L. Felicetti

University of Bologna — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

25h-index2.1kcitations68works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(17), Hemoglobinopathies and Related Disorders(14), RNA and protein synthesis mechanisms(10), Cardiomyopathy and Myosin Studies(8), DNA and Nucleic Acid Chemistry(7)

Publications68 total

Glycogenic acanthosis presenting as leukoplakia on the tongue
BMJ Case Reports·2010· 13 citedOpen Access
Predictive Role of p53 Protein as a Single Marker or Associated to Ki67 Antigen in Oral Carcinogenesis
The Open Dentistry Journal·2008· 19 citedOpen Access
P148 Static cytometry and classic G-banding cytogenetic procedures are both effective In detecting genetic alterations in oral pre-neoplastic lesions
Oral Oncology Supplement·2007
The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure
BMC Medical Genetics·2007· 28 citedOpen Access
Static cytometry and classic G-banding cytogenetic are both effective in detecting genetic alterations in oral pre-neoplastic lesions
Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna)·2007
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy
Annals of Neurology·2005· 135 cited
Pulse Field Gel Electrophoresis for the Detection of Facioscapulohumeral Muscular Dystrophy Gene Rearrangements
Neurogenetics·2003· 3 cited
Changes in motor cortex excitability in facioscapulohumeral muscular dystrophy
Neuromuscular Disorders·2003· 30 cited
Differential Segregation of β<sup>+</sup>IVS‐I‐110 (G→A),<sup>A</sup>γ − 117 (G→A), and<sup>G</sup>γ − 158 (C→T) Mutations in Members of an Albanian Family
Hemoglobin·2003
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype
Annals of Neurology·1999· 297 cited
Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
Neuromuscular Disorders·1999· 27 cited
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies
1999
Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy
The American Journal of Human Genetics·1998· 58 citedOpen Access
The impact of the molecular data on clinical practice in facio-scapulohumeral muscular dystrophy (FSHD)
Neuromuscular Disorders·1997
Mechanism of the 4q35 rearrangement in facio-scapulo-humeral muscular dystrophy (FSHD): sequence homology of 4qter and 10qter loci favors the instability of subtelomeric KpnI repeats
Neuromuscular Disorders·1997
Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).
Journal of Medical Genetics·1996· 142 citedOpen Access
Asymptomatic dystrophinopathies: analysis of DNA, mRNA and protein
Neuromuscular Disorders·1996
Molecular mechanism of DNA rearrangements implicated in FSH dystrophy and applications to the diagnosis of the disease
Neuromuscular Disorders·1996
Sickle cell anemia and β‐gene cluster haplotypes in Cuba
American Journal of Hematology·1995· 25 cited
Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter
European Journal of Human Genetics·1995· 102 cited
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Frequent Co-authors

B. Colombo(13), Giancarlo Deidda(12), Andrea Novelletto(10), S. Cacurri(7), Enzo Ricci(6), Giuliana Galluzzi(6), N. Piazzo(6), Corrado Baglioni(5), Anna Di Rienzo(5), Luca Colantoni(4), Eliana Vigneti(4), L. Terrenato(4), Barbara Merico(3), Serenella Servidei(3), P. Tonali(3), Youssef Al‐Tonbary(3), Salvatore Metafora(3), Roberto Gambino(3), Glauco P. Tocchini‐Valentini(3), Paola Amaldi(3)