Published in Am J Hum Genet on February 12, 2010
Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications. Nat Biotechnol (2010) 7.00
DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol (2011) 6.48
Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population. PLoS Genet (2012) 4.05
Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome. Cell (2012) 4.00
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome Biol (2012) 3.31
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder. Hum Mol Genet (2011) 2.99
Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood. Hum Mol Genet (2011) 2.48
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Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence. Genome Res (2012) 1.73
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Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development. BMC Genomics (2011) 1.56
MHC transmission: insights into gender bias in MS susceptibility. Neurology (2011) 1.49
Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing. BMC Bioinformatics (2010) 1.48
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Epigenetic mechanisms of depression and antidepressant action. Annu Rev Pharmacol Toxicol (2012) 1.45
Extensive sequence-influenced DNA methylation polymorphism in the human genome. Epigenetics Chromatin (2010) 1.43
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Accounting for population stratification in DNA methylation studies. Genet Epidemiol (2014) 1.25
The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue. PLoS One (2013) 1.25
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Genetic and epigenetic variations in inducible nitric oxide synthase promoter, particulate pollution, and exhaled nitric oxide levels in children. J Allergy Clin Immunol (2011) 1.21
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Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs. BMC Genomics (2014) 1.06
Global properties and functional complexity of human gene regulatory variation. PLoS Genet (2013) 1.02
Identification of imprinted genes subject to parent-of-origin specific expression in Arabidopsis thaliana seeds. BMC Plant Biol (2011) 1.02
Hypomethylation of the IGF2 DMR in colorectal tumors, detected by bisulfite pyrosequencing, is associated with poor prognosis. Gastroenterology (2010) 1.01
Tissue-specific Leptin promoter DNA methylation is associated with maternal and infant perinatal factors. Mol Cell Endocrinol (2013) 1.01
CpG methylation regulates allelic expression of GDF5 by modulating binding of SP1 and SP3 repressor proteins to the osteoarthritis susceptibility SNP rs143383. Hum Genet (2014) 1.01
Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes. Epigenetics (2015) 1.00
DNA methylation as a risk factor in the effects of early life stress. Brain Behav Immun (2011) 1.00
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DNA methylation and childhood maltreatment: from animal models to human studies. Neuroscience (2013) 0.98
The epigenomic interface between genome and environment in common complex diseases. Brief Funct Genomics (2010) 0.96
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci. Hum Mol Genet (2011) 0.95
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Power and sample size estimation for epigenome-wide association scans to detect differential DNA methylation. Int J Epidemiol (2015) 0.94
Epigenetic screen identifies genotype-specific promoter DNA methylation and oncogenic potential of CHRNB4. Oncogene (2012) 0.94
Genome-wide genetic variations are highly correlated with proximal DNA methylation patterns. Genome Res (2012) 0.93
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression. Genome Biol (2015) 0.91
Environmental risk, Oxytocin Receptor Gene (OXTR) methylation and youth callous-unemotional traits: a 13-year longitudinal study. Mol Psychiatry (2014) 0.90
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Epigenetic studies of schizophrenia: progress, predicaments, and promises for the future. Schizophr Bull (2012) 0.89
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Allele-specific, age-dependent and BMI-associated DNA methylation of human MCHR1. PLoS One (2011) 0.89
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DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro. Mov Disord (2013) 0.86
Putting epigenome comparison into practice. Nat Biotechnol (2010) 0.86
High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction. Genome Biol (2015) 0.85
