Published in Genet Epidemiol on January 01, 2002
Variance component model to account for sample structure in genome-wide association studies. Nat Genet (2010) 15.52
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet (2008) 12.07
A genomic background based method for association analysis in related individuals. PLoS One (2007) 3.46
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits. Am J Hum Genet (2014) 2.55
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. JAMA (2009) 2.10
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet (2012) 1.96
Rapid variance components-based method for whole-genome association analysis. Nat Genet (2012) 1.89
Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe). Hum Mol Genet (2011) 1.37
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
Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses. Heredity (Edinb) (2010) 1.11
Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia. Ann Hum Genet (2012) 1.08
Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset. J Invest Dermatol (2011) 1.08
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. PLoS One (2012) 1.07
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment. J Med Genet (2007) 1.07
Statistical distributions of test statistics used for quantitative trait association mapping in structured populations. Genet Sel Evol (2012) 1.01
Efficient calculation of P-value and power for quadratic form statistics in multilocus association testing. Ann Hum Genet (2010) 0.94
Pharmacogenetics of antipsychotic-induced weight gain. Psychopharmacology (Berl) (2004) 0.92
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates. Hum Mol Genet (2009) 0.91
Development and application of genomic control methods for genome-wide association studies using non-additive models. PLoS One (2013) 0.89
Gene by sex interaction for measures of obesity in the framingham heart study. J Obes (2010) 0.87
Comparing population structure as inferred from genealogical versus genetic information. Eur J Hum Genet (2009) 0.86
Influences of APOA5 variants on plasma triglyceride levels in Uyghur population. PLoS One (2014) 0.86
A genome-wide scan study identifies a single nucleotide substitution in ASIP associated with white versus non-white coat-colour variation in sheep (Ovis aries). Heredity (Edinb) (2013) 0.85
Permutation testing in the presence of polygenic variation. Genet Epidemiol (2015) 0.84
Genome-wide association analysis and genomic prediction of Mycobacterium avium subspecies paratuberculosis infection in US Jersey cattle. PLoS One (2014) 0.84
The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males. Hum Genet (2006) 0.83
Evaluating the accuracy of AIM panels at quantifying genome ancestry. BMC Genomics (2014) 0.80
Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia. PLoS One (2011) 0.80
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. Eur J Hum Genet (2011) 0.79
Assessing the joint effect of population stratification and sample selection in studies of gene-gene (environment) interactions. BMC Genet (2012) 0.77
European American stratification in ovarian cancer case control data: the utility of genome-wide data for inferring ancestry. PLoS One (2012) 0.76
A single-nucleotide polymorphism of human neuropeptide s gene originated from Europe shows decreased bioactivity. PLoS One (2013) 0.75
A Framework for Interpreting Type I Error Rates from a Product-Term Model of Interaction Applied to Quantitative Traits. Genet Epidemiol (2015) 0.75
Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. PLoS One (2017) 0.75
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature (2012) 13.71
De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature (2012) 13.61
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron (2011) 10.61
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature (2009) 9.47
Testing for an unusual distribution of rare variants. PLoS Genet (2011) 9.28
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Synaptic, transcriptional and chromatin genes disrupted in autism. Nature (2014) 5.30
Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Nat Genet (2010) 4.65
Genomic Control to the extreme. Nat Genet (2004) 4.19
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. Am J Hum Genet (2008) 3.95
HIGH DIMENSIONAL VARIABLE SELECTION. Ann Stat (2009) 3.72
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. Nat Genet (2009) 3.65
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. Am J Hum Genet (2003) 3.16
Discovering genetic ancestry using spectral graph theory. Genet Epidemiol (2010) 3.03
Characterization of multilocus linkage disequilibrium. Genet Epidemiol (2005) 3.03
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nat Genet (2011) 2.97
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell (2013) 2.94
Screen and clean: a tool for identifying interactions in genome-wide association studies. Genet Epidemiol (2010) 2.70
Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism (2012) 2.67
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron (2013) 2.45
