Genotype - Genetic Predisposition to Disease PubMed MeSh Term

Overview

subject area of

• DCDC2 is associated with reading disability and modulates neuronal development in the brain  Journal Article
• A Critical Review of the First 10 Years of Candidate Gene-by-Environment Interaction Research in Psychiatry  Journal Article
• A Preliminary Analysis of Interactions Between Genotype, Retrospective ADHD Symptoms, and Initial Reactions to Smoking in a Sample of Young Adults  Journal Article
• A Recessive Genetic Model and Runs of Homozygosity in Major Depressive Disorder  Journal Article
• A Risk Allele for Nicotine Dependence in CHRNA5 Is a Protective Allele for Cocaine Dependence  Journal Article
• A comparison of the cognitive deficits in reading disability and attention-deficit/hyperactivity disorder  Journal Article
• A computational language approach to modeling prose recall in schizophrenia  Journal Article
• A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.  Journal Article
• A genome-wide search for quantitative trait loci that influence antisocial drug dependence in adolescence  Journal Article
• A novel genetic marker of decreased inflammation and improved survival after acute myocardial infarction  Journal Article
• A twin study of drinking and smoking onset and latencies from first use to regular use  Journal Article
• ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of function  Journal Article
• Acquired and innate cardioprotection  Journal Article
• Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent  Journal Article
• All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs  Journal Article
• An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.  Journal Article
• An innate contribution of human nicotinic receptor polymorphisms to COPD-like lesions  Journal Article
• Are Rumination and Neuroticism Genetically or Environmentally Distinct Risk Factors for Psychopathology?  Journal Article
• Are endophenotypes based on measures of executive functions useful for molecular genetic studies of ADHD?  Journal Article
• Assessment and ascertainment in psychiatric molecular genetics: challenges and opportunities for cross-disorder research  Journal Article
• Association Analysis and Meta-Analysis of Multi-Allelic Variants for Large-Scale Sequence Data  Journal Article
• Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts  Journal Article
• Associations between Cannabinoid Receptor-1 (CNR1) Variation and Hippocampus and Amygdala Volumes in Heavy Cannabis Users  Journal Article
• Attention-deficit/hyperactivity disorder endophenotypes  Journal Article
• Bioinformatics assessment of β-myosin mutations reveals myosin's high sensitivity to mutations  Journal Article
• Biological insights from 108 schizophrenia-associated genetic loci  Journal Article
• Case-control and within-family tests for an association between conduct disorder and 5HTTLPR  Journal Article
• Case-control and within-family tests for an association between conduct disorder and DAT1  Journal Article
• Childhood maltreatment, subsequent antisocial behavior, and the role of monoamine oxidase A genotype  Journal Article
• Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices  Journal Article
• Cocaine'omics: Genome-wide and transcriptome-wide analyses provide biological insight into cocaine use and dependence  Journal Article
• Cohort Effects in the Genetic Influence on Smoking  Journal Article
• Collaborative analysis of DRD4 and DAT genotypes in population-defined ADHD subtypes  Journal Article
• Common and Rare Variants Genetic Association Analysis of Cigarettes per Day Among Ever-Smokers in Chronic Obstructive Pulmonary Disease Cases and Controls  Journal Article
• Common and drug-specific genetic influences on subjective effects to alcohol, tobacco and marijuana use  Journal Article
• Common and specific genetic influences on aggressive and nonaggressive conduct disorder domains  Journal Article
• Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.  Journal Article
• Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits  Journal Article
• Comparison of the multivariate genetic architecture of eight major psychiatric disorders across sex  Journal Article
• Confirmatory test of two factors and four subtypes of bipolar disorder based on lifetime psychiatric co-morbidity  Journal Article
• Connecting genetic risk to disease end points through the human blood plasma proteome  Journal Article
• Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects  Journal Article
• DeFries-Fulker Analysis of Longitudinal Reading Performance Data from Twin Pairs Ascertained for Reading Difficulties and from Their Nontwin Siblings  Journal Article
• Depression, Stressful Life Events, and the Impact of Variation in the Serotonin Transporter: Findings from the National Longitudinal Study of Adolescent to Adult Health (Add Health)  Journal Article
• Developmental Effects of Serotonin 1A Autoreceptors on Anxiety and Social Behavior  Journal Article
• Disentangling differing relationships between internalizing disorders and alcohol use  Journal Article
• Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking  Journal Article
• Dizziness and the genetic influences on subjective experiences to initial cigarette use  Journal Article
• Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale  Journal Article
• Dyslexia: nature and nurture.  Journal Article
• EXAMINING THE SHARED ETIOLOGY OF PSYCHOPATHOLOGY WITH GENOME-WIDE ASSOCIATION STUDIES  Journal Article
• Endophenotypes in the genetic analyses of mental disorders  Journal Article
• Enhancer RNA transcription pinpoints functional genetic variants linked to asthma  Journal Article
• Estimate of the abundance of cardiomyopathic mutations in the beta-myosin gene  Journal Article
• Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs  Journal Article
• Etiologies and Molecular Mechanisms of Communication Disorders  Journal Article
• Evaluation of the Potential Excess of Statistically Significant Findings in Published Genetic Association Studies: Application to Alzheimer's Disease  Journal Article
• Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence  Journal Article
• Evidence of Shared Genome-Wide Additive Genetic Effects on Interpersonal Trauma Exposure and Generalized Vulnerability to Drug Dependence in a Population of Substance Users  Journal Article
• Evolution of immune genes is associated with the Black Death  Journal Article
