Výsledky vyhľadávania - "Bis, Joshua C."
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Cholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease
ISSN: 2041-1723, 2041-1723Vydavateľské údaje: London Nature Publishing Group UK 24.09.2021Vydané v Nature communications (24.09.2021)“…Development of cholesteryl ester transfer protein (CETP) inhibitors for coronary heart disease (CHD) has yet to deliver licensed medicines. To distinguish…”
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The impact of APOE genotype on survival: Results of 38,537 participants from six population-based cohorts (E2-CHARGE)
ISSN: 1932-6203, 1932-6203Vydavateľské údaje: United States Public Library of Science 29.07.2019Vydané v PloS one (29.07.2019)“…Apolipoprotein E is a glycoprotein best known as a mediator and regulator of lipid transport and uptake. The APOE-ε4 allele has long been associated with…”
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Genomewide Association Study of Statin‐Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink
ISSN: 0009-9236, 1532-6535, 1532-6535Vydavateľské údaje: United States 01.12.2019Vydané v Clinical pharmacology and therapeutics (01.12.2019)“…Statins can be associated with myopathy. We have undertaken a genomewide association study (GWAS) to discover and validate genetic risk factors for…”
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Genetic evidence for a normal-weight "metabolically obese" phenotype linking insulin resistance, hypertension, coronary artery disease, and type 2 diabetes
ISSN: 1939-327X, 1939-327XVydavateľské údaje: United States 01.12.2014Vydané v Diabetes (New York, N.Y.) (01.12.2014)“…The mechanisms that predispose to hypertension, coronary artery disease (CAD), and type 2 diabetes (T2D) in individuals of normal weight are poorly understood…”
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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
ISSN: 1061-4036, 1546-1718, 1546-1718Vydavateľské údaje: New York Nature Publishing Group US 01.11.2009Vydané v Nature genetics (01.11.2009)“…Santhi Ganesh and colleagues report meta-analyses of genome-wide association studies of six erythrocyte traits within the CHARGE consortium, with replication…”
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Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology
ISSN: 1091-6490, 1091-6490Vydavateľské údaje: United States 18.05.2010Vydané v Proceedings of the National Academy of Sciences - PNAS (18.05.2010)“…Telomeres are engaged in a host of cellular functions, and their length is regulated by multiple genes. Telomere shortening, in the course of somatic cell…”
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Genome-Wide Association Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci
ISSN: 1553-7404, 1553-7390, 1553-7404Vydavateľské údaje: United States Public Library of Science 01.04.2011Vydané v PLoS genetics (01.04.2011)“…Soluble ICAM-1 (sICAM-1) is an endothelium-derived inflammatory marker that has been associated with diverse conditions such as myocardial infarction,…”
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Associations of Immune Cell Subsets With Coronary Artery Calcium Incidence and Progression in the Multi‐Ethnic Study of Atherosclerosis
ISSN: 2047-9980, 2047-9980Vydavateľské údaje: England Wiley 07.10.2025Vydané v Journal of the American Heart Association (07.10.2025)“…Limited data exist on associations of immune cell subsets with longitudinal changes in subclinical coronary artery disease. In the MESA (Multi-Ethnic Study of…”
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Effect of Alzheimer's disease risk genes on trajectories of cognitive function in the Cardiovascular Health Study
ISSN: 1535-7228, 1535-7228Vydavateľské údaje: United States 01.09.2012Vydané v The American journal of psychiatry (01.09.2012)“…The trajectory of cognitive decline in patients with late-onset Alzheimer's disease varies widely. Genetic variations in CLU, PICALM, and CR1 are associated…”
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Biomedical consequences of elevated cholesterol-containing lipoproteins and apolipoproteins on cardiovascular and non-cardiovascular outcomes
ISSN: 2730-664X, 2730-664XVydavateľské údaje: London Nature Publishing Group UK 20.01.2023Vydané v Communications medicine (20.01.2023)“…Background Higher concentrations of cholesterol-containing low-density lipoprotein (LDL-C) increase the risk of cardiovascular disease (CVD). The association…”
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Cerivastatin, genetic variants, and the risk of rhabdomyolysis
ISSN: 1744-6880, 1744-6880Vydavateľské údaje: United States 01.05.2011Vydané v Pharmacogenetics and genomics (01.05.2011)“…The withdrawal of cerivastatin involved an uncommon but serious adverse reaction, rhabdomyolysis. The bimodal response, rhabdomyolysis in a small proportion of…”
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Genes from a translational analysis support a multifactorial nature of white matter hyperintensities
ISSN: 1524-4628, 1524-4628Vydavateľské údaje: United States 01.02.2015Vydané v Stroke (1970) (01.02.2015)“…White matter hyperintensities (WMH) of presumed vascular origin increase the risk of stroke and dementia. Despite strong WMH heritability, few gene…”
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Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations
ISSN: 2666-2477, 2666-2477Vydavateľské údaje: United States Elsevier Inc 13.07.2023Vydané v HGG advances (13.07.2023)“…Alzheimer disease (AD) is the most common form of senile dementia, with high incidence late in life in many populations including Caribbean Hispanic (CH)…”
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Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease
ISSN: 1932-6203, 1932-6203Vydavateľské údaje: United States Public Library of Science 05.10.2018Vydané v PloS one (05.10.2018)“…We previously reported association of SCARB1 SNP rs10846744 with common carotid IMT (cIMT) and cardiovascular disease (CVD) events. Since rs10846744 has been…”
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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
ISSN: 1932-6203, 1932-6203Vydavateľské údaje: United States Public Library of Science 02.10.2014Vydané v PloS one (02.10.2014)“…Genome-wide association studies (GWAS) identified multiple loci for blood pressure (BP) and hypertension. Six genes--ATP2B1, CACNB2, CYP17A1, JAG1, PLEKHA7,…”
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Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease
ISSN: 2352-8729, 2352-8729“…Introduction Genes implicated by genome‐wide association studies and family‐based studies of Alzheimer's disease (AD) are largely discordant. We hypothesized…”Vydavateľské údaje: United States John Wiley & Sons, Inc 2021
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Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium
ISSN: 1523-6838, 1523-6838Vydavateľské údaje: United States 01.06.2013Vydané v American journal of kidney diseases (01.06.2013)“…Chronic kidney disease is associated with cardiovascular disease. We tested for evidence of a shared genetic basis to these traits. We conducted 2 targeted…”
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Twenty-seven-year time trends in dementia incidence in Europe and the United States: The Alzheimer Cohorts Consortium
ISSN: 1526-632X, 1526-632XVydavateľské údaje: United States 04.08.2020Vydané v Neurology (04.08.2020)“…To determine changes in the incidence of dementia between 1988 and 2015. This analysis was performed in aggregated data from individuals >65 years of age in 7…”
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Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study
ISSN: 1556-3871, 1556-3871Vydavateľské údaje: United States 01.03.2014Vydané v Heart rhythm (01.03.2014)“…Genome-wide association studies (GWAS) have identified common genetic variants that predispose to atrial fibrillation (AF). It is unclear whether rare and…”
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Associations of NINJ2 Sequence Variants with Incident Ischemic Stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) Consortium
ISSN: 1932-6203, 1932-6203Vydavateľské údaje: United States Public Library of Science 24.06.2014Vydané v PloS one (24.06.2014)“…Stroke, the leading neurologic cause of death and disability, has a substantial genetic component. We previously conducted a genome-wide association study…”
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