Published in Addict Biol on November 04, 2010
Polygenic risk scores for smoking: predictors for alcohol and cannabis use? Addiction (2014) 1.63
Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. Mol Psychiatry (2013) 1.38
The genetics of addiction-a translational perspective. Transl Psychiatry (2012) 1.30
The genetics of substance dependence. Annu Rev Genomics Hum Genet (2012) 1.25
The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addict Biol (2012) 1.01
Genetically informative research on adolescent substance use: methods, findings, and challenges. J Am Acad Child Adolesc Psychiatry (2010) 0.96
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. JAMA Psychiatry (2016) 0.93
Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample. Behav Genet (2015) 0.92
Genetics of dopamine receptors and drug addiction. Hum Genet (2012) 0.89
Linkage analysis followed by association show NRG1 associated with cannabis dependence in African Americans. Biol Psychiatry (2012) 0.88
A brief history of research on the genetics of alcohol and other drug use disorders. J Stud Alcohol Drugs Suppl (2014) 0.88
Whole exome sequencing in females with autism implicates novel and candidate genes. Int J Mol Sci (2015) 0.87
Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Transl Psychiatry (2016) 0.86
The Genetics, Neurogenetics and Pharmacogenetics of Addiction. Curr Behav Neurosci Rep (2014) 0.83
The Brisbane Longitudinal Twin Study: Pathways to Cannabis Use, Abuse, and Dependence project-current status, preliminary results, and future directions. Twin Res Hum Genet (2012) 0.82
DSM-5 cannabis use disorder: a phenotypic and genomic perspective. Drug Alcohol Depend (2013) 0.81
Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants. Mol Neurobiol (2013) 0.79
Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis. J Abnorm Psychol (2015) 0.79
Genetic imaging consortium for addiction medicine: From neuroimaging to genes. Prog Brain Res (2015) 0.78
Convergent functional genomics in addiction research - a translational approach to study candidate genes and gene networks. In Silico Pharmacol (2013) 0.76
Genetic and Environmental Factors Associated with Cannabis Involvement. Curr Addict Rep (2016) 0.75
DISC1 as a Possible Genetic Contribution to Opioid Dependence in a Polish Sample. J Stud Alcohol Drugs (2016) 0.75
A method to customize population-specific arrays for genome-wide association testing. Eur J Hum Genet (2016) 0.75
Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans. Drug Alcohol Depend (2016) 0.75
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet (2006) 115.71
A new, semi-structured psychiatric interview for use in genetic linkage studies: a report on the reliability of the SSAGA. J Stud Alcohol (1994) 12.91
Prevalence of marijuana use disorders in the United States: 1991-1992 and 2001-2002. JAMA (2004) 6.60
A genome-wide association study of alcohol dependence. Proc Natl Acad Sci U S A (2010) 4.94
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol (2010) 3.48
Ankyrin repeat: a unique motif mediating protein-protein interactions. Biochemistry (2006) 3.07
The genetic epidemiology of cannabis use, abuse and dependence. Addiction (2006) 2.93
Candidate genes for cannabis use disorders: findings, challenges and directions. Addiction (2009) 1.31
FN3: a new protein scaffold reaches the clinic. Drug Discov Today (2009) 1.23
Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes. Nucleic Acids Res (2009) 1.09
Heritability and a genome-wide linkage analysis of a Type II/B cluster construct for cannabis dependence in an American Indian community. Addict Biol (2009) 1.06
Convergent genome wide association results for bipolar disorder and substance dependence. Am J Med Genet B Neuropsychiatr Genet (2009) 0.99
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science (2007) 43.16
Replicating genotype-phenotype associations. Nature (2007) 16.11
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet (2009) 15.15
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nat Genet (2007) 13.76
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Hum Mol Genet (2006) 13.16
Gene expression during the life cycle of Drosophila melanogaster. Science (2002) 11.36
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet (2011) 10.07
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature (2009) 9.47
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet (2011) 9.23
Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet (2011) 8.57
Escalation of drug use in early-onset cannabis users vs co-twin controls. JAMA (2003) 8.29
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Novel genes identified in a high-density genome wide association study for nicotine dependence. Hum Mol Genet (2006) 7.90
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature (2009) 7.39
Common variants in the GDF5-UQCC region are associated with variation in human height. Nat Genet (2008) 7.31
Variants in nicotinic receptors and risk for nicotine dependence. Am J Psychiatry (2008) 6.73
The use of computed tomography in pediatrics and the associated radiation exposure and estimated cancer risk. JAMA Pediatr (2013) 6.18
Statistical analysis of rare sequence variants: an overview of collapsing methods. Genet Epidemiol (2011) 6.18
APOE predicts amyloid-beta but not tau Alzheimer pathology in cognitively normal aging. Ann Neurol (2010) 6.17
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet (2009) 5.62
TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol (2008) 5.58
Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet (2008) 5.04
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol (2007) 5.02
Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations. Am J Hum Genet (2004) 5.02
A genome-wide association study of alcohol dependence. Proc Natl Acad Sci U S A (2010) 4.94
Alzheimer's disease: the challenge of the second century. Sci Transl Med (2011) 4.88
Quality control and quality assurance in genotypic data for genome-wide association studies. Genet Epidemiol (2010) 4.83
Use of diagnostic imaging studies and associated radiation exposure for patients enrolled in large integrated health care systems, 1996-2010. JAMA (2012) 4.71
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (2013) 4.71
The role of childhood risk factors in initiation of alcohol use and progression to alcohol dependence. Addiction (2007) 4.55
Pittsburgh compound B imaging and prediction of progression from cognitive normality to symptomatic Alzheimer disease. Arch Neurol (2009) 4.55
ABC transporters: the power to change. Nat Rev Mol Cell Biol (2009) 4.48
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nat Genet (2010) 4.47
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A (2010) 4.30
Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nat Genet (2012) 4.08
Human apoE isoforms differentially regulate brain amyloid-β peptide clearance. Sci Transl Med (2011) 4.07
Cerebral air embolism following removal of central venous catheter. Mil Med (2009) 4.04
Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. PLoS Genet (2010) 3.91
Ascertainment of a mid-western US female adolescent twin cohort for alcohol studies: assessment of sample representativeness using birth record data. Twin Res (2002) 3.89
Effects of filtering by Present call on analysis of microarray experiments. BMC Bioinformatics (2006) 3.86
Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet (2010) 3.63
Association between self-reported childhood sexual abuse and adverse psychosocial outcomes: results from a twin study. Arch Gen Psychiatry (2002) 3.57
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol (2010) 3.48
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet (2009) 3.42
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet (2010) 3.37
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. Genome Res (2008) 3.33
Defining nicotine dependence for genetic research: evidence from Australian twins. Psychol Med (2004) 3.26
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. Am J Hum Genet (2005) 3.24