Julie A Johnson

Author PubWeight™ 156.90‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A pharmacogenetic versus a clinical algorithm for warfarin dosing. N Engl J Med 2013 7.09
2 CYP4F2 genetic variant alters required warfarin dose. Blood 2008 4.23
3 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. Blood 2008 4.02
4 Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study. Lancet 2013 3.21
5 Influence of coagulation factor, vitamin K epoxide reductase complex subunit 1, and cytochrome P450 2C9 gene polymorphisms on warfarin dose requirements. Clin Pharmacol Ther 2006 3.06
6 Preserving the genetic integrity of human embryonic stem cells. Nat Biotechnol 2005 3.03
7 Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups. Blood 2010 2.93
8 Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am J Hum Genet 2012 2.53
9 The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation. Clin Pharmacol Ther 2013 2.39
10 beta-Adrenergic receptor polymorphisms and responses during titration of metoprolol controlled release/extended release in heart failure. Clin Pharmacol Ther 2005 2.20
11 Regulatory polymorphism in vitamin K epoxide reductase complex subunit 1 (VKORC1) affects gene expression and warfarin dose requirement. Blood 2008 2.18
12 Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. Am J Hum Genet 2010 2.15
13 Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet 2012 1.96
14 Pharmacogenomics: challenges and opportunities. Ann Intern Med 2006 1.96
15 Plasma renin activity predicts blood pressure responses to beta-blocker and thiazide diuretic as monotherapy and add-on therapy for hypertension. Am J Hypertens 2010 1.90
16 Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. Stroke 2013 1.80
17 Statistical design of personalized medicine interventions: the Clarification of Optimal Anticoagulation through Genetics (COAG) trial. Trials 2010 1.72
18 Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease. Circ Cardiovasc Genet 2011 1.69
19 G protein receptor kinase 4 polymorphisms: β-blocker pharmacogenetics and treatment-related outcomes in hypertension. Hypertension 2012 1.59
20 Clinical pharmacogenetics implementation: approaches, successes, and challenges. Am J Med Genet C Semin Med Genet 2014 1.57
21 Beta1-adrenergic receptor polymorphisms and left ventricular remodeling changes in response to beta-blocker therapy. Pharmacogenet Genomics 2005 1.53
22 Hypertension susceptibility loci and blood pressure response to antihypertensives: results from the pharmacogenomic evaluation of antihypertensive responses study. Circ Cardiovasc Genet 2012 1.52
23 Pharmacogenomic association of nonsynonymous SNPs in SIGLEC12, A1BG, and the selectin region and cardiovascular outcomes. Hypertension 2013 1.52
24 Two CES1 gene mutations lead to dysfunctional carboxylesterase 1 activity in man: clinical significance and molecular basis. Am J Hum Genet 2008 1.50
25 TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives. J Hypertens 2015 1.43
26 Genetic warfarin dosing: tables versus algorithms. J Am Coll Cardiol 2011 1.43
27 Sustained restoration of autonomic balance with long- but not short-acting metoprolol in patients with heart failure. J Card Fail 2006 1.41
28 KCNMB1 genotype influences response to verapamil SR and adverse outcomes in the INternational VErapamil SR/Trandolapril STudy (INVEST). Pharmacogenet Genomics 2007 1.40
29 Genetic and pharmacogenetic associations between NOS3 polymorphisms, blood pressure, and cardiovascular events in hypertension. Am J Hypertens 2009 1.40
30 A haplotype-based algorithm for multilocus linkage disequilibrium mapping of quantitative trait loci with epistasis. Genetics 2003 1.31
31 Protocols for cytogenetic studies of human embryonic stem cells. Methods 2008 1.30
32 Collection of genomic DNA by the noninvasive mouthwash method for use in pharmacogenetic studies. Pharmacotherapy 2002 1.28
33 Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet 2013 1.27
34 Highly variable mRNA expression and splicing of L-type voltage-dependent calcium channel alpha subunit 1C in human heart tissues. Pharmacogenet Genomics 2006 1.27
