Lista de obras - Cristina Barlassina - Dominio Público Uruguay

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 principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A renal abnormality as a possible cause of "essential" hypertension ⬇️

artículo científico publicado el 27 de enero de 1979

ACE and α-Adducin Polymorphism as Markers of Individual Response to Diuretic Therapy

article

Active and Inactive Renin and Kidney Function in Young Subjects with Different Predisposition to Develop Essential Hypertension

scientific article published on 01 January 1982

Adducin in essential hypertension

artículo científico publicado en 1998

Alpha-adducin and angiotensin-converting enzyme polymorphisms in hypertension: evidence for a joint influence on albuminuria.

artículo científico publicado en 2006

Alpha-adducin polymorphisms and renal sodium handling in essential hypertensive patients.

artículo científico publicado en 1998

An overview of the genetic structure within the Italian population from genome-wide data

artículo científico publicado en 2012

Angiotensinogen gene polymorphism, again?

article

Carotid and femoral intima–media thickness in relation to three candidate genes in a Caucasian population

article

Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension

artículo científico publicado en 2007

Copy-number disorders are a common cause of congenital kidney malformations

artículo científico publicado en 2012

Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population

artículo científico publicado en 2015

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

artículo científico publicado en 2014

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

artículo científico publicado en 2014

Effects of three candidate genes on prevalence and incidence of hypertension in a Caucasian population.

artículo científico publicado en 2001

Endothelial nitric oxide synthase polymorphisms are associated with type 2 diabetes and the insulin resistance syndrome

artículo científico publicado en 2003

Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy.

artículo científico publicado en 2016

Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.

artículo científico publicado en 2015

Expression analysis of the human adducin gene family and evidence of ADD2 beta4 multiple splicing variants

artículo científico publicado en 2003

Familial Aggregation of Cation Transport Abnormalities and Essential Hypertension

scientific article published on 01 January 1981

Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.

artículo científico publicado en 2011

Genetic evidence of assortative mating in humans

article

Genetic models of arterial hypertension--role of tubular ion transport.

artículo científico publicado en 1993

Genetic polymorphism of the renin-angiotensin-aldosterone system and arterial hypertension in the Italian population: the GENIPER Project

scientific article published on 01 October 2003

Genetic polymorphism of the renin???angiotensin???aldosterone system and arterial hypertension in the Italian population

article

Genetics of renal mechanisms of primary hypertension: the role of adducin.

artículo científico publicado en 1997

Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.

artículo científico publicado en 2016

Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study.

artículo científico publicado en 2014

Genome-wide association study of kidney function decline in individuals of European descent

artículo científico publicado en 2014

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

artículo científico publicado en 2011

Gly460Trp alpha-adducin gene polymorphism and endothelial function in untreated hypertensive patients.

artículo científico publicado en 2007

Heritability estimate of erythrocyte Na-K-Cl cotransport in normotensive and hypertensive families.

artículo científico publicado en 1991

Identification of a transcriptome profile associated with improvement of organ function in septic shock patients after early supportive therapy

scientific article published on 21 November 2018

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Inactive Matrix Gla Protein Is Causally Related to Adverse Health Outcomes

article

Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study

scientific article published on 23 June 2016

Loss of mismatched HLA in leukemia after stem-cell transplantation.

artículo científico publicado en 2009

PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population.

artículo científico publicado en 2017

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.

artículo científico publicado en 2016

Pharmacogenomics considerations in the control of hypertension

artículo científico publicado en 2015

Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension

artículo científico publicado en 1997

Population Stratification Analysis in Genome-Wide Association Studies

Preliminary profiling of blood transcriptome in a rat model of hemorrhagic shock

artículo científico publicado en 2017

Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection.

artículo científico publicado en 2014

Self-renewal and phenotypic conversion are the main physiological responses of macrophages to the endogenous estrogen surge.

scientific article published on 20 March 2017

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

artículo científico publicado en 2013

ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock

artículo científico publicado en 2016

Synergistic effect of α-adducin and ACE genes causes blood pressure changes with body sodium and volume expansion

article

TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives.

