Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.
|
Nat Genet
|
2007
|
11.09
|
2
|
Genetic Analysis Workshop 17 mini-exome simulation.
|
BMC Proc
|
2011
|
9.16
|
3
|
Identification of common variants associated with human hippocampal and intracranial volumes.
|
Nat Genet
|
2012
|
3.73
|
4
|
High dimensional endophenotype ranking in the search for major depression risk genes.
|
Biol Psychiatry
|
2011
|
2.23
|
5
|
Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans.
|
Diabetes
|
2002
|
2.06
|
6
|
Genetic variation in selenoprotein S influences inflammatory response.
|
Nat Genet
|
2005
|
2.00
|
7
|
The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification.
|
BMC Genet
|
2005
|
1.98
|
8
|
Estimating the additive genetic effect of the X chromosome.
|
Genet Epidemiol
|
2005
|
1.95
|
9
|
Genetic variation at the FTO locus influences RBL2 gene expression.
|
Diabetes
|
2009
|
1.91
|
10
|
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
|
Brain Imaging Behav
|
2014
|
1.90
|
11
|
Amygdalar and hippocampal substrates of anxious temperament differ in their heritability.
|
Nature
|
2010
|
1.63
|
12
|
Quantitative trait nucleotide analysis using Bayesian model selection.
|
Hum Biol
|
2005
|
1.60
|
13
|
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.
|
Am J Hum Genet
|
2006
|
1.59
|
14
|
A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans.
|
Diabetes
|
2005
|
1.52
|
15
|
Plasma lipidomic profile signature of hypertension in Mexican American families: specific role of diacylglycerols.
|
Hypertension
|
2013
|
1.51
|
16
|
Quantitative trait nucleotide analysis using Bayesian model selection. 2005.
|
Hum Biol
|
2009
|
1.46
|
17
|
Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits.
|
BMC Proc
|
2007
|
1.36
|
18
|
Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans.
|
J Bone Miner Res
|
2003
|
1.25
|
19
|
A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees.
|
Adv Genet
|
2013
|
1.25
|
20
|
Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume.
|
Stroke
|
2009
|
1.24
|
21
|
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.
|
Hum Mol Genet
|
2013
|
1.23
|
22
|
Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes.
|
BMC Med Genomics
|
2010
|
1.22
|
23
|
Linkage analysis without defined pedigrees.
|
Genet Epidemiol
|
2011
|
1.20
|
24
|
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations.
|
Hum Genet
|
2009
|
1.20
|
25
|
Chemerin, a novel adipokine in the regulation of angiogenesis.
|
J Clin Endocrinol Metab
|
2010
|
1.20
|
26
|
A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).
|
PLoS Genet
|
2013
|
1.15
|
27
|
Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans.
|
Nat Genet
|
2001
|
1.14
|
28
|
Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree.
|
Invest Ophthalmol Vis Sci
|
2005
|
1.13
|
29
|
Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging.
|
Proc Natl Acad Sci U S A
|
2013
|
1.11
|
30
|
Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data.
|
BMC Proc
|
2009
|
1.11
|
31
|
Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses.
|
Stroke
|
2010
|
1.09
|
32
|
Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).
|
Eur J Hum Genet
|
2008
|
1.08
|
33
|
Strategy and model building in the fourth dimension: a null model for genotype x age interaction as a Gaussian stationary stochastic process.
|
BMC Genet
|
2003
|
1.08
|
34
|
Blood pressure and cerebral white matter share common genetic factors in Mexican Americans.
|
Hypertension
|
2010
|
1.07
|
35
|
Linkage disequilibrium across two different single-nucleotide polymorphism genome scans.
|
BMC Genet
|
2005
|
1.06
|
36
|
Genetic influences on type 2 diabetes and metabolic syndrome related quantitative traits in Mauritius.
|
Twin Res Hum Genet
|
2009
|
1.06
|
37
|
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
|
PLoS One
|
2012
|
1.05
|
38
|
A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study.
|
Am J Hum Genet
|
2007
|
1.04
|
39
|
P2 promoter variants of the hepatocyte nuclear factor 4alpha gene are associated with type 2 diabetes in Mexican Americans.
|
Diabetes
|
2007
|
1.01
|
40
|
Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study.
|
Hum Mol Genet
|
2010
|
1.00
|
41
|
Genetic determinants of mitochondrial content.
