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M. Serpente · SciRah

Researcher profile · Semantic Scholar

M. Serpente

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M. Serpente — researcher profile on SciRah

h-index: 34
Works: 139
Citations: 5,867

Most-cited papers

New insights into the genetic etiology of Alzheimer’s disease and related dementias
C. Bellenguez, F. Küçükali, I. Jansen, L. Kleineidam +496 more
2022Nature Genetics1,984 citations Open access
Semantic Scholar
Frontotemporal dementia and its subtypes: a genome-wide association study
R. Ferrari, D. Hernandez, M. Nalls, J. Rohrer +154 more
2014Lancet Neurology350 citations Open access
Semantic Scholar
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I. de Rojas, S. Moreno-Grau, N. Tesi, B. Grenier-Boley +496 more
2021Nature Communications295 citations Open access
Semantic Scholar
Circulating miRNAs as Potential Biomarkers in Alzheimer's Disease
D. Galimberti, C. Villa, C. Fenoglio, M. Serpente +5 more
2014Journal of Alzheimer's Disease205 citations
Semantic Scholar
The Role of Glymphatic System in Alzheimer’s and Parkinson’s Disease Pathogenesis
F. Buccellato, Marianna D’Anca, M. Serpente, A. Arighi +1 more
2022Biomedicines163 citations Open access
Semantic Scholar
Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases
Marianna D’Anca, C. Fenoglio, M. Serpente, B. Arosio +3 more
2019Frontiers in Aging Neuroscience144 citations Open access
Semantic Scholar
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.
D. Galimberti, C. Fenoglio, M. Serpente, C. Villa +38 more
2013Biological Psychiatry122 citations Open access
Semantic Scholar
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis
C. Fenoglio, E. Ridolfi, C. Cantoni, M. D. De Riz +12 more
2013Multiple Sclerosis117 citations
Semantic Scholar
MiRNA Profiling in Plasma Neural-Derived Small Extracellular Vesicles from Patients with Alzheimer’s Disease
M. Serpente, C. Fenoglio, Marianna D’Anca, M. Arcaro +12 more
2020Cells112 citations Open access
Semantic Scholar
Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis
E. Ridolfi, C. Fenoglio, C. Cantoni, A. Calvi +9 more
2013International Journal of Molecular Sciences89 citations Open access
Semantic Scholar
Innate Immune System and Inflammation in Alzheimer's Disease: From Pathogenesis to Treatment
M. Serpente, R. Bonsi, E. Scarpini, D. Galimberti
2014Neuroimmunomodulation84 citations Open access
Semantic Scholar
Role of Genetics and Epigenetics in the Pathogenesis of Alzheimer’s Disease and Frontotemporal Dementia
C. Fenoglio, E. Scarpini, M. Serpente, D. Galimberti
2018Journal of Alzheimer's Disease71 citations Open access
Semantic Scholar
Expression of the Transcription Factor Sp1 and its Regulatory hsa-miR-29b in Peripheral Blood Mononuclear Cells from Patients with Alzheimer's Disease
C. Villa, E. Ridolfi, C. Fenoglio, L. Ghezzi +14 more
2013Journal of Alzheimer's Disease70 citations
Semantic Scholar
The C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia
D. Galimberti, A. Reif, B. Dell'Osso, S. Kittel-Schneider +11 more
201466 citations
Semantic Scholar
Inflammatory molecules in Frontotemporal Dementia: cerebrospinal fluid signature of progranulin mutation carriers.
D. Galimberti, R. Bonsi, C. Fenoglio, M. Serpente +8 more
2015Brain, behavior, and immunity62 citations
Semantic Scholar
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study
D. Galimberti, G. Fumagalli, C. Fenoglio, Sara M. G. Cioffi +14 more
2018Neurobiology of Aging59 citations Open access
Semantic Scholar
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
R. Ferrari, M. Grassi, E. Salvi, B. Borroni +35 more
2015Neurobiology of Aging57 citations Open access
Semantic Scholar
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation
A. Arighi, M. Arcaro, G. Fumagalli, T. Carandini +9 more
2022Alzheimer's Research & Therapy51 citations Open access
Semantic Scholar
Altered Extracellular Vesicle miRNA Profile in Prodromal Alzheimer’s Disease
C. Visconte, C. Fenoglio, M. Serpente, P. Muti +10 more
2023International Journal of Molecular Sciences50 citations Open access
Semantic Scholar
LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients.
C. Fenoglio, E. Oldoni, M. Serpente, M. D. De Riz +12 more
2018Journal of Neuroimmunology48 citations Open access
Semantic Scholar
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.
S. Lattante, I. Le Ber, D. Galimberti, M. Serpente +7 more
2014Neurobiology of Aging43 citations
Semantic Scholar
Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis: correlation with CSF β-amyloid levels and brain volumes
A. Pietroboni, T. Carandini, A. Colombi, M. Mercurio +13 more
2018European Journal of Nuclear Medicine and Molecular Imaging40 citations Open access
Semantic Scholar
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
E. Taskesen, A. Mishra, S. van der Sluis, R. Ferrari +158 more
2017Scientific Reports40 citations Open access
Semantic Scholar
Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels in patients with multiple sclerosis.
C. Fenoglio, M. D. De Riz, A. Pietroboni, A. Calvi +6 more
2016Journal of Neuroimmunology40 citations
Semantic Scholar
Cerebrospinal Fluid Level of Aquaporin4: A New Window on Glymphatic System Involvement in Neurodegenerative Disease?
A. Arighi, A. Di Cristofori, C. Fenoglio, S. Borsa +14 more
2019Journal of Alzheimer's Disease36 citations
Semantic Scholar
C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder
D. Galimberti, A. Reif, B. Dell'Osso, C. Palazzo +9 more
2014Bipolar Disorders36 citations
Semantic Scholar
Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation
L. Ghezzi, T. Carandini, A. Arighi, C. Fenoglio +13 more
2017Neurology34 citations
Semantic Scholar
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect
C. Visconte, M. Golia, C. Fenoglio, M. Serpente +12 more
2023GeroScience33 citations Open access
Semantic Scholar
Incomplete Penetrance of the C9ORF72 Hexanucleotide Repeat Expansions: Frequency in a Cohort of Geriatric Non-Demented Subjects
D. Galimberti, B. Arosio, C. Fenoglio, M. Serpente +6 more
2014Journal of Alzheimer's Disease33 citations
Semantic Scholar
A “glympse” into neurodegeneration: Diffusion MRI and cerebrospinal fluid aquaporin‐4 for the assessment of glymphatic system in Alzheimer's disease and other dementias
L. Sacchi, Federico D'Agata, C. Campisi, M. Arcaro +15 more
2024Human Brain Mapping32 citations Open access
Semantic Scholar
miR-150-5p and let-7b-5p in Blood Myeloid Extracellular Vesicles Track Cognitive Symptoms in Patients with Multiple Sclerosis
Federica Scaroni, C. Visconte, M. Serpente, M. Golia +14 more
2022Cells26 citations Open access
Semantic Scholar
Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation
Sara M. G. Cioffi, D. Galimberti, F. Barocco, M. Spallazzi +6 more
2016Journal of Alzheimer's Disease25 citations
Semantic Scholar
author-version of: Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease
Irene Rosas, C. Martínez, J. Clarimón, A. Lleó +31 more
202323 citations Open access
Semantic Scholar
Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder.
D. Galimberti, C. Prunas, R. Paoli, B. Dell'Osso +8 more
2014Bipolar Disorders21 citations
Semantic Scholar
