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Genome-Wide Association Studies: Contribution of Genomics to Understanding Blood Pressure and Essential Hypertension

Current hypertension reports, 2010-02, Vol.12 (1), p.17-25

Ehret, Georg B.

2010

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Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

PLoS genetics, 2007-07, Vol.3 (7), p.e115-e115

2007

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A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability

American journal of human genetics, 2012-11, Vol.91 (5), p.863-871

2012

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Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency

PLoS computational biology, 2012-10, Vol.8 (10), p.e1002737-e1002737

2012

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Genes for blood pressure: an opportunity to understand hypertension

European heart journal, 2013-04, Vol.34 (13), p.951-961

2013

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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

Nature genetics, 2017-01, Vol.49 (1), p.54-64

2017

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The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility

Scientific reports, 2016-12, Vol.6 (1), p.38976-38976, Article 38976

2016

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Genetic Implication of a Novel Thiamine Transporter in Human Hypertension

Journal of the American College of Cardiology, 2014-04, Vol.63 (15), p.1542-1555

2014

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Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study

PloS one, 2014-10, Vol.9 (10), p.e109155-e109155

2014

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Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

European journal of human genetics : EJHG, 2008-12, Vol.16 (12), p.1507-1511

2008

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

Hypertension (Dallas, Tex. 1979), 2011-05, Vol.57 (5), p.903-910

2011

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Analysis of putative cis-regulatory elements regulating blood pressure variation

Human molecular genetics, 2020-07, Vol.29 (11), p.1922-1932

2020

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Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic Disorders

Journal of molecular biology, 2015-08, Vol.427 (16), p.2629-2646

2015

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Association Analysis of FOXO3 Longevity Variants With Blood Pressure and Essential Hypertension

American journal of hypertension, 2016-11, Vol.29 (11), p.1292-1300

2016

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Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study

European journal of human genetics : EJHG, 2009-12, Vol.17 (12), p.1650-1657

2009

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Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk

Circulation. Cardiovascular genetics, 2016-02, Vol.9 (1), p.64-70

2016

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Framingham's Contribution to Gene Identification for CV Risk Factors and Coronary Disease

Global heart, 2013-03, Vol.8 (1), p.59-65

Ehret, Georg B

2013

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The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart Disease

Global heart, 2013-03, Vol.8 (1), p.59-65

Ehret, Georg B

2013

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Positional identification of variants of Adamts16 linked to inherited hypertension

Human molecular genetics, 2009-08, Vol.18 (15), p.2825-2838

2009

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Effects of Rare and Common Blood Pressure Gene Variants on Essential Hypertension: Results From the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities Studies

Circulation research, 2013-01, Vol.112 (2), p.318-326

2013

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Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacology

Expert opinion on drug safety, 2007-05, Vol.6 (3), p.289-303

2007

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Influence of CYP2D6 activity on pre-emptive analgesia by the N-methyl-D-aspartate antagonist dextromethorphan in a randomized controlled trial of acute pain

Pain physician, 2013-01, Vol.16 (1), p.45-56

2013

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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Nature genetics, 2017-03, Vol.49 (3), p.403-415

2017

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Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

Science (American Association for the Advancement of Science), 2016-03, Vol.351 (6278), p.1166-1171

2016

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Genome-Wide Association Studies: Contribution of Genomics to Understanding Blood Pressure and Essential Hypertension

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability

Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency

Genes for blood pressure: an opportunity to understand hypertension

Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility

Genetic Implication of a Novel Thiamine Transporter in Human Hypertension

Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

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

Analysis of putative cis-regulatory elements regulating blood pressure variation

Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic Disorders

Association Analysis of FOXO3 Longevity Variants With Blood Pressure and Essential Hypertension

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk

Framingham's Contribution to Gene Identification for CV Risk Factors and Coronary Disease

The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart Disease

Positional identification of variants of Adamts16 linked to inherited hypertension

Effects of Rare and Common Blood Pressure Gene Variants on Essential Hypertension: Results From the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities Studies

Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacology

Influence of CYP2D6 activity on pre-emptive analgesia by the N-methyl-D-aspartate antagonist dextromethorphan in a randomized controlled trial of acute pain

Meeting highlights from the 2013 European Society of Cardiology Heart Failure Association Winter Meeting on Translational Heart Failure Research

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

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