| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Risk alleles for multiple sclerosis identified by a genomewide study.
|
N Engl J Med
|
2007
|
17.06
|
|
2
|
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
|
Nat Genet
|
2008
|
12.51
|
|
3
|
Common variants on chromosome 6p22.1 are associated with schizophrenia.
|
Nature
|
2009
|
8.12
|
|
4
|
Quality control and quality assurance in genotypic data for genome-wide association studies.
|
Genet Epidemiol
|
2010
|
4.83
|
|
5
|
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
|
Nat Genet
|
2012
|
3.68
|
|
6
|
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions.
|
Genet Epidemiol
|
2010
|
3.48
|
|
7
|
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
|
Genet Med
|
2012
|
3.29
|
|
8
|
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes.
|
Hum Mol Genet
|
2010
|
3.24
|
|
9
|
A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets.
|
Diabetes
|
2007
|
2.60
|
|
10
|
Quality control procedures for genome-wide association studies.
|
Curr Protoc Hum Genet
|
2011
|
2.48
|
|
11
|
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.
|
Proc Natl Acad Sci U S A
|
2009
|
2.31
|
|
12
|
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
|
Hum Genet
|
2011
|
2.00
|
|
13
|
Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes.
|
Hum Mol Genet
|
2010
|
1.89
|
|
14
|
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
|
Am J Hum Genet
|
2010
|
1.89
|
|
15
|
New susceptibility loci associated with kidney disease in type 1 diabetes.
|
PLoS Genet
|
2012
|
1.79
|
|
16
|
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA.
|
Hum Mol Genet
|
2011
|
1.77
|
|
17
|
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
|
PLoS Genet
|
2012
|
1.52
|
|
18
|
Association and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos.
|
Am J Hum Genet
|
2003
|
1.27
|
|
19
|
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
|
Genet Epidemiol
|
2011
|
1.26
|
|
20
|
Gene-environment interaction effects on the development of immune responses in the 1st year of life.
|
Am J Hum Genet
|
2005
|
1.19
|
|
21
|
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
|
Proc Natl Acad Sci U S A
|
2012
|
1.16
|
|
22
|
Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels.
|
Arterioscler Thromb Vasc Biol
|
2010
|
1.10
|
|
23
|
A polymorphism in the TCF7 gene, C883A, is associated with type 1 diabetes.
|
Diabetes
|
2003
|
1.09
|
|
24
|
Evaluating genetic risk for prostate cancer among Japanese and Latinos.
|
Cancer Epidemiol Biomarkers Prev
|
2012
|
1.08
|
|
25
|
Genetic variation associated with circulating monocyte count in the eMERGE Network.
|
Hum Mol Genet
|
2013
|
1.05
|
|
26
|
Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease.
|
J Lipid Res
|
2010
|
1.03
|
|
27
|
Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature.
|
Trends Genet
|
2012
|
1.00
|
|
28
|
Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol.
|
Arterioscler Thromb Vasc Biol
|
2013
|
0.93
|
|
29
|
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
|
Hum Mol Genet
|
2013
|
0.92
|
|
30
|
Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels.
|
Hum Mol Genet
|
2010
|
0.90
|
|
31
|
Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.
|
J Bone Miner Res
|
2015
|
0.78
|