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- gandreotti@icb.cnr.it
- 081 8675241
Researcher
1990, B.S. Chemistry (with top marks), University of Naples “Federico II”, Italy
1996, Ph.D. Biochemistry, University of Naples “Federico II”, Italy
From 27 December 2001, Researcher at the Institute of Biomolecular Chemistry- National Research Council of Italy
RECENT SCIENTIFIC INTERESTS
1. Monticelli M, Hay Mele B, Benetti E, Fallerini C, Baldassarri M, Furini S, Frullanti E, Mari F, GEN-COVID Multicenter Study, Andreotti G, Cubellis MV, Renieri A. Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women. Genes. 2021; 12(4):596. https://doi.org/10.3390/genes12040596
2. Monticelli M, Liguori L, Allocca M, Andreotti G*, Cubellis MV. β-Glucose-1,6-Bisphosphate Stabilizes Pathological Phophomannomutase2 Mutants In Vitro and Represents a Lead Compound to Develop Pharmacological Chaperones for the Most Common Disorder of Glycosylation, PMM2-CDG. Int. J. Mol. Sci. 2019, 20(17), 4164. https://doi.org/10.3390/ijms20174164
3. Citro V, Cimmaruta C, Monticelli M, Riccio G, Hay Mele B, Cubellis MV, Andreotti G. The Analysis of Variants in the General Population Reveals That PMM2 Is Extremely Tolerant to Missense Mutations and That Diagnosis of PMM2-CDG Can Benefit from the Identification of Modifiers. Int J Mol Sci. 2018 Jul 30;19(8). doi: 10.3390/ijms19082218
4. Citro V, Cammisa M, Liguori L, Cimmaruta C, Lukas J, Cubellis MV, and Andreotti G. The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense Mutations. Int. J. Mol. Sci. 2016, 17(12), 2010; doi:10.3390/ijms17122010
5. Citro V, Peña-Garcia J, den-Haan H, Perez-Sanchez H, Del Prete R, Liguori L, Cimmaruta C, Lukas J, Cubellis MV, Andreotti G. Identification of an Allosteric Binding Site on Human Lysosomal Alpha-Galactosidase Opens the Way to New Pharmacological Chaperones for Fabry Disease. PLOS ONE | DOI:10.1371/journal.pone.0165463 October 27, 2016
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