Published in BMC Bioinformatics on May 28, 2010
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet (2013) 9.46
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet (2012) 4.73
Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nat Genet (2012) 4.08
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
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. Nat Genet (2011) 3.06
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet (2015) 2.84
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity. Diabetes (2013) 2.70
Meta-analysis methods for genome-wide association studies and beyond. Nat Rev Genet (2013) 2.58
Transethnic meta-analysis of genomewide association studies. Genet Epidemiol (2011) 2.53
Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat Genet (2013) 2.43
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet (2013) 2.36
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes (2011) 2.21
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nat Genet (2010) 2.04
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain (2013) 1.95
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat Genet (2012) 1.90
FTO, type 2 diabetes, and weight gain throughout adult life: a meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies. Diabetes (2011) 1.75
Comprehensive literature review and statistical considerations for GWAS meta-analysis. Nucleic Acids Res (2012) 1.75
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Med (2013) 1.70
Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat Genet (2012) 1.64
Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data. Ann Rheum Dis (2012) 1.62
A variant in MCF2L is associated with osteoarthritis. Am J Hum Genet (2011) 1.60
Meta-analysis of sex-specific genome-wide association studies. Genet Epidemiol (2010) 1.56
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. PLoS Genet (2012) 1.55
Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study. PLoS One (2013) 1.55
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Nature (2015) 1.53
A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. Mol Psychiatry (2010) 1.52
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Stroke (2013) 1.51
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. Nat Genet (2016) 1.48
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium. Nephrol Dial Transplant (2015) 1.45
The Genetic Landscape of Renal Complications in Type 1 Diabetes. J Am Soc Nephrol (2016) 1.44
Genome-wide association meta-analysis identifies new endometriosis risk loci. Nat Genet (2012) 1.42
A genome-wide association study of anorexia nervosa. Mol Psychiatry (2014) 1.33
Coexpression network analysis in abdominal and gluteal adipose tissue reveals regulatory genetic loci for metabolic syndrome and related phenotypes. PLoS Genet (2012) 1.31
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. PLoS Genet (2014) 1.27
High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. Ann Rheum Dis (2014) 1.25
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat Genet (2016) 1.24
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nat Genet (2015) 1.23
The impact of low-frequency and rare variants on lipid levels. Nat Genet (2015) 1.20
Differential methylation of the TRPA1 promoter in pain sensitivity. Nat Commun (2014) 1.19
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nat Commun (2014) 1.18
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. PLoS One (2011) 1.18
Whole-genome sequence-based analysis of thyroid function. Nat Commun (2015) 1.16
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet (2012) 1.14
PCSK6 is associated with handedness in individuals with dyslexia. Hum Mol Genet (2010) 1.14
Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations. Eur J Hum Genet (2012) 1.09
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus. Gastroenterology (2014) 1.08
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Diabetologia (2013) 1.07
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. BMC Med Genet (2011) 1.02
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Mol Psychiatry (2014) 1.01
A central role for GRB10 in regulation of islet function in man. PLoS Genet (2014) 1.01
Variation in the ICAM1-ICAM4-ICAM5 locus is associated with systemic lupus erythematosus susceptibility in multiple ancestries. Ann Rheum Dis (2012) 0.96
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS Genet (2013) 0.94
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. Hum Mol Genet (2014) 0.94
Association study of genes controlling IL-12-dependent IFN-γ immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco. J Infect Dis (2014) 0.93
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Nat Commun (2015) 0.93
Identification of a candidate gene for astigmatism. Invest Ophthalmol Vis Sci (2013) 0.92
HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy. Am J Hum Genet (2015) 0.91
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2. Hum Mol Genet (2013) 0.91
DCAF4, a novel gene associated with leucocyte telomere length. J Med Genet (2015) 0.90
Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Hum Reprod Update (2014) 0.90
The neuropeptide galanin and variants in the GalR1 gene are associated with nicotine dependence. Neuropsychopharmacology (2011) 0.90
Trans-ethnic study design approaches for fine-mapping. Eur J Hum Genet (2016) 0.89
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Nat Commun (2016) 0.88
Genome-wide meta-analysis of common variant differences between men and women. Hum Mol Genet (2012) 0.88
Hypermethylation in the ZBTB20 gene is associated with major depressive disorder. Genome Biol (2014) 0.88
A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing. Front Genet (2015) 0.88
Genome-wide polygenic scoring for a 14-year long-term average depression phenotype. Brain Behav (2014) 0.88
Genome-wide associations for birth weight and correlations with adult disease. Nature (2016) 0.87
The α3β4* nicotinic ACh receptor subtype mediates physical dependence to morphine: mouse and human studies. Br J Pharmacol (2014) 0.86
Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. PLoS Genet (2014) 0.86
Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer. Nat Commun (2015) 0.85
Assessing the impact of missing genotype data in rare variant association analysis. BMC Proc (2011) 0.84
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. Pharmacogenomics J (2015) 0.84
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm. J Med Genet (2013) 0.83
Association between endometriosis and the interleukin 1A (IL1A) locus. Hum Reprod (2014) 0.83
An evaluation of different meta-analysis approaches in the presence of allelic heterogeneity. Eur J Hum Genet (2012) 0.83
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. Nat Genet (2016) 0.82
SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes. Diabetologia (2014) 0.82
Trans-ethnic meta-analysis of white blood cell phenotypes. Hum Mol Genet (2014) 0.82
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. Hum Mol Genet (2015) 0.82
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation. PLoS Genet (2015) 0.82
Performance of polygenic scores for predicting phobic anxiety. PLoS One (2013) 0.82
Epigenetic associations of type 2 diabetes and BMI in an Arab population. Clin Epigenetics (2016) 0.82
A genome-wide association study of pulmonary tuberculosis in Morocco. Hum Genet (2016) 0.81
Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci. Carcinogenesis (2015) 0.81
Nicotine reward and affective nicotine withdrawal signs are attenuated in calcium/calmodulin-dependent protein kinase IV knockout mice. PLoS One (2012) 0.81
Evaluating the Performance of Fine-Mapping Strategies at Common Variant GWAS Loci. PLoS Genet (2015) 0.81
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. Hum Mol Genet (2016) 0.81
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. PLoS Genet (2016) 0.80
Genome-wide association studies in nephrology: using known associations for data checks. Am J Kidney Dis (2014) 0.80
Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophr Res (2011) 0.80
Integrated genomic approaches identify major pathways and upstream regulators in late onset Alzheimer's disease. Sci Rep (2015) 0.80
ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. PLoS One (2011) 0.80
Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder. Psychiatr Genet (2013) 0.80
Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment. J Allergy Clin Immunol (2016) 0.80
Five endometrial cancer risk loci identified through genome-wide association analysis. Nat Genet (2016) 0.80
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: Comparison to myeloma. Leukemia (2016) 0.79
Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2. Sci Rep (2016) 0.79
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: a meta-analysis of three genome-wide association studies. Clin Pharmacol Ther (2016) 0.78
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children. Am J Hum Genet (2016) 0.78
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature (2007) 144.95
Meta-analysis in clinical trials. Control Clin Trials (1986) 144.91
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Quantifying heterogeneity in a meta-analysis. Stat Med (2002) 83.16
Genomic control for association studies. Biometrics (1999) 64.39
A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet (2007) 52.68
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet (2008) 35.06
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet (2007) 24.68
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet (2008) 22.35
Practical aspects of imputation-driven meta-analysis of genome-wide association studies. Hum Mol Genet (2008) 13.26
Variants in MTNR1B influence fasting glucose levels. Nat Genet (2008) 10.85
Assessing heterogeneity in meta-analysis: Q statistic or I2 index? Psychol Methods (2006) 8.42
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet (2009) 5.81
Heterogeneity in meta-analyses of genome-wide association investigations. PLoS One (2007) 5.77
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science (2007) 32.97
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet (2007) 12.62
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27
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
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet (2012) 6.15
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet (2009) 5.81
Two-stage two-locus models in genome-wide association. PLoS Genet (2006) 5.60
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nat Genet (2012) 5.55
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet (2012) 4.73
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet (2011) 4.50
Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes. Am J Hum Genet (2004) 4.44
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms. Am J Hum Genet (2008) 4.28
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet (2014) 4.13
Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice. Nat Genet (2004) 3.83
Data quality control in genetic case-control association studies. Nat Protoc (2010) 3.68
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet (2011) 3.46
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet (2013) 3.25
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
The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet (2004) 2.78
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets. Nat Genet (2005) 2.66
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
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nat Genet (2010) 2.04
Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. Am J Hum Genet (2013) 1.96
Basic statistical analysis in genetic case-control studies. Nat Protoc (2011) 1.86
A comparison of sample size and power in case-only association studies of gene-environment interaction. Am J Epidemiol (2010) 1.78
A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One (2012) 1.72
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry (2008) 1.69
