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Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications

artículo científico publicado en 2020

Application of Precision Medicine in Neurodegenerative Diseases

artículo científico publicado en 2018

Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations

scientific article published on 04 June 2019

Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in in a Family With FSHD

artículo científico publicado en 2018

Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era

scientific article published on 25 March 2019

Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis

scientific article published on 01 October 2019

Interpreting Mixture Profiles: Comparison between Precision ID GlobalFiler™ NGS STR Panel v2 and Traditional Methods

artículo científico publicado en 2020

Investigation of Genetic Variations of <i>IL6</i> and <i>IL6R</i> as Potential Prognostic and Pharmacogenetics Biomarkers: Implications for COVID-19 and Neuroinflammatory Disorders

artículo científico publicado en 2020

Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report

artículo científico publicado en 2019

P63 in health and cancer

artículo científico

RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects

scientific article published on 15 April 2020

The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of and ⬇️

artículo científico

Towards the application of precision medicine in Age-Related Macular Degeneration

artículo científico publicado en 2017

Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants.

artículo científico publicado en 2017

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