Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
|
Science
|
2007
|
51.70
|
2
|
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
|
Nat Genet
|
2008
|
35.06
|
3
|
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
|
Nat Genet
|
2008
|
22.35
|
4
|
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
|
Nat Genet
|
2008
|
20.73
|
5
|
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.
|
Lancet
|
2012
|
12.10
|
6
|
Polymorphisms associated with cholesterol and risk of cardiovascular events.
|
N Engl J Med
|
2008
|
9.83
|
7
|
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
|
Science
|
2010
|
9.61
|
8
|
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
|
Nat Genet
|
2008
|
7.07
|
9
|
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
|
PLoS Genet
|
2012
|
6.15
|
10
|
Transferability of tag SNPs in genetic association studies in multiple populations.
|
Nat Genet
|
2006
|
4.78
|
11
|
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals.
|
Diabetes
|
2006
|
4.36
|
12
|
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
|
PLoS Genet
|
2012
|
3.21
|
13
|
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
|
Nature
|
2013
|
2.57
|
14
|
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
|
Nat Genet
|
2011
|
2.42
|
15
|
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.
|
PLoS Genet
|
2012
|
2.34
|
16
|
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.
|
Nat Genet
|
2013
|
1.91
|
17
|
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants.
|
Genet Epidemiol
|
2011
|
1.78
|
18
|
A genome-wide association search for type 2 diabetes genes in African Americans.
|
PLoS One
|
2012
|
1.72
|
19
|
Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes.
|
Diabetes
|
2005
|
1.22
|
20
|
5' flanking variants of resistin are associated with obesity.
|
Diabetes
|
2002
|
1.16
|
21
|
Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis.
|
J Natl Cancer Inst
|
2005
|
1.05
|
22
|
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people.
|
Diabetes
|
2006
|
0.91
|
23
|
The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people.
|
Diabetes
|
2006
|
0.85
|
24
|
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people.
|
Diabetes
|
2005
|
0.85
|
25
|
Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes.
|
Diabetes
|
2006
|
0.85
|
26
|
Whole-genome amplification using Φ29 DNA polymerase.
|
Cold Spring Harb Protoc
|
2011
|
0.77
|
27
|
IGF2R missense single-nucleotide polymorphisms and breast cancer risk: the multiethnic cohort study.
|
Cancer Epidemiol Biomarkers Prev
|
2009
|
0.76
|