35 Genetics and cardiovascular disease: a policy statement from the American Heart Association. Circulation 2012 1.26
36 Creating and evaluating genetic tests predictive of drug response. Nat Rev Drug Discov 2008 1.24
37 Sequencing complex diseases With HapMap. Genetics 2004 1.22
38 Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. PLoS One 2012 1.21
39 Genetic and nongenetic factors associated with warfarin dose requirements in Egyptian patients. Pharmacogenet Genomics 2011 1.20
40 Pharmacokinetics and CYP2D6 genotypes do not predict metoprolol adverse events or efficacy in hypertension. Clin Pharmacol Ther 2004 1.20
41 Relation of beta(2)-adrenoceptor haplotype to risk of death and heart transplantation in patients with heart failure. Am J Cardiol 2006 1.19
42 Effects of high-fructose corn syrup and sucrose on the pharmacokinetics of fructose and acute metabolic and hemodynamic responses in healthy subjects. Metabolism 2011 1.15
43 Impact of abdominal obesity on incidence of adverse metabolic effects associated with antihypertensive medications. Hypertension 2009 1.15
44 Synergistic polymorphisms of beta1 and alpha2C-adrenergic receptors and the influence on left ventricular ejection fraction response to beta-blocker therapy in heart failure. Pharmacogenet Genomics 2007 1.15
45 Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide. Hypertension 2013 1.14
46 Pharmacogenetics of beta-blockers. Pharmacotherapy 2007 1.13
47 Chromosome 7 and 19 trisomy in cultured human neural progenitor cells. PLoS One 2009 1.13
48 Rationale and design of the Clarification of Optimal Anticoagulation through Genetics trial. Am Heart J 2013 1.12
49 Polymorphisms in genes coding for GRK2 and GRK5 and response differences in antihypertensive-treated patients. Pharmacogenet Genomics 2011 1.12
50 Pharmacometabolomics reveals racial differences in response to atenolol treatment. PLoS One 2013 1.10
51 Warfarin: an old drug but still interesting. Pharmacotherapy 2008 1.08
52 Modeling sequence-sequence interactions for drug response. Bioinformatics 2007 1.08
53 Role of carboxylesterase 1 and impact of natural genetic variants on the hydrolysis of trandolapril. Biochem Pharmacol 2009 1.08
54 Differences in drug pharmacokinetics between East Asians and Caucasians and the role of genetic polymorphisms. J Clin Pharmacol 2004 1.07
55 Alpha-adducin polymorphism associated with increased risk of adverse cardiovascular outcomes: results from GENEtic Substudy of the INternational VErapamil SR-trandolapril STudy (INVEST-GENES). Am Heart J 2008 1.05
56 Comparison of cytochrome P450 2C9 genotyping methods and implications for the clinical laboratory. Pharmacotherapy 2004 1.04
57 Human polymorphisms in the glutathione transferase zeta 1/maleylacetoacetate isomerase gene influence the toxicokinetics of dichloroacetate. J Clin Pharmacol 2011 1.03
58 Cardiovascular pharmacogenomics. Circ Res 2011 1.03
59 Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. J Am Coll Cardiol 2013 1.02
60 Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association. Circulation 2013 1.01
61 Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes. Circ Cardiovasc Genet 2013 0.99
62 Power to identify a genetic predictor of antihypertensive drug response using different methods to measure blood pressure response. J Transl Med 2012 0.97
63 Warfarin pharmacogenetics: a rising tide for its clinical value. Circulation 2012 0.97
64 Emerging roles for pharmacists in clinical implementation of pharmacogenomics. Pharmacotherapy 2014 0.96
65 Genetic influence on exercise-induced changes in physical function among mobility-limited older adults. Physiol Genomics 2014 0.95
66 Very important pharmacogene summary ADRB2. Pharmacogenet Genomics 2010 0.94
67 Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes. Stem Cell Res 2011 0.94
68 CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response. Circ Cardiovasc Genet 2009 0.94
69 Association of variants in NEDD4L with blood pressure response and adverse cardiovascular outcomes in hypertensive patients treated with thiazide diuretics. J Hypertens 2013 0.91
