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Pharmacogenomics|November 12, 2015
Pharmacogenomics considerations in the control of hypertensionSara Lupoli, Erika Salvi, Matteo Barcella, et al.BMC Bioinformatics|December 15, 2005
Modelling the interaction of steroid receptors with endocrine disrupting chemicalsPasqualina D'Ursi, Erika Salvi, Paola Fossa, et al.BMC Bioinformatics|April 18, 2008
SNPLims: a data management system for genome wide association studiesAlessandro Orro, Guia Guffanti, Erika Salvi, et al.Molecular Therapy. Methods & Clinical Development|October 9, 2023
Archival skin biopsy specimens as a tool for miRNA-based diagnosis: Technical and post-analytical considerationsMirna Andelic, Margherita Marchi, Stefania Marcuzzo, et al.Brain : a Journal of Neurology|October 31, 2019
Diagnostic criteria for small fibre neuropathy in clinical practice and researchGrazia Devigili, Sara Rinaldo, Raffaella Lombardi, et al.Pain|November 20, 2021
Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9AMargherita Marchi, Ilaria D'Amato, Mirna Andelic, et al.Gene|May 5, 2025
Pharmacogenetic pilot study of CYP2D6 and CYP1A2 genes in Italian patients with non-dystrophic myotonia and myotonic dystrophy treated with mexiletineRaffaella Brugnoni, Erika Salvi, Elisa Moresco, et al.Studies in Health Technology and Informatics|September 7, 2011
A standard based approach for biomedical knowledge representationAriel Farkash, Hani Neuvirth, Yaara Goldschmidt, et al.Journal of the Peripheral Nervous System : JPNS|July 7, 2018
A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusiaMargherita Marchi, Vincenzo Provitera, Maria Nolano, et al.Clinical Journal of the American Society of Nephrology : CJASN|September 21, 2018
Claudin-14 Gene Polymorphisms and Urine Calcium ExcretionTeresa Arcidiacono, Marco Simonini, Chiara Lanzani, et al.Pageof 10