Lista de obras - Cristina Agliardi - Dominio Público Uruguay

A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder

artículo científico publicado en 2006

A functional variant in ERAP1 predisposes to multiple sclerosis

artículo científico publicado en 2012

A role for activatory KIR/HLA complexes in HIV-associated Kaposi’s sarcoma development

artículo científico publicado en 2011

A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy

article

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

artículo científico publicado en 2012

Activating KIR molecules and their cognate ligands prevail in children with a diagnosis of ASD and in their mothers

artículo científico publicado en 2013

Activating KIR/HLA complexes in classic Kaposi's Sarcoma

artículo científico publicado en 2012

An HLA-G(∗)14bp insertion/deletion polymorphism associates with the development of autistic spectrum disorders

artículo científico publicado en 2014

An evolutionary analysis of RAC2 identifies haplotypes associated with human autoimmune diseases.

artículo científico publicado en 2011

Analysis of CCR5, CCR2, SDF1 and RANTES gene polymorphisms in subjects with HIV-related PML and not determined leukoencephalopathy

article

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensors.

artículo científico publicado en 2014

Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects

article

Association of HLA-DRB1 and -DQB1 with Classic Kaposi's Sarcoma in Mainland Italy

scientific article published on 01 January 2006

Association study of the HLA-A2 allele in Italian Alzheimer disease patients

artículo científico publicado en 2008

BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease.

artículo científico publicado en 2009

Blood extracellular vesicles (EVs) of central nervous system origin: a window into the brain

artículo científico publicado en 2020

Distribution, characterization and significance of polyomavirus genomic sequences in tumors of the brain and its covering

artículo científico publicado en 2005

Endoplasmic reticulum aminopeptidase 2 haplotypes play a role in modulating susceptibility to HIV infection.

artículo científico publicado en 2013

Epstein-Barr virus genetic variants are associated with multiple sclerosis

artículo científico publicado en 2015

Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders

artículo científico publicado en 2009

HLA alleles modulate EBV viral load in multiple sclerosis.

artículo científico publicado en 2018

HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study

artículo científico publicado en 2010

HLA-Cw allele frequencies in northern and southern Italy

artículo científico publicado en 2007

HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy.

artículo científico publicado en 2008

HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study

artículo científico publicado en 2019

HLA-G coding region polymorphism is skewed in autistic spectrum disorders.

artículo científico publicado en 2017

HLA-G∗14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum Disorders

artículo científico publicado en 2017

HLA-class I markers and multiple sclerosis susceptibility in the Italian population

artículo científico publicado en 2009

Human leukocyte antigen distribution analysis in North Italian brain Glioma patients: an association with HLA-DRB1*14.

artículo científico publicado en 2005

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

artículo científico publicado en 2011

Indoleamine-2,3-dioxygenase(IDO)2 polymorphisms are not associated with multiple sclerosis in Italians.

artículo científico publicado en 2017

Intrafamiliar transmission of Kaposi's sarcoma-associated herpesvirus and seronegative infection in family members of classic Kaposi's sarcoma patients

artículo científico publicado en 2011

KIRs and their HLA ligands in Remitting–Relapsing Multiple Sclerosis

scientific article published on 09 September 2010

Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease.

artículo científico publicado en 2013

Low frequency and rare coding variation contributes to multiple sclerosis risk

No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis

scientific article published on 16 April 2014

Oligomeric α-Syn and SNARE complex proteins in peripheral extracellular vesicles of neural origin are biomarkers for Parkinson's disease

artículo científico publicado en 2020

Possible association between SNAP-25 single nucleotide polymorphisms and alterations of categorical fluency and functional MRI parameters in Alzheimer's disease

artículo científico publicado en 2014

SNAP-25 in Serum Is Carried by Exosomes of Neuronal Origin and Is a Potential Biomarker of Alzheimer's Disease

artículo científico publicado en 2019

SNAP-25 single nucleotide polymorphisms are associated with hyperactivity in autism spectrum disorders

artículo científico publicado en 2011

SNAP25 Gene Polymorphisms Protect Against Parkinson's Disease and Modulate Disease Severity in Patients

article

TNF-α -308 G/A and -238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort.

