Published in Bioinformatics on December 29, 2009
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet (2011) 10.07
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation (2011) 3.68
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. PLoS Genet (2011) 3.07
Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet (2010) 2.91
β-Aminoisobutyric acid induces browning of white fat and hepatic β-oxidation and is inversely correlated with cardiometabolic risk factors. Cell Metab (2014) 2.86
CUBN is a gene locus for albuminuria. J Am Soc Nephrol (2011) 2.70
Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. Nat Genet (2010) 1.97
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Hum Mol Genet (2011) 1.77
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). PLoS Genet (2011) 1.75
Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease. Circ Cardiovasc Genet (2010) 1.64
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
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet (2013) 1.55
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Hum Genet (2010) 1.54
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Hum Mol Genet (2011) 1.54
Genome-wide association studies of the PR interval in African Americans. PLoS Genet (2011) 1.53
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. PLoS Genet (2012) 1.53
Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. PLoS Genet (2012) 1.53
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels. Blood (2014) 1.51
Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. Heart Rhythm (2012) 1.43
Network-driven plasma proteomics expose molecular changes in the Alzheimer's brain. Mol Neurodegener (2016) 1.41
A genome-wide association study of the human metabolome in a community-based cohort. Cell Metab (2013) 1.33
Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet (2013) 1.27
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
Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood (2012) 1.26
RNA-Seq identifies SNP markers for growth traits in rainbow trout. PLoS One (2012) 1.25
Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus. Circ Cardiovasc Genet (2012) 1.22
A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Mol Psychiatry (2012) 1.21
High-resolution linkage and quantitative trait locus mapping aided by genome survey sequencing: building up an integrative genomic framework for a bivalve mollusc. DNA Res (2013) 1.19
GEE-based SNP set association test for continuous and discrete traits in family-based association studies. Genet Epidemiol (2013) 1.14
A rapid generalized least squares model for a genome-wide quantitative trait association analysis in families. Hum Hered (2011) 1.14
Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. Blood (2011) 1.13
Genome-wide association study in a Chinese population with diabetic retinopathy. Hum Mol Genet (2013) 1.13
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. Hum Mol Genet (2011) 1.13
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Diabetes (2012) 1.12
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Hum Mol Genet (2011) 1.11
Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. Invest Ophthalmol Vis Sci (2012) 1.09
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. Am J Hum Genet (2011) 1.09
Analysis of family- and population-based samples in cohort genome-wide association studies. Hum Genet (2011) 1.09
Circulating CD34(+) progenitor cell frequency is associated with clinical and genetic factors. Blood (2013) 1.07
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. Hum Genet (2013) 1.06
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am J Hum Genet (2014) 1.06
Genetic predictors of fibrin D-dimer levels in healthy adults. Circulation (2011) 1.05
A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees. Genet Epidemiol (2011) 1.04
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J Clin Invest (2013) 1.04
A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability. Cornea (2012) 1.00
Polygenic risk for externalizing disorders: Gene-by-development and gene-by-environment effects in adolescents and young adults. Clin Psychol Sci (2015) 1.00
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA. PLoS One (2012) 0.99
Clinical and genetic correlates of growth differentiation factor 15 in the community. Clin Chem (2012) 0.99
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. PLoS One (2012) 0.98
APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema. Eur Respir J (2013) 0.97
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circ Cardiovasc Genet (2012) 0.97
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network. Hum Mol Genet (2013) 0.97
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels. Circ Res (2011) 0.97
Association of genetic loci with sleep apnea in European Americans and African-Americans: the Candidate Gene Association Resource (CARe). PLoS One (2012) 0.96
Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans. Alcohol Clin Exp Res (2014) 0.95
Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. PLoS One (2012) 0.95
