Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
New loci associated with kidney function and chronic kidney disease.
|
Nat Genet
|
2010
|
5.58
|
2
|
Lower estimated glomerular filtration rate and higher albuminuria are associated with mortality and end-stage renal disease. A collaborative meta-analysis of kidney disease population cohorts.
|
Kidney Int
|
2011
|
5.25
|
3
|
Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study.
|
J Am Soc Nephrol
|
2007
|
4.59
|
4
|
CUBN is a gene locus for albuminuria.
|
J Am Soc Nephrol
|
2011
|
2.70
|
5
|
Linking health-status measurements to the international classification of functioning, disability and health.
|
J Rehabil Med
|
2002
|
2.48
|
6
|
Serum creatinine, cystatin C, and beta-trace protein in diagnostic staging and predicting progression of primary nondiabetic chronic kidney disease.
|
Clin Chem
|
2010
|
1.95
|
7
|
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.
|
Circ Cardiovasc Genet
|
2008
|
1.82
|
8
|
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.
|
Atherosclerosis
|
2009
|
1.78
|
9
|
Genome-wide association and functional follow-up reveals new loci for kidney function.
|
PLoS Genet
|
2012
|
1.68
|
10
|
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.
|
PLoS Genet
|
2011
|
1.68
|
11
|
Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI.
|
Diabetes Care
|
2008
|
1.58
|
12
|
Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
|
Exp Gerontol
|
2008
|
1.41
|
13
|
Pro-A-type natriuretic peptide and pro-adrenomedullin predict progression of chronic kidney disease: the MMKD Study.
|
Kidney Int
|
2008
|
1.26
|
14
|
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.
|
Circ Cardiovasc Genet
|
2011
|
1.26
|
15
|
Uric acid as a risk factor for progression of non-diabetic chronic kidney disease? The Mild to Moderate Kidney Disease (MMKD) Study.
|
Exp Gerontol
|
2008
|
1.25
|
16
|
INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism.
|
Obesity (Silver Spring)
|
2008
|
1.24
|
17
|
Identification of relevant ICF categories in patients with chronic health conditions: a Delphi exercise.
|
J Rehabil Med
|
2004
|
1.22
|
18
|
Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?
|
PLoS Genet
|
2009
|
1.18
|
19
|
Validation of the International Classification of Functioning, Disability and Health (ICF) Core Set for rheumatoid arthritis from the patient perspective using focus groups.
|
Arthritis Res Ther
|
2006
|
1.16
|
20
|
A common variant in the adiponutrin gene influences liver enzyme values.
|
J Med Genet
|
2009
|
1.08
|
21
|
Predictive accuracy of the SCORE risk function for cardiovascular disease in clinical practice: a prospective evaluation of 44 649 Austrian men and women.
|
Eur J Cardiovasc Prev Rehabil
|
2005
|
1.08
|
22
|
B-type natriuretic peptide concentrations predict the progression of nondiabetic chronic kidney disease: the Mild-to-Moderate Kidney Disease Study.
|
Clin Chem
|
2007
|
1.00
|
23
|
Are the contents of treatment outcomes in fibromyalgia trials represented in the International Classification Of Functioning, Disability, and Health?
|
Clin J Pain
|
2007
|
0.99
|
24
|
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study.
|
Clin Chem
|
2008
|
0.94
|
25
|
Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease.
|
Exp Gerontol
|
2008
|
0.92
|
26
|
Evaluation of gene-obesity interaction effects on cholesterol levels: a genetic predisposition score on HDL-cholesterol is modified by obesity.
|
Atherosclerosis
|
2012
|
0.90
|
27
|
Measuring functioning in patients with hand osteoarthritis--content comparison of questionnaires based on the International Classification of Functioning, Disability and Health (ICF).
|
Rheumatology (Oxford)
|
2006
|
0.87
|
28
|
Homoarginine and progression of chronic kidney disease: results from the Mild to Moderate Kidney Disease Study.
|
PLoS One
|
2013
|
0.86
|
29
|
Cigarette smoking and chronic allograft nephropathy.
|
Nephrol Dial Transplant
|
2007
|
0.83
|
30
|
The association of relative telomere length with symptomatic peripheral arterial disease: results from the CAVASIC study.
|
Atherosclerosis
|
2013
|
0.83
|
31
|
Common variants in Mendelian kidney disease genes and their association with renal function.
|
J Am Soc Nephrol
|
2013
|
0.82
|
32
|
Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants.
|
Eur J Epidemiol
|
2014
|
0.81
|
33
|
Hydrogen breath testing versus LCT genotyping for the diagnosis of lactose intolerance: a matter of age?
|
Clin Chim Acta
|
2007
|
0.81
|
34
|
Plasma concentrations of the vitamin E-binding protein afamin are associated with overall and progression-free survival and platinum sensitivity in serous ovarian cancer--a study by the OVCAD consortium.
|
Gynecol Oncol
|
2012
|
0.81
|
35
|
Content validity of the Extended ICF Core Set for stroke: an international Delphi survey of physical therapists.
|
Phys Ther
|
2011
|
0.81
|
36
|
Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese persons.
|
Am J Clin Nutr
|
2008
|
0.80
|
37
|
Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations.
|
Eur J Hum Genet
|
2012
|
0.80
|
38
|
Content comparison of osteoporosis-targeted health status measures in relation to the International Classification of Functioning, Disability and Health (ICF).
|
Clin Rheumatol
|
2004
|
0.79
|
39
|
Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.
|
PLoS One
|
2012
|
0.79
|
40
|
Validation of the extended ICF core set for stroke from the patient perspective using focus groups.
|
Disabil Rehabil
|
2011
|
0.79
|
41
|
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium.
|
Atherosclerosis
|
2012
|
0.79
|
42
|
Visualizing interaction effects: a proposal for presentation and interpretation.
|
J Clin Epidemiol
|
2012
|
0.77
|
43
|
Influence of polymorphisms in genes encoding for insulin-like growth factor (IGF)-I, insulin, and IGF-binding protein (IGFBP)-3 on IGF-I, IGF-II, and IGFBP-3 levels in umbilical cord plasma.
|
Horm Res Paediatr
|
2012
|
0.77
|
44
|
What is our knowledge of functioning and disability in hand conditions based on?
|
Arch Phys Med Rehabil
|
2011
|
0.75
|