PubRank

Albert V Smith

Author PubWeight™ 211.43‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010 28.21
2 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011 13.25
3 Genome-wide association study of blood pressure and hypertension. Nat Genet 2009 11.54
4 Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 2010 9.52
5 The International HapMap Project Web site. Genome Res 2005 5.96
6 New loci associated with kidney function and chronic kidney disease. Nat Genet 2010 5.58
7 Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nat Genet 2012 5.48
8 Genomic inflation factors under polygenic inheritance. Eur J Hum Genet 2011 4.89
9 Multiple loci associated with indices of renal function and chronic kidney disease. Nat Genet 2009 4.78
10 Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet 2012 4.73
11 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science 2013 4.71
12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat Genet 2009 4.28
13 Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet 2010 3.97
14 Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genet 2011 3.92
15 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat Genet 2009 3.80
16 Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012 3.73
17 Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet 2012 3.71
18 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 2011 3.68
19 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 2011 3.40
20 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet 2010 3.37
21 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
22 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLoS Genet 2009 3.18
23 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet 2012 3.04
24 Genetic associations with valvular calcification and aortic stenosis. N Engl J Med 2013 3.02
25 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. Circ Cardiovasc Genet 2010 2.76
26 CUBN is a gene locus for albuminuria. J Am Soc Nephrol 2011 2.70
27 Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. PLoS One 2013 2.65
28 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. Nat Genet 2009 2.58
29 Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. Ann Neurol 2011 2.37
30 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet 2012 2.12
31 Genome-wide association meta-analysis for total serum bilirubin levels. Hum Mol Genet 2009 1.96
32 Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 2011 1.96
33 Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nat Genet 2011 1.92
34 Heterogeneity in white blood cells has potential to confound DNA methylation measurements. PLoS One 2012 1.91
35 Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels. PLoS Genet 2010 1.91
36 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. PLoS Genet 2012 1.84
37 Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet 2013 1.72
38 Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet 2012 1.68
39 Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum Mol Genet 2010 1.67
40 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. J Gerontol A Biol Sci Med Sci 2010 1.65
41 Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011 1.65
42 A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ Cardiovasc Genet 2011 1.63
43 A genome-wide association study of aging. Neurobiol Aging 2011 1.54
44 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. Hum Mol Genet 2010 1.53
45 Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS Genet 2012 1.52
46 Common variants at 6q22 and 17q21 are associated with intracranial volume. Nat Genet 2012 1.51
47 Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium. Stroke 2009 1.47
48 Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. PLoS Genet 2011 1.45
49 Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Am J Hum Genet 2012 1.29
50 Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Invest Ophthalmol Vis Sci 2011 1.22
51 HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination. Genome Res 2009 1.17
52 Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. PLoS One 2013 1.16
53 Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet 2012 1.14
54 Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. Ann Rheum Dis 2012 1.13
55 Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. Circ Cardiovasc Genet 2011 1.11
56 Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet 2012 1.09
57 Genetic variation associated with circulating monocyte count in the eMERGE Network. Hum Mol Genet 2013 1.05
58 Characterization of European ancestry nonalcoholic fatty liver disease-associated variants in individuals of African and Hispanic descent. Hepatology 2013 1.04
59 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. Eur J Hum Genet 2011 1.04
60 Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. Circ Cardiovasc Genet 2015 1.03
61 Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Hum Mol Genet 2014 1.02
62 Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. PLoS Genet 2013 1.02
63 The molecular genetic architecture of self-employment. PLoS One 2013 0.96
64 Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am J Epidemiol 2013 0.93
65 The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation. Hum Mutat 2009 0.91
66 Genome-wide profiling of blood pressure in adults and children. Hypertension 2011 0.89
67 Common variants in Mendelian kidney disease genes and their association with renal function. J Am Soc Nephrol 2013 0.82
68 Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet 2016 0.81
69 The distribution of a germline methylation marker suggests a regional mechanism of LINE-1 silencing by the piRNA-PIWI system. BMC Genet 2012 0.78
70 Lack of association between the MTHFR C677T variant and migraine with aura in an older population: could selective survival play a role? Cephalalgia 2012 0.77
71 Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genome. Gene 2011 0.76
72 A novel MALDI-TOF based methodology for genotyping single nucleotide polymorphisms. Nucleic Acids Res 2003 0.75
73 Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. Circ Cardiovasc Genet 2016 0.75
74 Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep 2017 0.75
75 Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet 2016 0.75
76 Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet 2017 0.75