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits. PLoS One (2013) 0.95
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. PLoS Genet (2014) 0.93
Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. Arterioscler Thromb Vasc Biol (2011) 0.93
Association of ANXA11 genetic variation with sarcoidosis in African Americans and European Americans. Genes Immun (2012) 0.90
Genome-wide association study of gene by smoking interactions in coronary artery calcification. PLoS One (2013) 0.90
High-density linkage mapping aided by transcriptomics documents ZW sex determination system in the Chinese mitten crab Eriocheir sinensis. Heredity (Edinb) (2015) 0.89
An association between the calpastatin (CAST) gene and keratoconus. Cornea (2013) 0.89
Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance. Diabetologia (2013) 0.89
Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study. PLoS One (2012) 0.86
Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. Invest Ophthalmol Vis Sci (2013) 0.86
Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology. PLoS One (2011) 0.85
Admixture fine-mapping in African Americans implicates XAF1 as a possible sarcoidosis risk gene. PLoS One (2014) 0.85
Dissecting ancestry genomic background in substance dependence genome-wide association studies. Pharmacogenomics (2015) 0.84
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. Pharmacogenomics J (2013) 0.84
Adjusting family relatedness in data-driven burden test of rare variants. Genet Epidemiol (2014) 0.84
A three-stage approach for genome-wide association studies with family data for quantitative traits. BMC Genet (2010) 0.84
Genome-wide association study in Han Chinese identifies three novel loci for human height. Hum Genet (2013) 0.83
Genome-wide association study of body mass index in subjects with alcohol dependence. Addict Biol (2015) 0.82
Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Transl Psychiatry (2015) 0.82
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans. Hum Genet (2014) 0.82
Cognitive mediators and disparities in the relation between teen depressiveness and smoking. Drug Alcohol Depend (2014) 0.82
Genetic variants at PSMD3 interact with dietary fat and carbohydrate to modulate insulin resistance. J Nutr (2013) 0.81
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. Drug Alcohol Depend (2014) 0.81
Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. Environ Health (2013) 0.81
A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium. Hum Mol Genet (2011) 0.81
A genome-wide association study of chronic obstructive pulmonary disease in Hispanics. Ann Am Thorac Soc (2015) 0.81
Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci. Am J Hypertens (2011) 0.80
Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis. Diabetologia (2012) 0.80
Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans. Am J Hematol (2015) 0.79
Native American ancestry, lung function, and COPD in Costa Ricans. Chest (2014) 0.79
A strategy analysis for genetic association studies with known inbreeding. BMC Genet (2011) 0.79
Genetic variants within the serotonin transporter associated with familial risk for major depression. Psychiatry Res (2015) 0.79
Common variants in DRD2 are associated with sleep duration: the CARe consortium. Hum Mol Genet (2015) 0.79
Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms. Genetics (2012) 0.79
CDKN2B expression in adipose tissue of familial combined hyperlipidemia patients. J Lipid Res (2013) 0.79
Genome-wide interaction of genotype by erythrocyte n-3 fatty acids contributes to phenotypic variance of diabetes-related traits. BMC Genomics (2014) 0.78
Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico. PLoS One (2014) 0.78
Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region. Ophthalmic Genet (2014) 0.78
An exome array study of the plasma metabolome. Nat Commun (2016) 0.78
The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene. Neuropsychopharmacology (2016) 0.78
The association of the vanin-1 N131S variant with blood pressure is mediated by endoplasmic reticulum-associated degradation and loss of function. PLoS Genet (2014) 0.78
Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Circ Cardiovasc Genet (2014) 0.78
Genomic control for association studies. Biometrics (1999) 64.39
Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet (1998) 40.97
Association analysis in a variance components framework. Genet Epidemiol (2001) 2.38
Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet (2008) 20.66
The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: design, recruitment, and initial examination. Am J Epidemiol (2007) 9.90
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. Lancet (2008) 5.89
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Genomewide association studies of stroke. N Engl J Med (2009) 5.29
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet (2007) 5.02
Multiple loci associated with indices of renal function and chronic kidney disease. Nat Genet (2009) 4.78
