Search Results - "Pullinger, R"
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A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
Published in PLoS genetics (01-04-2008)“…A genome-wide association study was performed to identify genetic factors involved in susceptibility to psoriasis (PS) and psoriatic arthritis (PSA),…”
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Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
Published in American journal of human genetics (04-05-2012)“…Psoriasis is a common inflammatory disorder of the skin and other organs. We have determined that mutations in CARD14, encoding a nuclear factor of kappa light…”
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KIBRA, MTNR1B, and FKBP5 genotypes are associated with decreased odds of incident delirium in elderly post-surgical patients
Published in Scientific reports (11-01-2022)“…Despite the association between cognitive impairment and delirium, little is known about whether genetic differences that confer cognitive resilience also…”
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Separation of postprandial lipoproteins: improved purification of chylomicrons using an ApoB100 immunoaffinity method
Published in Journal of lipid research (01-03-2020)“…Elevated levels of triglyceride-rich lipoproteins (TRLs), both fasting and postprandial, are associated with increased risk for atherosclerosis. However,…”
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APOL1 Risk Variants Associate With the Prevalence of Stroke in African American Current and Past Smokers
Published in Journal of the American Heart Association (19-12-2023)“…African American smokers have 2.5 times higher risk for stroke compared with nonsmokers (higher than other races). About 50% of the African American population…”
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Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia
Published in Journal of lipid research (01-11-2019)“…Severe hypertriglyceridemia (HTG) is a relatively common form of dyslipidemia with a complex pathophysiology and serious health complications. HTG can develop…”
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Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
Published in Journal of lipid research (01-06-2022)“…Low levels of high density lipoprotein-cholesterol (HDL-C) are associated with an elevated risk of arteriosclerotic coronary heart disease. Heritability of…”
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Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case–control study
Published in Human molecular genetics (15-03-2009)“…Functionally significant heterozygous mutations in the Melanocortin-4 receptor (MC4R) have been implicated in 2.5% of early onset obesity cases in European…”
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Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal function
Published in JAMA neurology (01-10-2014)“…The identification of a patient with a rare form of severe dysbetalipoproteinemia allowed the study of the consequences of total absence of apolipoprotein E…”
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An internal promoter underlies the difference in disease severity between N- and C-terminal truncation mutations of Titin in zebrafish
Published in eLife (16-10-2015)“…Truncating mutations in the giant sarcomeric protein Titin result in dilated cardiomyopathy and skeletal myopathy. The most severely affected dilated…”
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Apolipoprotein E e4 allele increases the risk of early postoperative delirium in older patients undergoing noncardiac surgery
Published in Anesthesiology (Philadelphia) (01-09-2007)“…Whether patients who subsequently develop early postoperative delirium have a genetic predisposition that renders them at risk for postoperative delirium has…”
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Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia
Published in Nature genetics (01-12-2007)“…Hypertriglyceridemia is a hallmark of many disorders, including metabolic syndrome, diabetes, atherosclerosis and obesity. A well-known cause is the deficiency…”
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The acute wheezy adult with airways disease in the emergency department: a retrospective case-note review of exacerbations of COPD
Published in International journal of chronic obstructive pulmonary disease (01-05-2019)“…There has been an increase in interest in the peripheral blood eosinophil count as a biomarker in COPD. Few studies have examined the eosinophil count in…”
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Levels of Prebeta-1 High-Density Lipoprotein Are a Strong Independent Positive Risk Factor for Coronary Heart Disease and Myocardial Infarction: A Meta-Analysis
Published in Journal of the American Heart Association (06-04-2021)“…Background We previously showed that levels of prebeta-1 high-density lipoprotein (HDL), the principal acceptor of cholesterol effluxed from cells, including…”
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Relation of Increased Prebeta-1 High-Density Lipoprotein Levels to Risk of Coronary Heart Disease
Published in The American journal of cardiology (01-08-2011)“…Preβ-1 high-density lipoprotein (HDL) plays a key role in reverse cholesterol transport by promoting cholesterol efflux. Our aims were (1) to test previous…”
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Symptom Experience in HIV-Infected Adults: A Function of Demographic and Clinical Characteristics
Published in Journal of pain and symptom management (01-12-2009)“…Abstract Personal characteristics that interact with both HIV diagnosis and its medical management can influence symptom experience. Little is known about how…”
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Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia
Published in The New England journal of medicine (27-04-2017)“…Six patients with severe hypertriglyceridemia (chylomicronemia) were found to have autoantibodies against a capillary endothelial-cell protein (GPIHBP1) that…”
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Assessing the Role of the Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1) Three-finger Domain in Binding Lipoprotein Lipase
Published in The Journal of biological chemistry (03-06-2011)“…Glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) is an endothelial cell protein that transports lipoprotein lipase…”
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Cytokine Polymorphisms are Associated with Daytime Napping in Adults Living with HIV
Published in Sleep medicine (01-04-2017)“…Abstract Objective/Background Daytime napping longer than one hour has been associated with an increased risk for all-cause mortality. Associations between…”
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Identification of Four Gene Variants Associated with Myocardial Infarction
Published in American journal of human genetics (01-10-2005)“…Family history is a major risk factor for myocardial infarction (MI). However, known gene variants associated with MI cannot fully explain the genetic…”
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