artículo científico publicado en 2015

Target sequencing, cell experiments, and a population study establish endothelial nitric oxide synthase (eNOS) gene as hypertension susceptibility gene

artículo científico publicado en 2013

The -665 C>T polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans

artículo científico publicado en 2014

The 460Trp allele of α-adducin increases carotid intima–media thickness in young adult males

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The burden of multiple sclerosis variants in continental Italians and Sardinians

artículo científico publicado en 2015

The role of adducin in hypertension

Transcapillary protein escape in arterial hypertension

artículo científico publicado en 1980

Xanthine oxidase gene variants and their association with blood pressure and incident hypertension: a population study

artículo científico publicado en 2016

alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy

artículo científico publicado en 2009

α-Adducin 460Trp Allele Is Associated With Erythrocyte Na Transport Rate in North Sardinian Primary Hypertensives

artículo científico publicado en 2002

Lista de obras de Cristina Barlassina

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

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

A renal abnormality as a possible cause of "essential" hypertension ⬇️

ACE and α-Adducin Polymorphism as Markers of Individual Response to Diuretic Therapy

Active and Inactive Renin and Kidney Function in Young Subjects with Different Predisposition to Develop Essential Hypertension

Adducin in essential hypertension

Alpha-adducin and angiotensin-converting enzyme polymorphisms in hypertension: evidence for a joint influence on albuminuria.

Alpha-adducin polymorphisms and renal sodium handling in essential hypertensive patients.

An overview of the genetic structure within the Italian population from genome-wide data

Angiotensinogen gene polymorphism, again?

Carotid and femoral intima–media thickness in relation to three candidate genes in a Caucasian population

Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension

Copy-number disorders are a common cause of congenital kidney malformations

Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Effects of three candidate genes on prevalence and incidence of hypertension in a Caucasian population.

Endothelial nitric oxide synthase polymorphisms are associated with type 2 diabetes and the insulin resistance syndrome

Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy.

Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.

Expression analysis of the human adducin gene family and evidence of ADD2 beta4 multiple splicing variants

Familial Aggregation of Cation Transport Abnormalities and Essential Hypertension

Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.

Genetic evidence of assortative mating in humans

Genetic models of arterial hypertension--role of tubular ion transport.

Genetic polymorphism of the renin-angiotensin-aldosterone system and arterial hypertension in the Italian population: the GENIPER Project

Genetic polymorphism of the renin???angiotensin???aldosterone system and arterial hypertension in the Italian population

Genetics of renal mechanisms of primary hypertension: the role of adducin.

Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.

Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study.

Genome-wide association study of kidney function decline in individuals of European descent

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

Gly460Trp alpha-adducin gene polymorphism and endothelial function in untreated hypertensive patients.

Heritability estimate of erythrocyte Na-K-Cl cotransport in normotensive and hypertensive families.

Identification of a transcriptome profile associated with improvement of organ function in septic shock patients after early supportive therapy

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Inactive Matrix Gla Protein Is Causally Related to Adverse Health Outcomes

Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study

Loss of mismatched HLA in leukemia after stem-cell transplantation.

PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population.

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.

Pharmacogenomics considerations in the control of hypertension

Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension

Population Stratification Analysis in Genome-Wide Association Studies

Preliminary profiling of blood transcriptome in a rat model of hemorrhagic shock

Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection.

Self-renewal and phenotypic conversion are the main physiological responses of macrophages to the endogenous estrogen surge.

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock

Synergistic effect of α-adducin and ACE genes causes blood pressure changes with body sodium and volume expansion

TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives.

Target sequencing, cell experiments, and a population study establish endothelial nitric oxide synthase (eNOS) gene as hypertension susceptibility gene

The -665 C>T polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans

The 460Trp allele of α-adducin increases carotid intima–media thickness in young adult males

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

The burden of multiple sclerosis variants in continental Italians and Sardinians

The role of adducin in hypertension

Transcapillary protein escape in arterial hypertension

Xanthine oxidase gene variants and their association with blood pressure and incident hypertension: a population study

alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy

α-Adducin 460Trp Allele Is Associated With Erythrocyte Na Transport Rate in North Sardinian Primary Hypertensives