Alessia Mauri

Molecular genetics of GLUT1DS Italian pediatric cohort: 10 novel related-disease variants and structural analysis

C. Cereda, F. Coscia, S. Benedetti, 2022, bioRxiv.

Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology

G. Scuvera, M. Bedeschi, D. Milani, 2022, Genes & Genomics.

Investigating the role of social behavior in financial markets through agent-based simulation

Andrea Tettamanzi, Alessia Mauri, A. Tettamanzi, 2012, AAMAS.

Cognitive-Agent-Based Modeling of a Financial Market

Célia da Costa Pereira, Andrea Tettamanzi, Alessia Mauri, 2009, 2009 IEEE/WIC/ACM International Joint Conference on Web Intelligence and Intelligent Agent Technology.

Redox Imbalance in Neurological Disorders in Adults and Children

G. Zuccotti, S. Carelli, C. Berardo, 2023, Antioxidants.

Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study

V. Calcaterra, G. Zuccotti, S. Carelli, 2023, Cells.

Menkes disease complicated by concurrent ACY1 deficiency: A case report

P. Veggiotti, E. Cattaneo, L. Antonelli, 2023, Frontiers in Genetics.

Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis

F. Coscia, S. Benedetti, P. Veggiotti, 2022, International journal of molecular sciences.

Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome.

S. Bertoli, R. De Amicis, C. Doneda, 2024, Pediatric neurology.

Role of epigenetics and alterations in RNA metabolism in leukodystrophies

S. Carelli, Federica Rey, Alessia Mauri, 2024, Wiley interdisciplinary reviews. RNA.