List of works by Chiara Villa

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

scientific article

Analysis of Human Papillomavirus (HPV) 16 Variants Associated with Cervical Infection in Italian Women

scientific article published on 01 January 2020

Arylsulfatase A (ASA) in Parkinson's Disease: From Pathogenesis to Biomarker Potential

scientific article published on 07 October 2020

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

scientific article

Biomarkers for Alzheimer's Disease: Where Do We Stand and Where Are We Going?

scientific article published on 20 November 2020

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

scientific article published on 16 December 2013

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

scientific article

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

scientific article

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

scientific article (publication date: August 2009)

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

scientific article

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

scientific article published on 25 February 2009

Candidate gene analysis of semaphorins in patients with Alzheimer's disease.

scientific article published on 3 December 2009

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

scientific article

Circulating miRNAs as potential biomarkers in Alzheimer's disease

scientific article

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

scientific article

Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis.

scientific article published in December 2013

Ehlers-Danlos syndromes and epilepsy: An updated review

scientific article published on 02 March 2018

Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

scientific article published on 02 January 2019

Epileptic seizures in autosomal dominant forms of Alzheimer's disease

scientific article published on 19 July 2018

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

scientific article published on 25 February 2013

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

scientific article published on 19 August 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

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

scientific article published on 01 January 2010

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

scientific article published in January 2011

GRN variability contributes to sporadic frontotemporal lobar degeneration

scientific article

GSK3β genetic variability in patients with Multiple Sclerosis

scientific article

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

Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration

scientific article

Investigating Cardiac Morphological Alterations in a Pentylenetetrazol-Kindling Model of Epilepsy

scientific article published on 09 June 2020

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

scientific article

Lymphocyte-Activation Gene 3 (LAG3) Protein as a Possible Therapeutic Target for Parkinson's Disease: Molecular Mechanisms Connecting Neuroinflammation to α-Synuclein Spreading Pathology

scientific article published on 23 April 2020

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels

scientific article

Molecular and Imaging Biomarkers in Alzheimer's Disease: A Focus on Recent Insights

scientific article published on 10 July 2020

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration

scientific article published on 27 November 2007

Novel exon 1 progranulin gene variant in Alzheimer's disease.

scientific article published on 26 August 2008

Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia

scientific article

Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

scientific article

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

scientific article published on 6 February 2014

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

scientific article published in January 2011

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

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

scientific article

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration

scientific article

The Progranulin (GRN) Cys157LysfsX97 Mutation is Associated with Nonfluent Variant of Primary Progressive Aphasia Clinical Phenotype

The Synergistic Relationship between Alzheimer's Disease and Sleep Disorders: An Update

scientific article published on 02 April 2015

Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing

scientific article published on 02 March 2019

and Nocturnal Frontal Lobe Epilepsy: Identification and Characterization of a Novel Loss of Function Mutation

scientific article published on 12 February 2019

Paulina is supported by:

About Paulina

Help