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List of works by Elisa Rubino

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

scientific article

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

scientific article

Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: a meta-analysis.

scientific article published on 18 May 2013

Association between major mood disorders and the hypocretin receptor 1 gene

scientific article published on 10 November 2010

Association between migraine and HLA-DRB1 gene polymorphisms.

scientific article

Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache: a meta-analysis.

scientific article published on 11 June 2007

Association of the C677T Polymorphism in the MTHFR Gene with Migraine: A Meta-Analysis

scientific article published in August 2009

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

scientific article

Brain arteriovenous malformations are associated with interleukin-1 cluster gene polymorphisms.

scientific article published in January 2012

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

scientific article published on 17 September 2020

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

scientific article published on 7 June 2021

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

scientific article published on 23 January 2017

Endocrine Function Is Altered in Chronic Migraine Patients with Medication-Overuse

scientific article published on 01 April 2006

Evidence for an association between migraine and the hypocretin receptor 1 gene

scientific article

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

scientific article

Genetics of cluster headache: an update

scientific article

HLA-DRB1 genotyping in Italian migraine patients

scientific article published in January 2006

Haemochromatosis Gene (HFE) Polymorphisms and Migraine: An Association Study

scientific article published in January 2007

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

scientific article published on 24 July 2011

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

scientific article published on 6 June 2014

Interleukin 6 gene polymorphisms are not associated with aneurysmal subarachnoid haemorrhage in an Italian population

scientific article published in April 2008

Interleukin-1 cluster gene polymorphisms and aneurysmal subarachnoid hemorrhage.

scientific article published in June 2010

Investigating the genetic role of aquaporin4 gene in migraine

scientific article

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

scientific article

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

scientific article

Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: A comprehensive meta-analysis

article

Lack of association between the 3092 T-->C Clock gene polymorphism and cluster headache.

scientific article

Mutation analysis of CHCHD10 in different neurodegenerative diseases

scientific article published on 31 March 2015

Neurofunctional Signature of Hyperfamiliarity for Unknown Faces

scientific article published on 8 July 2015

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

scientific article published on 7 May 2016

Novel mutation of SLC20A2 in an Italian patient presenting with migraine

scientific article

O056. Migraine as presenting symptom of SLC20A2gene mutations

scientific article published on December 2015

O057. Altered plasma adipokines concentrations in chronic migraine

scientific article published on December 2015

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

scientific article published on 6 January 2016

Prevalence of HFE (Hemochromatosis) Gene Mutations in Patients With Cluster Headache

scientific article published in October 2005

Pro-Inflammatory Cytokine Genes Influence the Clinical Features of Frontotemporal Lobar Degeneration

scientific article published in 2009

Proinflammatory cytokine gene polymorphisms and susceptibility to Paget's disease of bone: an association study.

scientific article published on 13 September 2011

Resolution of cluster headache after closure of an anterior communicating artery aneurysm: the role of pericarotid sympathetic fibres

scientific article published in February 2006

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

scientific article published on 12 September 2012

TUMOR NECROSIS FACTOR-α GENE AND CEREBRAL ANEURYSMS

scientific article published in April 2007

The 1246 G/A polymorphism of the HCRTR2 gene is not associated with migraine

scientific article published in August 2007

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

scientific article

Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation

scientific article published on 17 February 2010

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