Lista de obras -

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

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

artículo científico publicado en 2015

A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia

artículo científico publicado en 2017

Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration.

artículo científico publicado en 2009

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

artículo científico publicado en 2013

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

scientific article published on 01 January 2011

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

scientific article published on 17 September 2020

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

artículo científico publicado en 2009

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

artículo científico publicado en 2011

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

scientific article published on 01 January 2010

Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration

artículo científico publicado en 2010

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

artículo científico publicado en 2014

GRN variability contributes to sporadic frontotemporal lobar degeneration

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene

artículo científico publicado en 2011

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients

artículo científico publicado en 2014

Investigation of c9orf72 in 4 neurodegenerative disorders

artículo científico publicado en 2012

Is HCRTR2 a genetic risk factor for Alzheimer's disease?

artículo científico publicado en 2014

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

artículo científico publicado en 2010

Mutation analysis of CHCHD10 in different neurodegenerative diseases

artículo científico publicado en 2015

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 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.

artículo científico publicado en 2011

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

artículo científico publicado en 2012

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients

artículo científico publicado en 2015

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

artículo científico publicado en 2007

Lista de obras de

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

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

A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia

Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration.

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

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

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

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

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

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

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

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration

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

GRN variability contributes to sporadic frontotemporal lobar degeneration

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

Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients

Investigation of c9orf72 in 4 neurodegenerative disorders

Is HCRTR2 a genetic risk factor for Alzheimer's disease?

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

Mutation analysis of CHCHD10 in different neurodegenerative diseases

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

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

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

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

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease