Noël P Burtt

Author PubWeight™ 201.37‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 2007 51.70
2 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008 35.06
3 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 2008 22.35
4 Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet 2008 20.73
5 Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet 2012 12.10
6 Polymorphisms associated with cholesterol and risk of cardiovascular events. N Engl J Med 2008 9.83
7 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science 2010 9.61
8 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet 2008 7.07
9 The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet 2012 6.15
10 Transferability of tag SNPs in genetic association studies in multiple populations. Nat Genet 2006 4.78
11 Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals. Diabetes 2006 4.36
12 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet 2012 3.21
13 Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Nature 2013 2.57
14 Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction. Nat Genet 2011 2.42
15 Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. PLoS Genet 2012 2.34
16 Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. Nat Genet 2013 1.91
17 Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. Genet Epidemiol 2011 1.78
18 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
19 Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes. Diabetes 2005 1.22
20 5' flanking variants of resistin are associated with obesity. Diabetes 2002 1.16
21 Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis. J Natl Cancer Inst 2005 1.05
22 High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people. Diabetes 2006 0.91
23 The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people. Diabetes 2006 0.85
24 Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people. Diabetes 2005 0.85
25 Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes. Diabetes 2006 0.85
26 Whole-genome amplification using Φ29 DNA polymerase. Cold Spring Harb Protoc 2011 0.77
27 IGF2R missense single-nucleotide polymorphisms and breast cancer risk: the multiethnic cohort study. Cancer Epidemiol Biomarkers Prev 2009 0.76