PubRank

Devin Absher

Author PubWeight™ 124.85‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
2 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 13.25
3 Signals of recent positive selection in a worldwide sample of human populations. Genome Res 2009 8.38
4 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
5 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 2010 7.94
6 Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet 2012 7.59
7 Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet 2009 6.79
8 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Proc Natl Acad Sci U S A 2009 3.49
9 The role of geography in human adaptation. PLoS Genet 2009 3.41
10 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet 2013 3.25
11 Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls. Circ Cardiovasc Genet 2010 3.15
12 Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet 2013 2.92
13 Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet 2013 2.83
14 Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet 2008 2.71
15 Genomic patterns of homozygosity in worldwide human populations. Am J Hum Genet 2012 2.30
16 Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J Am Coll Cardiol 2010 2.17
17 Age-related somatic structural changes in the nuclear genome of human blood cells. Am J Hum Genet 2012 2.15
18 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Diabetes 2011 2.09
19 Characterizing the admixed African ancestry of African Americans. Genome Biol 2009 2.01
20 Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet 2013 1.72
21 Differential DNA methylation with age displays both common and dynamic features across human tissues that are influenced by CpG landscape. Genome Biol 2013 1.69
22 Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. PLoS Genet 2013 1.57
23 Epigenome-wide association study of fasting measures of glucose, insulin, and HOMA-IR in the Genetics of Lipid Lowering Drugs and Diet Network study. Diabetes 2013 1.38
24 Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging. PLoS Genet 2009 1.30
25 Whole-genome sequencing: a step closer to personalized medicine. JAMA 2011 1.13
26 Randomized trial of personal genomics for preventive cardiology: design and challenges. Circ Cardiovasc Genet 2012 1.06
27 Characterization of X-linked SNP genotypic variation in globally distributed human populations. Genome Biol 2010 1.02
28 Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime. J Med Genet 2012 0.99
29 Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation. Am J Med Genet A 2010 0.95
30 Risk variants for psoriasis vulgaris in a large case-control collection and association with clinical subphenotypes. Hum Mol Genet 2012 0.95
31 A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. Gut 2012 0.90
32 Statistical quantification of methylation levels by next-generation sequencing. PLoS One 2011 0.84
33 Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population. Diabetologia 2013 0.83
34 Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime. Postgrad Med J 2013 0.77
35 Potential of whole-genome sequencing for determining risk and personalizing therapy: focus on AML. Expert Rev Anticancer Ther 2012 0.77
36 Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet 2016 0.75
37 Post-zygotic and inter-individual structural genetic variation in a presumptive enhancer element of the locus between the IL10Rβ and IFNAR1 genes. PLoS One 2013 0.75