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KIBRA, MTNR1B, and FKBP5 genotypes are associated with decreased odds of incident delirium in elderly post-surgical patients

Scientific reports, 2022-01, Vol.12 (1), p.556-6, Article 556

2022

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Association between regulator of G protein signaling 9-2 and body weight

PloS one, 2011-11, Vol.6 (11), p.e27984

2011

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Moderate statin treatment reduces prebeta-1 high-density lipoprotein levels in dyslipidemic patients

Journal of clinical lipidology, 2017-07, Vol.11 (4), p.908-914

2017

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HDL Cholesterol Efflux Capacity and Cardiovascular Events

The New England journal of medicine, 2015-05, Vol.372 (19), p.1869-1872

2015

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A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components

Scientific reports, 2013-03, Vol.3 (1), p.1491-1491, Article 1491

2013

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Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

The Journal of clinical investigation, 2002-07, Vol.110 (1), p.109-117

2002

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CLN8: AN ATORVASTATIN-SPECIFIC MARKER FOR COMMON MYALGIA

Journal of the American College of Cardiology, 2014-04, Vol.63 (12), p.A1285-A1285

2014

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Sex Bias in Cytokines Transported by High‐Density Lipoproteins in Patients with Coronary Artery Disease

The FASEB journal, 2018-04, Vol.32 (S1), p.813.4-813.4

2018

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Abstract P201: Separation of Postprandial Lipoproteins: Purification of Chylomicrons Using an ApoB100 Immunoaffinity Method

Circulation (New York, N.Y.), 2019-03, Vol.139 (Suppl_1)

2019

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Primary hypercholesterolemia: genetic causes and treatment of five monogenic disorders

Expert review of cardiovascular therapy, 2003-05, Vol.1 (1), p.107-119

2003

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Gene Variants in Caveolin-1 and Caveolin-2 in Patients with Idiopathic Pulmonary Arterial Hypertension

Journal of cardiac failure, 2008-08, Vol.14 (6), p.S8-S8

2008

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An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patientss

Journal of lipid research, 2008-08, Vol.49 (8), p.1846-1854

2008

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Abstract 20918: Cytokines Involved in Arterial Wall Inflammation Are Transported by High Density Lipoprotein Particles

Circulation (New York, N.Y.), 2017-11, Vol.136 (suppl_1)

2017

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Human cholesterol 7α-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

The Journal of clinical investigation, 2002-07, Vol.110 (1), p.109-117

2002

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Comment on: Marquez et al. Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk. Diabetes 2012;61:524–530

Diabetes (New York, N.Y.), 2012-05, Vol.61 (5), p.e3-e3

2012

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Rare and Common Variants in CARD 14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis

American journal of human genetics, 2012, Vol.90 (5), p.796-808

2012

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Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the

Pharmacogenomics, 2010-07, Vol.11 (7), p.959-971

2010

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Apolipoprotein L, a New Human High Density Lipoprotein Apolipoprotein Expressed by the Pancreas

The Journal of biological chemistry, 1997-10, Vol.272 (41), p.25576-25582

1997

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Comment on: Marquez et al. Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes 2012;61:524-530

Diabetes (New York, N.Y.), 2012-05, Vol.61 (5), p.e3-e3

2012

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Apolipoprotein E e4 auele increases the risk of early postoperative delirium in older patients undergoing noncardiac surgery

Anesthesiology (Philadelphia), 2007, Vol.107 (3), p.406-411

2007

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Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia. Commentary

European heart journal, 2008, Vol.29 (18)

2008

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Genetic Variation in PLTP Modulates Lipoprotein Profiles in Hyperalphalipoproteinemia

Metabolism, clinical and experimental, 2008-12, Vol.57 (12), p.1719-1724

2008

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Human cholesterol 7(alpha)-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

The Journal of clinical investigation, 2002-07, Vol.110 (1), p.109

2002

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A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci: e1000041

PLoS genetics, 2008-04, Vol.4 (4)

2008

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KIBRA, MTNR1B, and FKBP5 genotypes are associated with decreased odds of incident delirium in elderly post-surgical patients

An internal promoter underlies the difference in disease severity between N- and C-terminal truncation mutations of Titin in zebrafish

Association between regulator of G protein signaling 9-2 and body weight

Moderate statin treatment reduces prebeta-1 high-density lipoprotein levels in dyslipidemic patients

HDL Cholesterol Efflux Capacity and Cardiovascular Events

A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components

Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

CLN8: AN ATORVASTATIN-SPECIFIC MARKER FOR COMMON MYALGIA

Sex Bias in Cytokines Transported by High‐Density Lipoproteins in Patients with Coronary Artery Disease

Abstract P201: Separation of Postprandial Lipoproteins: Purification of Chylomicrons Using an ApoB100 Immunoaffinity Method

Primary hypercholesterolemia: genetic causes and treatment of five monogenic disorders

Gene Variants in Caveolin-1 and Caveolin-2 in Patients with Idiopathic Pulmonary Arterial Hypertension

An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patientss

Abstract 20918: Cytokines Involved in Arterial Wall Inflammation Are Transported by High Density Lipoprotein Particles

Human cholesterol 7α-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

Comment on: Marquez et al. Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk. Diabetes 2012;61:524–530

Rare and Common Variants in CARD 14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis

Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the

Apolipoprotein L, a New Human High Density Lipoprotein Apolipoprotein Expressed by the Pancreas

Comment on: Marquez et al. Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes 2012;61:524-530

Apolipoprotein E e4 auele increases the risk of early postoperative delirium in older patients undergoing noncardiac surgery

Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia. Commentary

Genetic Variation in PLTP Modulates Lipoprotein Profiles in Hyperalphalipoproteinemia

Human cholesterol 7(alpha)-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci: e1000041

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