| Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients S Gambardella, F Rinaldi, SM Lepore, A Viola, E Loro, C Angelini, ... Journal of translational medicine 8, 1-9, 2010 | 141 | 2010 |
| Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells E Loro, F Rinaldi, A Malena, E Masiero, G Novelli, C Angelini, V Romeo, ... Cell Death & Differentiation 17 (8), 1315-1324, 2010 | 100 | 2010 |
| Stem cells for skeletal muscle regeneration: therapeutic potential and roadblocks F Rinaldi, RCR Perlingeiro Translational Research 163 (4), 409-417, 2014 | 66 | 2014 |
| Novel mutations of TCOF1 gene in European patients with treacher Collins syndrome C Conte, MR D'Apice, F Rinaldi, S Gambardella, F Sangiuolo, G Novelli BMC Medical Genetics 12, 1-6, 2011 | 60 | 2011 |
| Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2 A Botta, L Vallo, F Rinaldi, E Bonifazi, F Amati, M Biancolella, ... Gene expression 13 (6), 339, 2007 | 60 | 2007 |
| The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients A Botta, F Rinaldi, C Catalli, L Vergani, E Bonifazi, V Romeo, E Loro, ... Journal of medical genetics 45 (10), 639-646, 2008 | 58 | 2008 |
| Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2 R Cardani, M Giagnacovo, A Botta, F Rinaldi, A Morgante, B Udd, ... Journal of neurology 259, 2090-2099, 2012 | 52 | 2012 |
| Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes S Selvaraj, R Mondragon-Gonzalez, B Xu, A Magli, H Kim, J Lainé, J Kiley, ... Elife 8, e47970, 2019 | 50 | 2019 |
| Functional dissection of Pax3 in paraxial mesoderm development and myogenesis A Magli, E Schnettler, F Rinaldi, P Bremer, RCR Perlingeiro Stem Cells 31 (1), 59-70, 2013 | 40 | 2013 |
| Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2 R Cardani, S Baldassa, A Botta, F Rinaldi, G Novelli, E Mancinelli, ... Neuromuscular Disorders 19 (5), 335-343, 2009 | 36 | 2009 |
| Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues F Rinaldi, C Terracciano, V Pisani, R Massa, E Loro, L Vergani, ... Neurobiology of disease 45 (1), 264-271, 2012 | 28 | 2012 |
| Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) C Catalli, A Morgante, R Iraci, F Rinaldi, A Botta, G Novelli The Journal of Molecular Diagnostics 12 (5), 601-606, 2010 | 27 | 2010 |
| Screening of EDA1 Gene in X-Linked Anhidrotic Ectodermal Dysplasia Using DHPLC: Identification of 14 Novel Mutations in Italian Patients C Conte, S Gambardella, C Bulli, F Rinaldi, D Di Marino, M Falconi, ... Genetic Testing 12 (3), 437-442, 2008 | 24 | 2008 |
| Pax3-induced expansion enables the genetic correction of dystrophic satellite cells A Filareto, F Rinaldi, RW Arpke, R Darabi, JJ Belanto, EA Toso, AZ Miller, ... Skeletal Muscle 5, 1-11, 2015 | 20 | 2015 |
| Treatment with rGDF11 does not improve the dystrophic muscle pathology of mdx mice F Rinaldi, Y Zhang, R Mondragon-Gonzalez, J Harvey, RCR Perlingeiro Skeletal muscle 6, 1-8, 2016 | 18 | 2016 |
| An efficient method for cloning gastrointestinal stem cells from patients via endoscopic biopsies M Duleba, Y Qi, R Mahalingam, AA Liew, R Neupane, K Flynn, F Rinaldi, ... Gastroenterology 156 (1), 20-23, 2019 | 7 | 2019 |
| Gene targeting methods and tools R Perlingeiro, M Kyba, F Rinaldi, DF Voytas US Patent 9,850,497, 2017 | 6 | 2017 |
| Activation, Expansion, and In Vivo Regenerative Potential of Pax3-Transduced Satellite Cells: A Potential Cell-Based Therapy for Duchenne Muscular Dystrophy A Filareto, RW Arpke, D Bosnakovski, R Darabi, F Rinaldi, A Miller, ... Molecular Therapy 21, S66-S67, 2013 | 1 | 2013 |
| Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in … F Rinaldi, A Botta, L Vallo, G Contino, A Morgante, R Iraci, C Catalli, ... Acta Myologica 27 (3), 82, 2008 | 1 | 2008 |
| Genome Wide Analysis of PAX7-Induced Myogenesis Identifies CD54 as a Novel Marker for cGMP-Compatible Purification of Human PS Cell-Derived Myogenic Progenitors T Incitti, A Magli, J Kiley, SA Swanson, R Darabi, F Rinaldi, S Selvaraj, ... MOLECULAR THERAPY 25 (5), 195-196, 2017 | | 2017 |
