzi, Alessandro Rimini, Paola G Marchisio, Domenico Coviello, Anna Colli, Donatella Milani
Aortic dilation in Sotos syndrome: An underestimated feature? American journal of medical genetics. Part A 182 (7) (2020)
Chiara Leoni, Valentina Giorgio, Roberta Onesimo, Luigi Tarani, Mauro Celli, Angelo Selicorni, Giuseppe Zampino
The dark side of COVID-19: The need of integrated medicine for children with special care needs. American journal of medical genetics. Part A 182 (8) (2020)
Ilana Chilton, Volkan Okur, Giuseppina Vitiello, Angelo Selicorni, Milena Mariani, Alice Goldenberg, Thomas Husson, Dominique Campion, Klaske D Lichtenbelt, Koen van Gassen, Michelle Steinraths, Jennifer Rice, Elizabeth R Roeder, Rebecca O Littlejohn, Myriam Srour, Guillaume Sebire, Andrea Accogli, Delphine Héron, Solveig Heide, Caroline Nava, Christel Depienne, Austin Larson, Dmitriy Niyazov, Meron Azage, George Hoganson, Jennifer Burton, Eric T Rush, Janda L Jenkins, Carol J Saunders, Isabelle Thiffault, Joseph T Alaimo, Julie Fleischer, Daniel Groepper, Karen W Gripp, Wendy K Chung
De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 182 (5) (2020)
Barbara Parma, Paola Cianci, Valentina Decimi, Milena Mariani, Maria Cristina Provero, Caterina Funari, Silvia Tajè, Erika Apuril, Anna Cereda, Roberto Panceri, Silvia Maitz, Chiara Fossati, Angelo Selicorni
Complex nutritional deficiencies in a large cohort of Italian patients with Cornelia de Lange syndrome spectrum. American journal of medical genetics. Part A 182 (9) (2020)
Paola Cianci, Valeria D'Apolito, Alex Moretti, Massimo Barbagallo, Sabrina Paci, Maria Teresa Carbone, Riccardo Lubrano, Antonio Urbino, Carlo Dionisi Vici, Luigi Memo, Giuseppe Zampino, Giancarlo La Marca, Alberto Villani, Giovanni Corsello, Angelo Selicorni, null null, null null, null null
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases. Italian journal of pediatrics 46 (1) (2020)
Elisabetta Pangallo, Paola Cianci, Filippo Favuzza, Donatella Milani, Chiara Vimercati, Alex Moretti, Raffaella Picchi, Anita De Paoli, Massimo Agosti, Angelo Selicorni
Pulmonary function in Williams-Beuren syndrome: Spirometric data of 22 Italian patients. American journal of medical genetics. Part A 185 (2) (2020)
Barbara Parma, Paola Cianci, Milena Mariani, Anna Cereda, Roberto Panceri, Chiara Fossati, Luciano Maestri, Francesco Macchini, Roberta Onesimo, Giuseppe Zampino, Pietro Betalli, Maurizio Cheli, Angelo Selicorni
Nissen fundoplication in Cornelia de Lange syndrome spectrum: Who are the potential candidates? American journal of medical genetics. Part A 182 (7) (2020)
Valentina Decimi, Barbara Parma, Roberto Panceri, Chiara Fossati, Milena Mariani, Silvia Russo, Cristina C Gervasini, Maurizio Cheli, Anna Cereda, Angelo Selicorni
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohort. American journal of medical genetics. Part A 176 (9) (2018)