Tight junction protein expression and barrier properties of immortalized mouse brain microvessel endothelial cells. Brain Res (2006) 1.65
Fine mapping versus replication in whole-genome association studies. Am J Hum Genet (2007) 1.64
Meta-analysis of sex-specific genome-wide association studies. Genet Epidemiol (2010) 1.56
The inheritance of resistance alleles in multiple sclerosis. PLoS Genet (2007) 1.54
Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis. Am J Clin Nutr (2008) 1.49
Genome-wide association meta-analysis identifies new endometriosis risk loci. Nat Genet (2012) 1.42
Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples. Hum Mol Genet (2004) 1.41
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Diabetes (2013) 1.36
Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Am J Hum Genet (2012) 1.29
DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry (2011) 1.29
Natriuretic peptides and nitric oxide stimulate cGMP synthesis in different cellular compartments. J Gen Physiol (2006) 1.27
Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany. Eur J Hum Genet (2010) 1.26
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studies. BMC Bioinformatics (2010) 1.26
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants. Genome Res (2005) 1.25
Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk. Diabetes (2009) 1.25
AF17 competes with AF9 for binding to Dot1a to up-regulate transcription of epithelial Na+ channel alpha. J Biol Chem (2009) 1.22
Gearing up for genome-wide gene-association studies. Hum Mol Genet (2005) 1.21
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. PLoS One (2011) 1.18
Genotype prediction using a dense map of SNPs. Genet Epidemiol (2004) 1.16
PCSK6 is associated with handedness in individuals with dyslexia. Hum Mol Genet (2010) 1.14
Marker selection for genetic case-control association studies. Nat Protoc (2009) 1.12
Dual alterations in casein kinase I-epsilon and GSK-3beta modulate beta-catenin stability in hyperproliferating colonic epithelia. Am J Physiol Gastrointest Liver Physiol (2006) 1.06
Genome-wide association analysis of imputed rare variants: application to seven common complex diseases. Genet Epidemiol (2012) 1.06
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data. Hum Hered (2012) 1.05
Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. Diabetes (2011) 1.05
Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets. Diabetes (2012) 1.02
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. PLoS Genet (2013) 1.02
Goldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies. BMC Bioinformatics (2008) 1.00
Clinical and genetic correlates of growth differentiation factor 15 in the community. Clin Chem (2012) 0.99
Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group. Genet Epidemiol (2010) 0.99
Promising hypotensive effect of hawthorn extract: a randomized double-blind pilot study of mild, essential hypertension. Phytother Res (2002) 0.96
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS Genet (2013) 0.94
Genome-wide association scan allowing for epistasis in type 2 diabetes. Ann Hum Genet (2010) 0.93
Linkage disequilibrium mapping via cladistic analysis of phase-unknown genotypes and inferred haplotypes in the Genetic Analysis Workshop 14 simulated data. BMC Genet (2005) 0.91
Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits. Brief Funct Genomics (2014) 0.91
Examining the statistical properties of fine-scale mapping in large-scale association studies. Genet Epidemiol (2008) 0.90
Expression of rotavirus NSP4 alters the actin network organization through the actin remodeling protein cofilin. J Virol (2007) 0.90
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene. J Clin Invest (2015) 0.90
A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traits. PLoS Genet (2013) 0.88
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. PLoS One (2012) 0.86
Chronic PKC-beta activation in HT-29 Cl.19a colonocytes prevents cAMP-mediated ion secretion by inhibiting apical membrane current generation. Am J Physiol Gastrointest Liver Physiol (2006) 0.86
How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage. Genet Epidemiol (2005) 0.86
Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis. Hum Genet (2010) 0.85
Assessing the impact of missing genotype data in rare variant association analysis. BMC Proc (2011) 0.84
Assessment of sex-specific effects in a genome-wide association study of rheumatoid arthritis. BMC Proc (2009) 0.84
Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes. Genet Epidemiol (2011) 0.83
A TNF region haplotype offers protection from typhoid fever in Vietnamese patients. Hum Genet (2007) 0.82
Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis. Clin Endocrinol (Oxf) (2014) 0.81
A comparison of case-only designs for detecting gene x gene interaction in rheumatoid arthritis using genome-wide case-control data in Genetic Analysis Workshop 16. BMC Proc (2009) 0.80
Chronic PKC-beta2 activation in HT-29 Cl.19a colonocytes prevents cAMP-mediated ion secretion by inhibiting apical membrane CFTR targeting. Am J Physiol Gastrointest Liver Physiol (2006) 0.78
Genetic variation in the CYP2B6 gene is related to circulating 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) concentrations: an observational population-based study. Environ Health (2014) 0.77
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene. J Clin Invest (2016) 0.76
Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. PLoS One (2013) 0.76
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
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J Clin Invest (2017) 0.75
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet (2017) 0.75
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Circ Cardiovasc Genet (2017) 0.75
Physicomechanical properties of sintered scaffolds formed from porous and protein-loaded poly(DL-lactic-co-glycolic acid) microspheres for potential use in bone tissue engineering. J Biomater Sci Polym Ed (2015) 0.75
Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat Commun (2017) 0.75