Published in Nat Genet on May 01, 1999
Control of confounding of genetic associations in stratified populations. Am J Hum Genet (2003) 7.99
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. N Engl J Med (2006) 7.75
False-positive results in cancer epidemiology: a plea for epistemological modesty. J Natl Cancer Inst (2008) 3.72
Population stratification confounds genetic association studies among Latinos. Hum Genet (2005) 3.19
STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement. PLoS Med (2009) 2.39
Testing for population subdivision and association in four case-control studies. Am J Hum Genet (2002) 2.26
Most published research findings are false-but a little replication goes a long way. PLoS Med (2007) 2.26
Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations. Am J Respir Cell Mol Biol (2005) 2.08
Replication in genome-wide association studies. Stat Sci (2009) 1.89
STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement. Eur J Clin Invest (2009) 1.82
Lack of support for the association between GAD2 polymorphisms and severe human obesity. PLoS Biol (2005) 1.59
Common variants in HSPB7 and FRMD4B associated with advanced heart failure. Circ Cardiovasc Genet (2010) 1.51
Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement. Hum Genet (2009) 1.47
Comprehensive testing of positionally cloned asthma genes in two populations. Am J Respir Crit Care Med (2007) 1.32
Genetic studies of IgA nephropathy: past, present, and future. Pediatr Nephrol (2010) 1.30
Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement. Eur J Epidemiol (2009) 1.25
Genetics and genomics in pediatric septic shock. Crit Care Med (2012) 1.23
Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research. Genet Med (2007) 1.16
Generating genetic risk scores from intermediate phenotypes for use in association studies of clinically significant endpoints. Ann Hum Genet (2005) 1.13
Supportive evidence for a genetic association of the FCRL3 promoter polymorphism with rheumatoid arthritis. Ann Rheum Dis (2005) 1.11
Power consequences of linkage disequilibrium variation between populations. Genet Epidemiol (2009) 1.08
Methodological Issues in Multistage Genome-wide Association Studies. Stat Sci (2009) 1.06
A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance. Am J Hum Genet (2002) 1.05
Genetics of liver disease: immunogenetics and disease pathogenesis. Gut (2004) 1.04
Replication of the genetic effects of IFN regulatory factor 5 (IRF5) on systemic lupus erythematosus in a Korean population. Arthritis Res Ther (2007) 1.00
P-value based analysis for shared controls design in genome-wide association studies. Genet Epidemiol (2010) 1.00
Searching for genes that matter in acute kidney injury: a systematic review. Clin J Am Soc Nephrol (2009) 0.99
Genetics of arterial hypertension and hypotension. Naunyn Schmiedebergs Arch Pharmacol (2007) 0.97
The genomic architecture of sporadic heart failure. Circ Res (2011) 0.95
Protective effect of the Nramp1 BB genotype against Brucella abortus in the water buffalo (Bubalus bubalis). Infect Immun (2006) 0.94
Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis. Mutat Res (2011) 0.90
Genetic aspects in attention-deficit/hyperactivity disorder. J Neural Transm (Vienna) (2008) 0.90
Ethical issues of predictive genetic testing for diabetes. J Diabetes Sci Technol (2009) 0.89
Transcriptomic biomarkers of cardiovascular disease. Prog Cardiovasc Dis (2012) 0.88
Host susceptibility to persistent hepatitis B virus infection. World J Gastroenterol (2006) 0.88
Dopamine genes and schizophrenia: case closed or evidence pending? Schizophr Bull (2007) 0.88
Impact of common genetic variation on neonatal disease and outcome. Arch Dis Child Fetal Neonatal Ed (2007) 0.88
Cis sequence effects on gene expression. BMC Genomics (2007) 0.85
A functional polymorphism in the interleukin-1 receptor-1 gene is associated with increased risk of Helicobacter pylori infection but not with gastric cancer. Dig Dis Sci (2004) 0.84
Selection of extreme phenotypes: the role of clinical observation in translational research. Clin Transl Oncol (2010) 0.83
Pseudosibship methods in the case-parents design. Stat Med (2011) 0.82
Ranking bias in association studies. Hum Hered (2009) 0.80
Opportunities and limitations of genetic analysis of hypertensive rat strains. J Hypertens (2009) 0.79
Polymorphisms in tumour necrosis factor (TNF) are associated with risk of bladder cancer and grade of tumour at presentation. Br J Cancer (2003) 0.79
A powerful statistical framework for generalization testing in GWAS, with application to the HCHS/SOL. Genet Epidemiol (2017) 0.78
The Nramp1AA genotype confers susceptibility to Brucella abortus in water buffalo. Mamm Genome (2007) 0.78
Assessing the quality of case-control association studies on the genetic basis of sepsis. Pediatr Crit Care Med (2005) 0.78
Genetics in psychiatry: common variant association studies. Mol Autism (2010) 0.78
The interleukin-6 gene promoter polymorphism -174 and atherosclerotic events in overweight transplanted patients. J Transplant (2011) 0.77
Assessment of systematic effects of methodological characteristics on candidate genetic associations. Hum Genet (2012) 0.77
Pharmacogenetics of cardiovascular drug therapy. Clin Cases Miner Bone Metab (2009) 0.75
Is anti-cyclic citrullinated Peptide antibody a good value biomarker for Alzheimer disease? Int J Prev Med (2013) 0.75
Heterozygosity at the A625C polymorphic site of the MyD88 gene is associated with Mycobacterium bovis infection in cattle. Infect Immun (2013) 0.75
Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese. Sci Rep (2017) 0.75
An unvarnished truth. J Clin Invest (1999) 0.75
Relationship of five inflammatory gene polymorphisms with morbidity and mortality in 533 patients admitted to an ICU. Inflammation (2005) 0.75
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease. Nat Genet (1999) 2.01
Alpha-2 macroglobulin polymorphism and Alzheimer disease risk in the UK. Nat Genet (1999) 1.79
Alpha-2 macroglobulin gene and Alzheimer disease. Nat Genet (1999) 1.73