Published in Am J Hum Genet on July 22, 2004
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Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS Genet (2010) 5.79
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Evaluating historical candidate genes for schizophrenia. Mol Psychiatry (2015) 1.26
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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. PLoS One (2014) 1.11
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. Am J Hum Genet (2009) 1.11
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Ethnicity-specific gene-gene interaction between IL-13 and IL-4Ralpha among African Americans with asthma. Am J Respir Crit Care Med (2007) 1.10
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A quality assessment of genetic association studies supporting susceptibility and outcome in acute lung injury. Crit Care (2008) 1.08
Regulatory polymorphisms in the cyclophilin A gene, PPIA, accelerate progression to AIDS. PLoS Pathog (2007) 1.08
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment. J Med Genet (2007) 1.07
Association of bone morphogenetic proteins with otosclerosis. J Bone Miner Res (2008) 1.07
Linkage-disequilibrium-based binning affects the interpretation of GWASs. Am J Hum Genet (2012) 1.07
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Genetic association test for multiple traits at gene level. Genet Epidemiol (2012) 1.06
A simple method for assessing the strength of evidence for association at the level of the whole gene. Adv Appl Bioinform Chem (2008) 1.04
Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. PLoS One (2014) 1.04
Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. PLoS One (2012) 1.03
A network-based approach to prioritize results from genome-wide association studies. PLoS One (2011) 1.03
Association study of clock gene (CLOCK) and schizophrenia and mood disorders in the Japanese population. Eur Arch Psychiatry Clin Neurosci (2009) 1.02
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. J Alzheimers Dis (2012) 1.02
Gene-based interaction analysis by incorporating external linkage disequilibrium information. Eur J Hum Genet (2010) 1.02
Gene-based analysis suggests association of the nicotinic acetylcholine receptor beta1 subunit (CHRNB1) and M1 muscarinic acetylcholine receptor (CHRM1) with vulnerability for nicotine dependence. Hum Genet (2006) 1.01
Cannabinoid receptor 1 gene association with nicotine dependence. Arch Gen Psychiatry (2008) 1.01
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Am J Hum Genet (2011) 1.01
Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations. Am J Respir Crit Care Med (2005) 1.00
Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility. Carcinogenesis (2012) 0.99
Detecting multiple associations in genome-wide studies. Hum Genomics (2006) 0.99
Common variants of inflammatory cytokine genes are associated with risk of nephropathy in type 2 diabetes among Asian Indians. PLoS One (2009) 0.97
A gene-based method for detecting gene-gene co-association in a case-control association study. Eur J Hum Genet (2009) 0.96
The role of LTA4H and ALOX5AP genes in the risk for asthma in Latinos. Clin Exp Allergy (2010) 0.96
Association study of CSF2RB with schizophrenia in Irish family and case - control samples. Mol Psychiatry (2007) 0.95
Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. Eur J Hum Genet (2012) 0.95
Neuregulin 1 genotype and schizophrenia. Schizophr Bull (2007) 0.95
The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits. Front Genet (2013) 0.94
Gene-environment interactions in genome-wide association studies: current approaches and new directions. J Child Psychol Psychiatry (2013) 0.93
Gene association studies in acute lung injury: replication and future direction. Am J Physiol Lung Cell Mol Physiol (2009) 0.93
Gene expression in the etiology of schizophrenia. Schizophr Bull (2008) 0.93
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity. Hum Mol Genet (2013) 0.93
Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations. Eur J Hum Genet (2008) 0.93
Genetic influences on heart rate variability at rest and during stress. Psychophysiology (2009) 0.93
No association of genetic variants in BDNF with major depression: a meta- and gene-based analysis. Am J Med Genet B Neuropsychiatr Genet (2012) 0.92
Nonlinear tests for genomewide association studies. Genetics (2006) 0.92
Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults. Atherosclerosis (2007) 0.92
Genetic associations with hypoxemia and pulmonary arterial pressure in COPD. Chest (2008) 0.91
Gene hunting of the Genetic Analysis Workshop 16 rheumatoid arthritis data using rough set theory. BMC Proc (2009) 0.91
Genetics of obsessive-compulsive disorder. Psychiatr Clin North Am (2010) 0.90
Identification of genetic associations of SP110/MYBBP1A/RELA with pulmonary tuberculosis in the Chinese Han population. Hum Genet (2012) 0.90
Genetic variation in APOJ, LPL, and TNFRSF10B affects plasma fatty acid distribution in Alaskan Eskimos. Am J Clin Nutr (2010) 0.89
Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Front Genet (2014) 0.89
Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population. PLoS One (2013) 0.89
Gene- or region-based association study via kernel principal component analysis. BMC Genet (2011) 0.89
MEGF10 association with schizophrenia. Biol Psychiatry (2008) 0.89
Unraveling the genetic basis of asthma and allergic diseases. Allergy Asthma Immunol Res (2010) 0.89
Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort. Hum Genet (2013) 0.88
Mapping the new frontier: complex genetic disorders. J Clin Invest (2005) 0.88
The interaction between coagulation factor 2 receptor and interleukin 6 haplotypes increases the risk of myocardial infarction in men. PLoS One (2010) 0.88
A gene-wide investigation on polymorphisms in the taste receptor 2R14 (TAS2R14) and susceptibility to colorectal cancer. BMC Med Genet (2010) 0.87
The nature of nurture: a genomewide association scan for family chaos. Behav Genet (2008) 0.87
A kernel regression approach to gene-gene interaction detection for case-control studies. Genet Epidemiol (2013) 0.87
Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes. BMC Proc (2009) 0.87
Unraveling genetic origin of aging-related traits: evolving concepts. Rejuvenation Res (2013) 0.86
Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS19. PLoS One (2009) 0.86
SNP-set analysis replicates acute lung injury genetic risk factors. BMC Med Genet (2012) 0.86
Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia. Schizophr Res (2008) 0.86
Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes. Schizophr Bull (2015) 0.86
Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease. Hum Mutat (2012) 0.86
Assessment of possible association between rs3787016 and prostate cancer risk in Serbian population. Int J Clin Exp Med (2012) 0.85
Individualized risk for statin-induced myopathy: current knowledge, emerging challenges and potential solutions. Pharmacogenomics (2012) 0.85
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Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening. Am J Hum Genet (2011) 1.26
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Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships. Hum Mol Genet (2004) 1.14
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Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. PLoS One (2012) 1.03
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Association analysis of the DRD4 and COMT genes in methamphetamine abuse. Am J Med Genet B Neuropsychiatr Genet (2004) 1.00
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Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk association. J Clin Endocrinol Metab (2008) 0.98
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Single-nucleotide polymorphism-mass array reveals commonly deleted regions at 3p22 and 3p14.2 associate with poor clinical outcome in esophageal squamous cell carcinoma. Int J Cancer (2008) 0.97
Artificial neural networks and decision tree model analysis of liver cancer proteomes. Biochem Biophys Res Commun (2007) 0.97
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Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population. Am J Med Genet B Neuropsychiatr Genet (2004) 0.96
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Regression-based sib pair linkage analysis for binary traits. Hum Hered (2003) 0.95
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Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing. Hum Mol Genet (2013) 0.95
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