Published in Psychiatr Genet on December 01, 2007
Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission. Hum Genet (2008) 2.18
Gene × environment interaction studies have not properly controlled for potential confounders: the problem and the (simple) solution. Biol Psychiatry (2013) 1.88
Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. Drug Alcohol Depend (2012) 1.88
MAOA, childhood maltreatment, and antisocial behavior: meta-analysis of a gene-environment interaction. Biol Psychiatry (2013) 1.79
Gene-environment interaction in psychological traits and disorders. Annu Rev Clin Psychol (2011) 1.40
Gene x disease interaction on orbitofrontal gray matter in cocaine addiction. Arch Gen Psychiatry (2011) 1.14
Measuring addiction propensity and severity: the need for a new instrument. Drug Alcohol Depend (2010) 1.05
Serotonin pathway gene-gene and gene-environment interactions influence behavioral stress response in infant rhesus macaques. Dev Psychopathol (2010) 1.02
The AVPR1A gene and substance use disorders: association, replication, and functional evidence. Biol Psychiatry (2011) 1.02
Neurobehavior disinhibition, parental substance use disorder, neighborhood quality and development of cannabis use disorder in boys. Drug Alcohol Depend (2009) 0.99
The impact of gene-environment interaction on alcohol use disorders. Alcohol Res (2012) 0.99
Does the "gateway" sequence increase prediction of cannabis use disorder development beyond deviant socialization? Implications for prevention practice and policy. Drug Alcohol Depend (2012) 0.95
Impact of behavioral genetic evidence on the adjudication of criminal behavior. J Am Acad Psychiatry Law (2014) 0.94
Moderating role of the MAOA genotype in antisocial behaviour. Br J Psychiatry (2012) 0.91
Effects of MAOA-genotype, alcohol consumption, and aging on violent behavior. Alcohol Clin Exp Res (2008) 0.91
Parental care moderates the influence of MAOA-uVNTR genotype and childhood stressors on trait impulsivity and aggression in adult women. Psychiatr Genet (2009) 0.90
Deviant peer affiliation and antisocial behavior: interaction with Monoamine Oxidase A (MAOA) genotype. J Abnorm Child Psychol (2011) 0.86
Pharmacogenetics: a tool for identifying genetic factors in drug dependence and response to treatment. Addict Sci Clin Pract (2010) 0.85
Family-based association analysis of alcohol dependence in the COGA sample and replication in the Australian twin-family study. J Neural Transm (Vienna) (2011) 0.82
Ethical concerns related to developing pharmacogenomic treatment strategies for addiction. Addict Sci Clin Pract (2011) 0.82
Advances in genetic studies of substance abuse in China. Shanghai Arch Psychiatry (2013) 0.81
Effects of Behavioral Genetic Evidence on Perceptions of Criminal Responsibility and Appropriate Punishment. Psychol Public Policy Law (2015) 0.81
Epigenetics in Developmental Disorder: ADHD and Endophenotypes. J Genet Syndr Gene Ther (2011) 0.81
Association of positive and negative parenting behavior with childhood ADHD: interactions with offspring monoamine oxidase A (MAO-A) genotype. J Abnorm Child Psychol (2012) 0.81
The dopamine receptor D1 gene is associated with the length of interval between first heroin use and onset of dependence in Chinese Han heroin addicts. J Neural Transm (Vienna) (2013) 0.78
The role of the monoamine oxidase A gene in moderating the response to adversity and associated antisocial behavior: a review. Psychol Res Behav Manag (2014) 0.78
Impact of behavioral genetic evidence on the perceptions and dispositions of child abuse victims. Public Health Genomics (2014) 0.77
Underlying Mechanisms of Gene-Environment Interactions in Externalizing Behavior: A Systematic Review and Search for Theoretical Mechanisms. Clin Child Fam Psychol Rev (2015) 0.77
Gene by Social-Environment Interaction for Youth Delinquency and Violence: Thirty-Nine Aggression-related Genes. Soc Forces (2015) 0.76
Familiality of addiction and its developmental mechanisms in girls. Drug Alcohol Depend (2014) 0.76
Monoamine oxidase A genotype, childhood trauma, and subclinical atherosclerosis: a twin study. Psychosom Med (2013) 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
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med (2004) 7.91
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet (2008) 6.72
Synaptic, transcriptional and chromatin genes disrupted in autism. Nature (2014) 5.30
Susceptibility genes for age-related maculopathy on chromosome 10q26. Am J Hum Genet (2005) 4.91
Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes. Diabetes (2005) 4.31
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers. PLoS Genet (2009) 4.22
Neurobehavioral disinhibition in childhood predicts early age at onset of substance use disorder. Am J Psychiatry (2003) 4.07
Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor. EMBO J (2002) 3.99
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. Am J Hum Genet (2008) 3.95
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Discovering genetic ancestry using spectral graph theory. Genet Epidemiol (2010) 3.03
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nat Genet (2011) 2.97
Impaired FGF signaling contributes to cleft lip and palate. Proc Natl Acad Sci U S A (2007) 2.94
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell (2013) 2.94
Item response theory analysis of diagnostic criteria for alcohol and cannabis use disorders in adolescents: implications for DSM-V. J Abnorm Psychol (2006) 2.92
An application of item response theory analysis to alcohol, cannabis, and cocaine criteria in DSM-IV. J Abnorm Psychol (2004) 2.90
Racial differences in the relation between uncoupling protein genes and resting energy expenditure. Am J Clin Nutr (2002) 2.84
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
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet (2004) 2.65
Genetic variation in human NPY expression affects stress response and emotion. Nature (2008) 2.65
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. BMC Med Genet (2008) 2.63
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions. Am J Hum Genet (2004) 2.58
