John H Eckfeldt

Author PubWeight™ 153.52‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Estimating glomerular filtration rate from serum creatinine and cystatin C. N Engl J Med 2012 14.99
2 Recommendations for improving serum creatinine measurement: a report from the Laboratory Working Group of the National Kidney Disease Education Program. Clin Chem 2005 8.93
3 Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circ Cardiovasc Genet 2010 6.74
4 Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med 2005 5.78
5 Reporting genetic results in research studies: summary and recommendations of an NHLBI working group. Am J Med Genet A 2006 4.56
6 Performance in Measurement of Serum Cystatin C by Laboratories Participating in the College of American Pathologists 2014 CYS Survey. Arch Pathol Lab Med 2015 3.36
7 Leukocyte telomeres are longer in African Americans than in whites: the National Heart, Lung, and Blood Institute Family Heart Study and the Bogalusa Heart Study. Aging Cell 2008 3.24
8 Renal outcomes in high-risk hypertensive patients treated with an angiotensin-converting enzyme inhibitor or a calcium channel blocker vs a diuretic: a report from the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). Arch Intern Med 2005 3.18
9 Cardiovascular outcomes in high-risk hypertensive patients stratified by baseline glomerular filtration rate. Ann Intern Med 2006 2.81
10 Circulating TNF receptors 1 and 2 predict ESRD in type 2 diabetes. J Am Soc Nephrol 2012 2.75
11 Risk for ESRD in type 1 diabetes remains high despite renoprotection. J Am Soc Nephrol 2011 2.50
12 Clinical significance of incident hypokalemia and hyperkalemia in treated hypertensive patients in the antihypertensive and lipid-lowering treatment to prevent heart attack trial. Hypertension 2012 2.42
13 Plasma fatty acid composition and incidence of diabetes in middle-aged adults: the Atherosclerosis Risk in Communities (ARIC) Study. Am J Clin Nutr 2003 2.41
14 Roadmap for harmonization of clinical laboratory measurement procedures. Clin Chem 2011 2.34
15 High-normal serum uric acid increases risk of early progressive renal function loss in type 1 diabetes: results of a 6-year follow-up. Diabetes Care 2010 2.12
16 Dietary linolenic acid is inversely associated with calcified atherosclerotic plaque in the coronary arteries: the National Heart, Lung, and Blood Institute Family Heart Study. Circulation 2005 2.03
17 Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study. Am J Nephrol 2009 1.80
18 Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults. Am J Med Sci 2003 1.76
19 NHANES monitoring of serum 25-hydroxyvitamin D: a roundtable summary. J Nutr 2010 1.74
20 Biological variability of transferrin saturation and unsaturated iron-binding capacity. Am J Med 2007 1.72
21 Genome scan of glomerular filtration rate and albuminuria: the HyperGEN study. Nephrol Dial Transplant 2006 1.59
22 Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study. J Hypertens 2010 1.55
23 Trends in the prevalence of reduced GFR in the United States: a comparison of creatinine- and cystatin C-based estimates. Am J Kidney Dis 2013 1.54
24 HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study. Circ Cardiovasc Genet 2009 1.45
25 Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study. Circulation 2003 1.44
26 Biomarkers of vitamin B-12 status in NHANES: a roundtable summary. Am J Clin Nutr 2011 1.43
27 Biomarkers of folate status in NHANES: a roundtable summary. Am J Clin Nutr 2011 1.43
28 Alcohol consumption and metabolic syndrome: does the type of beverage matter? Obes Res 2004 1.38
29 Pharmacogenetic association of the angiotensin-converting enzyme insertion/deletion polymorphism on blood pressure and cardiovascular risk in relation to antihypertensive treatment: the Genetics of Hypertension-Associated Treatment (GenHAT) study. Circulation 2005 1.30
30 Pharmacogenetic association of the NPPA T2238C genetic variant with cardiovascular disease outcomes in patients with hypertension. JAMA 2008 1.30
31 Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Am J Hum Genet 2012 1.29
32 An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study. BMC Genet 2007 1.27
33 Serum concentration of cystatin C and risk of end-stage renal disease in diabetes. Diabetes Care 2012 1.26
34 HFE C282Y homozygotes have reduced low-density lipoprotein cholesterol: the Atherosclerosis Risk in Communities (ARIC) Study. Transl Res 2008 1.20
