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Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration

Scientific reports, 2021-02, Vol.11 (1), p.3639-21, Article 3639

2021

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Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

Journal of lipid research, 1990-03, Vol.31 (3), p.545-548

1990

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Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in chinese population

Journal of human hypertension, 2011-08, Vol.25 (8), p.500-508

2011

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A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

Nature genetics, 1997-03, Vol.15 (3), p.273-276

1997

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Normal Variation in Leptin Levels Is Associated with Polymorphisms in the Proopiomelanocortin Gene, POMC

The journal of clinical endocrinology and metabolism, 1999-09, Vol.84 (9), p.3187-3191

1999

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A quantitative trait locus on chromosome 16q influences variation in plasma HDL-C levels in Mexican Americans

Arteriosclerosis, thrombosis, and vascular biology, 2003-02, Vol.23 (2), p.339

2003

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Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans : The San Antonio Family Heart Study

Circulation (New York, N.Y.), 1996-11, Vol.94 (9), p.2159-2170

1996

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QTL-specific genotype-by-smoking interaction and burden of calcified coronary atherosclerosis: The NHLBI Family Heart Study

Atherosclerosis, 2007-07, Vol.193 (1), p.11-19

2007

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A quantitative trait locus influencing BMI maps to the region of the beta-3 adrenergic receptor

Diabetes (New York, N.Y.), 1999-09, Vol.48 (9), p.1863

1999

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The contribution of individual and pairwise combinations of SNPs in the APOA1 and APOC3 genes to interindividual HDL-C variability

Journal of molecular medicine (Berlin, Germany), 2006-07, Vol.84 (7), p.561-572

2006

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The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study

The pharmacogenomics journal, 2013-08, Vol.13 (4), p.312-317

2013

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Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study

Journal of human hypertension, 2016-09, Vol.30 (9), p.543-548

2016

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Common Genetic Variants in the Endothelial System Predict Blood Pressure Response to Sodium Intake: The GenSalt Study

American journal of hypertension, 2013-05, Vol.26 (5), p.643-656

2013

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Associations of epithelial sodium channel genes with blood pressure: the GenSalt study

Journal of human hypertension, 2015-04, Vol.29 (4), p.224-228

2015

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The Pro12Ala variant of peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with measures of obesity in Mexican Americans

International Journal of Obesity, 2000-05, Vol.24 (4), p.522-524

2000

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Human Pedigree-Based Quantitative-Trait–Locus Mapping: Localization of Two Genes Influencing HDL-Cholesterol Metabolism

American journal of human genetics, 1999-06, Vol.64 (6), p.1686-1693

1999

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Baboons as an Animal Model for Genetic Studies of Common Human Disease

American journal of human genetics, 1997-09, Vol.61 (3), p.489-493

1997

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A genome search identifies major quantitative trait loci on human chromosomes 3 and 4 that influence cholesterol concentrations in small LDL particles

Arteriosclerosis, thrombosis, and vascular biology, 1999-03, Vol.19 (3), p.777

1999

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Molecular basis for "null" lipoprotein(a) phenotypes and the influence of apolipoprotein(a) size on plasma lipoprotein(a) level in the baboon

The Journal of biological chemistry, 1994-03, Vol.269 (12), p.9060-9066

1994

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A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans

The Journal of clinical investigation, 1998-02, Vol.101 (3), p.584-587

1998

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Association of Genetic Variants in the Apelin–APJ System and ACE2 With Blood Pressure Responses to Potassium Supplementation: The GenSalt Study

American journal of hypertension, 2010-06, Vol.23 (6), p.606-613

2010

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Linkage of serum insulin concentrations to chromosome 3p in Mexican Americans

Diabetes (New York, N.Y.), 2000-03, Vol.49 (3), p.513-516

2000

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Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans

International Journal of Obesity, 2000-08, Vol.24 (8), p.1065-1068

2000

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Genetics of Atherosclerosis Risk Factors in Mexican Americans

Nutrition reviews, 1999-05, Vol.57 (5), p.59-65

1999

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Analysis of Sex Hormone Genes Reveals Gender Differences in the Genetic Etiology of Blood Pressure Salt Sensitivity: The GenSalt Study

American journal of hypertension, 2013-02, Vol.26 (2), p.191-200

2013

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Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration

Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in chinese population

A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

Normal Variation in Leptin Levels Is Associated with Polymorphisms in the Proopiomelanocortin Gene, POMC

A quantitative trait locus on chromosome 16q influences variation in plasma HDL-C levels in Mexican Americans

Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans : The San Antonio Family Heart Study

QTL-specific genotype-by-smoking interaction and burden of calcified coronary atherosclerosis: The NHLBI Family Heart Study

A quantitative trait locus influencing BMI maps to the region of the beta-3 adrenergic receptor

The contribution of individual and pairwise combinations of SNPs in the APOA1 and APOC3 genes to interindividual HDL-C variability

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study

Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study

Common Genetic Variants in the Endothelial System Predict Blood Pressure Response to Sodium Intake: The GenSalt Study

Associations of epithelial sodium channel genes with blood pressure: the GenSalt study

The Pro12Ala variant of peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with measures of obesity in Mexican Americans

Human Pedigree-Based Quantitative-Trait–Locus Mapping: Localization of Two Genes Influencing HDL-Cholesterol Metabolism

Baboons as an Animal Model for Genetic Studies of Common Human Disease

A genome search identifies major quantitative trait loci on human chromosomes 3 and 4 that influence cholesterol concentrations in small LDL particles

Molecular basis for "null" lipoprotein(a) phenotypes and the influence of apolipoprotein(a) size on plasma lipoprotein(a) level in the baboon

A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans

Association of Genetic Variants in the Apelin–APJ System and ACE2 With Blood Pressure Responses to Potassium Supplementation: The GenSalt Study

Linkage of serum insulin concentrations to chromosome 3p in Mexican Americans

Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans

Genetics of Atherosclerosis Risk Factors in Mexican Americans

Analysis of Sex Hormone Genes Reveals Gender Differences in the Genetic Etiology of Blood Pressure Salt Sensitivity: The GenSalt Study

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