Genome-Wide Association Study of Copy Number Variations (CNVs) with Opioid Dependence

Fragile X Mental Retardation Protein Regulates Synaptic and Behavioral Plasticity to Repeated Cocaine Administration

(2014) Laura N. Smith et al.   NEURON

Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia

(2013) Caitlin Rippey et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide Association Study Identifies New Susceptibility Loci for Posttraumatic Stress Disorder

(2013) Pingxing Xie et al.   BIOLOGICAL PSYCHIATRY

Genome-Wide Association Study of Opioid Dependence: Multiple Associations Mapped to Calcium and Potassium Pathways

(2013) Joel Gelernter et al.   BIOLOGICAL PSYCHIATRY

Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants

(2013) Can Yang et al.   HUMAN GENETICS

Association of the HTR2A gene with alcohol and heroin abuse

(2013) Jian Cao et al.   HUMAN GENETICS

Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci

(2013) J Gelernter et al.   MOLECULAR PSYCHIATRY

Significant association of CHRNB3 variants with nicotine dependence in multiple ethnic populations

(2013) W Y Cui et al.   MOLECULAR PSYCHIATRY

Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene

(2013) J Gelernter et al.   MOLECULAR PSYCHIATRY

Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence

(2012) Lingjun Zuo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Association of COL25A1 with Comorbid Antisocial Personality Disorder and Substance Dependence

(2012) Dawei Li et al.   BIOLOGICAL PSYCHIATRY

Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients

(2012) Richard B. Kennedy et al.   HUMAN GENETICS

A genome-wide association meta-analysis identifies new childhood obesity loci

(2012)   NATURE GENETICS

Genome-wide efficient mixed-model analysis for association studies

(2012) Xiang Zhou et al.   NATURE GENETICS

Deletion of LCE3C_LCE3B is associated with rheumatoid arthritis and systemic lupus erythematosus in the Chinese Han population

(2011) X. Lu et al.   ANNALS OF THE RHEUMATIC DISEASES

A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications

(2011) Andrew C. Heath et al.   BIOLOGICAL PSYCHIATRY

Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass

(2011) Rong Hai et al.   JOURNAL OF HUMAN GENETICS

Genome structural variation discovery and genotyping

(2011) Can Alkan et al.   NATURE REVIEWS GENETICS

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Incorporating age at onset of smoking into genetic models for nicotine dependence: evidence for interaction with multiple genes

(2010) Richard A. Grucza et al.   ADDICTION BIOLOGY

Structural Variation in the Human Genome and its Role in Disease

(2010) Paweł Stankiewicz et al.   Annual Review of Medicine

Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis

(2010) Elisa Docampo et al.   ARTHRITIS AND RHEUMATISM

Genetic variants of human urea transporter-2 are associated with metabolic syndrome in Asian population

(2010) Hui-Ju Tsai et al.   CLINICA CHIMICA ACTA

Meta-Analysis Confirms the LCE3C_LCE3B Deletion as a Risk Factor for Psoriasis in Several Ethnic Groups and Finds Interaction with HLA-Cw6

(2010) Eva Riveira-Munoz et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

(2010) R. G. Walters et al.   NATURE

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

(2010)   NATURE

Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population

(2010) Donald J. MacIntyre et al.   NEUROSCIENCE LETTERS

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function

(2010) David Warde-Farley et al.   NUCLEIC ACIDS RESEARCH

Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population

(2010) Pauline Chaste et al.   PLoS One

Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease

(2009) Andy Itsara et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Copy Number Variation in Human Health, Disease, and Evolution

(2009) Feng Zhang et al.   Annual Review of Genomics and Human Genetics

Copy number variation in the human genome and its implication in autoimmunity

(2009) H. Schaschl et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

(2009) H. C. Mefford et al.   GENOME RESEARCH

Genomic copy number variation, human health, and disease

(2009) Louise V Wain et al.   LANCET

Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma

(2009) Taketoshi Yasuda et al.   MODERN PATHOLOGY

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Large, rare chromosomal deletions associated with severe early-onset obesity

(2009) Elena G. Bochukova et al.   NATURE

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

(2009) Rafael de Cid et al.   NATURE GENETICS

The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line

(2009) Harukazu Suzuki et al.   NATURE GENETICS

Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array

(2008) C. A. Hodgkinson et al.   ALCOHOL AND ALCOHOLISM

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family

(2008) Janet M. Young et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

(2008) Terry Vrijenhoek et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Establishment of a novel specific ELISA system for rat N- and C-ERC/mesothelin. Rat ERC/mesothelin in the body fluids of mice bearing mesothelioma

(2008) Yoshiaki Hagiwara et al.   CANCER SCIENCE

Reduced purifying selection prevails over positive selection in human copy number variant evolution

(2008) D.-Q. Nguyen et al.   GENOME RESEARCH

Copy-number variations associated with neuropsychiatric conditions

(2008) Edwin H. Cook Jr et al.   NATURE

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

A robust statistical method for case-control association testing with copy number variation

(2008) Chris Barnes et al.   NATURE GENETICS

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

(2008) Gregory M Cooper et al.   NATURE GENETICS

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Integrated detection and population-genetic analysis of SNPs and copy number variation

(2008) Steven A McCarroll et al.   NATURE GENETICS

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE

Meta-study on association between the monoamine oxidase A gene (MAOA) and schizophrenia

(2007) Dawei Li et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS