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List of works by Maria Serpente

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

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

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

scientific article published on 19 August 2011
Circulating miRNAs as potential biomarkers in Alzheimer's disease

scientific article
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

scientific article
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis

scientific article published in December 2013
MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers

scientific article published on 07 November 2011
Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

scientific article published on 25 February 2013
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.

scientific article published on 6 May 2011
Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease

scientific article published in January 2013
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

scientific article
Innate immune system and inflammation in Alzheimer's disease: from pathogenesis to treatment

scientific article
C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

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

scientific article published in January 2012
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred

article
Cerebrospinal fluid biomarkers in Progranulin mutations carriers

scientific article published in January 2011
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

scientific article
C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

scientific article published on 16 December 2013
GRN variability contributes to sporadic frontotemporal lobar degeneration

scientific article
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

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

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

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

scientific article published on 28 June 2014
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.

scientific article published in January 2011
Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway?

scientific article published on 28 November 2015
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

scientific article published on 13 November 2017
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

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

scientific article published on 6 February 2014
GSK3β genetic variability in patients with Multiple Sclerosis

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

scientific article published in January 2013
Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutations

scientific article
Candidate gene analysis of selectin cluster in patients with multiple sclerosis

scientific article published on 25 February 2009
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

scientific article published on 6 January 2016
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

scientific article published on 01 January 2011
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration

scientific article published in January 2012
Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation.

scientific article published on 15 November 2017
LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

scientific article published on 27 August 2018
Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism†

scientific article published on 01 January 2014
Candidate gene analysis of semaphorins in patients with Alzheimer's disease

scientific article published on 3 December 2009
Novel evidence of phenotypical variability in the hexanucleotide repeat expansion in chromosome 9.

scientific article published on January 2013
Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation

scientific article published on 15 November 2016
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

scientific article published on 23 January 2017
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration

scientific article (publication date: August 2009)
Transmembrane protein 106B gene (TMEM106B) variability and influence on progranulin plasma levels in patients with Alzheimer's disease

scientific article published in January 2015
Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

scientific article published on 10 August 2016
Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficits

scientific article published on January 2014
C9ORF72 repeat expansion not detected in patients with multiple sclerosis

scientific article
C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020
Profiling of Specific Gene Expression Pathways in Peripheral Cells from Prodromal Alzheimer's Disease Patients.

scientific article published in January 2018
Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset

scientific article published on 01 January 2019

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