|
1
|
Identification of common variants associated with human hippocampal and intracranial volumes.
|
Nat Genet
|
2012
|
3.73
|
|
2
|
High dimensional endophenotype ranking in the search for major depression risk genes.
|
Biol Psychiatry
|
2011
|
2.23
|
|
3
|
Genetic variation at the FTO locus influences RBL2 gene expression.
|
Diabetes
|
2009
|
1.91
|
|
4
|
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
|
Brain Imaging Behav
|
2014
|
1.90
|
|
5
|
Assessment of gene-by-sex interaction effect on bone mineral density.
|
J Bone Miner Res
|
2012
|
1.58
|
|
6
|
Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women.
|
J Bone Miner Res
|
2013
|
1.16
|
|
7
|
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
|
|
8
|
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
|
|
9
|
Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain.
|
Front Neurosci
|
2011
|
1.09
|
|
10
|
Blood pressure and cerebral white matter share common genetic factors in Mexican Americans.
|
Hypertension
|
2010
|
1.07
|
|
11
|
Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease.
|
Eur J Hum Genet
|
2011
|
0.93
|
|
12
|
Cytogenetic alterations in nonmelanoma skin cancer: a review.
|
Genes Chromosomes Cancer
|
2005
|
0.92
|
|
13
|
Influence of age, sex and genetic factors on the human brain.
|
Brain Imaging Behav
|
2014
|
0.92
|
|
14
|
Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits.
|
Am J Hum Genet
|
2013
|
0.92
|
|
15
|
Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a Northern European family population.
|
BMC Med Genomics
|
2013
|
0.89
|
|
16
|
Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos.
|
Front Genet
|
2012
|
0.89
|
|
17
|
Genetic architecture of carotid artery intima-media thickness in Mexican Americans.
|
Circ Cardiovasc Genet
|
2013
|
0.85
|
|
18
|
Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans.
|
Eur J Hum Genet
|
2012
|
0.85
|
|
19
|
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm.
|
J Med Genet
|
2013
|
0.83
|
|
20
|
Novel associations of nonstructural Loci with paraoxonase activity.
|
J Lipids
|
2012
|
0.83
|
|
21
|
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
|
|
22
|
Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines.
|
BMC Med Genomics
|
2012
|
0.81
|
|
23
|
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
|
|
24
|
Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity.
|
J Clin Endocrinol Metab
|
2014
|
0.79
|
|
25
|
Identification of pleiotropic genetic effects on obesity and brain anatomy.
|
Hum Hered
|
2013
|
0.78
|
|
26
|
The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome.
|
Metabolism
|
2009
|
0.77
|
|
27
|
Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.
|
Genet Epidemiol
|
2014
|
0.77
|
|
28
|
Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage.
|
Am J Psychiatry
|
2014
|
0.76
|
|
29
|
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
|
|
30
|
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
|
|
31
|
Cytogenetics of melanoma and nonmelanoma skin cancer.
|
Adv Exp Med Biol
|
2014
|
0.75
|