Resolving the variable genome and epigenome in human disease. J Intern Med (2012) 0.85
Dark matters in AMD genetics: epigenetics and stochasticity. Invest Ophthalmol Vis Sci (2011) 0.84
Genome-wide DNA methylation map of human neutrophils reveals widespread inter-individual epigenetic variation. Sci Rep (2015) 0.84
Identification of methylation quantitative trait loci (mQTLs) influencing promoter DNA methylation of alcohol dependence risk genes. Hum Genet (2014) 0.84
A genetic association study of DNA methylation levels in the DRD4 gene region finds associations with nearby SNPs. Behav Brain Funct (2012) 0.83
Epigenetic Regulation of Infant Neurobehavioral Outcomes. Med Epigenet (2014) 0.83
Premature aging of leukocyte DNA methylation is associated with type 2 diabetes prevalence. Clin Epigenetics (2015) 0.83
β-2 adrenergic receptor gene methylation is associated with decreased asthma severity in inner-city schoolchildren: asthma and rhinitis. Clin Exp Allergy (2014) 0.82
Genome-wide analysis of DNA methylation in five tissues of Zhikong scallop, Chlamys farreri. PLoS One (2014) 0.82
Allele-specific methylation occurs at genetic variants associated with complex disease. PLoS One (2014) 0.82
Epigenetic mechanisms, T-cell activation, and CCR5 genetics interact to regulate T-cell expression of CCR5, the major HIV-1 coreceptor. Proc Natl Acad Sci U S A (2015) 0.82
DNA methylation: conducting the orchestra from exposure to phenotype? Clin Epigenetics (2016) 0.81
Allele-specific gene expression in a wild nonhuman primate population. Mol Ecol (2011) 0.80
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Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation. Am J Hum Genet (2016) 0.80
Analysis of a four generation family reveals the widespread sequence-dependent maintenance of allelic DNA methylation in somatic and germ cells. Sci Rep (2016) 0.79
HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS. Depress Anxiety (2015) 0.79
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease. PLoS Genet (2014) 0.79
Genome-wide DNA methylation analyses in the brain reveal four differentially methylated regions between humans and non-human primates. BMC Evol Biol (2012) 0.79
Exploring the effects of polymorphisms on cis-regulatory signal transduction response. Trends Mol Med (2012) 0.79
The Future is The Past: Methylation QTLs in Schizophrenia. Genes (Basel) (2016) 0.78
Systematic chromatin state comparison of epigenomes associated with diverse properties including sex and tissue type. Nat Commun (2015) 0.78
PON1 as a model for integration of genetic, epigenetic, and expression data on candidate susceptibility genes. Environ Epigenet (2015) 0.78
Characterization of genome-methylome interactions in 22 nuclear pedigrees. PLoS One (2014) 0.78
Identification of specific DNA methylation sites on the Y-chromosome as biomarker in prostate cancer. Oncotarget (2015) 0.78
Epigenetic modification of the repair donor regulates targeted gene correction. Mol Ther Nucleic Acids (2012) 0.77
Epigenetic regulation of differential HLA-A allelic expression levels. Hum Mol Genet (2015) 0.77
Variations in discovery-based preeclampsia candidate genes. Clin Transl Sci (2012) 0.77
Combined epigenetic and intraspecific variation of the DRD4 and SERT genes influence novelty seeking behavior in great tit Parus major. Epigenetics (2015) 0.77
Allele-Skewed DNA Modification in the Brain: Relevance to a Schizophrenia GWAS. Am J Hum Genet (2016) 0.76
Genome-wide methylation data mirror ancestry information. Epigenetics Chromatin (2017) 0.76
Intronic parent-of-origin dependent differential methylation at the Actn1 gene is conserved in rodents but is not associated with imprinted expression. PLoS One (2012) 0.76
Measurements of DNA methylation at seven loci in various tissues of CD1 mice. PLoS One (2012) 0.76
Tissue-specific patterns of allelically-skewed DNA methylation. Epigenetics (2016) 0.76
Comparative epigenomics: defining and utilizing epigenomic variations across species, time-course, and individuals. Wiley Interdiscip Rev Syst Biol Med (2014) 0.75
Finding the missing heritability of complex diseases. Nature (2009) 67.95
Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science (2003) 28.61
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet (2003) 25.57
DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis. BMC Bioinformatics (2007) 12.76
Genomic imprinting: parental influence on the genome. Nat Rev Genet (2001) 11.50