A systematic review of progranulin concentrations in biofluids in over 7,000 people—assessing the pathogenicity of GRN mutations and other influencing factors
Imogen J. Swift, R. Rademakers, N. Finch, Matt Baker +93 more
2024Alzheimer's Research & Therapy20 citations Open access
Semantic Scholar
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Claudia Manzoni, D. Kia, Raffaele Ferrari, G. Leonenko +133 more
2024American Journal of Human Genetics19 citations Open access
Semantic Scholar
A Novel Automated Chemiluminescence Method for Detecting Cerebrospinal Fluid Amyloid-Beta 1-42 and 1-40, Total Tau and Phosphorylated-Tau: Implications for Improving Diagnostic Performance in Alzheimer’s Disease
M. Arcaro, C. Fenoglio, M. Serpente, A. Arighi +9 more
2022Biomedicines19 citations Open access
Semantic Scholar
Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway?
S. Gazzina, E. Premi, I. Zanella, G. Biasiotto +8 more
2015Neurodegenerative Diseases19 citations
Semantic Scholar
Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism
M. Carecchio, D. Galimberti, C. Fenoglio, M. Serpente +4 more
2013Journal of Alzheimer's Disease19 citations Open access
Semantic Scholar
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population
E. Oldoni, G. Fumagalli, M. Serpente, C. Fenoglio +24 more
2016Journal of Alzheimer's Disease18 citations Open access
Semantic Scholar
Novel Evidence of Phenotypical Variability in the Hexanucleotide Repeat Expansion in Chromosome 9
C. Cerami, A. Marcone, D. Galimberti, M. Zamboni +4 more
2013Journal of Alzheimer's Disease17 citations
Semantic Scholar
Profiling of Ubiquitination Pathway Genes in Peripheral Cells from Patients with Frontotemporal Dementia due to C9ORF72 and GRN Mutations
M. Serpente, C. Fenoglio, S. Cioffi, R. Bonsi +5 more
2015International Journal of Molecular Sciences16 citations Open access
Semantic Scholar
GRN Thr272fs Clinical Heterogeneity: A Case with Atypical Late Onset Presenting with a Dementia with Lewy Bodies Phenotype
B. Arosio, C. Abbate, D. Galimberti, P. Rossi +10 more
2013Journal of Alzheimer's Disease15 citations
Semantic Scholar
Association between enlarged perivascular spaces and cerebrospinal fluid aquaporin-4 and tau levels: report from a memory clinic
L. Sacchi, M. Arcaro, T. Carandini, A. Pietroboni +12 more
2023Frontiers in Aging Neuroscience13 citations Open access
Semantic Scholar
Niemann-Pick Type C 1 (NPC1) and NPC2 Gene Variability in Demented Patients with Evidence of Brain Amyloid Deposition
F. Sorrentino, A. Arighi, M. Serpente, B. Arosio +11 more
2021Journal of Alzheimer's Disease13 citations
Semantic Scholar
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia.
Irene Rosas, C. Martínez, E. Coto, J. Clarimón +34 more
2020Neurobiology of Aging13 citations Open access
Semantic Scholar
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
L. Bonham, Natasha Z. R. Steele, C. Karch, Iris J. Broce +166 more
2019Scientific Reports13 citations Open access
Semantic Scholar
C9ORF72 repeat expansion not detected in patients with multiple sclerosis.
C. Fenoglio, M. D. De Riz, C. Villa, M. Serpente +8 more
2014Neurobiology of Aging12 citations
Semantic Scholar
Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia - A GENFI study.
C. Fenoglio, M. Serpente, M. Arcaro, T. Carandini +37 more
2024Brain, behavior, and immunity11 citations Open access
Semantic Scholar
The Novel GRN g.1159_1160delTG Mutation is Associated with Behavioral Variant Frontotemporal Dementia
A. Calvi, Sara M. G. Cioffi, P. Caffarra, C. Fenoglio +7 more
2015Journal of Alzheimer's Disease11 citations Open access
Semantic Scholar

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