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
Liability to substance use disorders: 1. Common mechanisms and manifestations. Neurosci Biobehav Rev (2003) 2.32
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol Psychiatry (2011) 2.28
Effects of exercise on mitochondrial content and function in aging human skeletal muscle. J Gerontol A Biol Sci Med Sci (2006) 2.23
Decreased STAT1 expression by promoter methylation in squamous cell carcinogenesis. J Natl Cancer Inst (2006) 2.21
Association studies for quantitative traits in structured populations. Genet Epidemiol (2002) 2.13
Haptoglobin genotype and functional outcome after aneurysmal subarachnoid hemorrhage. J Neurosurg (2013) 2.05
Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Hum Mol Genet (2005) 2.04
Efficacy of valproate maintenance in patients with bipolar disorder and alcoholism: a double-blind placebo-controlled study. Arch Gen Psychiatry (2005) 1.99
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. Bipolar Disord (2009) 1.90
Analysis of risk factors for adverse drug events in critically ill patients*. Crit Care Med (2012) 1.89
Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. Drug Alcohol Depend (2012) 1.88
Childhood risk categories for adolescent substance involvement: a general liability typology. Drug Alcohol Depend (2005) 1.86
Characteristics of skeletal muscle mitochondrial biogenesis induced by moderate-intensity exercise and weight loss in obesity. J Appl Physiol (1985) (2007) 1.86
C-reactive protein genotypes affect baseline, but not exercise training-induced changes, in C-reactive protein levels. Arterioscler Thromb Vasc Biol (2004) 1.81
HGF and MET mutations in primary and secondary lymphedema. Lymphat Res Biol (2008) 1.80
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nat Genet (2010) 1.79
Divergent effects of genetic variation in endocannabinoid signaling on human threat- and reward-related brain function. Biol Psychiatry (2008) 1.79
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
Measurement of the risk for substance use disorders: phenotypic and genetic analysis of an index of common liability. Behav Genet (2009) 1.76
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b. Am J Med Genet A (2003) 1.74
Identification and replication of a combined epigenetic and genetic biomarker predicting suicide and suicidal behaviors. Am J Psychiatry (2014) 1.73
Neurobehavior disinhibition in childhood predisposes boys to substance use disorder by young adulthood: direct and mediated etiologic pathways. Drug Alcohol Depend (2004) 1.72
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Hum Hered (2009) 1.71
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
Insulin resistance is associated with higher intramyocellular triglycerides in type I but not type II myocytes concomitant with higher ceramide content. Diabetes (2009) 1.67
Risk for depression during interferon-alpha treatment is affected by the serotonin transporter polymorphism. Biol Psychiatry (2008) 1.66
Effects of weight loss and physical activity on skeletal muscle mitochondrial function in obesity. Am J Physiol Endocrinol Metab (2004) 1.64
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatr Res (2004) 1.64
Predictors of marijuana use in adolescents before and after licit drug use: examination of the gateway hypothesis. Am J Psychiatry (2006) 1.63
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
Haptoglobin genotype: a determinant of cardiovascular complication risk in type 1 diabetes. Diabetes (2008) 1.62
Nephropathy in type 1 diabetes: a manifestation of insulin resistance and multiple genetic susceptibilities? Further evidence from the Pittsburgh Epidemiology of Diabetes Complication Study. Kidney Int (2002) 1.62
Liability to substance use disorders: 2. A measurement approach. Neurosci Biobehav Rev (2003) 1.59
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Hum Mol Genet (2006) 1.58
Personality characteristics of women before and after recovery from an eating disorder. Psychol Med (2004) 1.57
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. PLoS Genet (2013) 1.53
Variability within alpha- and beta-adrenoreceptor genes as a predictor of cardiovascular function at rest and in response to mental challenge. J Hypertens (2002) 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
Effects of HTR1A C(-1019)G on amygdala reactivity and trait anxiety. Arch Gen Psychiatry (2009) 1.51
Estimates of African, European and Native American ancestry in Afro-Caribbean men on the island of Tobago. Hum Hered (2005) 1.51
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics (2013) 1.51
Comparing intravenous amiodarone or lidocaine, or both, outcomes for inpatients with pulseless ventricular arrhythmias. Crit Care Med (2006) 1.49
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. PLoS Genet (2013) 1.48
Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate. Am J Med Genet A (2007) 1.48
Origins and consequences of child neglect in substance abuse families. Clin Psychol Rev (2002) 1.48
Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. Am J Hum Genet (2002) 1.44
High and low neurobehavior disinhibition clusters within locales: implications for community efforts to prevent substance use disorder. Am J Drug Alcohol Abuse (2013) 1.43
A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Hum Mol Genet (2007) 1.43
Outcomes and costs of abciximab versus eptifibatide for percutaneous coronary intervention. Ann Pharmacother (2005) 1.43
Multilocus genetic profile for dopamine signaling predicts ventral striatum reactivity. Neuropsychopharmacology (2011) 1.41
Angiotensinogen M235T polymorphism associates with exercise hemodynamics in postmenopausal women. Physiol Genomics (2002) 1.40
Salivary cortisol, personality, and aggressive behavior in adolescent boys: a 5-year longitudinal study. J Am Acad Child Adolesc Psychiatry (2003) 1.38
Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome. Mol Cell Endocrinol (2011) 1.38
Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis. Psychiatr Genet (2002) 1.32
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