Common regulatory variation impacts gene expression in a cell type-dependent manner. Science (2009) 11.28
Phenotypic plasticity and the epigenetics of human disease. Nature (2007) 10.37
Widespread monoallelic expression on human autosomes. Science (2007) 7.12
BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing. Bioinformatics (2005) 5.95
Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation. Nat Genet (2008) 5.66
Allelic variation in gene expression is common in the human genome. Genome Res (2003) 5.50
Mechanisms regulating imprinted genes in clusters. Curr Opin Cell Biol (2007) 5.49
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis. Nat Genet (2009) 4.72
Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet (2008) 4.71
Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human. Nat Methods (2009) 4.38
Twins' Early Development Study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems from childhood through adolescence. Twin Res Hum Genet (2007) 4.19
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Computational and experimental identification of novel human imprinted genes. Genome Res (2007) 3.50
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry (2007) 3.49
DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping. Behav Genet (2003) 3.42
Cis-acting variation in the expression of a high proportion of genes in human brain. Hum Genet (2003) 3.07
The role of DNA methylation in setting up chromatin structure during development. Nat Genet (2003) 3.06
Allele-specific gene expression uncovered. Trends Genet (2004) 2.92
A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q. Genome Res (2004) 2.56
DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution. PLoS Genet (2009) 2.37
Environmental epigenomics in human health and disease. Environ Mol Mutagen (2008) 2.06
Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation. Genome Res (2008) 2.03
Allele-specific DNA methylation in mouse strains is mainly determined by cis-acting sequences. Genome Res (2009) 1.80
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting. Hum Mol Genet (2000) 1.76
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Mol Psychiatry (2007) 1.68
Non-imprinted allele-specific DNA methylation on human autosomes. Genome Biol (2009) 1.64
Epigenetic heterogeneity at imprinted loci in normal populations. Biochem Biophys Res Commun (2001) 1.47
The SNPMaP package for R: a framework for genome-wide association using DNA pooling on microarrays. Bioinformatics (2008) 1.15
Single nucleotide extension technology for quantitative site-specific evaluation of metC/C in GC-rich regions. Nucleic Acids Res (2005) 1.01
Loss of OPCML expression and the correlation with CpG island methylation and LOH in ovarian serous carcinoma. Eur J Gynaecol Oncol (2007) 0.92
Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 months. Twin Res Hum Genet (2009) 0.83
Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science (2003) 28.61
Role of genotype in the cycle of violence in maltreated children. Science (2002) 13.50
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature (2011) 13.23
Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature (2011) 10.16
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nat Genet (2010) 8.48
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nat Genet (2011) 5.56
The genetic and environmental origins of learning abilities and disabilities in the early school years. Monogr Soc Res Child Dev (2007) 5.54
Evidence for a strong genetic influence on childhood adiposity despite the force of the obesogenic environment. Am J Clin Nutr (2008) 4.79
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Nat Genet (2009) 4.61
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat Genet (2010) 4.42
Twins early development study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems in childhood. Twin Res (2002) 4.32
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Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population. PLoS Genet (2012) 4.05
Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome. Cell (2012) 4.00
Time to give up on a single explanation for autism. Nat Neurosci (2006) 3.87
Obesity associated genetic variation in FTO is associated with diminished satiety. J Clin Endocrinol Metab (2008) 3.80
A data-driven approach to preprocessing Illumina 450K methylation array data. BMC Genomics (2013) 3.59
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet (2012) 3.40
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet (2010) 3.34
