Published in Bioinformatics on May 25, 2010
Genetic variation predicting cisplatin cytotoxicity associated with overall survival in lung cancer patients receiving platinum-based chemotherapy. Clin Cancer Res (2011) 1.32
IL1RN coding variant is associated with lower risk of acute respiratory distress syndrome and increased plasma IL-1 receptor antagonist. Am J Respir Crit Care Med (2013) 1.03
A genome-wide association study identifies two novel promising candidate genes affecting Escherichia coli F4ab/F4ac susceptibility in swine. PLoS One (2012) 0.98
Genome wide association study for drought, aflatoxin resistance, and important agronomic traits of maize hybrids in the sub-tropics. PLoS One (2015) 0.82
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers. Bioinformatics (2015) 0.78
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature (2001) 33.12
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet (2008) 30.20
Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet (2005) 25.34
New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nat Genet (2007) 13.76
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. Nat Genet (2008) 8.63
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Genotyping errors: causes, consequences and solutions. Nat Rev Genet (2005) 5.00
A method to address differential bias in genotyping in large-scale association studies. PLoS Genet (2007) 4.51
Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Mol Psychiatry (2008) 3.85
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet (2001) 2.68
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Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification. Hum Mol Genet (2004) 1.38
Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure. Curr Opin Lipidol (2008) 1.34
Quantification of the power of Hardy-Weinberg equilibrium testing to detect genotyping error. Hum Hered (2006) 1.32
Allowing for genotyping error in analysis of unmatched case-control studies. Ann Hum Genet (2003) 1.21
On the usage of HWE for identifying genotyping errors. Ann Hum Genet (2007) 1.08
Goldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies. BMC Bioinformatics (2008) 1.00
Incorporating individual error rate into association test of unmatched case-control design. Hum Hered (2004) 0.99
On quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data. PLoS Genet (2009) 0.88
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies. Am J Med Genet B Neuropsychiatr Genet (2008) 0.85
Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies. Ann Hum Genet (2008) 0.81
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nat Genet (2007) 13.76
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet (2009) 12.96
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. N Engl J Med (2014) 6.89
A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry (2012) 6.34
Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet (2009) 6.13
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet (2012) 5.78
Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am J Psychiatry (2009) 4.74
Exome sequencing and the genetic basis of complex traits. Nat Genet (2012) 4.11
The Swedish Twin Registry in the third millennium: an update. Twin Res Hum Genet (2006) 3.58
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. Am J Hum Genet (2012) 3.50
Genome-wide association study of alcohol dependence. Arch Gen Psychiatry (2009) 3.08
Prevalence, heritability, and prospective risk factors for anorexia nervosa. Arch Gen Psychiatry (2006) 3.02
A twin study of genetic and environmental influences on tobacco initiation, regular tobacco use and nicotine dependence. Psychol Med (2004) 2.98
Recurrence risks for schizophrenia in a Swedish national cohort. Psychol Med (2006) 2.75
Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects. Eur J Hum Genet (2008) 2.75
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies. Nat Genet (2012) 2.50
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. PLoS Genet (2009) 2.27
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genet (2013) 2.08
Evidence of soil nutrient availability as the proximate constraint on growth of treeline trees in northwest Alaska. Ecology (2015) 2.05
False discoveries and models for gene discovery. Trends Genet (2003) 2.03
zCall: a rare variant caller for array-based genotyping: genetics and population analysis. Bioinformatics (2012) 1.87
Genome-wide association study of suicide attempts in mood disorder patients. Am J Psychiatry (2010) 1.85
Meta-analysis of genome-wide association studies with overlapping subjects. Am J Hum Genet (2009) 1.83
Simulating association studies: a data-based resampling method for candidate regions or whole genome scans. Bioinformatics (2007) 1.77
seeQTL: a searchable database for human eQTLs. Bioinformatics (2011) 1.72
Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression. Am J Hum Genet (2011) 1.71
The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: a transdisciplinary perspective. Am Psychol (2005) 1.71
Estimation of SNP heritability from dense genotype data. Am J Hum Genet (2013) 1.64
TAMAL: an integrated approach to choosing SNPs for genetic studies of human complex traits. Bioinformatics (2006) 1.57
Irritable bowel syndrome: a co-twin control analysis. Am J Gastroenterol (2007) 1.56
Chronic widespread pain and its comorbidities: a population-based study. Arch Intern Med (2006) 1.49
Cigarettes and oral snuff use in Sweden: Prevalence and transitions. Addiction (2006) 1.48
Extensions to the modeling of initiation and progression: applications to substance use and abuse. Behav Genet (2006) 1.48
Population structure, migration, and diversifying selection in the Netherlands. Eur J Hum Genet (2013) 1.47
Medical and psychiatric morbidity in obese women with and without binge eating. Int J Eat Disord (2002) 1.46
Schizophrenia genetics: where next? Schizophr Bull (2011) 1.42
The relation between eating disorders and components of perfectionism. Am J Psychiatry (2003) 1.41
Importance of genetic influences on chronic widespread pain. Arthritis Rheum (2006) 1.41
Association of ADH and ALDH genes with alcohol dependence in the Irish Affected Sib Pair Study of alcohol dependence (IASPSAD) sample. Alcohol Clin Exp Res (2008) 1.41