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat Genet (2009) 4.28
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet (2012) 3.04
Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet (2010) 2.91
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation (2010) 2.78
CUBN is a gene locus for albuminuria. J Am Soc Nephrol (2011) 2.70
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. Ann Neurol (2011) 2.37
Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study. J Am Soc Nephrol (2004) 2.36
Chemokine receptor mutant CX3CR1-M280 has impaired adhesive function and correlates with protection from cardiovascular disease in humans. J Clin Invest (2003) 2.27
Description of the Framingham Heart Study data for Genetic Analysis Workshop 13. BMC Genet (2003) 2.17
Elevated ATPase activity of KaiC applies a circadian checkpoint on cell division in Synechococcus elongatus. Cell (2010) 2.15
Heritable stochastic switching revealed by single-cell genealogy. PLoS Biol (2007) 2.11
Uromodulin levels associate with a common UMOD variant and risk for incident CKD. J Am Soc Nephrol (2009) 2.10
Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. Nat Genet (2010) 1.97
Genome-wide association meta-analysis for total serum bilirubin levels. Hum Mol Genet (2009) 1.96
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. PLoS Genet (2011) 1.94
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels. PLoS Genet (2010) 1.91
Heritability of age at natural menopause in the Framingham Heart Study. J Clin Endocrinol Metab (2005) 1.80
CCL2 polymorphisms are associated with serum monocyte chemoattractant protein-1 levels and myocardial infarction in the Framingham Heart Study. Circulation (2005) 1.76
Modeling the cell cycle: why do certain circuits oscillate? Cell (2011) 1.72
The MYH9/APOL1 region and chronic kidney disease in European-Americans. Hum Mol Genet (2011) 1.71
Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet (2012) 1.68
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. PLoS Genet (2011) 1.68
Multiple loci are associated with white blood cell phenotypes. PLoS Genet (2011) 1.65
Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease. Circ Cardiovasc Genet (2010) 1.64
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. Hum Mol Genet (2010) 1.53
Rapid, simple, and high-throughput antimicrobial susceptibility testing and antibiotics screening. Angew Chem Int Ed Engl (2011) 1.50
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arterioscler Thromb Vasc Biol (2014) 1.45
A combined epidemiologic and metabolomic approach improves CKD prediction. J Am Soc Nephrol (2013) 1.42
A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. BMC Med Genet (2007) 1.42
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. Circ Cardiovasc Genet (2009) 1.41
Water-soluble conjugated polymers for imaging, diagnosis, and therapy. Chem Rev (2012) 1.40
Common genetic variation in five thrombosis genes and relations to plasma hemostatic protein level and cardiovascular disease risk. Arterioscler Thromb Vasc Biol (2006) 1.36
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. Am J Hum Genet (2011) 1.35
Expansion of monocytic myeloid-derived suppressor cells dampens T cell function in HIV-1-seropositive individuals. J Virol (2012) 1.32
Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood (2012) 1.26
Comprehensive survey of common genetic variation at the plasminogen activator inhibitor-1 locus and relations to circulating plasminogen activator inhibitor-1 levels. Circulation (2005) 1.21
Common genetic variants associate with serum phosphorus concentration. J Am Soc Nephrol (2010) 1.20
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics (2004) 1.19
Sex-specific association between estrogen receptor-alpha gene variation and measures of adiposity: the Framingham Heart Study. J Clin Endocrinol Metab (2005) 1.17
CDKN1C/p57kip2 is a candidate tumor suppressor gene in human breast cancer. BMC Cancer (2008) 1.17
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet (2012) 1.14
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. Hum Mol Genet (2011) 1.13
Evidence for linkage of red blood cell size and count: genome-wide scans in the Framingham Heart Study. Am J Hematol (2007) 1.12
Meta-analysis on inoperable pancreatic cancer: a comparison between gemcitabine-based combination therapy and gemcitabine alone. World J Gastroenterol (2006) 1.11
Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks. BMC Proc (2007) 1.11
Circulating insulin-like growth factor-1 and its binding protein-3: metabolic and genetic correlates in the community. Arterioscler Thromb Vasc Biol (2010) 1.11
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. Hum Mol Genet (2011) 1.10
Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study. Kidney Int (2005) 1.09
Genome-wide linkage analysis to age at natural menopause in a community-based sample: the Framingham Heart Study. Fertil Steril (2005) 1.08
ADAR1 is required for hematopoietic progenitor cell survival via RNA editing. Proc Natl Acad Sci U S A (2009) 1.07
