Published in Am J Hum Genet on March 01, 2008
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Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. PLoS Genet (2011) 1.38
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Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families. Neurogenetics (2006) 1.24
Association testing in a linked region using large pedigrees. Am J Hum Genet (2005) 1.23
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Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21. Genome Res (2005) 1.20
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Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population. Diabetes (2007) 1.16
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Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome. Diabetes (2006) 1.15
The SLC6A14 gene shows evidence of association with obesity. J Clin Invest (2003) 1.15
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The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans. J Clin Invest (2011) 1.12
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WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. Am J Hum Genet (2008) 1.06
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USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease. Arterioscler Thromb Vasc Biol (2007) 1.01
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A Path Algorithm for Constrained Estimation. J Comput Graph Stat (2013) 0.97
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Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. PLoS One (2010) 0.96
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A Poisson model for random multigraphs. Bioinformatics (2010) 0.94
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Modeling maternal-offspring gene-gene interactions: the extended-MFG test. Genet Epidemiol (2010) 0.93
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Niche adaptation by expansion and reprogramming of general transcription factors. Mol Syst Biol (2011) 0.92
Association of ketone body levels with hyperglycemia and type 2 diabetes in 9,398 Finnish men. Diabetes (2013) 0.92
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Upstream transcription factor 1 influences plasma lipid and metabolic traits in mice. Hum Mol Genet (2009) 0.91
Powerful allele sharing statistics for nonparametric linkage analysis. Hum Hered (2004) 0.91
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia. Circ Res (2002) 0.90
Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes. BMC Med Genomics (2012) 0.90
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans. Arterioscler Thromb Vasc Biol (2009) 0.90
A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia. Hum Genet (2009) 0.89
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A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians. Atherosclerosis (2005) 0.88
Galanin preproprotein is associated with elevated plasma triglycerides. Arterioscler Thromb Vasc Biol (2008) 0.88
Merging microsatellite data. J Comput Biol (2006) 0.88
Reconstructing ancestral haplotypes with a dictionary model. J Comput Biol (2006) 0.87
Evidence for a gene influencing high-density lipoprotein cholesterol on chromosome 4q31.21. Arterioscler Thromb Vasc Biol (2005) 0.87
Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels. Circ Cardiovasc Genet (2009) 0.87
Unraveling the complex genetics of familial combined hyperlipidemia. Ann Med (2006) 0.87
A heterozygote-homozygote test of Hardy-Weinberg equilibrium. Eur J Hum Genet (2009) 0.87