Patrizia Zavattari

9PUBLICATIONS
14CO-AUTHORS
NeonatologyNeurogeneticsGene mappingGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Apr 09, 2026
Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.

Amber S E van Oirsouw, Tzung-Chien Hsieh, Martijn Koetsier

|Mar 28, 2026
So Fragile, So Human: Noncoding DNA Regions Orchestrating Gene Expression Involved in Neurodevelopmental Disorders and in Human Brain Evolution.

Carolina Marenco, Giorgia Pozzolini, Martina Casciaro

|Mar 23, 2024
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.

Marta Viggiano, Fabiola Ceroni, Paola Visconti

|Nov 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.

Elena Bacchelli, Marta Viggiano, Fabiola Ceroni

|Jan 21, 2021
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.

Cinzia Cameli, Marta Viggiano, Magali J Rochat

|Oct 21, 2020
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old.

Magali Jane Rochat, Giacomo Distefano, Monica Maffei

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Frequent Collaborators

3 joint publications

Elena Maestrini

2 joint publications

Cinzia Cameli

1 joint publications

Annio Posar

1 joint publications

Marta Viggiano