Author

Donatella Milani

Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoORCID 0000-0002-3087-8514Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alessandra GaspariniiD· 1 shared Alessandra MurgiaiD· 1 shared Angela PeroniD· 1 shared Camilla CeccaraniiD· 1 shared Chiara ParodiiD· 1 shared Cristina GervasiniiD· 1 shared Cristina Marino‐BusljeiD· 1 shared Elisa Adele ColomboiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetics

Alessandra GaspariniORCID

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2 papers

Recent·Most cited

Exogenous and endogenous HDAC inhibitor effects in Rubinstein-Taybi syndrome models

Elisabetta Di Fede, Emerenziana Ottaviano, Paolo Grazioli, Camilla Ceccarani, Chiara Parodi, Elisa Adele Colombo, G. Bassanini, Marco Severgnini, Donatella Milani, Elvira Verduci, Thomas Vaccari, Valentina Massa, Elisa Borghi, Cristina Gervasini

This study investigates the effects of HDAC inhibitors in RSTS models, showing molecular rescue and microbiota changes, and highlights the role of gut microbiota in chromatinopathy.

bioRxiv · Mar 31, 2020 · PreprintGenetics

Characterization of Intellectual disability and Autism comorbidity through gene panel sequencing

Maria Cristina Aspromonte, Mariagrazia Bellini, Alessandra Gasparini, Marco Carraro, Elisa Bettella, Roberta Polli, Federica Cesca, Stefania Bigoni, Stefania Boni, Ombretta Carlet, Susanna Negrin, Isabella Mammi, Donatella Milani, Angela Peron, Stefano Sartori, , Emanuela Leonardi

The paper develops a low-cost NGS gene panel for diagnosing intellectual disability and autism spectrum disorder, achieving a 27% diagnostic yield in 150 patients.

Human Mutation · Jun 18, 2019Peer-reviewedGenetics