70 Discordant beta-blocker effects on clinic, ambulatory, resting, and exercise hemodynamics in patients with hypertension. Pharmacotherapy 2006 0.91
71 Lack of correlation between thiazide-induced hyperglycemia and hypokalemia: subgroup analysis of results from the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. Pharmacotherapy 2009 0.90
72 Simplified method for determination of clarithromycin in human plasma using protein precipitation in a 96-well format and liquid chromatography-tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci 2008 0.90
73 Very important pharmacogene summary: thiopurine S-methyltransferase. Pharmacogenet Genomics 2010 0.90
74 Very important pharmacogene summary: sulfotransferase 1A1. Pharmacogenet Genomics 2009 0.89
75 Genetic nondiscrimination legislation: a critical prerequisite for pharmacogenomics data sharing. Pharmacogenomics 2007 0.89
76 Factors influencing blood pressure response to trandolapril add-on therapy in patients taking verapamil SR (from the International Verapamil SR/Trandolapril [INVEST] Study). Am J Cardiol 2007 0.89
77 Genetic variation in the beta2 subunit of the voltage-gated calcium channel and pharmacogenetic association with adverse cardiovascular outcomes in the INternational VErapamil SR-Trandolapril STudy GENEtic Substudy (INVEST-GENES). Circ Cardiovasc Genet 2010 0.89
78 Aromatase gene polymorphisms are associated with survival among patients with cardiovascular disease in a sex-specific manner. PLoS One 2010 0.89
79 CYP2C19 polymorphisms and therapeutic drug monitoring of voriconazole: are we ready for clinical implementation of pharmacogenomics? Pharmacotherapy 2014 0.88
80 Is diabetes mellitus-linked amino acid signature associated with β-blocker-induced impaired fasting glucose? Circ Cardiovasc Genet 2014 0.88
81 Urate transporter gene SLC22A12 polymorphisms associated with obesity and metabolic syndrome in Caucasians with hypertension. Kidney Blood Press Res 2012 0.88
82 Effect of cytochrome P450 3A5 genotype on atorvastatin pharmacokinetics and its interaction with clarithromycin. Pharmacotherapy 2011 0.88
83 Pharmacogenetics of chronic cardiovascular drugs: applications and implications. Expert Opin Pharmacother 2006 0.88
84 Pathway analysis of genome-wide data improves warfarin dose prediction. BMC Genomics 2013 0.87
85 Effects of genetic variation in H3K79 methylation regulatory genes on clinical blood pressure and blood pressure response to hydrochlorothiazide. J Transl Med 2012 0.87
86 Blood pressure responses and metabolic effects of hydrochlorothiazide and atenolol. Am J Hypertens 2011 0.86
87 Adrenergic gene polymorphisms and cardiovascular risk in the NHLBI-sponsored Women's Ischemia Syndrome Evaluation. J Transl Med 2008 0.86
88 Carvedilol reduces aortic wave reflection and improves left ventricular/vascular coupling: a comparison with atenolol (CENTRAL Study). J Clin Hypertens (Greenwich) 2011 0.86
89 Comparison of office, ambulatory, and home blood pressure antihypertensive response to atenolol and hydrochlorthiazide. J Clin Hypertens (Greenwich) 2010 0.85
90 Single nucleotide polymorphism discovery and haplotype analysis of Ca2+-dependent K+ channel beta-1 subunit. Pharmacogenet Genomics 2007 0.85
91 The evolving role of nesiritide in advanced or decompensated heart failure. Pharmacotherapy 2003 0.85
92 Predictors for glucose change in hypertensive participants following short-term treatment with atenolol or hydrochlorothiazide. Pharmacotherapy 2014 0.84
93 Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Hum Mol Genet 2013 0.84
94 Pharmacogenetics, pharmacogenomics, and cardiovascular therapeutics: the way forward. Am J Cardiovasc Drugs 2002 0.84
95 Systolic blood pressure and subjective well-being in patients with coronary artery disease. Clin Cardiol 2009 0.83
96 The influence of the CYP2C19*10 allele on clopidogrel activation and CYP2C19*2 genotyping. Pharmacogenet Genomics 2014 0.83
97 Association of beta1-adrenergic receptor genetic polymorphism with mental stress-induced myocardial ischemia in patients with coronary artery disease. Arch Intern Med 2008 0.83
98 A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian population. Mol Genet Metab 2011 0.83
