Samuli Ripatti

Author PubWeight™ 309.27‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010 28.21
2 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010 23.08
3 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
4 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
5 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet 2008 12.32
6 Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet 2012 12.10
7 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet 2008 12.07
8 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 2012 11.09
9 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
10 Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet 2012 7.59
11 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet 2010 6.49
12 Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet 2012 4.73
13 Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. PLoS Genet 2009 4.71
14 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science 2013 4.71
15 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet 2014 4.13
16 Genome-wide association study identifies five loci associated with lung function. Nat Genet 2009 4.10
17 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Arterioscler Thromb Vasc Biol 2010 4.08
18 Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nat Genet 2012 4.08
19 Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes 2010 4.07
20 Identification of seven loci affecting mean telomere length and their association with disease. Nat Genet 2013 3.87
21 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 2011 3.68
22 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet 2013 3.25
23 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
24 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet 2012 3.04
25 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet 2011 3.03
26 Geographical structure and differential natural selection among North European populations. Genome Res 2009 3.03
27 Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet 2013 2.92
28 Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet 2013 2.83
29 The genome-wide patterns of variation expose significant substructure in a founder population. Am J Hum Genet 2008 2.79
30 FTO genotype is associated with phenotypic variability of body mass index. Nature 2012 2.77
31 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nat Genet 2011 2.73
32 Genetically determined height and coronary artery disease. N Engl J Med 2015 2.24
33 Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15. Hum Mol Genet 2009 2.22
34 Metabonomic, transcriptomic, and genomic variation of a population cohort. Mol Syst Biol 2010 2.17
35 Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. Am J Respir Crit Care Med 2011 2.07
36 Childhood adversities are associated with shorter telomere length at adult age both in individuals with an anxiety disorder and controls. PLoS One 2010 2.03
37 Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. PLoS Genet 2012 1.97
38 Metabolic signatures of insulin resistance in 7,098 young adults. Diabetes 2012 1.80
39 An immune response network associated with blood lipid levels. PLoS Genet 2010 1.74
40 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
41 The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Med 2013 1.70
42 Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. Circ Cardiovasc Genet 2012 1.60
43 Impact of common variation in bone-related genes on type 2 diabetes and related traits. Diabetes 2012 1.42
44 Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus. Hum Mol Genet 2002 1.42
45 Distinct variants at LIN28B influence growth in height from birth to adulthood. Am J Hum Genet 2010 1.37
46 Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. Genome Res 2010 1.32
47 Gender differences in genetic risk profiles for cardiovascular disease. PLoS One 2008 1.31
48 A P3G generic access agreement for population genomic studies. Nat Biotechnol 2013 1.28
49 Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer. Anesthesiology 2013 1.27
50 Pain in 1,000 women treated for breast cancer: a prospective study of pain sensitivity and postoperative pain. Anesthesiology 2013 1.24
51 Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes. PLoS Genet 2010 1.24
52 Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits. Nicotine Tob Res 2012 1.22
53 Determinants of the progression in lumbar degeneration: a 5-year follow-up study of adult male monozygotic twins. Spine (Phila Pa 1976) 2006 1.20
54 Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Hum Mol Genet 2013 1.19
55 Association of variants in DISC1 with psychosis-related traits in a large population cohort. Arch Gen Psychiatry 2009 1.19
56 SAIL--a software system for sample and phenotype availability across biobanks and cohorts. Bioinformatics 2010 1.15
57 Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide. Hypertension 2013 1.14
58 Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease. Arterioscler Thromb Vasc Biol 2013 1.13
59 Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci. Hum Mol Genet 2011 1.13
60 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
61 NordicDB: a Nordic pool and portal for genome-wide control data. Eur J Hum Genet 2010 1.07
62 The genetic structure of the Swedish population. PLoS One 2011 1.05
63 Pubertal timing and growth influences cardiometabolic risk factors in adult males and females. Diabetes Care 2012 1.04
64 From genetic discovery to future personalized health research. N Biotechnol 2012 0.98
65 A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genet 2011 0.97
66 Work-related exhaustion and telomere length: a population-based study. PLoS One 2012 0.97
67 Adipose tissue gene expression analysis reveals changes in inflammatory, mitochondrial respiratory and lipid metabolic pathways in obese insulin-resistant subjects. BMC Med Genomics 2012 0.96
68 The molecular genetic architecture of self-employment. PLoS One 2013 0.96
69 A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Res Hum Genet 2012 0.95
70 A random change point model for assessing variability in repeated measures of cognitive function. Stat Med 2008 0.95
71 Association of known loci with lipid levels among children and prediction of dyslipidemia in adults. Circ Cardiovasc Genet 2011 0.93
72 Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol. Arterioscler Thromb Vasc Biol 2013 0.93
73 Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study. Hypertension 2011 0.91
74 European lactase persistence genotype shows evidence of association with increase in body mass index. Hum Mol Genet 2009 0.91
75 Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--a meta-analysis of three independent studies. PLoS One 2012 0.90
76 Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humans. PLoS One 2013 0.89
77 Missing value imputation in longitudinal measures of alcohol consumption. Int J Methods Psychiatr Res 2011 0.88
78 Genome-wide meta-analysis of common variant differences between men and women. Hum Mol Genet 2012 0.88
79 Genetic architecture of circulating lipid levels. Eur J Hum Genet 2011 0.88
80 Phenotype mining in CNV carriers from a population cohort. Hum Mol Genet 2011 0.87
81 Genetic association and interaction analysis of USF1 and APOA5 on lipid levels and atherosclerosis. Arterioscler Thromb Vasc Biol 2009 0.87
82 Psychiatric comorbidity in couples: a longitudinal study of 202,959 married and cohabiting individuals. Soc Psychiatry Psychiatr Epidemiol 2010 0.87
83 A longitudinal Swedish study on screening for squamous cell carcinoma and adenocarcinoma: evidence of effectiveness and overtreatment. Cancer Epidemiol Biomarkers Prev 2007 0.86
84 Associations of nicotine intake measures with CHRN genes in Finnish smokers. Nicotine Tob Res 2011 0.86
85 A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe. PLoS One 2013 0.83
86 Towards a molecular systems model of coronary artery disease. Curr Cardiol Rep 2014 0.82
87 Support for involvement of glutamate decarboxylase 1 and neuropeptide Y in anxiety susceptibility. Am J Med Genet B Neuropsychiatr Genet 2012 0.81
88 Further evidence for the role of ENPP1 in obesity: association with morbid obesity in Finns. Obesity (Silver Spring) 2008 0.80
89 Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs. J Am Heart Assoc 2015 0.79
90 A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. Heart Rhythm 2012 0.78
91 Diagnostic efficacy of myeloperoxidase to identify acute coronary syndrome in subjects with chest pain. Ann Med 2013 0.77
92 The influence of mortality on twin models of change: addressing missingness through multiple imputation. Behav Genet 2003 0.77
93 Does expecting more pain make it more intense? Factors associated with the first week pain trajectories after breast cancer surgery. Pain 2017 0.75
94 Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data. Genet Epidemiol 2014 0.75
95 [Genetics of multifactorial diseases]. Duodecim 2010 0.75
96 Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study. PLoS Genet 2017 0.75
97 Bayesian latent variable collapsing model for detecting rare variant interaction effect in twin study. Genet Epidemiol 2014 0.75
98 Determinants of changes in bone density: a 5-year follow-up study of adult male monozygotic twins. J Clin Densitom 2007 0.75