Paola Prandini
Publications by Year
Research Areas
Muscle Physiology and Disorders, Autism Spectrum Disorder Research, RNA Research and Splicing, Antiplatelet Therapy and Cardiovascular Diseases, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan(2001)596 cited
- → Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance(2007)198 cited
- → A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome(2009)120 cited
- → Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy(2005)101 cited
- → Clinical and Molecular Characterization of Patients With Limb-Girdle Muscular Dystrophy Type 2I(2005)92 cited
- → A molecular signature associated with prolonged survival in glioblastoma patients treated with regorafenib(2020)76 cited
- → Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21(2007)64 cited
- → Integrin α7β1 in Muscular Dystrophy/Myopathy of Unknown Etiology(2002)62 cited
- → Impact of Insulin Receptor Substrate-1 Genotypes on Platelet Reactivity and Cardiovascular Outcomes in Patients With Type 2 Diabetes Mellitus and Coronary Artery Disease(2011)58 cited
- → Clinical and molecular study in congenital muscular dystrophy with partial laminin ?2 (LAMA2) deficiency(2003)52 cited