| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Biological, clinical and population relevance of 95 loci for blood lipids.
|
Nature
|
2010
|
28.21
|
|
2
|
Relative impact of nucleotide and copy number variation on gene expression phenotypes.
|
Science
|
2007
|
23.38
|
|
3
|
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
|
Nat Genet
|
2008
|
22.35
|
|
4
|
Genome-wide associations of gene expression variation in humans.
|
PLoS Genet
|
2005
|
17.27
|
|
5
|
Genome-wide association analysis identifies 20 loci that influence adult height.
|
Nat Genet
|
2008
|
16.92
|
|
6
|
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
|
Nat Genet
|
2009
|
15.15
|
|
7
|
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
|
Nat Genet
|
2011
|
9.23
|
|
8
|
A genotype calling algorithm for the Illumina BeadArray platform.
|
Bioinformatics
|
2007
|
8.03
|
|
9
|
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
|
Am J Hum Genet
|
2008
|
7.33
|
|
10
|
LDL-cholesterol concentrations: a genome-wide association study.
|
Lancet
|
2008
|
6.44
|
|
11
|
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
|
Nat Genet
|
2009
|
5.32
|
|
12
|
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
|
Arterioscler Thromb Vasc Biol
|
2010
|
4.08
|
|
13
|
Bayesian refinement of association signals for 14 loci in 3 common diseases.
|
Nat Genet
|
2012
|
3.31
|
|
14
|
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
|
|
15
|
Genetic variation in LIN28B is associated with the timing of puberty.
|
Nat Genet
|
2009
|
3.09
|
|
16
|
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.
|
Nat Genet
|
2010
|
2.99
|
|
17
|
Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture.
|
Ann Intern Med
|
2009
|
2.80
|
|
18
|
A genome-wide association study of testicular germ cell tumor.
|
Nat Genet
|
2009
|
2.79
|
|
19
|
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.
|
Nature
|
2012
|
2.66
|
|
20
|
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.
|
Hum Mol Genet
|
2002
|
2.65
|
|
21
|
Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.
|
Diabetes
|
2004
|
2.43
|
|
22
|
High-throughput genotyping of Salmonella enterica serovar Typhi allowing geographical assignment of haplotypes and pathotypes within an urban District of Jakarta, Indonesia.
|
J Clin Microbiol
|
2008
|
2.14
|
|
23
|
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
|
Nat Genet
|
2012
|
2.12
|
|
24
|
Gene expression changes with age in skin, adipose tissue, blood and brain.
|
Genome Biol
|
2013
|
1.34
|
|
25
|
Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.
|
Diabetes
|
2008
|
1.33
|
|
26
|
Facilitating genome navigation: survey sequencing and dense radiation-hybrid gene mapping.
|
Nat Rev Genet
|
2005
|
1.33
|
|
27
|
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.
|
Am J Hum Genet
|
2008
|
1.27
|
|
28
|
Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response.
|
Proc Natl Acad Sci U S A
|
2006
|
1.23
|
|
29
|
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders.
|
Trends Biochem Sci
|
2002
|
1.11
|
|
30
|
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.
|
Hum Mol Genet
|
2013
|
1.10
|
|
31
|
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.
|
J Alzheimers Dis
|
2012
|
1.02
|
|
32
|
Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
|
Genomics
|
2004
|
0.94
|
|
33
|
Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.
|
BMC Genet
|
2007
|
0.83
|
|
34
|
Data analysis issues for allele-specific expression using Illumina's GoldenGate assay.
|
BMC Bioinformatics
|
2010
|
0.79
|
|
35
|
A histone map of human chromosome 20q13.12.
|
PLoS One
|
2009
|
0.77
|