Published in BMC Proc on December 15, 2009
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Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet (2012) 3.73
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Long-term changes in adiposity and glycemic control are associated with past adenovirus infection. Diabetes Care (2012) 1.63
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On the genetic architecture of cortical folding and brain volume in primates. Neuroimage (2010) 1.62
Quantitative trait nucleotide analysis using Bayesian model selection. Hum Biol (2005) 1.60
Linkage analysis of glomerular filtration rate in American Indians. Kidney Int (2008) 1.59
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet (2006) 1.59
Assessment of gene-by-sex interaction effect on bone mineral density. J Bone Miner Res (2012) 1.58
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
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Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families. Arch Gen Psychiatry (2010) 1.50
Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence. Am J Hum Genet (2005) 1.49
Adjudicating neurocognitive endophenotypes for schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2007) 1.48
A quantitative trait locus influencing free plasma protein S levels on human chromosome 1q: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) project. Arterioscler Thromb Vasc Biol (2003) 1.48
Heritability of brain volume, surface area and shape: an MRI study in an extended pedigree of baboons. Hum Brain Mapp (2007) 1.47
A genome search for genetic determinants that influence plasma fibrinogen levels. Arterioscler Thromb Vasc Biol (2005) 1.47
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Variance component methods for analysis of complex phenotypes. Cold Spring Harb Protoc (2010) 1.44
The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005. Hum Biol (2009) 1.43
Linkage of the cholesterol 7alpha-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: the National Heart, Lung, and Blood Institute Family Heart Study. Chin Med J (Engl) (2005) 1.42
Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction. J Stud Alcohol (2006) 1.42
The functional connectivity of the human caudate: an application of meta-analytic connectivity modeling with behavioral filtering. Neuroimage (2011) 1.41
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nat Genet (2013) 1.39
Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits. BMC Proc (2007) 1.36
Plasma lipid profiling in a large population-based cohort. J Lipid Res (2013) 1.35
The baboon as a nonhuman primate model for the study of the genetics of obesity. Obes Res (2003) 1.34
Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism. Behav Genet (2005) 1.32
Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring) (2007) 1.32
SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse. Diabetes (2007) 1.30
Heritability of left ventricular dimensions and mass in American Indians: The Strong Heart Study. J Hypertens (2004) 1.30
Genes on chromosomes 1 and 13 have significant effects on Ascaris infection. Proc Natl Acad Sci U S A (2002) 1.28