Author

Sara Bardi

Observed name: S. Bardi

Institution: Ospedale Misericordia - Grosseto

Observed institutions: University of Padua, Azienda Ospedaliero-Universitaria Careggi, Ospedale di Parma, Ospedale Misericordia - Grosseto, University of Florence

ORCID: 0009-0006-0376-5924

Observed ORCID: 0009-0006-0376-5924

OpenAlex ID: A5012642592

Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

2014 · Raffaele Coppini, Carolyn Y. Ho, et al. · Journal of the American College of Cardiology · 183

Novel α-Actinin 2 Variant Associated With Familial Hypertrophic Cardiomyopathy and Juvenile Atrial Arrhythmias: A Massively Parallel Sequencing Study

2014 · Francesca Girolami, Maria Iascone, et al. · Circulation Cardiovascular Genetics · 89

Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center

2018 · Francesco Mazzarotto, Francesca Girolami, et al. · Genetics in Medicine · 75

Impact of Genotype on the Occurrence of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy

2016 · Carolina Bongini, Cecilia Ferrantini, et al. · The American Journal of Cardiology · 35

Diagnostic Performance of Next-Generation Sequencing (NGS) in Indeterminate Thyroid Nodules: A Single Hospital Experience

2025 · Marco Capezzone, Maja Rossi, et al. · International Journal of Molecular Sciences · 8

A novel desmoplakin dominant mutation responsible for Carvajal/Naxos syndrome identified by exome sequencing

2013 · B. Tomberli, A. Fornaro, et al. · European Heart Journal · 3

Identification of a Novel Non-V600E BRAF Mutation in Papillary Thyroid Cancer

2024 · Marco Capezzone, Maja Rossi, et al. · Case Reports in Endocrinology · 2

BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological Settings

2023 · Alessandro Pancrazzi, Francesco Bloise, et al. · Global Medical Genetics · 2

Impact of E163R cTnT Mutation on Cardiac Mechanics and Energetics in a Murine Model

2014 · Benedetta Tosi, Cecilia Ferrantini, et al. · Biophysical Journal

Genetic causes of cardiomyopathies identified by Whole Exome Sequencing

2013 · B. Tomberli, F. Girolami, et al. · European Heart Journal

Rilevanza clinica del test genetico nella cardiomiopatia ipertrofica

2011 · Francesca Girolami, Sara Bardi, et al. · Recenti Progressi in Medicina

Works count: 11

Citation count: 397

H-index: 5

I10-index: 4