1
|
New loci associated with kidney function and chronic kidney disease.
|
Nat Genet
|
2010
|
5.58
|
2
|
The -256T>C polymorphism in the apolipoprotein A-II gene promoter is associated with body mass index and food intake in the genetics of lipid lowering drugs and diet network study.
|
Clin Chem
|
2007
|
2.03
|
3
|
High-throughput discovery of rare insertions and deletions in large cohorts.
|
Genome Res
|
2010
|
1.83
|
4
|
A family longevity selection score: ranking sibships by their longevity, size, and availability for study.
|
Am J Epidemiol
|
2009
|
1.81
|
5
|
Genome-wide association and functional follow-up reveals new loci for kidney function.
|
PLoS Genet
|
2012
|
1.68
|
6
|
Using tree-based recursive partitioning methods to group haplotypes for increased power in association studies.
|
Ann Hum Genet
|
2005
|
1.15
|
7
|
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.
|
Hum Mol Genet
|
2012
|
1.14
|
8
|
Genome-wide linkage analysis for loci affecting pulse pressure: the Family Blood Pressure Program.
|
Hypertension
|
2005
|
1.07
|
9
|
Polyunsaturated fatty acids modulate the effect of TCF7L2 gene variants on postprandial lipemia.
|
J Nutr
|
2009
|
1.01
|
10
|
Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.
|
BMC Genomics
|
2012
|
0.99
|
11
|
Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study.
|
Pharmacogenet Genomics
|
2009
|
0.97
|
12
|
An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP).
|
Am J Hypertens
|
2006
|
0.95
|
13
|
Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states.
|
Am J Clin Nutr
|
2008
|
0.94
|
14
|
Postprandial triacylglycerol metabolism is modified by the presence of genetic variation at the perilipin (PLIN) locus in 2 white populations.
|
Am J Clin Nutr
|
2008
|
0.93
|
15
|
Apolipoprotein E and familial longevity.
|
Neurobiol Aging
|
2012
|
0.93
|
16
|
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses.
|
BMC Proc
|
2009
|
0.91
|
17
|
The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions.
|
J Hum Genet
|
2008
|
0.90
|
18
|
Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q.
|
Atherosclerosis
|
2004
|
0.87
|
19
|
Genetic variants at the PDZ-interacting domain of the scavenger receptor class B type I interact with diet to influence the risk of metabolic syndrome in obese men and women.
|
J Nutr
|
2009
|
0.87
|
20
|
Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study.
|
Am J Clin Nutr
|
2009
|
0.84
|
21
|
Functional genomics of critical illness and injury.
|
Crit Care Med
|
2002
|
0.84
|
22
|
Epistatic interactions of CDKN2B-TCF7L2 for risk of type 2 diabetes and of CDKN2B-JAZF1 for triglyceride/high-density lipoprotein ratio longitudinal change: evidence from the Framingham Heart Study.
|
BMC Proc
|
2009
|
0.83
|
23
|
Functional genomics of critical illness and injury.
|
Crit Care Med
|
2002
|
0.82
|
24
|
A haplotype similarity based transmission/disequilibrium test under founder heterogeneity.
|
Ann Hum Genet
|
2005
|
0.82
|
25
|
Common variants in Mendelian kidney disease genes and their association with renal function.
|
J Am Soc Nephrol
|
2013
|
0.82
|
26
|
Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.
|
Hum Genet
|
2004
|
0.82
|
27
|
Inheritance pattern of Beckwith-Wiedemann syndrome is heterogeneous in 291 families with an affected proband.
|
Am J Med Genet A
|
2005
|
0.75
|