Maria Clara Bonaglia

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 9

Top Venues

Genes & genomics

Nutritional neuroscience

Epilepsia open

Molecular cytogenetics

Istituto di Ricovero e Cura a Carattere Scientifico Eugenio Medea

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

Affiliation History

Istituto di Ricovero e Cura a Carattere Scientifico Eugenio Medea

Italy

Scientist and Head of Cytogenetics and Molecular Cytogenetics Laboratory :: Genetic Laboratory

Publications

Martina Miceli, Pinella Failla, Lucia Saccuzzo, Ornella Galesi, Silvestra Amata, Corrado Romano, Maria Clara Bonaglia, Marco Fichera
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & genomics 45 (4) (2023)
Martina Miceli, Pinella Failla, Lucia Saccuzzo, Ornella Galesi, Silvestra Amata, Corrado Romano, Maria Clara Bonaglia, Marco Fichera
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & genomics 45 (4) (2023)
Martina Miceli, Pinella Failla, Lucia Saccuzzo, Ornella Galesi, Silvestra Amata, Corrado Romano, Maria Clara Bonaglia, Marco Fichera
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & genomics 45 (4) (2023)
Martina Miceli, Pinella Failla, Lucia Saccuzzo, Ornella Galesi, Silvestra Amata, Corrado Romano, Maria Clara Bonaglia, Marco Fichera
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & genomics (2023)
Martina Miceli, Pinella Failla, Lucia Saccuzzo, Ornella Galesi, Silvestra Amata, Corrado Romano, Maria Clara Bonaglia, Marco Fichera
Trait - driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & genomics 45 (4) (2023)
Maria Clara Bonaglia, Sara Bertuzzo, Anna Maria Ciaschini, Giancarlo Discepoli, Lucia Castiglia, Romina Romaniello, Orsetta Zuffardi, Marco Fichera
Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome. Molecular cytogenetics 13 (2020)
Maria Clara Bonaglia, Nehir Edibe Kurtas, Edoardo Errichiello, Sara Bertuzzo, Silvana Beri, Mana M Mehrjouy, Aldesia Provenzano, Debora Vergani, Vanna Pecile, Francesca Novara, Paolo Reho, Marilena Carmela Di Giacomo, Giancarlo Discepoli, Roberto Giorda, Micheala A Aldred, Cíntia Barros Santos-Rebouças, Andressa Pereira Goncalves, Diane N Abuelo, Sabrina Rita Giglio, Ivana Ricca, Fabrizia Franchi, Philippos C Patsalis, Carolina Sismani, María Angeles Morí, Julián Nevado, Niels Tommerup, Orsetta Zuffardi
De novo unbalanced translocations have a complex history/aetiology. Human genetics 137 (10) (2018)
Barbara De Santis, Carlo Brera, Alessandra Mezzelani, Sabina Soricelli, Francesca Ciceri, Giorgio Moretti, Francesca Debegnach, Maria Clara Bonaglia, Laura Villa, Massimo Molteni, Maria Elisabetta Raggi
Role of mycotoxins in the pathobiology of autism: A first evidence. Nutritional neuroscience 22 (2) (2017)
Maria Clara Bonaglia, Roberto Giorda, Roberta Epifanio, Sara Bertuzzo, Susan Marelli, Marion Gerard, Joris Andrieux, Nicoletta Zanotta, Claudio Zucca
Partial deletion of DEPDC5 in a child with focal epilepsy. Epilepsia open 1 (3-4) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Maria Clara Bonaglia