Lista de obras - Elisa Rubino - Dominio Público Uruguay

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

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

artículo científico publicado en 2009

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

artículo científico

Association between major mood disorders and the hypocretin receptor 1 gene

artículo científico publicado en 2010

Association between migraine and HLA-DRB1 gene polymorphisms.

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

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

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

artículo científico publicado en 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

artículo científico publicado en 2021

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

artículo científico publicado en 2017

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

artículo científico publicado en 2006

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

Genetic variants in the NOTCH4 gene influence the clinical features of migraine ⬇️

artículo científico publicado el 26 de marzo de 2013

Genetics of cluster headache: an update

artículo científico publicado en 2005

HLA-DRB1 genotyping in Italian migraine patients

artículo científico publicado en 2006

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

artículo científico publicado en 2007

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

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

artículo científico publicado en 2008

Interleukin-1 cluster gene polymorphisms and aneurysmal subarachnoid hemorrhage.

artículo científico publicado en 2010

Investigating the genetic role of aquaporin4 gene in migraine

artículo científico publicado en 2009

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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.

artículo científico publicado en 2005

Mutation analysis of CHCHD10 in different neurodegenerative diseases

artículo científico publicado en 2015

Neurofunctional Signature of Hyperfamiliarity for Unknown Faces

artículo científico publicado en 2015

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

artículo científico publicado en 2016

Novel mutation of SLC20A2 in an Italian patient presenting with migraine

artículo científico publicado en 2014

O056. Migraine as presenting symptom of SLC20A2gene mutations

artículo científico publicado en 2015

O057. Altered plasma adipokines concentrations in chronic migraine

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2005

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2006

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

artículo científico publicado en 2012

TUMOR NECROSIS FACTOR-α GENE AND CEREBRAL ANEURYSMS

artículo científico publicado en 2007

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

artículo científico publicado en 2007

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Lista de obras de 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

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

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

Association between major mood disorders and the hypocretin receptor 1 gene

Association between migraine and HLA-DRB1 gene polymorphisms.

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

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

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

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

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

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.

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

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

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

Genetic variants in the NOTCH4 gene influence the clinical features of migraine ⬇️

Genetics of cluster headache: an update

HLA-DRB1 genotyping in Italian migraine patients

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

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

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

Interleukin-1 cluster gene polymorphisms and aneurysmal subarachnoid hemorrhage.

Investigating the genetic role of aquaporin4 gene in migraine

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

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

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

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

Mutation analysis of CHCHD10 in different neurodegenerative diseases

Neurofunctional Signature of Hyperfamiliarity for Unknown Faces

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

Novel mutation of SLC20A2 in an Italian patient presenting with migraine

O056. Migraine as presenting symptom of SLC20A2gene mutations

O057. Altered plasma adipokines concentrations in chronic migraine

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

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

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

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

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

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

TUMOR NECROSIS FACTOR-α GENE AND CEREBRAL ANEURYSMS

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

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

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