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EJIFCC|November 28, 2018
Next Generation Sequencing: From Research Area to Clinical PracticeChiara Di Resta, Maurizio FerrariClinical Biochemistry|April 25, 2019
New molecular approaches to Alzheimer's diseaseChiara Di Resta, Maurizio FerrariEJIFCC|May 17, 2018
Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunitiesChiara Di Resta, Silvia Galbiati, Paola Carrera, et al.Neural Regeneration Research|September 28, 2020
Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencingChiara Di Resta, Giovanni Battista Pipitone, Paola Carrera, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|June 11, 2014
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratoriesChiara Di Resta, Martina Manzoni, Massimo Zoni Berisso, et al.Human Molecular Genetics|July 30, 2015
High-throughput genetic characterization of a cohort of Brugada syndrome patientsChiara Di Resta, Alessandro Pietrelli, Simone Sala, et al.Advances in Experimental Medicine and Biology|June 17, 2010
Introduction to ion channelsChiara Di Resta, Andrea BecchettiClinica Chimica Acta; International Journal of Clinical Chemistry|January 13, 2015
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot studyPaola Carrera, Chiara Di Resta, Chiara Volonteri, et al.Biomolecules|October 28, 2023
Advance in Genomics of Rare Genetic DiseasesElena Sommariva, Milena Bellin, Chiara Di RestaPageof 22