Published in Dev Psychopathol on November 01, 2013
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Genetic link between family socioeconomic status and children's educational achievement estimated from genome-wide SNPs. Mol Psychiatry (2015) 1.10
Strong genetic influence on a UK nationwide test of educational achievement at the end of compulsory education at age 16. PLoS One (2013) 1.08
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Genotype-environment correlation in the era of DNA. Behav Genet (2014) 0.92
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Nature, Nurture, and Expertise. Intelligence (2014) 0.80
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Publication Trends Over 55 Years of Behavioral Genetic Research. Behav Genet (2016) 0.75
Genetic Influence on Intergenerational Educational Attainment. Psychol Sci (2017) 0.75
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
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Origins and functional impact of copy number variation in the human genome. Nature (2009) 23.63
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet (2010) 20.73
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature (2010) 16.86
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet (2013) 13.17
Five years of GWAS discovery. Am J Hum Genet (2012) 12.97
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet (2009) 12.96
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Genomewide association studies and assessment of the risk of disease. N Engl J Med (2010) 11.51
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Genome-wide association study identifies five new schizophrenia loci. Nat Genet (2011) 9.07
Estimating missing heritability for disease from genome-wide association studies. Am J Hum Genet (2011) 8.95
Polygenic susceptibility to breast cancer and implications for prevention. Nat Genet (2002) 8.89
A versatile gene-based test for genome-wide association studies. Am J Hum Genet (2010) 8.44
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet (2011) 7.80
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Data and theory point to mainly additive genetic variance for complex traits. PLoS Genet (2008) 7.15
Rare and common variants: twenty arguments. Nat Rev Genet (2012) 6.67
A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry (2012) 6.34
DNA methylation profiles in monozygotic and dizygotic twins. Nat Genet (2009) 5.99
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet (2012) 5.78
The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood. Am J Psychiatry (2010) 4.92
Epigenetic inheritance and the missing heritability problem. Genetics (2009) 4.90
CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell (2012) 4.81
Candidate-gene approaches for studying complex genetic traits: practical considerations. Nat Rev Genet (2002) 4.76
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (2013) 4.71
Generalist genes and learning disabilities. Psychol Bull (2005) 4.48
Pervasive sharing of genetic effects in autoimmune disease. PLoS Genet (2011) 4.42
Phenotypic heterogeneity of genomic disorders and rare copy-number variants. N Engl J Med (2012) 4.36
Common disorders are quantitative traits. Nat Rev Genet (2009) 4.34
Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Mol Psychiatry (2011) 4.16
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics (2012) 3.97
De novo mutations in human genetic disease. Nat Rev Genet (2012) 3.81
Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet (2012) 3.73
Power and predictive accuracy of polygenic risk scores. PLoS Genet (2013) 3.72
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. PLoS Genet (2011) 3.68
Improved heritability estimation from genome-wide SNPs. Am J Hum Genet (2012) 3.48
Germline DNA demethylation dynamics and imprint erasure through 5-hydroxymethylcytosine. Science (2012) 3.45
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry (2010) 3.13
Family-based designs for genome-wide association studies. Nat Rev Genet (2011) 3.12
Polygenic risk, rapid childhood growth, and the development of obesity: evidence from a 4-decade longitudinal study. Arch Pediatr Adolesc Med (2012) 2.70
Genetic contributions to stability and change in intelligence from childhood to old age. Nature (2012) 2.63
Genetics of autism spectrum disorders. Trends Cogn Sci (2011) 2.61
Polygenic modeling with bayesian sparse linear mixed models. PLoS Genet (2013) 2.59
MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS. PLoS One (2012) 2.56
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet (2012) 2.55
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry (2012) 2.48
A twin approach to unraveling epigenetics. Trends Genet (2011) 2.38
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Mol Psychiatry (2013) 2.15
Most reported genetic associations with general intelligence are probably false positives. Psychol Sci (2012) 2.10
A longitudinal study of epigenetic variation in twins. Epigenetics (2010) 2.06
Genomics. ENCODE project writes eulogy for junk DNA. Science (2012) 2.05
Phenotypic impact of genomic structural variation: insights from and for human disease. Nat Rev Genet (2013) 1.98
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet (2012) 1.96
The genetic architecture of economic and political preferences. Proc Natl Acad Sci U S A (2012) 1.89
The continuing value of twin studies in the omics era. Nat Rev Genet (2012) 1.88
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Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet (2010) 1.87
Pathway analysis of genomic data: concepts, methods, and prospects for future development. Trends Genet (2012) 1.86
Estimating the genetic variance of major depressive disorder due to all single nucleotide polymorphisms. Biol Psychiatry (2012) 1.86
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Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression. Am J Psychiatry (2010) 1.82
Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies. Eur J Hum Genet (2010) 1.79
No genetic influence for childhood behavior problems from DNA analysis. J Am Acad Child Adolesc Psychiatry (2013) 1.79
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Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Mol Psychiatry (2010) 1.63
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Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study. Genet Epidemiol (2011) 1.61
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits. Mol Psychiatry (2013) 1.60
Common DNA markers can account for more than half of the genetic influence on cognitive abilities. Psychol Sci (2013) 1.57
An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions. Genet Med (2004) 1.57
Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Transl Psychiatry (2012) 1.52
Linking prenatal maternal adversity to developmental outcomes in infants: the role of epigenetic pathways. Dev Psychopathol (2012) 1.39
Don't give up on GWAS. Mol Psychiatry (2011) 1.27
DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities. Behav Genet (2013) 1.26
Child development and molecular genetics: 14 years later. Child Dev (2012) 1.23
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. Genet Med (2011) 1.22
The epigenetics of maternal cigarette smoking during pregnancy and effects on child development. Dev Psychopathol (2012) 1.22
DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12. Mol Psychiatry (2013) 1.19
Little epistasis for anxiety-related measures in the DeFries strains of laboratory mice. Mamm Genome (2004) 1.18
Recent advances in nanopore sequencing. Electrophoresis (2012) 1.16
Disease model distortion in association studies. Genet Epidemiol (2011) 1.14
Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world. Dev Psychopathol (2012) 1.10
Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nat Genet (2013) 1.10
Exome sequencing and the genetics of intellectual disability. Clin Genet (2011) 1.08
Twin registries worldwide: an important resource for scientific research. Twin Res Hum Genet (2013) 1.07
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Quantitative genetics in the era of molecular genetics: learning abilities and disabilities as an example. J Am Acad Child Adolesc Psychiatry (2010) 1.05
A beginners guide to SNP calling from high-throughput DNA-sequencing data. Hum Genet (2012) 1.05
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Genome-Wide Polygenic Scores Predict Reading Performance Throughout the School Years. Sci Stud Read (2017) 0.75