PubRank

Clive R Pullinger

Author PubWeight™ 55.14‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. PLoS Genet 2008 5.85
2 Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia. Nat Genet 2007 2.60
3 A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol 2007 2.47
4 Functional variants of the HMGA1 gene and type 2 diabetes mellitus. JAMA 2011 2.00
5 Identification of four gene variants associated with myocardial infarction. Am J Hum Genet 2005 1.89
6 Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis. Am J Hum Genet 2012 1.88
7 Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia. Eur Heart J 2008 1.80
8 Symptom experience in HIV-infected adults: a function of demographic and clinical characteristics. J Pain Symptom Manage 2009 1.72
9 Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction. Arterioscler Thromb Vasc Biol 2006 1.60
10 Lack of support for the association between GAD2 polymorphisms and severe human obesity. PLoS Biol 2005 1.59
11 Exome sequencing in suspected monogenic dyslipidemias. Circ Cardiovasc Genet 2015 1.51
12 Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm 2012 1.49
13 Genetic analysis of a polymorphism in the human apoA-V gene: effect on plasma lipids. J Lipid Res 2003 1.32
14 Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case-control study. Hum Mol Genet 2008 1.30
15 Risk factors and symptoms associated with pain in HIV-infected adults. J Assoc Nurses AIDS Care 2010 1.21
16 Relation of increased prebeta-1 high-density lipoprotein levels to risk of coronary heart disease. Am J Cardiol 2011 1.09
17 Self-reported medication adherence and symptom experience in adults with HIV. J Assoc Nurses AIDS Care 2011 1.07
18 Assessing the role of the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) three-finger domain in binding lipoprotein lipase. J Biol Chem 2011 1.07
19 WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. Am J Hum Genet 2008 1.06
20 Mechanisms of statin-induced myalgia assessed by physiogenomic associations. Atherosclerosis 2011 1.05
21 Types of sleep problems in adults living with HIV/AIDS. J Clin Sleep Med 2012 1.00
22 Apolipoprotein E e4 allele increases the risk of early postoperative delirium in older patients undergoing noncardiac surgery. Anesthesiology 2007 0.99
23 Regulation of apoAI processing by procollagen C-proteinase enhancer-2 and bone morphogenetic protein-1. J Lipid Res 2009 0.95
24 Apolipoprotein L-I is positively associated with hyperglycemia and plasma triglycerides in CAD patients with low HDL. J Lipid Res 2004 0.91
25 A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components. Sci Rep 2013 0.90
26 The lipoprotein lipase gene in combined hyperlipidemia: evidence of a protective allele depletion. Lipids Health Dis 2006 0.90
27 HDL cholesterol efflux capacity and cardiovascular events. N Engl J Med 2015 0.89
28 Galanin preproprotein is associated with elevated plasma triglycerides. Arterioscler Thromb Vasc Biol 2008 0.88
29 Genetic variation of PLTP modulates lipoprotein profiles in hypoalphalipoproteinemia. J Lipid Res 2005 0.86
30 Variations in human HM74 (GPR109B) and HM74A (GPR109A) niacin receptors. Hum Mutat 2005 0.85
31 No influence of the VAMP8 rs1010 single nucleotide polymorphism on platelet functions in vitro. J Cell Mol Med 2009 0.84
32 Polymorphisms of interleukin-1 Beta and interleukin-17Alpha genes are associated with restless legs syndrome. Biol Res Nurs 2013 0.84
33 Arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene and coronary heart disease risk in familial hypercholesterolemia. Atherosclerosis 2008 0.83
34 Comment on: Marquez et al. Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes 2012;61:524-530. Diabetes 2012 0.83
35 Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia. Metabolism 2008 0.82
36 Regulation of ATP-binding cassette transporter A1 transcription by thyroid hormone receptor. Biochemistry 2004 0.82
37 The I4399M variant of apolipoprotein(a) is associated with increased oxidized phospholipids on apolipoprotein B-100 particles. Atherosclerosis 2009 0.82
38 Genetic variants of the ENPP1/PC-1 gene are associated with hypertriglyceridemia in male subjects. Metab Syndr Relat Disord 2009 0.81
39 Evaluation of polymorphisms in EWSR1 and risk of Ewing sarcoma: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer 2011 0.81
40 Association between regulator of G protein signaling 9-2 and body weight. PLoS One 2011 0.80
41 Deficiency of TDAG51 protects against atherosclerosis by modulating apoptosis, cholesterol efflux, and peroxiredoxin-1 expression. J Am Heart Assoc 2013 0.79
42 Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol? Pharmacogenomics 2010 0.79
43 Polymorphisms and noncardioembolic stroke in three case-control studies. Cerebrovasc Dis 2011 0.76
44 Influence of an asparagine to lysine mutation at amino acid 3516 of apolipoprotein B on low-density lipoprotein receptor binding. Clin Chim Acta 2002 0.75
45 Epigenetic regulation and measurement of epigenetic changes. Biol Res Nurs 2012 0.75
46 Dynamic regulation of alternative ATP-binding cassette transporter A1 transcripts. Biochem Biophys Res Commun 2003 0.75