Verdiana Pullano

6PUBLICATIONS
55CO-AUTHORS
NeurogeneticsHaematological tumoursBiomedical instrumentationGene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapy
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Publications (6)

|Jul 08, 2026
The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

|May 25, 2026
Utility of combined CD39/CD73/CD38 expression for the detection of malignant T cells in Sézary syndrome.

|Feb 09, 2026
MK4 Repositioning for IAHSP: Overcoming In Vivo Data Gaps through In Silico Refinement and In Vitro Validation.

Matteo Rossi Sebastiano, Antonio Vicidomini, Serena Francisco

|Oct 29, 2025
Expanding Clinical and Genetic Landscape of SATB2-Associated Syndrome.

Verdiana Pullano, Federico Rondot, Ilaria Carelli

|Feb 13, 2024
Identification of the DNA methylation signature of Mowat-Wilson syndrome.

Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney

|Mar 06, 2023
Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.

Chiara Giovenino, Slavica Trajkova, Lisa Pavinato

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Frequent Collaborators

4 joint publications

Alfredo Brusco

3 joint publications

Marco Tartaglia

3 joint publications

Lisa Pavinato

3 joint publications

Diana Carli