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Whole-genome association study identifies STK39 as a hypertension susceptibility gene

Proceedings of the National Academy of Sciences - PNAS, 2009-01, Vol.106 (1), p.226-231

2009

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Disruption of ldlr causes increased LDL-c and vascular lipid accumulation in a zebrafish model of hypercholesterolemia[S]

Journal of lipid research, 2014-11, Vol.55 (11), p.2242-2253

2014

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OPRM1 rs1799971 - COMT rs4680 - FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia

Pain (Amsterdam), 2019-08, Vol.160 (8), p.1824-1834

2019

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A polymorphic 3'UTR element in ATP1B1 regulates alternative polyadenylation and is associated with blood pressure

PloS one, 2013-10, Vol.8 (10), p.e76290-e76290

2013

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Identification and characterization of alternative STK39 transcripts within human and mouse kidneys reveals species‐specific regulation of blood pressure

Physiological reports, 2020-02, Vol.8 (4), p.e14379-n/a

2020

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Multigene kinase network, kidney transport, and salt in essential hypertension

Kidney international, 2010-06, Vol.77 (12), p.1063-1069

2010

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Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples

The Journal of nutrition, 2020-10, Vol.150 (10), p.2635-2645

2020

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Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion

PLoS genetics, 2005-12, Vol.1 (6), p.e82-e82

2005

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Determinants of Blood Pressure Response to Low‐Salt Intake in a Healthy Adult Population

The journal of clinical hypertension (Greenwich, Conn.), 2011-11, Vol.13 (11), p.795-800

2011

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Hypertrophy-Associated Polymorphisms Ascertained in a Founder Cohort Applied to Heart Failure Risk and Mortality

Clinical and translational science, 2011-02, Vol.4 (1), p.17-23

2011

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Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program

Genome research, 2003-02, Vol.13 (2), p.173-181

2003

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Associations Between Hypertension and Genes in the Renin-Angiotensin System

Hypertension (Dallas, Tex. 1979), 2003-05, Vol.41 (5), p.1027-1034

2003

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Nicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study

BMC medical genetics, 2008-07, Vol.9 (1), p.67-67, Article 67

2008

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Heritability of serum sodium concentration: evidence for sex- and ethnic-specific effects

Physiological genomics, 2012-02, Vol.44 (3), p.220-228

2012

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Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Diabetes (New York, N.Y.), 2007-12, Vol.56 (12), p.3053-3062

2007

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Identification of Novel Candidate Genes for Type 2 Diabetes From a Genome-Wide Association Scan in the Old Order Amish

Diabetes (New York, N.Y.), 2007-12, Vol.56 (12), p.3053-3062

2007

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An APOO Pseudogene on Chromosome 5q is Associated with LDL-C Levels

Circulation (New York, N.Y.), 2018-09, Vol.138 (13), p.1343-1355

2018

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The genetic response to short-term interventions affecting cardiovascular function: Rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

The American heart journal, 2008-05, Vol.155 (5), p.823-828

2008

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Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

Archives of internal medicine (1960), 2010-11, Vol.170 (20), p.1850

2010

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Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish

Arthritis and rheumatism, 2008-09, Vol.58 (9), p.2874-2881

2008

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OPRM1 rs1799971, COMT rs4680, and FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia

Pain (Amsterdam), 2019-08, Vol.160 (8), p.1824-1834

2019

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Haplotype Association Analysis of AGT Variants with Hypertension-Related Traits: The HyperGEN Study

Human heredity, 2005-01, Vol.60 (3), p.164-176

2005

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Polymorphisms in the SOCS7 gene and glucose homeostasis traits

BMC research notes, 2013-06, Vol.6 (1), p.235-235, Article 235

2013

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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Nature genetics, 2011-11, Vol.43 (11), p.1131-1138

2011

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A Population Association Study of Angiotensinogen Polymorphisms and Haplotypes With Left Ventricular Phenotypes

Hypertension (Dallas, Tex. 1979), 2005-12, Vol.46 (6), p.1294-1299

2005

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Whole-genome association study identifies STK39 as a hypertension susceptibility gene

Disruption of ldlr causes increased LDL-c and vascular lipid accumulation in a zebrafish model of hypercholesterolemia[S]

OPRM1 rs1799971 - COMT rs4680 - FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia

A polymorphic 3'UTR element in ATP1B1 regulates alternative polyadenylation and is associated with blood pressure

Identification and characterization of alternative STK39 transcripts within human and mouse kidneys reveals species‐specific regulation of blood pressure

Multigene kinase network, kidney transport, and salt in essential hypertension

Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples

Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion

Determinants of Blood Pressure Response to Low‐Salt Intake in a Healthy Adult Population

Hypertrophy-Associated Polymorphisms Ascertained in a Founder Cohort Applied to Heart Failure Risk and Mortality

Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program

Associations Between Hypertension and Genes in the Renin-Angiotensin System

Nicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study

Heritability of serum sodium concentration: evidence for sex- and ethnic-specific effects

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Identification of Novel Candidate Genes for Type 2 Diabetes From a Genome-Wide Association Scan in the Old Order Amish

An APOO Pseudogene on Chromosome 5q is Associated with LDL-C Levels

The genetic response to short-term interventions affecting cardiovascular function: Rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish

OPRM1 rs1799971, COMT rs4680, and FAAH rs324420 genes interact with placebo procedures to induce hypoalgesia

Haplotype Association Analysis of AGT Variants with Hypertension-Related Traits: The HyperGEN Study

Polymorphisms in the SOCS7 gene and glucose homeostasis traits

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

A Population Association Study of Angiotensinogen Polymorphisms and Haplotypes With Left Ventricular Phenotypes

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