|
Hum Mol Genet
|
2007
|
0.99
|
42
|
Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans.
|
Laterality
|
2006
|
0.99
|
43
|
Type I error rates in association versus joint linkage/association tests in related individuals.
|
Genet Epidemiol
|
2007
|
0.97
|
44
|
X chromosome effects and their interactions with mitochondrial effects.
|
BMC Genet
|
2005
|
0.96
|
45
|
A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies.
|
Hum Mol Genet
|
2006
|
0.96
|
46
|
Bivariate linkage analysis of the insulin resistance syndrome phenotypes on chromosome 7q.
|
Hum Biol
|
2005
|
0.95
|
47
|
Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans.
|
Atherosclerosis
|
2006
|
0.94
|
48
|
Waist circumference independently associates with the risk of insulin resistance and type 2 diabetes in mexican american families.
|
PLoS One
|
2013
|
0.93
|
49
|
Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress.
|
Am J Hum Genet
|
2006
|
0.93
|
50
|
Influence of age, sex and genetic factors on the human brain.
|
Brain Imaging Behav
|
2014
|
0.92
|
51
|
A comparison of univariate, bivariate, and trivariate whole-genome linkage screens of genetically correlated electrophysiological endophenotypes.
|
BMC Genet
|
2005
|
0.91
|
52
|
Gene-by-age effects on BMI from birth to adulthood: the Fels Longitudinal Study.
|
Obesity (Silver Spring)
|
2013
|
0.90
|
53
|
Mitochondrial genetic effects on latent class variables associated with susceptibility to alcoholism.
|
BMC Genet
|
2005
|
0.89
|
54
|
Hepatic gene networks in morbidly obese patients with nonalcoholic fatty liver disease.
|
Obes Surg
|
2010
|
0.89
|
55
|
A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.
|
Neurogenetics
|
2012
|
0.88
|
56
|
The positive association of obesity variants with adulthood adiposity strengthens over an 80-year period: a gene-by-birth year interaction.
|
Hum Hered
|
2013
|
0.88
|
57
|
Genotype×age interaction in human transcriptional ageing.
|
Mech Ageing Dev
|
2012
|
0.88
|
58
|
Genome-wide discovery of maternal effect variants.
|
BMC Proc
|
2009
|
0.88
|
59
|
Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a major susceptibility locus on chromosome 6q14.1.
|
Hum Hered
|
2011
|
0.87
|
60
|
Fasting insulin and obesity-related phenotypes are linked to chromosome 2p: the Strong Heart Family Study.
|
Diabetes
|
2006
|
0.87
|
61
|
The association of genetic variants of type 2 diabetes with kidney function.
|
Kidney Int
|
2012
|
0.87
|
62
|
Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults.
|
Calcif Tissue Int
|
2008
|
0.87
|
63
|
A gene expression signature for insulin resistance.
|
Physiol Genomics
|
2010
|
0.86
|
64
|
Genetic effects on DNA methylation and its potential relevance for obesity in Mexican Americans.
|
PLoS One
|
2013
|
0.86
|
65
|
Metabolic syndrome is linked to chromosome 7q21 and associated with genetic variants in CD36 and GNAT3 in Mexican Americans.
|
Obesity (Silver Spring)
|
2012
|
0.86
|
66
|
On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis.
|
BMC Genet
|
2003
|
0.85
|
67
|
Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans Administration Genetic Epidemiology Study.
|
Diabetes
|
2008
|
0.85
|
68
|
Genetic architecture of carotid artery intima-media thickness in Mexican Americans.
|
Circ Cardiovasc Genet
|
2013
|
0.85
|
69
|
Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease.
|
Mol Hum Reprod
|
2013
|
0.84
|
70
|
Heritability of brachydactyly type A3 in children, adolescents, and young adults from an endogamous population in eastern Nepal.
|
Hum Biol
|
2007
|
0.84
|
71
|
Social- and behavioral-specific genetic effects on blood pressure traits: the Strong Heart Family Study.
|
Circ Cardiovasc Genet
|
2009
|
0.84
|
72
|
Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island.
|
Gene
|
2011
|
0.83
|
73
|
Novel associations of nonstructural Loci with paraoxonase activity.
|
J Lipids
|
2012
|
0.83
|
74
|
Plasma dihydroceramide species associate with waist circumference in Mexican American families.
