Lista de obras - Erika Salvi - Dominio Público Uruguay

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

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 regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosis

artículo científico publicado en 2013

Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2: clinical studies

artículo científico publicado en 2010

Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort

artículo científico publicado en 2016

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

Copy number variations and cognitive phenotypes in unselected populations

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Effect of intravenous l-carnitine in Chinese patients with chronic heart failure

article

Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: association with the functional IRAK1 196Phe/532Ser haplotype

artículo científico publicado en 2011

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

artículo científico publicado en 2017

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification

artículo científico publicado en 2013

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

artículo científico publicado en 2021

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 74 loci associated with educational attainment

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

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

artículo científico publicado en 2012

Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis

artículo científico publicado en 2011

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

Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

artículo científico publicado en 2009

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis

artículo científico publicado en 2015

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

Left ventricular diastolic function associated with common genetic variation in ATP12A in a general population.

artículo científico publicado en 2014

Modelling the interaction of steroid receptors with endocrine disrupting chemicals

artículo científico publicado en 2005

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

artículo científico publicado en 2014

PEAR1is not a human hypertension-susceptibility gene

article

Pharmacogenomics considerations in the control of hypertension

artículo científico publicado en 2015

Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs

artículo científico publicado en 2015

Population Stratification Analysis in Genome-Wide Association Studies

Response to Endothelial Nitric Oxide Synthase Polymorphism rs3918226 Associated With Hypertension Does Not Affect Plasma Nitrite Levels in Healthy Subjects

SNPLims: a data management system for genome wide association studies

artículo científico publicado en 2008

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

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

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

artículo científico publicado en 2016

Lista de obras de Erika Salvi

A catalog of genetic loci associated with kidney function from analyses of a million individuals

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 regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosis

Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2: clinical studies

Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort

Associations of autozygosity with a broad range of human phenotypes

Blood pressure loci identified with a gene-centric array

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Copy number variations and cognitive phenotypes in unselected populations

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

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

Directional dominance on stature and cognition in diverse human populations

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

Effect of intravenous l-carnitine in Chinese patients with chronic heart failure

Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: association with the functional IRAK1 196Phe/532Ser haplotype

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence

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

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

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

Genome-wide association study identifies 74 loci associated with educational attainment

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

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis

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

Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Identification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis

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

Left ventricular diastolic function associated with common genetic variation in ATP12A in a general population.

Modelling the interaction of steroid receptors with endocrine disrupting chemicals

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

PEAR1is not a human hypertension-susceptibility gene

Pharmacogenomics considerations in the control of hypertension

Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs

Population Stratification Analysis in Genome-Wide Association Studies

Response to Endothelial Nitric Oxide Synthase Polymorphism rs3918226 Associated With Hypertension Does Not Affect Plasma Nitrite Levels in Healthy Subjects

SNPLims: a data management system for genome wide association studies

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

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

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