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Elena Piccoli

Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study
2011 · Roberta Ghidoni, Elena Stoppani, et al. · Neurodegenerative Diseases · 96
C9ORF72 Hexanucleotide Repeat Number in Frontotemporal Lobar Degeneration: A Genotype-Phenotype Correlation Study
2013 · Luisa Benussi, Giacomina Rossi, et al. · Journal of Alzheimer s Disease · 55
Mutations in MAPT Gene Cause Chromosome Instability and Introduce Copy Number Variations Widely in the Genome
2013 · Giacomina Rossi, Donatella Conconi, et al. · Journal of Alzheimer s Disease · 50
New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterization
2011 · Giacomina Rossi, Antonio Bastone, et al. · Neurobiology of Aging · 46
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features
2013 · Giacomina Rossi, Antonio Bastone, et al. · Neurobiology of Aging · 41
Infectivity in Skeletal Muscle of Cattle with Atypical Bovine Spongiform Encephalopathy
2012 · Silvia Suardi, Chiara Vimercati, et al. · PLoS ONE · 30
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Mutations in MAPT give rise to aneuploidy in animal models of tauopathy
2013 · Giacomina Rossi, Donatella Conconi, et al. · Neurogenetics · 23
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Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks ( TAR DNA ‐binding protein 43 inclusions) in missense progranulin mutation C ys139 A rg
2016 · Veronica Redaelli, Giacomina Rossi, et al. · Brain Pathology · 22
Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features
2015 · Celeste M. Karch, Lubov Ezerskiy, et al. · Neurobiology of Aging · 21
A Novel Progranulin Mutation Causing Frontotemporal Lobar Degeneration with Heterogeneous Phenotypic Expression
2011 · Giacomina Rossi, Elena Piccoli, et al. · Journal of Alzheimer s Disease · 17
Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing
2016 · Elena Piccoli, Giacomina Rossi, et al. · Neurobiology of Aging · 15
Variability of the Clinical Phenotype in an Italian Family with Dementia Associated with an Intronic Deletion in the GRN Gene
2011 · Gabriella Marcon, Giacomina Rossi, et al. · Journal of Alzheimer s Disease · 11
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration
2011 · Cinzia Coppola, Giacomina Rossi, et al. · Neurological Sciences · 11
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations
2016 · Cinzia Coppola, Dario Saracino, et al. · Neurobiology of Aging · 8
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?
2015 · Cinzia Coppola, Dario Saracino, et al. · Journal of the Neurological Sciences · 2
Erratum
2012 · Rajat Sandhir, Aditi Sood, et al. · Neurodegenerative Diseases
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Front & Back Matter
2012 · Rajat Sandhir, Aditi Sood, et al. · Neurodegenerative Diseases
P1‐160: Clinical phenotypic variability in an Italian family bearing the IVS6+5_8delGTGA mutation in PGRN gene
2011 · Gabriella Marcon, Fabrizio Tagliavini, et al. · Alzheimer s & Dementia
O1‐07‐07: Tau mutations lead to chromosome aberrations: A new role of tau in the pathogenesis of genetic tauopathies?
2010 · Fabrizio Tagliavini, Elena Piccoli, et al. · Alzheimer s & Dementia
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Works count: 19
Citation count: 448
H-index: 11
I10-index: 13
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