35 Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening. Can J Gastroenterol 2008 1.19
36 A genome-wide affected sibpair linkage analysis of hypertension: the HyperGEN network. Am J Hypertens 2003 1.12
37 Serum ferritin and transferrin saturation in Asians and Pacific Islanders. Arch Intern Med 2007 1.12
38 Interactions between the single nucleotide polymorphisms in the homocysteine pathway (MTHFR 677C>T, MTHFR 1298 A>C, and CBSins) and the efficacy of HMG-CoA reductase inhibitors in preventing cardiovascular disease in high-risk patients of hypertension: the GenHAT study. Pharmacogenet Genomics 2008 1.12
39 Comparison of serum concentrations of β-trace protein, β2-microglobulin, cystatin C, and creatinine in the US population. Clin J Am Soc Nephrol 2013 1.11
40 Comparison of the unsaturated iron-binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for hemochromatosis in 101,168 participants in the hemochromatosis and iron overload screening (HEIRS) study. Clin Chem 2005 1.09
41 Association of low-grade albuminuria with adverse cardiac mechanics: findings from the hypertension genetic epidemiology network (HyperGEN) study. Circulation 2013 1.07
42 Familial clustering for features of the metabolic syndrome: the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study. Diabetes Care 2006 1.06
43 The prevalence of reduced glomerular filtration rate in older hypertensive patients and its association with cardiovascular disease: a report from the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial. Arch Intern Med 2004 1.06
44 Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations. PLoS One 2012 1.03
45 Liver diseases in the hemochromatosis and iron overload screening study. Clin Gastroenterol Hepatol 2006 1.02
46 Genome-wide association study identifies genetic loci associated with iron deficiency. PLoS One 2011 1.01
47 Dietary linolenic acid is inversely associated with plasma triacylglycerol: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr 2003 1.01
48 Relation of the metabolic syndrome to calcified atherosclerotic plaque in the coronary arteries and aorta. Am J Cardiol 2005 1.00
49 Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study. Atherosclerosis 2003 0.98
50 Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care population. Am J Hematol 2008 0.98
51 HAMP promoter mutation nc.-153C>T in 785 HEIRS study participants. Haematologica 2009 0.97
52 Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis 2007 0.97
53 Influence of apolipoprotein E, smoking, and alcohol intake on carotid atherosclerosis: National Heart, Lung, and Blood Institute Family Heart Study. Stroke 2002 0.96
54 Association study of CRP gene polymorphisms with serum CRP level and cardiovascular risk in the NHLBI Family Heart Study. Am J Physiol Heart Circ Physiol 2006 0.95
55 Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study. Can J Gastroenterol 2009 0.95
56 HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants. Am J Hematol 2009 0.94
57 Advances in standardization of laboratory measurement procedures: implications for measuring biomarkers of folate and vitamin B-12 status in NHANES. Am J Clin Nutr 2011 0.94
58 Alcohol consumption and plasma atrial natriuretic peptide (from the HyperGEN study). Am J Cardiol 2006 0.93
59 Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants. Blood Cells Mol Dis 2009 0.92
60 Genetic and Adverse Health Outcome Associations with Treatment Resistant Hypertension in GenHAT. Int J Hypertens 2013 0.92
61 A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Hum Genet 2002 0.91
62 The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13 ) on the effectiveness of statins: the GenHAT study. Pharmacogenet Genomics 2009 0.91
63 Serum β-trace protein and risk of mortality in incident hemodialysis patients. Clin J Am Soc Nephrol 2012 0.91
64 The effects of freeze-thaw on β-trace protein and β2-microglobulin assays after long-term sample storage. Clin Biochem 2012 0.89
65 Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study. Hepatology 2012 0.89
66 Interarm differences in seated systolic and diastolic blood pressure: the Hypertension Genetic Epidemiology Network study. J Hypertens 2005 0.89
67 Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening. Am J Hematol 2008 0.88
