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S. Curcio · SciRah

Researcher profile · Semantic Scholar

S. Curcio

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S. Curcio — researcher profile on SciRah

h-index: 18
Works: 34
Citations: 958

Most-cited papers

Mutation analysis of CHCHD10 in different neurodegenerative diseases.
Ming Zhang, Zhengrui Xi, L. Zinman, A. Bruni +20 more
2015Brain : a journal of neurology108 citations Open access
Semantic Scholar
Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia
V. Laganà, Francesco Bruno, Natalia Altomari, Giulia Bruni +15 more
2022Frontiers in Neurology98 citations Open access
Semantic Scholar
Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.
A. Bruni, J. Takahashi‐Fujigasaki, F. Maltecca, J. Foncin +9 more
2004Archives of Neurology89 citations Open access
Semantic Scholar
Heterogeneity within a large kindred with frontotemporal dementia
A. C. Bruni, P. Momeni, L. Bernardi, C. Tomaino +20 more
2007Neurology81 citations
Semantic Scholar
The effects of APOE and tau gene variability on risk of frontotemporal dementia.
L. Bernardi, R. Maletta, C. Tomaino, N. Smirne +13 more
2006Neurobiology of Aging64 citations
Semantic Scholar
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
L. Bernardi, C. Tomaino, M. Anfossi, M. Gallo +11 more
2009Neurobiology of Aging62 citations
Semantic Scholar
A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer’s Disease
Natalia Altomari, Francesco Bruno, V. Laganà, N. Smirne +7 more
2021Journal of Alzheimer's Disease49 citations Open access
Semantic Scholar
Epidemiology and genetics of FTD: a door-to-door survey in Southern Italy
L. Bernardi, F. Frangipane, N. Smirne, R. Colao +24 more
2012Neurobiology of Aging48 citations Open access
Semantic Scholar
Worldwide distribution of PSEN1 Met146Leu mutation
A. Bruni, L. Bernardi, R. Colao, E. Rubino +31 more
2010Neurology42 citations Open access
Semantic Scholar
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
M. E. Conidi, L. Bernardi, G. Puccio, N. Smirne +17 more
2015Neurology32 citations Open access
Semantic Scholar
Role of Niemann-Pick Type C Disease Mutations in Dementia
C. Cupidi, F. Frangipane, M. Gallo, A. Clodomiro +17 more
2016Journal of Alzheimer's Disease29 citations
Semantic Scholar
AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions
L. Bernardi, S. Geracitano, R. Colao, G. Puccio +10 more
2009Journal of Alzheimer's Disease28 citations
Semantic Scholar
Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease
C. Tomaino, L. Bernardi, M. Anfossi, A. Costanzo +15 more
2007Journal of Neurology23 citations
Semantic Scholar
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
M. Gallo, F. Frangipane, C. Cupidi, M. De Bartolo +22 more
2017Neurobiology of Aging21 citations
Semantic Scholar
MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia: Variable Penetrant Mutation or Rare Polymorphism?
M. Anfossi, L. Bernardi, M. Gallo, S. Geracitano +9 more
2011Alzheimer Disease and Associated Disorders20 citations
Semantic Scholar
A large Calabrian kindred segregating frontotemporal dementia
S. Curcio, T. Kawarai, A. Paterson, R. Maletta +7 more
2002Journal of Neurology20 citations
Semantic Scholar
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.
L. Bernardi, C. Cupidi, F. Frangipane, M. Anfossi +12 more
2014Neurobiology of Aging18 citations
Semantic Scholar
A Novel Pathogenic PSEN1 Mutation in a Family with Alzheimer's Disease: Phenotypical and Neuropathological Features
M. Gallo, N. Marcello, S. Curcio, R. Colao +17 more
2011Journal of Alzheimer's Disease18 citations
Semantic Scholar
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia.
M. Anfossi, R. Vuono, R. Maletta, K. Virdee +15 more
2011Neurobiology of Aging18 citations
Semantic Scholar
Role of TOMM40 rs10524523 Polymorphism in Onset of Alzheimer's Disease Caused by the PSEN1 M146L Mutation
L. Bernardi, M. Gallo, M. Anfossi, M. E. Conidi +11 more
2013Journal of Alzheimer's Disease17 citations
Semantic Scholar
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia
M. Gallo, C. Tomaino, G. Puccio, F. Frangipane +10 more
2010Neurological Sciences17 citations
Semantic Scholar
A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family
Francesco Bruno, M. E. Conidi, G. Puccio, F. Frangipane +9 more
2021Frontiers in Genetics16 citations Open access
Semantic Scholar
PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype
L. Bernardi, M. Anfossi, M. Gallo, S. Geracitano +11 more
2011Journal of Alzheimer's Disease10 citations
Semantic Scholar
Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairment
R. Perri, Marco Monaco, L. Fadda, L. Serra +6 more
2015Journal of Neurology8 citations
Semantic Scholar
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia
R. Maletta, N. Smirne, L. Bernardi, M. Anfossi +17 more
2018Journal of Alzheimer's Disease6 citations
Semantic Scholar
Identification of Three Novel LRRK2 Mutations associated with Parkinson's Disease in a Calabrian Population
M. Anfossi, R. Colao, M. Gallo, L. Bernardi +12 more
2013Journal of Alzheimer's Disease6 citations
Semantic Scholar
Genetic variability in ADAM17/TACE is associated with sporadic Alzheimer’s disease risk, neuropsychiatric symptoms and cognitive performance on the Rey Auditory Verbal Learning and Clock Drawing Tests
Francesco Bruno, M. A. Aceto, Ersilia Paparazzo, Domenico Arcuri +22 more
2025PLoS ONE5 citations Open access
Semantic Scholar
Using the Theory of Planned Behavior and Past Behavior to Explain the Intention to Receive a Seasonal Influenza Vaccine among Family Caregivers of People with Dementia
Francesco Bruno, Paolo Abondio, V. Laganà, R. Colao +6 more
2023International Journal of Translational Medicine2 citations Open access
Semantic Scholar
Phenotypic expressions of Alzheimer’s disease: a gender perspective
N. Smirne, P. Notaro, Desirée Addesi, V. Laganà +19 more
20182 citations
Semantic Scholar
P3–193: Genotype–phenotype relationship is lacking in families with PS1–Met146Leu founder mutation
A. C. Bruni, B. Terni, L. Bernardi, C. Tomaino +14 more
20061 citations
Semantic Scholar
Primary progressive crossed aphasia in dextrals: report of three cases
T. Piccoli, S. Realmuto, S. Curcio, C. Cupidi +9 more
20130 citations
Semantic Scholar
P3–404: Presenilins mutations are frequent in early–onset familial frontotemporal dementia
R. Maletta, R. Colao, S. Curcio, F. Frangipane +12 more
20060 citations
Semantic Scholar
P3-401 CHARACTERIZATION OF GAMMA-SECRETASE USING A RECOMBINANT APP C99 SUBSTRATE AND COMPARTIVE ANALYSIS OF GAMMA- ACTIVITY IN MOUSE TISSUES
Michael Ho, Nancy T. Ilaya, D. Hoke, Anthony R. White +14 more
20060 citations
Semantic Scholar
P2–405: Achei efficacy in familial Alzheimer's disease
G. Puccio, R. Colao, F. Frangipane, S. Curcio +5 more
20060 citations
Semantic Scholar

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G. Puccio×31
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R. Colao×30
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M. Mirabelli×25

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M. Anfossi — researcher profile on SciRah

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Raffaele Di Lorenzo×14

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S. Geracitano×13

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