Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Biological, clinical and population relevance of 95 loci for blood lipids.
|
Nature
|
2010
|
28.21
|
2
|
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
|
Nat Genet
|
2010
|
23.08
|
3
|
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
|
Nat Genet
|
2008
|
22.35
|
4
|
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
|
Nat Genet
|
2010
|
17.89
|
5
|
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
|
Nat Genet
|
2008
|
12.32
|
6
|
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
|
Nat Genet
|
2010
|
7.94
|
7
|
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.
|
Lancet
|
2010
|
6.07
|
8
|
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.
|
PLoS Genet
|
2009
|
5.81
|
9
|
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
|
Nat Genet
|
2012
|
4.08
|
10
|
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
|
11
|
Common variants associated with plasma triglycerides and risk for coronary artery disease.
|
Nat Genet
|
2013
|
2.92
|
12
|
High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools.
|
Proc Natl Acad Sci U S A
|
2002
|
2.32
|
13
|
Metabonomic, transcriptomic, and genomic variation of a population cohort.
|
Mol Syst Biol
|
2010
|
2.17
|
14
|
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.
|
Am J Hum Genet
|
2009
|
1.81
|
15
|
Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans.
|
Am J Clin Nutr
|
2012
|
1.80
|
16
|
An immune response network associated with blood lipid levels.
|
PLoS Genet
|
2010
|
1.74
|
17
|
A genome-wide association search for type 2 diabetes genes in African Americans.
|
PLoS One
|
2012
|
1.72
|
18
|
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.
|
Circ Cardiovasc Genet
|
2011
|
1.63
|
19
|
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.
|
Genet Epidemiol
|
2009
|
1.43
|
20
|
The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study.
|
PLoS Med
|
2011
|
1.36
|
21
|
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
|
Ann Neurol
|
2013
|
1.30
|
22
|
Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.
|
Hum Mol Genet
|
2007
|
1.28
|
23
|
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.
|
Hum Mol Genet
|
2006
|
1.28
|
24
|
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.
|
PLoS Genet
|
2011
|
1.27
|
25
|
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.
|
Hum Genet
|
2007
|
1.17
|
26
|
The SLC6A14 gene shows evidence of association with obesity.
|
J Clin Invest
|
2003
|
1.15
|
27
|
Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.
|
PLoS One
|
2012
|
1.13
|
28
|
Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
|
PLoS Genet
|
2006
|
1.13
|
29
|
The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland.
|
Schizophr Res
|
2007
|
1.04
|
30
|
Combined effects of thrombosis pathway gene variants predict cardiovascular events.
|
PLoS Genet
|
2007
|
1.03
|
31
|
Assessment of the neuropeptide S system in anxiety disorders.
|
Biol Psychiatry
|
2010
|
0.99
|
32
|
Variation in resistin gene promoter not associated with polycystic ovary syndrome.
|
Diabetes
|
2003
|
0.97
|
33
|
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.
|
Twin Res Hum Genet
|
2012
|
0.95
|
34
|
An association analysis of circadian genes in anxiety disorders.
|
Biol Psychiatry
|
2010
|
0.95
|
35
|
C-reactive protein-associated genetic variants and cancer risk: findings from FINRISK 1992, FINRISK 1997 and Health 2000 studies.
|
Eur J Cancer
|
2010
|
0.95
|
36
|
Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
|
PLoS Genet
|
2011
|
0.94
|
37
|
Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample.
|
Biol Psychiatry
|
2008
|
0.93
|
38
|
Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort.
|
Diabetes
|
2002
|
0.92
|
39
|
Contribution of adenosine related genes to the risk of depression with disturbed sleep.
|
J Affect Disord
|
2010
|
0.91
|
40
|
European lactase persistence genotype shows evidence of association with increase in body mass index.
|
Hum Mol Genet
|
2009
|
0.91
|
41
|
An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders.
|
Biol Psychiatry
|
2008
|
0.90
|
42
|
Active and low-active forms of serum phospholipid transfer protein in a normal Finnish population sample.
|
J Lipid Res
|
2004
|
0.87
|
43
|
Genetic association and interaction analysis of USF1 and APOA5 on lipid levels and atherosclerosis.
|
Arterioscler Thromb Vasc Biol
|
2009
|
0.87
|
44
|
Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins.
|
Am J Med Genet B Neuropsychiatr Genet
|
2009
|
0.86
|
45
|
Genome-wide association study of sleep duration in the Finnish population.
|
J Sleep Res
|
2014
|
0.84
|
46
|
Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population.
|
Am J Med Genet B Neuropsychiatr Genet
|
2010
|
0.81
|
47
|
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.
|
Heart Rhythm
|
2012
|
0.81
|
48
|
μ-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption.
|
Alcohol Alcohol
|
2013
|
0.81
|
49
|
Further evidence for the role of ENPP1 in obesity: association with morbid obesity in Finns.
|
Obesity (Silver Spring)
|
2008
|
0.80
|
50
|
Ethical issues and GenomEUtwin.
|
Twin Res
|
2003
|
0.80
|
51
|
The enhancement of homogenous mass extension reaction: comparison of two enzymes.
|
Mol Cell Probes
|
2007
|
0.79
|
52
|
ESR1 genetic variants, haplotypes and the risk of coronary heart disease and ischemic stroke in the Finnish population: a prospective follow-up study.
|
Atherosclerosis
|
2010
|
0.77
|
53
|
Subsets of Finns with high HDL to total cholesterol ratio show evidence for linkage to type 2 diabetes on chromosome 6q.
|
Hum Hered
|
2006
|
0.75
|
54
|
Common genetic variation near melatonin receptor 1A gene linked to job-related exhaustion in shift workers.
|
Sleep
|
2016
|
0.75
|