Published in Am J Hum Genet on April 12, 2000
Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. PLoS Genet (2006) 7.13
Parental phenotypes in family-based association analysis. Am J Hum Genet (2004) 6.35
Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet (2002) 5.20
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations. Diabetes (2008) 4.20
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat Genet (2015) 3.82
Leveraging the HapMap correlation structure in association studies. Am J Hum Genet (2007) 3.57
Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs. Am J Hum Genet (2006) 3.25
A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biol Psychiatry (2011) 2.87
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet (2001) 2.50
Polysubstance abuse-vulnerability genes: genome scans for association, using 1,004 subjects and 1,494 single-nucleotide polymorphisms. Am J Hum Genet (2001) 2.26
Pooled association genome scanning for alcohol dependence using 104,268 SNPs: validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism. Am J Med Genet B Neuropsychiatr Genet (2006) 2.09
Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays. Genes Brain Behav (2008) 2.08
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Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples. PLoS Genet (2014) 1.92
A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples. Behav Genet (2009) 1.75
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The IMAGE project: methodological issues for the molecular genetic analysis of ADHD. Behav Brain Funct (2006) 1.37
The power of multivariate quantitative-trait loci linkage analysis is influenced by the correlation between variables. Am J Hum Genet (2002) 1.35
Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping. PLoS One (2012) 1.34
Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet (2002) 1.31
Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting. Am J Hum Genet (2002) 1.30
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A genome-wide linkage scan for age at menarche in three populations of European descent. J Clin Endocrinol Metab (2008) 1.19
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The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies. Hum Genet (2006) 0.96
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Power calculations using exact data simulation: a useful tool for genetic study designs. Behav Genet (2007) 0.87
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Combined linkage and association mapping of quantitative trait loci by multiple markers. Genetics (2005) 0.86
Twin studies and their implications for molecular genetic studies: endophenotypes integrate quantitative and molecular genetics in ADHD research. J Am Acad Child Adolesc Psychiatry (2010) 0.86
Association mapping in outbred populations: power and efficiency when genotyping parents and phenotyping progeny. Genetics (2008) 0.84
Incorporating parental information into family-based association tests. Biostatistics (2012) 0.82
Quantitative similarity-based association tests using population samples. Am J Hum Genet (2001) 0.81
Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophr Res (2011) 0.80
Co-segregation of social cognition, executive function and local processing style in children with ASD, their siblings and normal controls. J Autism Dev Disord (2013) 0.80
Replicated analysis of the genetic architecture of quantitative traits in two wild great tit populations. Mol Ecol (2015) 0.80
Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. Eur J Hum Genet (2012) 0.79
Theoretical and empirical power of regression and maximum-likelihood methods to map quantitative trait loci in general pedigrees. Am J Hum Genet (2004) 0.79
An unbiased index to quantify participant's phenotypic contribution to an open-access cohort. Sci Rep (2017) 0.75
Variance components linkage analysis with repeated measurements. Hum Hered (2008) 0.75
Quantitative trait locus analysis of hybrid pedigrees: variance-components model, inbreeding parameter, and power. BMC Genet (2007) 0.75
Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. Am J Med Genet B Neuropsychiatr Genet (2017) 0.75
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Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet (1998) 40.97
Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nat Genet (1999) 25.93
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Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet (1995) 12.78
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Extended multipoint identity-by-descent analysis of human quantitative traits: efficiency, power, and modeling considerations. Am J Hum Genet (1993) 4.13
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A twin-pronged attack on complex traits. Nat Genet (1997) 3.63
Genome screens using linkage disequilibrium tests: optimal marker characteristics and feasibility. Am J Hum Genet (1998) 2.86
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Multivariate multipoint linkage analysis of quantitative trait loci. Behav Genet (1996) 2.24
Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations. Am J Hum Genet (1996) 1.90
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The effect of marker heterozygosity on the power to detect linkage disequilibrium. Genetics (1997) 1.33
Optimal selection of sib pairs from random samples for linkage analysis of a QTL using the EDAC test. Behav Genet (1998) 1.19
