Lista de obras - Aravinda Chakravarti - Dominio Público Uruguay

52 Genetic Loci Influencing Myocardial Mass

artículo científico publicado en 2016

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

artículo científico publicado en 2006

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

artículo científico publicado en 2005

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery

artículo científico publicado en 2007

An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval

artículo científico publicado en 2014

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

artículo científico publicado en 2011

Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals

artículo científico publicado en 2011

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

artículo científico publicado en 2007

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Bethesda Statement on Open Access Publishing

copyright manifesto

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

artículo científico publicado en 2011

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

artículo científico publicado en 2010

Common variants in KCNN3 are associated with lone atrial fibrillation

artículo científico publicado en 2010

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

artículo científico publicado en 2018

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

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

artículo científico publicado en 2014

Estimating the prior probability of paternity from the results of exclusion tests

scientific article published on 01 February 1984

Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer

artículo científico publicado en 2005

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

artículo científico publicado en 2008

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

artículo científico publicado en 2014

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

artículo científico publicado en 2013

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study of PR interval

artículo científico publicado en 2010

Genome-wide association study of blood pressure and hypertension

scientific journal article

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

artículo científico publicado en 2011

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Global implementation of genomic medicine: We are not alone

artículo científico publicado en 2015

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

artículo científico publicado en 2011

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays

artículo científico publicado en 2006

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

artículo científico publicado en 2016

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

artículo científico publicado en 2012

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

artículo científico publicado en 2009

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence

artículo científico publicado en 2005

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

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 association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study

artículo científico publicado en 2009

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

artículo científico publicado en 2018

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

The road ahead in genetics and genomics

artículo científico publicado en 2020

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained

artículo científico publicado en 2013

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

artículo científico publicado en 2016

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

scientific article published on 13 July 2009

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

artículo científico publicado en 2017

Lista de obras de Aravinda Chakravarti

52 Genetic Loci Influencing Myocardial Mass

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

A second generation human haplotype map of over 3.1 million SNPs

Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery

An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

Bethesda Statement on Open Access Publishing

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

Common variants associated with plasma triglycerides and risk for coronary artery disease

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Common variants in KCNN3 are associated with lone atrial fibrillation

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

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

Defining the role of common variation in the genomic and biological architecture of adult human height

Directional dominance on stature and cognition in diverse human populations

Discovery and refinement of loci associated with lipid levels

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

Estimating the prior probability of paternity from the results of exclusion tests

Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genetic studies of body mass index yield new insights for obesity biology

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Genome-wide association study of PR interval

Genome-wide association study of blood pressure and hypertension

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

Genome-wide detection and characterization of positive selection in human populations

Global implementation of genomic medicine: We are not alone

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Multiple loci are associated with white blood cell phenotypes

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

New genetic loci link adipose and insulin biology to body fat distribution

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

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

The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

The road ahead in genetics and genomics

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes