M. Serpente

发表

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Demis A. Kia, O. Andreassen, B. Miller, 2020, Neurology.

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Nick C Fox, Cory C. Funk, D. G. Clark, 2017, Nature Genetics.

MiRNA Profiling in Plasma Neural-Derived Small Extracellular Vesicles from Patients with Alzheimer’s Disease

D. Galimberti, C. Fenoglio, E. Scarpini, 2020, Cells.

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer ' s disease

D. G. Clark, M. Fornage, A. Hofman, 2022 .

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Timothy A. Miller, Jennifer E. Phillips-Cremins, Lilah M. Besser, 2020, Neuron.

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Nick C Fox, Alan J. Thomas, D. Hernandez, 2020, Scientific Reports.

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

D. Mari, S. Sorbi, C. Mariani, 2016, Journal of Alzheimer's disease : JAD.

Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis: correlation with CSF β-amyloid levels and brain volumes

M. Bozzali, D. Galimberti, C. Fenoglio, 2018, European Journal of Nuclear Medicine and Molecular Imaging.

miR-150-5p and let-7b-5p in Blood Myeloid Extracellular Vesicles Track Cognitive Symptoms in Patients with Multiple Sclerosis

D. Galimberti, C. Fenoglio, E. Scarpini, 2022, Cells.

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

C. Broeckhoven, S. Sorbi, V. Álvarez, 2020, Neurobiology of Aging.

Frontotemporal Lobar Degeneration: Genetics and Clinical Phenotypes

D. Galimberti, M. Serpente, 2014 .

A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

N. Bresolin, S. Cappa, D. Galimberti, 2011, Alzheimer's & Dementia.

Profiling of Ubiquitination Pathway Genes in Peripheral Cells from Patients with Frontotemporal Dementia due to C9ORF72 and GRN Mutations

D. Galimberti, C. Fenoglio, E. Scarpini, 2015, International journal of molecular sciences.

Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.

N. Bresolin, D. Galimberti, C. Fenoglio, 2011, Journal of Alzheimer's disease : JAD.

Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions

S. Rivaud-Pechoux, D. Galimberti, C. Fenoglio, 2014, Neurobiology of Aging.

GRN Thr272fs clinical heterogeneity: a case with atypical late onset presenting with a dementia with Lewy bodies phenotype.

D. Mari, D. Galimberti, C. Fenoglio, 2013, Journal of Alzheimer's disease : JAD.

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, M. Bocchetta, J. Rohrer, 2018, Neurobiology of Aging.

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

D. Galimberti, C. Fenoglio, E. Scarpini, 2016, Journal of Alzheimer's disease : JAD.

CCL8/MCP-2 association analysis in patients with Alzheimer’s disease and frontotemporal lobar degeneration

N. Bresolin, S. Cappa, F. Clerici, 2009, Journal of Neurology.

Inflammatory molecules in Frontotemporal Dementia: Cerebrospinal fluid signature of progranulin mutation carriers

D. Galimberti, C. Fenoglio, E. Scarpini, 2015, Brain, Behavior, and Immunity.

Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects.

D. Mari, D. Galimberti, C. Fenoglio, 2014, Journal of Alzheimer's disease : JAD.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation

F. Turkheimer, D. Galimberti, C. Fenoglio, 2022, Alzheimer's Research & Therapy.

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Timothy A. Miller, Sonja W. Scholz, Jennifer E. Phillips-Cremins, 2020, Neuron.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

M. Nalls, A. Ramasamy, P. Pietrini, 2019, Scientific Reports.

Novel evidence of phenotypical variability in the hexanucleotide repeat expansion in chromosome 9.

S. Cappa, D. Galimberti, C. Fenoglio, 2013, Journal of Alzheimer's disease : JAD.

GRN variability contributes to sporadic frontotemporal lobar degeneration.