Exploiting pleiotropy to map genes for oligogenic phenotypes using extended pedigree data. Genet Epidemiol (1997) 1.01
Testing causal hypotheses in multivariate linkage analysis of quantitative traits: general formulation and application to sibpair data. Genet Epidemiol (1998) 0.97
A multivariate model for the analysis of sibship covariance structure using marker information and multiple quantitative traits. Genet Epidemiol (1997) 0.88
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics (2003) 17.92
Combined linkage and association sib-pair analysis for quantitative traits. Am J Hum Genet (1999) 11.22
GRR: graphical representation of relationship errors. Bioinformatics (2001) 6.09
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Mol Psychiatry (2011) 4.91
Multipoint interval mapping of quantitative trait loci, using sib pairs. Am J Hum Genet (1995) 4.29
An improved multipoint sib-pair analysis of quantitative traits. Behav Genet (1996) 3.91
Genetic and environmental influences on behavioral disinhibition. Am J Med Genet (2000) 3.61
High-resolution mapping of quantitative trait loci in outbred mice. Nat Genet (1999) 2.69
Genetics and developmental psychopathology: 2. The main effects of genes and environment on behavioral problems in the Virginia Twin Study of Adolescent Behavioral Development. J Child Psychol Psychiatry (1997) 2.65
The heritability of general cognitive ability increases linearly from childhood to young adulthood. Mol Psychiatry (2009) 2.52
Association analysis in a variance components framework. Genet Epidemiol (2001) 2.38
Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet (1999) 2.26
Amisulpride augmentation of clozapine: an open non-randomized study in patients with schizophrenia partially responsive to clozapine. Acta Psychiatr Scand (2004) 2.24
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Mol Psychiatry (2010) 2.21
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Mol Psychiatry (2012) 2.20
Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs. Am J Hum Genet (2001) 2.16
The impact of genotyping error on family-based analysis of quantitative traits. Eur J Hum Genet (2001) 2.12
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Genetic influence on language delay in two-year-old children. Nat Neurosci (1998) 2.06
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Polymorphisms in FKBP5 are associated with peritraumatic dissociation in medically injured children. Mol Psychiatry (2005) 1.91
A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behav Genet (2001) 1.86
Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Mol Psychiatry (2011) 1.84
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A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Neurology (2009) 1.67
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Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Mol Psychiatry (2010) 1.63
Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry (2012) 1.57
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Testing structural equation models for twin data using LISREL. Behav Genet (1989) 1.46
Support for involvement of neuregulin 1 in schizophrenia pathophysiology. Mol Psychiatry (2005) 1.44
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. J Med Genet (2006) 1.42
Genome-wide association study of Tourette's syndrome. Mol Psychiatry (2012) 1.42
Analytic power calculation for QTL linkage analysis of small pedigrees. Eur J Hum Genet (2001) 1.39
Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia. Mol Psychiatry (2005) 1.34
Parent ratings of temperament in twins: explaining the 'too low' DZ correlations. Twin Res (2000) 1.26
Replication study of SNP associations for colorectal cancer in Hong Kong Chinese. Br J Cancer (2010) 1.24
Optimal sibship selection for genotyping in quantitative trait locus linkage analysis. Hum Hered (2001) 1.22
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Fitting genetic models with LISREL: hypothesis testing. Behav Genet (1989) 1.17
Familial association between allergic disorders and depression in adult Finnish twins. Am J Med Genet (2000) 1.17
Polygenic dissection of the bipolar phenotype. Br J Psychiatry (2011) 1.17
Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Mol Psychiatry (2012) 1.16
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Parent-offspring resemblance for reading performance at 7, 12 and 16 years of age in the Colorado Adoption Project. J Child Psychol Psychiatry (2002) 1.13
A twin study of drinking and smoking onset and latencies from first use to regular use. Behav Genet (1999) 1.12
GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Res (2000) 1.10
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Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Diabetologia (2013) 1.07
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A genome-wide association study of attempted suicide. Mol Psychiatry (2011) 1.04
The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample. Mol Psychiatry (2003) 1.03
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Further evidence of association between two NET single-nucleotide polymorphisms with ADHD. Mol Psychiatry (2007) 0.99
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Investigation of variation in SNAP-25 and ADHD and relationship to co-morbid major depressive disorder. Am J Med Genet B Neuropsychiatr Genet (2007) 0.94
OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays. BMC Genomics (2008) 0.94
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