Francesca Torricelli

Author

Azienda Ospedaliero-Universitaria Careggi

Also Known As

F Torricelli, F. TORRICELLI, F. Torricelli, FRANCESCA TORRICELLI, Francesca Torricelli, Giancarlo Isaia, Maria Pia Micieli, Torricelli, F.

131

Publications

Citations

H-Index

164

Concepts

All Affiliations

Azienda Ospedaliero-Universitaria Careggi University of Florence Mayo Clinic University of Siena Vita-Salute San Raffaele University

About

Francesca Torricelli is an author at Azienda Ospedaliero-Universitaria Careggi specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	46	3.2K
2	Health Sciences	5	5	233
3	Arts	3	3	152
4	Engineering	2	2	28
5	Law	1	1	25

Francesca Torricelli

Publications

4.8K

Citations

H-Index

Page 1

	Year	Citations
Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy Iacopo Olivotto, Francesca Girolami, Michael J. Ackerman, Mayo Clinic Proceedings Cardiac MuscleCardiomyopathyHeart FailureStructural Heart DiseaseGenetics	2008	325
Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy Iacopo Olivotto, Francesca Girolami, Michael J. Ackerman, Mayo Clinic Proceedings Cardiac MuscleCardiomyopathyHeart FailureStructural Heart DiseaseGenetics	2008	296
Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations Francesca Girolami, Carolyn Y. Ho, Christopher Semsarian, Journal of the American College of Cardiology Cardiac MuscleCardiomyopathyGeneticsPathologyClinical Features	2010	294
Relevance of Coronary Microvascular Flow Impairment to Long-Term Remodeling and Systolic Dysfunction in Hypertrophic Cardiomyopathy Iacopo Olivotto, Franco Cecchi, Roberto Gistri, Journal of the American College of Cardiology CardiomyopathyCardiovascular DiseaseLong-term RemodelingPhysiologySystolic Dysfunction	2006	238
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript Matteo Benelli, Chiara Pescucci, Giuseppina Marseglia, Bioinformatics	2012	225
Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations Iacopo Olivotto, Francesca Girolami, Roberto Sciagrà, Journal of the American College of Cardiology Cardiac MuscleCardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular Disease	2011	168
Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations Raffaele Coppini, Carolyn Y. Ho, Euan A. Ashley, Journal of the American College of Cardiology	2014	163
Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications Rosaria A.M.S. Casano, David Johnson, Yelena Bykhovskaya, American Journal of Otolaryngology AllergyMedicineInherited Metabolic DiseaseGenetic EpidemiologyGenetic Heterogeneity	1999	145
<i>De novo</i> balanced chromosome rearrangements in prenatal diagnosis Daniela Giardino, Cecilia Corti, Lucia Ballarati, Prenatal Diagnosis	2009	139
Th2‐oriented profile of male offspring T cells present in women with systemic sclerosis and reactive with maternal major histocompatibility complex antigens Cristina Scaletti, Alessandra Vultaggio, Stefania Bonifacio, Arthritis & Rheumatism	2002	132

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