Weight lifting in women with breast-cancer-related lymphedema. N Engl J Med (2009) 3.33
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome Biol (2012) 3.31
Genetic heterogeneity between the three components of the autism spectrum: a twin study. J Am Acad Child Adolesc Psychiatry (2006) 3.16
Twins Early Development Study (TEDS): a genetically sensitive investigation of cognitive and behavioral development from childhood to young adulthood. Twin Res Hum Genet (2012) 3.00
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder. Hum Mol Genet (2011) 2.99
Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins. J Child Psychol Psychiatry (2005) 2.85
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Evidence for substantial genetic risk for psychopathy in 7-year-olds. J Child Psychol Psychiatry (2005) 2.64
Internet cognitive testing of large samples needed in genetic research. Twin Res Hum Genet (2007) 2.45
Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans. Nucleic Acids Res (2006) 2.33
Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample. J Child Psychol Psychiatry (2008) 2.21
Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits. Behav Genet (2004) 2.14
Parental feeding style and the inter-generational transmission of obesity risk. Obes Res (2002) 2.10
Genetic and environmental influences on adolescent attachment. J Child Psychol Psychiatry (2013) 2.09
A longitudinal study of epigenetic variation in twins. Epigenetics (2010) 2.06
Outcomes of early language delay: I. Predicting persistent and transient language difficulties at 3 and 4 years. J Speech Lang Hear Res (2003) 2.01
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus. PLoS One (2010) 1.93
Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%). Arch Gen Psychiatry (2011) 1.91
SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. Hum Mol Genet (2005) 1.91
An interdisciplinary approach to introducing professionalism. Am J Pharm Educ (2006) 1.89
Commentary: The seven plagues of epigenetic epidemiology. Int J Epidemiol (2012) 1.88
A three-stage genome-wide association study of general cognitive ability: hunting the small effects. Behav Genet (2010) 1.85
Weight lifting for women at risk for breast cancer-related lymphedema: a randomized trial. JAMA (2010) 1.83
No genetic influence for childhood behavior problems from DNA analysis. J Am Acad Child Adolesc Psychiatry (2013) 1.79
Increasing heritability of BMI and stronger associations with the FTO gene over childhood. Obesity (Silver Spring) (2008) 1.77
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
Identical genetic influences underpin behavior problems in adolescence and basic traits of personality. J Child Psychol Psychiatry (2013) 1.74
Relationships between parental negativity and childhood antisocial behavior over time: a bidirectional effects model in a longitudinal genetically informative design. J Abnorm Child Psychol (2007) 1.71
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Genetic and environmental contributions to general cognitive ability through the first 16 years of life. Dev Psychol (2004) 1.68
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The ABCs of Math: A Genetic Analysis of Mathematics and Its Links With Reading Ability and General Cognitive Ability. J Educ Psychol (2009) 1.66
Effects of seating position and appropriate restraint use on the risk of injury to children in motor vehicle crashes. Pediatrics (2005) 1.66
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A novel strategy for the identification of genomic islands by comparative analysis of the contents and contexts of tRNA sites in closely related bacteria. Nucleic Acids Res (2006) 1.60
Genetic, environmental and gender influences on attachment disorder behaviours. Br J Psychiatry (2007) 1.60
Common DNA markers can account for more than half of the genetic influence on cognitive abilities. Psychol Sci (2013) 1.57
Socioeconomic status (SES) and children's intelligence (IQ): in a UK-representative sample SES moderates the environmental, not genetic, effect on IQ. PLoS One (2012) 1.56
Genetic support for the dual nature of attention deficit hyperactivity disorder: substantial genetic overlap between the inattentive and hyperactive-impulsive components. J Abnorm Child Psychol (2007) 1.55
Protection from genetic diathesis in attention-deficit/hyperactivity disorder: possible complementary roles of exercise. J Am Acad Child Adolesc Psychiatry (2013) 1.54