68 Pharmacogenetic effect of the stromelysin (MMP3) polymorphism on stroke risk in relation to antihypertensive treatment: the genetics of hypertension associated treatment study. Stroke 2010 0.88
69 Novel association between plasma matrix metalloproteinase-9 and risk of incident atrial fibrillation in a case-cohort study: the Atherosclerosis Risk in Communities study. PLoS One 2013 0.88
70 Pharmacogenetic associations of MMP9 and MMP12 variants with cardiovascular disease in patients with hypertension. PLoS One 2011 0.87
71 Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study. Am J Hum Genet 2002 0.85
72 Dietary linolenic acid and fasting glucose and insulin: the National Heart, Lung, and Blood Institute Family Heart Study. Obesity (Silver Spring) 2006 0.85
73 Vitamin D-Binding Protein Concentrations Quantified by Mass Spectrometry. N Engl J Med 2015 0.84
74 Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study. Thyroid 2008 0.83
75 Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study. Pharmacogenet Genomics 2012 0.83
76 Pharmacogenetic association of NOS3 variants with cardiovascular disease in patients with hypertension: the GenHAT study. PLoS One 2012 0.83
77 Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study. Am J Hematol 2010 0.83
78 Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians. Clin Gastroenterol Hepatol 2013 0.83
79 Dietary linolenic acid and adjusted QT and JT intervals in the National Heart, Lung, and Blood Institute Family Heart study. J Am Coll Cardiol 2005 0.82
80 HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening. Genet Test 2007 0.82
81 Exceptional memory performance in the Long Life Family Study. Neurobiol Aging 2013 0.82
82 TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study. Atherosclerosis 2004 0.82
83 Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Hum Genet 2004 0.82
84 Absence of an interaction between the angiotensin-converting enzyme insertion-deletion polymorphism and pravastatin on cardiovascular disease in high-risk hypertensive patients: the Genetics of Hypertension-Associated Treatment (GenHAT) study. Am Heart J 2007 0.81
85 Mixture models of serum iron measures in population screening for hemochromatosis and iron overload. Transl Res 2006 0.80
86 Hemochromatosis (HFE) gene splice site mutation IVS5+1 G/A in North American Vietnamese with and without phenotypic evidence of iron overload. Transl Res 2007 0.79
87 Comparison of cystatin C and creatinine-based equations for GFR estimation after living kidney donation. Transplantation 2014 0.79
88 Antihypertensive pharmacogenetic effect of fibrinogen-beta variant -455G>A on cardiovascular disease, end-stage renal disease, and mortality: the GenHAT study. Pharmacogenet Genomics 2009 0.78
89 Apolipoprotein E polymorphism modifies the alcohol-HDL association observed in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr 2004 0.78
90 Health-related quality of life in a racially diverse population screened for hemochromatosis: results from the Hemochromatosis and Iron Overload Screening (HEIRS) study. Genet Med 2007 0.78
91 Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. Eur J Hum Genet 2002 0.78
92 Estimated plasma stearoyl co-A desaturase-1 activity and risk of incident diabetes: the Atherosclerosis Risk in Communities (ARIC) study. Metabolism 2012 0.77
93 HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L. Can J Gastroenterol 2013 0.77
94 Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN Study. Hum Genet 2007 0.77
95 Dietary iron intake and serum ferritin concentration in 213 patients homozygous for the HFEC282Y hemochromatosis mutation. Can J Gastroenterol 2012 0.76
96 Comment on "Multidimensional results reporting to participants in genomic studies: getting it right". Sci Transl Med 2011 0.76
97 Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study. Pharmacogenet Genomics 2014 0.75
98 Tumor necrosis factor-alpha promoter variants and iron phenotypes in 785 hemochromatosis and iron overload screening (HEIRS) study participants. Blood Cells Mol Dis 2010 0.75
99 The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. Am J Hypertens 2009 0.75
100 Interlaboratory variation of plasma total homocysteine measurements: results of three successive homocysteine proficiency testing surveys. Clin Chem 2002 0.75
101 Cystatin C enhances glomerular filtration rate estimating equations in kidney transplant recipients. Am J Nephrol 2014 0.75