Transcriptome analysis of Pacific white shrimp (Litopenaeus vannamei) hepatopancreas in response to Taura syndrome Virus (TSV) experimental infection. PLoS One (2013) 1.05
Genetic predictors of fibrin D-dimer levels in healthy adults. Circulation (2011) 1.05
A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees. Genet Epidemiol (2011) 1.04
Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China. Mov Disord (2013) 1.04
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. Circ Cardiovasc Genet (2015) 1.03
Quantitative DNA fingerprinting may distinguish new primary breast cancer from disease recurrence. J Clin Oncol (2004) 1.03
Global protein-protein interaction network in the human pathogen Mycobacterium tuberculosis H37Rv. J Proteome Res (2010) 1.02
Resistance to Bombyx mori nucleopolyhedrovirus via overexpression of an endogenous antiviral gene in transgenic silkworms. Arch Virol (2012) 1.02
Clinical significance and functional studies of myeloid-derived suppressor cells in chronic hepatitis C patients. J Clin Immunol (2013) 1.02
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. PLoS Genet (2013) 1.02
Impact of renal denervation on renalase expression in adult rats with spontaneous hypertension. Exp Ther Med (2012) 0.99
The carboxyl terminus of the Galpha-subunit is the latch for triggered activation of heterotrimeric G proteins. Mol Pharmacol (2005) 0.98
Flexible semiparametric analysis of longitudinal genetic studies by reduced rank smoothing. J R Stat Soc Ser C Appl Stat (2011) 0.97
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels. Circ Res (2011) 0.97
Weaning of extracorporeal membrane oxygenation using continuous hemodynamic transesophageal echocardiography. J Thorac Cardiovasc Surg (2013) 0.96
Performance of a genetic risk score for CKD stage 3 in the general population. Am J Kidney Dis (2011) 0.96
Conjugated polymer nanoparticles for drug delivery and imaging. ACS Appl Mater Interfaces (2010) 0.94
Clinical correlates and heritability of cystatin C (from the Framingham Offspring Study). Am J Cardiol (2008) 0.94
Thyroid function and lipid subparticle sizes in patients with short-term hypothyroidism and a population-based cohort. J Clin Endocrinol Metab (2007) 0.93
Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. Arterioscler Thromb Vasc Biol (2011) 0.93
Pharmacochaperoning of the A1 adenosine receptor is contingent on the endoplasmic reticulum. Mol Pharmacol (2010) 0.91
Oridonin induces apoptosis in gastric cancer through Apaf-1, cytochrome c and caspase-3 signaling pathway. World J Gastroenterol (2012) 0.91
Comparison of factors that may affect the inhibitory efficacy of transgenic RNAi targeting of baculoviral genes in silkworm, Bombyx mori. Antiviral Res (2012) 0.90
Transcriptome analysis of Litopenaeus vannamei in response to white spot syndrome virus infection. PLoS One (2013) 0.90
PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sample. Obesity (Silver Spring) (2006) 0.90
Joint rare variant association test of the average and individual effects for sequencing studies. PLoS One (2012) 0.90
Resistance to BmNPV via overexpression of an exogenous gene controlled by an inducible promoter and enhancer in transgenic silkworm, Bombyx mori. PLoS One (2012) 0.89
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc (2007) 0.89
Association of estimated glomerular filtration rate and urinary uromodulin concentrations with rare variants identified by UMOD gene region sequencing. PLoS One (2012) 0.89
Clinical and genetic correlates of circulating angiopoietin-2 and soluble Tie-2 in the community. Circ Cardiovasc Genet (2010) 0.89
The RAGE Gly82Ser polymorphism is not associated with cardiovascular disease in the Framingham offspring study. Atherosclerosis (2005) 0.89
The presence of serum anti-p53 antibodies from patients with invasive ductal carcinoma of breast: correlation to other clinical and biological parameters. Breast Cancer Res Treat (2005) 0.88
Gemcitabine-based cytotoxic doublets chemotherapy for advanced pancreatic cancer: updated subgroup meta-analyses of overall survival. Jpn J Clin Oncol (2010) 0.86
Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study. PLoS One (2012) 0.86
Postoperative chemoradiotherapy versus postoperative chemotherapy for completely resected gastric cancer with D2 Lymphadenectomy: a meta-analysis. PLoS One (2013) 0.86
Handling linkage disequilibrium in linkage analysis using dense single-nucleotide polymorphisms. BMC Proc (2007) 0.86
The human D2 dopamine receptor synergizes with the A2A adenosine receptor to stimulate adenylyl cyclase in PC12 cells. Neuropsychopharmacology (2003) 0.86
Upregulated expression of annexin II is a prognostic marker for patients with gastric cancer. World J Surg Oncol (2012) 0.86
Thyroid function and left ventricular structure and function in the Framingham Heart Study. Thyroid (2010) 0.85
Renalase gene polymorphism in patients with hypertension and concomitant coronary heart disease. Kidney Blood Press Res (2014) 0.85
A highly emissive conjugated polyelectrolyte vector for gene delivery and transfection. Adv Mater (2012) 0.85