N. Bresolin, S. Cappa, F. Clerici, 2010, Journal of Alzheimer's disease : JAD.

miRNA Expression Is Increased in Serum from Patients with Semantic Variant Primary Progressive Aphasia

D. Galimberti, C. Fenoglio, M. Serpente, 2022, International journal of molecular sciences.

The C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

D. Galimberti, C. Fenoglio, E. Scarpini, 2014, Neurobiology of Aging.

Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations.

N. Bresolin, D. Galimberti, C. Fenoglio, 2012, Journal of Alzheimer's disease : JAD.

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

A. Singleton, J. Hardy, B. Nacmias, 2016, Journal of Alzheimer's disease : JAD.

The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia.

D. Galimberti, C. Fenoglio, E. Scarpini, 2015, Journal of Alzheimer's disease : JAD.

The Role of Glymphatic System in Alzheimer’s and Parkinson’s Disease Pathogenesis

D. Galimberti, M. Serpente, M. D’Anca, 2022, Biomedicines.

Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation

D. Galimberti, C. Fenoglio, E. Scarpini, 2017, Neurology.

Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset.

D. Galimberti, C. Fenoglio, E. Scarpini, 2019, Journal of Alzheimer's disease : JAD.

Evidence of pre-synaptic dopaminergic deficit in a patient with a novel progranulin mutation presenting with atypical parkinsonism.

D. Galimberti, C. Fenoglio, E. Scarpini, 2013, Journal of Alzheimer's disease : JAD.

Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia

Y. Pijnenburg, S. Mead, J. Veldink, 2022, Acta Neuropathologica Communications.

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

D. Galimberti, C. Fenoglio, E. Scarpini, 2022, Biomedicines.

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

A. Altamura, D. Galimberti, C. Fenoglio, 2014, Bipolar disorders.

C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone

D. Galimberti, C. Fenoglio, E. Scarpini, 2020, Neurobiology of Aging.

CIRCULATING AND INTRATHECAL MIRNAS AS POTENTIAL BIOMARKERS FOR ALZHEIMER'S DISEASE

D. Galimberti, C. Fenoglio, E. Scarpini, 2014, Alzheimer's & Dementia.

Y. Pijnenburg, S. Mead, J. Veldink, 2022, Acta Neuropathologica Communications.

Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway?

D. Galimberti, E. Scarpini, B. Borroni, 2015, Neurodegenerative Diseases.

Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect

Arosio, D. Galimberti, C. Fenoglio, 2023, GeroScience.

Progranulin Gene Variability and Plasma Levels in Bipolar Disorder and Schizophrenia

N. Bresolin, A. Altamura, D. Galimberti, 2012, PloS one.

Role of Genetics and Epigenetics in the Pathogenesis of Alzheimer’s Disease and Frontotemporal Dementia

D. Galimberti, C. Fenoglio, E. Scarpini, 2018, Journal of Alzheimer's disease : JAD.

MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers

V. Martinelli, G. Comi, D. Galimberti, 2012, Neuroscience Letters.

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

N. Bresolin, D. Galimberti, C. Fenoglio, 2011, Neuroscience Letters.

Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort

G. Comi, V. Martinelli, G. Comi, 2010, European journal of neurology.

Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

Nick C Fox, Alan J. Thomas, D. Hernandez, 2021, Biological Psychiatry.

Circulating Non-Coding RNA Levels Are Altered in Autosomal Dominant Frontotemporal Dementia

D. Galimberti, C. Fenoglio, E. Scarpini, 2022, International journal of molecular sciences.

Autosomal Dominant Frontotemporal Lobar Degeneration: From Genotype to Phenotype

D. Galimberti, M. Serpente, 2018 .

across RNA cell death gene networks is implicated in the semantic variant of primary progressive aphasia.