Pleiotropy and principal components of heritability combine to increase power for association analysis. Genet Epidemiol (2008) 2.39
Analysis of multilocus models of association. Genet Epidemiol (2003) 2.33
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol Psychiatry (2011) 2.28
SNP-based analysis of genetic substructure in the German population. Hum Hered (2006) 2.21
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. Bipolar Disord (2009) 1.90
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association. Genomics (2007) 1.78
Evolutionary-based association analysis using haplotype data. Genet Epidemiol (2003) 1.73
The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders. Neuron (2012) 1.71
Association and linkage analyses of RGS4 polymorphisms in schizophrenia. Hum Mol Genet (2002) 1.68
Novel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samples. Biol Psychiatry (2006) 1.63
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nat Genet (2012) 1.63
Personality characteristics of women before and after recovery from an eating disorder. Psychol Med (2004) 1.57
African ancestry and lung function in Puerto Rican children. J Allergy Clin Immunol (2012) 1.54
Eating disorder symptoms among college students: prevalence, persistence, correlates, and treatment-seeking. J Am Coll Health (2011) 1.54
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. PLoS Genet (2013) 1.53
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. Am J Hum Genet (2012) 1.52
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics (2013) 1.51
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. PLoS Genet (2013) 1.48
Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genet Epidemiol (2011) 1.47
Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. Am J Respir Crit Care Med (2012) 1.46
Do common variants play a role in risk for autism? Evidence and theoretical musings. Brain Res (2010) 1.44
A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Hum Mol Genet (2007) 1.43
Circadian phase variation in bipolar I disorder. Chronobiol Int (2005) 1.31
Integration of association statistics over genomic regions using Bayesian adaptive regression splines. Hum Genomics (2003) 1.28
Alcohol use disorder comorbidity in eating disorders: a multicenter study. J Clin Psychiatry (2004) 1.26
Unintentional overdose and suicide among substance users: a review of overlap and risk factors. Drug Alcohol Depend (2010) 1.26
Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees. Biol Psychiatry (2011) 1.25
Association of FKBP5 polymorphisms with suicidal events in the Treatment of Resistant Depression in Adolescents (TORDIA) study. Am J Psychiatry (2009) 1.21
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Mol Autism (2014) 1.20
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): recruitment and assessment methods. Schizophr Res (2006) 1.19
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients. Am J Psychiatry (2010) 1.15
The genetics of anorexia nervosa collaborative study: methods and sample description. Int J Eat Disord (2008) 1.12
Genetic analysis of bulimia nervosa: methods and sample description. Int J Eat Disord (2004) 1.11
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biol Psychiatry (2013) 1.11
Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies. Stat Med (2010) 1.11
Incomplete response in late-life depression: getting to remission. Dialogues Clin Neurosci (2008) 1.10
High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. J Bone Miner Res (2009) 1.09
The MAOA promoter polymorphism, disruptive behavior disorders, and early onset substance use disorder: gene-environment interaction. Psychiatr Genet (2007) 1.08
Association of multiple DRD2 polymorphisms with anorexia nervosa. Neuropsychopharmacology (2005) 1.06
Heritability of psychosis in Alzheimer disease. Am J Geriatr Psychiatry (2005) 1.06
Trajectories of cognitive decline in Alzheimer's disease. Int Psychogeriatr (2009) 1.06
Mixture models for linkage analysis of affected sibling pairs and covariates. Genet Epidemiol (2002) 1.06
TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease. Neurobiol Aging (2011) 1.05
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses. Am J Med Genet B Neuropsychiatr Genet (2005) 1.05
The AVPR1A gene and substance use disorders: association, replication, and functional evidence. Biol Psychiatry (2011) 1.02
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biol Psychiatry (2006) 1.00
Consanguinity associated with increased risk for bipolar I disorder in Egypt. Am J Med Genet B Neuropsychiatr Genet (2009) 0.99
ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR. Genomics (2004) 0.98
Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates. Am J Med Genet B Neuropsychiatr Genet (2005) 0.98
Heterogeneous association between engrailed-2 and autism in the CPEA network. Am J Med Genet B Neuropsychiatr Genet (2008) 0.97
Intellectual disability is associated with increased runs of homozygosity in simplex autism. Am J Hum Genet (2013) 0.96
Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk. Schizophr Res (2007) 0.95