Published in Nucleic Acids Res on September 29, 2006
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Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med (2012) 10.16
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet (2010) 6.49
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. Nat Genet (2009) 5.32
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Nat Genet (2009) 5.06
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet (2009) 3.46
Several common variants modulate heart rate, PR interval and QRS duration. Nat Genet (2010) 3.34
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A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Nat Genet (2011) 2.43
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. Nat Genet (2012) 2.29
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Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. Nat Genet (2009) 1.73
Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease. Nat Genet (2016) 1.71
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Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. PLoS Genet (2010) 1.57
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Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry. J Clin Endocrinol Metab (2012) 1.44
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A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. Nat Genet (2013) 1.23
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HABP2 G534E Variant in Papillary Thyroid Carcinoma. PLoS One (2016) 1.16
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. Hum Mol Genet (2011) 1.03
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk. Cancer Res (2011) 0.92
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Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. Hum Mol Genet (2014) 0.90
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A genetic risk variant for myocardial infarction on chromosome 6p24 is associated with impaired central hemodynamic indexes. Am J Hypertens (2012) 0.84
HLA class II sequence variants influence tuberculosis risk in populations of European ancestry. Nat Genet (2016) 0.80
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease. PLoS Genet (2015) 0.79
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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Mol Psychiatry (2016) 0.75
Replication study of 34 common SNPs associated with prostate cancer in the Romanian population. J Cell Mol Med (2016) 0.75
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis. Nat Commun (2016) 0.75
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. PLoS One (2016) 0.75
A genome-wide association study yields five novel thyroid cancer risk loci. Nat Commun (2017) 0.75
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