L. Ferrucci, A. Ramasamy, E. Haan, 2019 .

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

D. Hernandez, M. Nalls, L. Ferrucci, 2017, bioRxiv.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

A. Goris, D. Galimberti, C. Fenoglio, 2018, Journal of Neuroimmunology.

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

Daniele Pepe, Erika Salvi, Fernando Palluzzi, 2015, Neurobiology of Aging.

Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.

N. Bresolin, S. Cappa, M. Franceschi, 2011, Rejuvenation research.

Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.

N. Bresolin, S. Cappa, M. Franceschi, 2011, Journal of Alzheimer's disease : JAD.

Innate Immune System and Inflammation in Alzheimer's Disease: From Pathogenesis to Treatment

D. Galimberti, E. Scarpini, M. Serpente, 2014, Neuroimmunomodulation.

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

D. Galimberti, C. Fenoglio, E. Scarpini, 2014, Neurobiology of Aging.

BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease.

N. Bresolin, S. Cappa, M. Franceschi, 2011, Journal of Alzheimer's disease : JAD.

Exosome Determinants of Physiological Aging and Age-Related Neurodegenerative Diseases

M. Cesari, D. Galimberti, C. Fenoglio, 2019, Front. Aging Neurosci..

Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficits.

D. Mari, D. Galimberti, C. Fenoglio, 2014, Journal of Alzheimer's disease : JAD.

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

G. Comi, S. Cappa, M. Filippi, 2013, Biological Psychiatry.

GSK3β genetic variability in patients with Multiple Sclerosis

D. Comings, N. Bresolin, D. Galimberti, 2011, Neuroscience Letters.

Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis

N. Bresolin, D. Galimberti, C. Fenoglio, 2013, Multiple sclerosis.

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

N. Bresolin, D. Galimberti, C. Fenoglio, 2009, Journal of Neurology.

Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease.

S. Cappa, M. Franceschi, F. Clerici, 2013, Journal of Alzheimer's disease : JAD.

A Case with Early Onset Alzheimer's Disease, Frontotemporal Hypometabolism, ApoE Genotype ɛ4/ɛ4 and C9ORF72 Intermediate Expansion: A Treviso Dementia (TREDEM) Registry Case Report.

D. Galimberti, C. Fenoglio, M. Gregianin, 2019, Journal of Alzheimer's disease : JAD.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Nature Medicine.

Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer’s disease

N. Bresolin, F. Clerici, C. Mariani, 2011, Journal of Neurology.

Analysis of C9orf72 Intermediate Alleles in a Retrospective Cohort of Neurological Patients: Risk Factors for Alzheimer's Disease?

D. Galimberti, C. Fenoglio, E. Scarpini, 2021, Journal of Alzheimer's disease : JAD.

Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder.

A. Altamura, D. Galimberti, C. Fenoglio, 2014, Bipolar disorders.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Brain : a journal of neurology.

Circulating miRNAs as potential biomarkers in Alzheimer's disease.

D. Galimberti, C. Fenoglio, E. Scarpini, 2014, Journal of Alzheimer's disease : JAD.

Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration.

N. Bresolin, S. Cappa, M. Franceschi, 2012, Journal of Alzheimer's Disease.

Late‐onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation

Y. Pijnenburg, D. Galimberti, C. Fenoglio, 2020, European journal of neurology.

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.

N. Bresolin, A. Goate, K. Mayo, 2009, Journal of Alzheimer's disease : JAD.

Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu‐Hakola Disease

D. Galimberti, C. Fenoglio, L. Piccio, 2019, Cytokine.

author-version of: Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

C. van Broeckhoven, S. Sorbi, V. Álvarez, 2022 .

Cerebrospinal fluid biomarkers in Progranulin mutations carriers.

N. Bresolin, M. Franceschi, D. Galimberti, 2011, Journal of Alzheimer's disease : JAD.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Nick C Fox, D. Hernandez, M. Nalls, 2017, Scientific Reports.

Anti-Cholinergic Derangement of Cortical Metabolism on 18F-FDG PET in a Patient with Frontotemporal Lobar Degeneration Dementia: A Case of the TREDEM Registry.

