Ilaria Catusi

6PUBLICATIONS
22CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMedical infection agents (incl. prions)Infant and child health
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Publications (6)

|May 28, 2022
12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature.

Maria Paola Recalcati, Ilaria Catusi, Maria Garzo

|Mar 25, 2022
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region.

Serena Redaelli, Donatella Conconi, Elena Sala

|Jun 02, 2021
Histone Deacetylase Inhibitors Ameliorate Morphological Defects and Hypoexcitability of iPSC-Neurons from Rubinstein-Taybi Patients.

Valentina Alari, Paolo Scalmani, Paola Francesca Ajmone

|Apr 30, 2021
8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature.

Ilaria Catusi, Maria Garzo, Anna Paola Capra

|Nov 14, 2020
Recombinant Chromosome 7 Driven by Maternal Chromosome 7 Pericentric Inversion in a Girl with Features of Silver-Russell Syndrome.

Ilaria Catusi, Maria Teresa Bonati, Ester Mainini

|Dec 19, 2019
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate.

Ilaria Catusi, Maria Paola Recalcati, Ilaria Bestetti

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Frequent Collaborators

4 joint publications

Maria Paola Recalcati

3 joint publications

Lidia Larizza

2 joint publications

Silvia Russo

2 joint publications

Anna Paola Capra