| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A second generation human haplotype map of over 3.1 million SNPs.
|
Nature
|
2007
|
85.39
|
|
2
|
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
|
Science
|
2007
|
51.70
|
|
3
|
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
|
Nat Genet
|
2008
|
35.06
|
|
4
|
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
|
Nat Genet
|
2010
|
17.89
|
|
5
|
Genome-wide detection and characterization of positive selection in human populations.
|
Nature
|
2007
|
17.27
|
|
6
|
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
|
Nat Genet
|
2010
|
16.96
|
|
7
|
Variants in MTNR1B influence fasting glucose levels.
|
Nat Genet
|
2008
|
10.85
|
|
8
|
A common variant of HMGA2 is associated with adult and childhood height in the general population.
|
Nat Genet
|
2007
|
6.87
|
|
9
|
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
|
PLoS Genet
|
2012
|
6.15
|
|
10
|
Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines.
|
PLoS Genet
|
2008
|
5.08
|
|
11
|
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
|
Nat Genet
|
2008
|
4.84
|
|
12
|
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
|
Nat Genet
|
2012
|
4.37
|
|
13
|
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations.
|
Diabetes
|
2008
|
4.20
|
|
14
|
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.
|
Diabetes
|
2010
|
4.07
|
|
15
|
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.
|
J Clin Invest
|
2008
|
3.51
|
|
16
|
TXNIP regulates peripheral glucose metabolism in humans.
|
PLoS Med
|
2007
|
3.27
|
|
17
|
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
|
|
18
|
Common variants associated with plasma triglycerides and risk for coronary artery disease.
|
Nat Genet
|
2013
|
2.92
|
|
19
|
Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program.
|
Diabetes
|
2011
|
2.17
|
|
20
|
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.
|
PLoS Genet
|
2009
|
2.09
|
|
21
|
Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program.
|
Diabetes
|
2010
|
2.02
|
|
22
|
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.
|
Am J Hum Genet
|
2012
|
1.96
|
|
23
|
Tissue-specific alternative splicing of TCF7L2.
|
Hum Mol Genet
|
2009
|
1.80
|
|
24
|
A genome-wide association search for type 2 diabetes genes in African Americans.
|
PLoS One
|
2012
|
1.72
|
|
25
|
Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program.
|
Diabetes
|
2008
|
1.71
|
|
26
|
DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation.
|
Am J Hum Genet
|
2011
|
1.62
|
|
27
|
Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry.
|
J Clin Endocrinol Metab
|
2012
|
1.44
|
|
28
|
Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity.
|
Diabetes
|
2006
|
1.26
|
|
29
|
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study.
|
Diabetes
|
2012
|
1.12
|
|
30
|
Pleiotropic effects of GIP on islet function involve osteopontin.
|
Diabetes
|
2011
|
1.08
|
|
31
|
Principal-component analysis for assessment of population stratification in mitochondrial medical genetics.
|
Am J Hum Genet
|
2010
|
1.02
|
|
32
|
Triglyceride response to an intensive lifestyle intervention is enhanced in carriers of the GCKR Pro446Leu polymorphism.
|
J Clin Endocrinol Metab
|
2011
|
1.00
|
|
33
|
Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.
|
PLoS One
|
2012
|
0.99
|
|
34
|
Common mitochondrial sequence variants in ischemic stroke.
|
Ann Neurol
|
2010
|
0.97
|
|
35
|
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage.
|
Stroke
|
2013
|
0.86
|
|
36
|
The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people.
|
Diabetes
|
2006
|
0.85
|
|
37
|
Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population.
|
PLoS One
|
2013
|
0.82
|
|
38
|
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort.
|
Circ Cardiovasc Genet
|
2014
|
0.81
|
|
39
|
Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study.
|
PLoS One
|
2012
|
0.79
|
|
40
|
Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes.
|
Diabetologia
|
2013
|
0.79
|
|
41
|
Surgical Intensive Care Unit Optimal Mobilisation Score (SOMS) trial: a protocol for an international, multicentre, randomised controlled trial focused on goal-directed early mobilisation of surgical ICU patients.
|
BMJ Open
|
2013
|
0.79
|
|
42
|
Common variants in CLOCK are not associated with measures of sleep duration in people of european ancestry from the sleep heart health study.
|
Biol Psychiatry
|
2013
|
0.78
|
|
43
|
Environmental and genetic factors influence age at menarche in women with polycystic ovary syndrome.
|
J Pediatr Endocrinol Metab
|
2012
|
0.78
|
|
44
|
Evaluating reported candidate gene associations with polycystic ovary syndrome.
|
Fertil Steril
|
2013
|
0.77
|
|
45
|
Variation in the human genome and risk to common disease. Keystone Symposium on 'Human Genome Sequence Variation and the Inherited Basis of Common Diseases'. January 8-13, Breckenridge, Colorado, USA.
|
Pharmacogenomics
|
2004
|
0.77
|
|
46
|
Rv3080c regulates the rate of inhibition of mycobacteria by isoniazid through FabD.
|
Mol Cell Biochem
|
2012
|
0.76
|
|
47
|
IBC CARe microarray allelic population prevalences in an American Indian population.
|
PLoS One
|
2013
|
0.75
|
|
48
|
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections.
|
medRxiv
|
2022
|
0.75
|
|
49
|
Quantitative analysis of conjugated and free estrogens in swine manure: solutions to overcome analytical problems due to matrix effects.
|
J Chromatogr A
|
2013
|
0.75
|
|
50
|
Correction: Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population.
|
PLoS One
|
2013
|
0.75
|