D. Galimberti, C. Fenoglio, L. Bonanni, 2020, Journal of Alzheimer's disease : JAD.

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

D. Galimberti, C. Fenoglio, E. Scarpini, 2013, International journal of molecular sciences.

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation

B. Ghetti, D. Galimberti, C. Fenoglio, 2017, Movement Disorders.

Theme 08 - Clinical Imaging and Electrophysiology

Jennifer M. Nicholas, M. Freedman, R. Keren, 2022, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.

Niemann-Pick Type C 1 (NPC1) and NPC2 Gene Variability in Demented Patients with Evidence of Brain Amyloid Deposition.

D. Galimberti, C. Fenoglio, E. Scarpini, 2021, Journal of Alzheimer's disease : JAD.

Detection of the SQSTM1 Mutation in a Patient with Early-Onset Hippocampal Amnestic Syndrome.

D. Galimberti, C. Fenoglio, E. Scarpini, 2020, Journal of Alzheimer's disease : JAD.

Profiling of Specific Gene Expression Pathways in Peripheral Cells from Prodromal Alzheimer's Disease Patients.

D. Galimberti, C. Fenoglio, E. Scarpini, 2018, Journal of Alzheimer's disease : JAD.

DCUN1D1 is a risk factor for frontotemporal lobar degeneration

N. Bresolin, S. Cappa, F. Clerici, 2009, European journal of neurology.

Cerebrospinal Fluid Level of Aquaporin4: A New Window on Glymphatic System Involvement in Neurodegenerative Disease?

D. Galimberti, C. Fenoglio, E. Scarpini, 2019, Journal of Alzheimer's disease : JAD.

Candidate gene analysis of semaphorins in patients with Alzheimer’s disease

N. Bresolin, D. Galimberti, C. Fenoglio, 2010, Neurological Sciences.

CXCR4 involvement in neurodegenerative diseases

O. Andreassen, G. Schellenberg, A. Dale, 2017, bioRxiv.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Klotho Gene Expression Is Decreased in Peripheral Blood Mononuclear Cells in Patients with Alzheimer's Disease and Frontotemporal Dementia.

D. Galimberti, C. Fenoglio, E. Scarpini, 2023, Journal of Alzheimer's disease : JAD.

Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels in patients with multiple sclerosis

D. Galimberti, C. Fenoglio, E. Scarpini, 2016, Journal of Neuroimmunology.

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

M. Filippi, M. Franceschi, F. Agosta, 2013, Biological Psychiatry.

Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.

N. Bresolin, D. Galimberti, C. Fenoglio, 2011, Journal of Alzheimer's disease : JAD.

Altered Extracellular Vesicle miRNA Profile in Prodromal Alzheimer’s Disease

D. Galimberti, C. Fenoglio, E. Scarpini, 2023, International journal of molecular sciences.

Circulating miRNAs as potential biomarkers in Alzheimer’s disease

D. Galimberti, C. Fenoglio, E. Scarpini, 2013 .

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

A. Singleton, B. Nacmias, D. Galimberti, 2016, Journal of Alzheimer's disease : JAD.

Long Non-Coding RNA Profile in Genetic Symptomatic and Presymptomatic Frontotemporal Dementia: A GENFI Study.

C. Fenoglio, R. Laforce, M. Tartaglia, 2024, Journal of Alzheimer's disease : JAD.

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

D. Galimberti, C. Fenoglio, E. Scarpini, 2016, Journal of Alzheimer's Disease.

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

H. Leonard, D. Knopman, C. van Broeckhoven, 2024, American journal of human genetics.

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

A. Altamura, D. Galimberti, C. Fenoglio, 2014, Bipolar disorders.

Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia − A GENFI study

C. Fenoglio, R. Laforce, J. V. van Swieten, 2024, Brain, Behavior, and Immunity.