artículo científico publicado en 2017

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease

scientific article published on 01 June 2019

Vitamin D Receptor Gene Polymorphisms and HLA DRB1*04 Cosegregation in Saudi Type 2 Diabetes Patients

article

Vitamin D Receptor Polymorphisms Associated with Autism Spectrum Disorder

artículo científico publicado en 2020

Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB1*15-positive individuals

article

Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity

artículo científico publicado en 2014

Vitamin D-binding protein gene polymorphisms are not associated with MS risk in an Italian cohort

artículo científico publicado en 2017

Whole-blood global DNA methylation is increased in amyotrophic lateral sclerosis independently of age of onset

artículo científico publicado en 2013

Lista de obras de Cristina Agliardi

A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder

A functional variant in ERAP1 predisposes to multiple sclerosis

A role for activatory KIR/HLA complexes in HIV-associated Kaposi’s sarcoma development

A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

Activating KIR molecules and their cognate ligands prevail in children with a diagnosis of ASD and in their mothers

Activating KIR/HLA complexes in classic Kaposi's Sarcoma

An HLA-G(∗)14bp insertion/deletion polymorphism associates with the development of autistic spectrum disorders

An evolutionary analysis of RAC2 identifies haplotypes associated with human autoimmune diseases.

Analysis of CCR5, CCR2, SDF1 and RANTES gene polymorphisms in subjects with HIV-related PML and not determined leukoencephalopathy

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensors.

Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects

Association of HLA-DRB1 and -DQB1 with Classic Kaposi's Sarcoma in Mainland Italy

Association study of the HLA-A2 allele in Italian Alzheimer disease patients

BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease.

Blood extracellular vesicles (EVs) of central nervous system origin: a window into the brain

Distribution, characterization and significance of polyomavirus genomic sequences in tumors of the brain and its covering

Endoplasmic reticulum aminopeptidase 2 haplotypes play a role in modulating susceptibility to HIV infection.

Epstein-Barr virus genetic variants are associated with multiple sclerosis

Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders

HLA alleles modulate EBV viral load in multiple sclerosis.

HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study

HLA-Cw allele frequencies in northern and southern Italy

HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy.

HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study

HLA-G coding region polymorphism is skewed in autistic spectrum disorders.

HLA-G∗14bp Insertion and the KIR2DS1-HLAC2 Complex Impact on Behavioral Impairment in Children with Autism Spectrum Disorders

HLA-class I markers and multiple sclerosis susceptibility in the Italian population

Human leukocyte antigen distribution analysis in North Italian brain Glioma patients: an association with HLA-DRB1*14.

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

Indoleamine-2,3-dioxygenase(IDO)2 polymorphisms are not associated with multiple sclerosis in Italians.

Intrafamiliar transmission of Kaposi's sarcoma-associated herpesvirus and seronegative infection in family members of classic Kaposi's sarcoma patients

KIRs and their HLA ligands in Remitting–Relapsing Multiple Sclerosis

Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease.

Low frequency and rare coding variation contributes to multiple sclerosis risk

No association of IFI16 (interferon-inducible protein 16) variants with susceptibility to multiple sclerosis

Oligomeric α-Syn and SNARE complex proteins in peripheral extracellular vesicles of neural origin are biomarkers for Parkinson's disease

Possible association between SNAP-25 single nucleotide polymorphisms and alterations of categorical fluency and functional MRI parameters in Alzheimer's disease

SNAP-25 in Serum Is Carried by Exosomes of Neuronal Origin and Is a Potential Biomarker of Alzheimer's Disease

SNAP-25 single nucleotide polymorphisms are associated with hyperactivity in autism spectrum disorders

SNAP25 Gene Polymorphisms Protect Against Parkinson's Disease and Modulate Disease Severity in Patients

TNF-α -308 G/A and -238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort.

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease

Vitamin D Receptor Gene Polymorphisms and HLA DRB1*04 Cosegregation in Saudi Type 2 Diabetes Patients

Vitamin D Receptor Polymorphisms Associated with Autism Spectrum Disorder

Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB1*15-positive individuals

Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity

Vitamin D-binding protein gene polymorphisms are not associated with MS risk in an Italian cohort

Whole-blood global DNA methylation is increased in amyotrophic lateral sclerosis independently of age of onset