|
Obesity (Silver Spring)
|
2013
|
0.83
|
75
|
Do rare variant genotypes predict common variant genotypes?
|
BMC Proc
|
2011
|
0.83
|
76
|
Genetic variation in PARL influences mitochondrial content.
|
Hum Genet
|
2009
|
0.83
|
77
|
Plasma lipidome is independently associated with variability in metabolic syndrome in Mexican American families.
|
J Lipid Res
|
2014
|
0.82
|
78
|
Heritable changes in regional cortical thickness with age.
|
Brain Imaging Behav
|
2014
|
0.82
|
79
|
Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition.
|
Am J Med Genet B Neuropsychiatr Genet
|
2013
|
0.81
|
80
|
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.
|
PLoS One
|
2012
|
0.81
|
81
|
A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens).
|
Anat Rec (Hoboken)
|
2011
|
0.81
|
82
|
Multiple QTLs influence variation in paraoxonase 1 activity in Mexican Americans.
|
Hum Biol
|
2006
|
0.81
|
83
|
Sex-specific QTL effects on variation in paraoxonase 1 (PON1) activity in Mexican Americans.
|
Genet Epidemiol
|
2007
|
0.80
|
84
|
A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation.
|
BMC Med Genomics
|
2013
|
0.80
|
85
|
Introduction to genetic analysis workshop 17 summaries.
|
Genet Epidemiol
|
2011
|
0.79
|
86
|
Genetic risk for earlier menarche also influences peripubertal body mass index.
|
Am J Phys Anthropol
|
2013
|
0.79
|
87
|
Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity.
|
J Clin Endocrinol Metab
|
2014
|
0.79
|
88
|
A comparison of discrete versus continuous environment in a variance components-based linkage analysis of the COGA data.
|
BMC Genet
|
2005
|
0.78
|
89
|
Variability in associations of phosphatidylcholine molecular species with metabolic syndrome in Mexican-American families.
|
Lipids
|
2013
|
0.78
|
90
|
Identification of pleiotropic genetic effects on obesity and brain anatomy.
|
Hum Hered
|
2013
|
0.78
|
91
|
Smoothing of the bivariate LOD score for non-normal quantitative traits.
|
BMC Genet
|
2005
|
0.77
|
92
|
Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate.
|
Eur J Hum Genet
|
2010
|
0.77
|
93
|
Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES).
|
Hum Hered
|
2013
|
0.77
|
94
|
Association of genetic variation within UBL5 with phenotypes of metabolic syndrome.
|
Hum Biol
|
2006
|
0.77
|
95
|
Admixture effects in the traditional linkage analysis of admixed families.
|
Ethn Dis
|
2002
|
0.77
|
96
|
Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.
|
Genet Epidemiol
|
2014
|
0.77
|
97
|
Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders.
|
Am J Med Genet B Neuropsychiatr Genet
|
2014
|
0.76
|
98
|
Genetic signal maximization using environmental regression.
|
BMC Proc
|
2011
|
0.76
|
99
|
Effect of genotype x alcoholism interaction on linkage analysis of an alcoholism-related quantitative phenotype.
|
BMC Genet
|
2005
|
0.76
|
100
|
Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage.
|
Am J Psychiatry
|
2014
|
0.76
|
101
|
Increased waist circumference is independently associated with hypothyroidism in Mexican Americans: replicative evidence from two large, population-based studies.
|
BMC Endocr Disord
|
2014
|
0.75
|
102
|
Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cells.
|
Cancer Chemother Pharmacol
|
2013
|
0.75
|
103
|
Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging.
|
Mech Ageing Dev
|
2011
|
0.75
|
104
|
Comparison of strategies for identification of regulatory quantitative trait loci of transcript expression traits.
|
BMC Proc
|
2007
|
0.75
|
105
|
Presentation, heritability, and genome-wide linkage analysis of the midchildhood growth spurt in healthy children from the Fels Longitudinal Study.
|
Hum Biol
|
2008
|
0.75
|
106
|
Association mapping: methodologies, strategies, and issues.
|
Genet Epidemiol
|
2005
|
0.75
|
107
|
Autosomal genome-wide linkage analysis to identify loci for gallbladder wall thickness in Mexican Americans.
|
Hum Biol
|
2008
|
0.75
|
108
|
Unifying ideas for non-parametric linkage analysis.
|
Hum Hered
|
2011
|
0.75
|