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We investigate the role of genetics in rare diseases, with a particular focus on neurodevelopmental and psychiatric disorders.

We are a group of physicians, biologists and biotechnologists, putting our knowledge together and acting at the meeting point between research and clinical care. 

Our research lines

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NEURODEVELOPMENTAL DISORDERS

Identification and functional characterization of novel disease-related genes through Whole Exome Sequencing.

A list of our last publications.
Click on the title to directly open Pubmed link.

2022, Nat Gen, doi: 10.1038/s41588-022-01104-0.

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Full Professor

Principal Investigator

ALFREDO BRUSCO, PHD

©2020 di Medical Genetics and Rare Diseases.
Università degli Studi di Torino | Via Verdi, 8 - 10124 Torino | P.I. 02099550010 | C.F. 80088230018

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