Phenotypic and genetic overlap between autistic traits at the extremes of the general population. J Am Acad Child Adolesc Psychiatry (2006) 1.54
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nat Genet (2012) 1.52
DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage. Am J Med Genet B Neuropsychiatr Genet (2008) 1.50
A twin study of anxiety-related behaviours in pre-school children. J Child Psychol Psychiatry (2003) 1.48
The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism. Dev Sci (2005) 1.47
A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. Hum Mol Genet (2011) 1.47
Epigenetic mediation of environmental influences in major psychotic disorders. Schizophr Bull (2009) 1.47
Genetic evidence for bidirectional effects of early lexical and grammatical development. Child Dev (2003) 1.46
Prosocial behavior from early to middle childhood: genetic and environmental influences on stability and change. Dev Psychol (2006) 1.46
Nonshared environmental influences on individual differences in early behavioral development: a monozygotic twin differences study. Child Dev (2003) 1.43
Learning abilities and disabilities: generalist genes in early adolescence. Cogn Neuropsychiatry (2009) 1.42
Genetic influences in different aspects of language development: the etiology of language skills in 4.5-year-old twins. Child Dev (2005) 1.41
The etiology of behavior problems in 7-year-old twins: substantial genetic influence and negligible shared environmental influence for parent ratings and ratings by same and different teachers. J Abnorm Child Psychol (2005) 1.38
Genetic influences on the stability of attention-deficit/hyperactivity disorder symptoms from early to middle childhood. Biol Psychiatry (2005) 1.37
Allele-specific methylation in the human genome: implications for genetic studies of complex disease. Epigenetics (2010) 1.37
Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia. Genome Biol (2014) 1.37
Genetic and environmental influences in adolescent peer socialization: evidence from two genetically sensitive designs. Child Dev (2004) 1.35
Knockdown of the psychosis susceptibility gene ZNF804A alters expression of genes involved in cell adhesion. Hum Mol Genet (2011) 1.35
Genetic predictors of response to antidepressants in the GENDEP project. Pharmacogenomics J (2009) 1.35
Automated ventricular systems segmentation in brain CT images by combining low-level segmentation and high-level template matching. BMC Med Inform Decis Mak (2009) 1.34
Mathematical ability of 10-year-old boys and girls: genetic and environmental etiology of typical and low performance. J Learn Disabil (2007) 1.34
In silico identified CCR4 antagonists target regulatory T cells and exert adjuvant activity in vaccination. Proc Natl Acad Sci U S A (2008) 1.34
Gene expression changes with age in skin, adipose tissue, blood and brain. Genome Biol (2013) 1.34
From learning to read to reading to learn: substantial and stable genetic influence. Child Dev (2007) 1.33
The structure of language abilities at 4 years: a twin study. Dev Psychol (2002) 1.32
Differential epigenomic and transcriptomic responses in subcutaneous adipose tissue between low and high responders to caloric restriction. Am J Clin Nutr (2009) 1.30
Bisulfite-based epityping on pooled genomic DNA provides an accurate estimate of average group DNA methylation. Epigenetics Chromatin (2009) 1.29
Dramatic increase in heritability of cognitive development from early to middle childhood: an 8-year longitudinal study of 8,700 pairs of twins. Psychol Sci (2009) 1.28
Learning Abilities and Disabilities: Generalist Genes, Specialist Environments. Curr Dir Psychol Sci (2007) 1.28
Effects of cis-regulatory variation differ across regions of the adult human brain. Hum Mol Genet (2010) 1.27
A longitudinal twin study on the association between ADHD symptoms and reading. J Child Psychol Psychiatry (2011) 1.26
DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities. Behav Genet (2013) 1.26
Etiologies of associations between childhood sleep and behavioral problems in a large twin sample. J Am Acad Child Adolesc Psychiatry (2004) 1.25
Moderation of antidepressant response by the serotonin transporter gene. Br J Psychiatry (2009) 1.25
The etiology of variation in language skills changes with development: a longitudinal twin study of language from 2 to 12 years. Dev Sci (2012) 1.25
Genetic etiology in cases of recovered and persistent stuttering in an unselected, longitudinal sample of young twins. Am J Speech Lang Pathol (2007) 1.25