99 Liver X receptor α gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study. Pharmacogenet Genomics 2011 0.82
100 Genetic predictors of glucocorticoid-induced hypertension in children with acute lymphoblastic leukemia. Pharmacogenet Genomics 2008 0.81
101 Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide. Pharmacogenet Genomics 2010 0.81
102 Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association. Circulation 2015 0.81
103 Beta-blocker pharmacogenetics in heart failure. Heart Fail Rev 2008 0.81
104 Assessment of human serotonin 1A receptor polymorphisms and SSRI responsiveness. Mol Diagn Ther 2007 0.80
105 Influence of gender and race on hemodynamic response to dobutamine during dobutamine stress echocardiography. Am J Cardiol 2004 0.80
106 Atenolol exposure and risk for development of adverse metabolic effects: a pilot study. Pharmacotherapy 2010 0.80
107 PROX1 gene variant is associated with fasting glucose change after antihypertensive treatment. Pharmacotherapy 2013 0.80
108 Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs. J Am Heart Assoc 2015 0.79
109 Impact of TCF7L2 single nucleotide polymorphisms on hydrochlorothiazide-induced diabetes. Pharmacogenet Genomics 2013 0.79
110 Genotyping the GGGCGG tandem repeat promoter polymorphism in the 5-lipoxygenase enzyme gene (ALOX5) by pyrosequencing assay. Genet Test Mol Biomarkers 2009 0.78
111 Association of diurnal blood pressure pattern with risk of hospitalization or death in men with heart failure. J Card Fail 2007 0.78
112 Comparing marginal structural models to standard methods for estimating treatment effects of antihypertensive combination therapy. BMC Med Res Methodol 2012 0.78
113 VKORC1 Asp36Tyr geographic distribution and its impact on warfarin dose requirements in Egyptians. Thromb Haemost 2013 0.78
114 PharmGKB submission update: IX. ADRB1 gene summary. Pharmacol Rev 2007 0.78
115 Altered beta-2 adrenergic receptor gene expression in human clinical hypertension. Biol Res Nurs 2009 0.78
116 University of Florida Clinical and Translational Science Institute: transformation and translation in personalized medicine. Clin Transl Sci 2011 0.78
117 Heart failure pharmacogenetics: past, present, and future. Curr Cardiol Rep 2011 0.78
118 Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. PLoS One 2013 0.77
119 Association of branched and aromatic amino acids levels with metabolic syndrome and impaired fasting glucose in hypertensive patients. Metab Syndr Relat Disord 2015 0.77
120 Night blood pressure responses to atenolol and hydrochlorothiazide in black and white patients with essential hypertension. Am J Hypertens 2013 0.77
121 Impact of genetic polymorphisms of SLC2A2, SLC2A5, and KHK on metabolic phenotypes in hypertensive individuals. PLoS One 2013 0.77
122 PTPRD gene associated with blood pressure response to atenolol and resistant hypertension. J Hypertens 2015 0.76
123 Lack of association of the HMGA1 IVS5-13insC variant with type 2 diabetes in an ethnically diverse hypertensive case control cohort. J Transl Med 2013 0.76
124 CYP2C9 promoter variable number tandem repeat polymorphism regulates mRNA expression in human livers. Drug Metab Dispos 2012 0.76
125 Impact of the CYP2C19 genotype on voriconazole exposure in adults with invasive fungal infections. Pharmacogenet Genomics 2017 0.75
126 Genome-Wide Prioritization and Transcriptomics Reveal Novel Signatures Associated With Thiazide Diuretics Blood Pressure Response. Circ Cardiovasc Genet 2017 0.75
127 Re: Meckley LM, Veenstra DL. Screening for the alpha-adducin Gly460Trp variant in hypertensive patients: a cost-effectiveness analysis. Pharmacogenet Genom 2006; 16:139-147. Pharmacogenet Genomics 2006 0.75
128 Clopidogrel and warfarin pharmacogenetic tests: what is the evidence for use in clinical practice? Curr Opin Cardiol 2013 0.75
129 Combination antihypertensive treatment: is initiation order important? J Clin Hypertens (Greenwich) 2010 0.75
130 Dobutamine pharmacodynamics during dobutamine stress echocardiography and the impact of beta-blocker withdrawal: a report from the Women's Ischemic Syndrome Evaluation Study. Pharmacotherapy 2002 0.75