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. PLoS Genet (2012) 1.40
Premorbid predictors of chronic fatigue. Arch Gen Psychiatry (2006) 1.40
LifeGene--a large prospective population-based study of global relevance. Eur J Epidemiol (2010) 1.38
Psychiatric and medical symptoms in binge eating in the absence of compensatory behaviors. Obes Res (2004) 1.38
The Irish Affected Sib Pair Study of Alcohol Dependence: study methodology and validation of diagnosis by interview and family history. Alcohol Clin Exp Res (2005) 1.33
Genetic and environmental contributions to obesity and binge eating. Int J Eat Disord (2003) 1.33
The epidemiology of chronic fatigue in the Swedish Twin Registry. Psychol Med (2005) 1.31
A searchable database of genetic evidence for psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet (2008) 1.31
A systematic method for estimating individual responses to treatment with antipsychotics in CATIE. Schizophr Res (2008) 1.30
Multivariate phenotype association analysis by marker-set kernel machine regression. Genet Epidemiol (2012) 1.29
Current developments in the genetics of autism: from phenome to genome. J Neuropathol Exp Neurol (2008) 1.26
A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects. Hum Mol Genet (2013) 1.24
Genome-wide association study of exercise behavior in Dutch and American adults. Med Sci Sports Exerc (2009) 1.22
Feeling bad in more ways than one: comorbidity patterns of medically unexplained and psychiatric conditions. J Gen Intern Med (2007) 1.20
Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence. Alcohol Clin Exp Res (2006) 1.20
Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. Neuropsychopharmacology (2010) 1.19
MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples. Epigenomics (2012) 1.16
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Hum Mol Genet (2013) 1.14
Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia. Hum Mol Genet (2006) 1.14
Sex differences in the human peripheral blood transcriptome. BMC Genomics (2014) 1.13
Causes and recovery in anorexia nervosa: the patient's perspective. Int J Eat Disord (2003) 1.12
A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. Biol Psychol (2010) 1.12
The genetics of anorexia nervosa. Annu Rev Nutr (2007) 1.12
Association study of 182 candidate genes in anorexia nervosa. Am J Med Genet B Neuropsychiatr Genet (2010) 1.11
Familial clustering of major depression and anxiety disorders in Australian and Dutch twins and siblings. Twin Res Hum Genet (2005) 1.11
Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia. Biol Psychiatry (2007) 1.10
Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression. Nat Genet (2011) 1.10
Comment on a simple and improved correction for population stratification. Am J Hum Genet (2008) 1.09
Genomewide association study of movement-related adverse antipsychotic effects. Biol Psychiatry (2009) 1.09
Pharmacogenomic genome-wide association studies: lessons learned thus far. Pharmacogenomics (2009) 1.08
MethylPCA: a toolkit to control for confounders in methylome-wide association studies. BMC Bioinformatics (2013) 1.06
Interactions among shrub cover and the soil microclimate may determine future Arctic carbon budgets. Ecol Lett (2012) 1.06
The genetic structure of the Swedish population. PLoS One (2011) 1.05
Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry (2013) 1.05
Genetic and phenotypic stability of measures of neuroticism over 22 years. Twin Res Hum Genet (2007) 1.04
Six months of treatment for depression: outcome and predictors of the course of illness. Am J Psychiatry (2006) 1.02
The STAGE cohort: a prospective study of tobacco use among Swedish twins. Nicotine Tob Res (2008) 1.02
The genomics of schizophrenia: update and implications. J Clin Invest (2013) 0.98
Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentation. Nucleic Acids Res (2012) 0.98
A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder. Alcohol Clin Exp Res (2006) 0.98
A framework for controlling false discovery rates and minimizing the amount of genotyping in the search for disease mutations. Hum Hered (2003) 0.98
A genome scan of neuroticism in nicotine dependent smokers. Am J Med Genet B Neuropsychiatr Genet (2005) 0.98
The neuregulin 1 promoter polymorphism rs6994992 is not associated with chronic schizophrenia or neurocognition. Am J Med Genet B Neuropsychiatr Genet (2008) 0.97
The types of regular cigarette smokers: a latent class analysis. Nicotine Tob Res (2005) 0.97
Modifiers and subtype-specific analyses in whole-genome association studies: a likelihood framework. Hum Hered (2011) 0.96
Patterns and predictors of remission, response and recovery in major depression treated with fluoxetine or nortriptyline. Aust N Z J Psychiatry (2002) 0.96
Temperament, childhood environment and psychopathology as risk factors for avoidant and borderline personality disorders. Aust N Z J Psychiatry (2003) 0.95
Melancholia: definitions, risk factors, personality, neuroendocrine markers and differential antidepressant response. Aust N Z J Psychiatry (2002) 0.95
Association of RGS2 and RGS5 variants with schizophrenia symptom severity. Schizophr Res (2008) 0.94
Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Arch Gen Psychiatry (2008) 0.94
Anxiety and comorbid measures associated with PLXNA2. Arch Gen Psychiatry (2007) 0.93
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol (2015) 0.93
SNP-based analysis of neuroactive ligand-receptor interaction pathways implicates PGE2 as a novel mediator of antipsychotic treatment response: data from the CATIE study. Schizophr Res (2011) 0.93
Transcriptome atlases of mouse brain reveals differential expression across brain regions and genetic backgrounds. G3 (Bethesda) (2012) 0.92
The prevalence of self-reported chronic fatigue in a U.S. twin registry. J Psychosom Res (2005) 0.92
Gene expression in peripheral blood leukocytes in monozygotic twins discordant for chronic fatigue: no evidence of a biomarker. PLoS One (2009) 0.92
Genetic determinants of variable metabolism have little impact on the clinical use of leading antipsychotics in the CATIE study. Genet Med (2008) 0.92