• Examining associations between disordered eating and serotonin transporter gene polymorphisms  Journal Article
• Examining the role of common genetic variants on alcohol, tobacco, cannabis and illicit drug dependence: genetics of vulnerability to drug dependence  Journal Article
• Executive Functions and Substance Use: Relations in Late Adolescence and Early Adulthood  Journal Article
• Exploring How Symptoms of Attention-Deficit/Hyperactivity Disorder Are Related to Reading and Mathematics Performance: General Genes, General Environments  Journal Article
• Exploring candidate gene associations with neuropsychological performance  Journal Article
• Familial aggregation for conduct disorder symptomatology: the role of genes, marital discord and family adaptability  Journal Article
• Family-based association test of the 5HTTLPR and aggressive behavior in a general population sample of children  Journal Article
• Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1  Journal Article
• Functional Analyses of Endometriosis-Related Polymorphisms in the Estrogen Synthesis and Metabolism-Related Genes  Journal Article
• Functional and structural assessment of retinal sheet allograft transplantation in feline hereditary retinal degeneration  Journal Article
• GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium  Journal Article
• Gene by environment interactions influencing reading disability and the inattentive symptom dimension of attention deficit/hyperactivity disorder  Journal Article
• Gene expression imputation across multiple brain regions provides insights into schizophrenia risk  Journal Article
• Gene x Environment Interaction Studies Have Not Properly Controlled for Potential Confounders: The Problem and the (Simple) Solution  Journal Article
• Gene x environment interactions in speech sound disorder predict language and preliteracy outcomes  Journal Article
• Gene-Environment Interplay in Common Complex Diseases: Forging an Integrative Model-Recommendations From an NIH Workshop  Journal Article
• Genetic Architecture and Molecular Neuropathology of Human Cocaine Addiction  Journal Article
• Genetic Association of the CHRNA6 and CHRNB3 Genes with Tobacco Dependence in a Nationally Representative Sample  Journal Article
• Genetic Etiologies of Comorbidity and Stability for Reading Difficulties and ADHD: A Replication Study  Journal Article
• Genetic Influences on Pubertal Development and Links to Behavior Problems  Journal Article
• Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume  Journal Article
• Genetic analysis of low-dose ethanol-induced activation (LDA) in inbred long sleep (ILS) and inbred short sleep (ISS) mice  Journal Article
• Genetic and environmental contributions to common psychopathologies of childhood and adolescence: A study of twins and their siblings  Journal Article
• Genetic and environmental influences on antisocial behavior: A meta-analysis of twin and adoption studies  Journal Article
• Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities  Journal Article
• Genetic and environmental influences on substance initiation, use, and problem use in adolescents  Journal Article
• Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis  Journal Article
• Genetic architecture of four smoking behaviors using partitioned SNP heritability  Journal Article
• Genetic dissection of quantitative trait locus for ethanol sensitivity in long- and short-sleep mice  Journal Article
• Genetic diversity fuels gene discovery for tobacco and alcohol use  Journal Article
• Genetic etiology of the common liability to drug dependence: Evidence of common and specific mechanisms for DSM-IV dependence symptoms  Journal Article
• Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability  Journal Article
• Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs  Journal Article
• Genetic variation links creativity to psychiatric disorders  Journal Article
• Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample  Journal Article
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences  Journal Article
• Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence  Journal Article
• Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia  Journal Article
• Genome-wide association study identifies five new schizophrenia loci  Journal Article
• Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia  Journal Article
• Genome-wide single nucleotide polymorphism heritability of nicotine dependence as a multidimensional phenotype  Journal Article
• Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan  Journal Article
• Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders  Journal Article
• Human gamma-aminobutyric acid A receptor alpha 2 gene moderates the acute effects of alcohol and brain mRNA expression  Journal Article
• Identical and Nonidentical Twins: Risk and Factors Involved in Development of Islet Autoimmunity and Type 1 Diabetes  Journal Article
• Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18  Journal Article
• Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors  Journal Article
• Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers  Journal Article
• Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment  Journal Article
• Inherited causes of clonal haematopoiesis in 97,691 whole genomes  Journal Article
• Insights into Human β-Cardiac Myosin Function from Single Molecule and Single Cell Studies  Journal Article
• Integrated analysis of direct and proxy genome wide association studies highlights polygenicity of Alzheimer's disease outside of the APOE region  Journal Article
• Interaction between MAO-A genotype and maltreatment in the risk for conduct disorder: Failure to confirm in adolescent patients  Journal Article
• Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets  Journal Article
• Large-scale genomics unveils the genetic architecture of psychiatric disorders  Journal Article
• Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium  Journal Article
• Life events, genetic susceptibility, and smoking among adolescents  Journal Article
• Linkage Disequilibrium Mapping of The Chromosome 6q21-22.31 Bipolar I Disorder Susceptibility Locus  Journal Article
• Little Evidence of Modified Genetic Effect of rs16969968 on Heavy Smoking Based on Age of Onset of Smoking  Journal Article
• Loci on chromosome 20 interact with rs16969968 to influence cigarettes per day in European ancestry individuals  Journal Article
• MAOA Genotype, Childhood Maltreatment, and Their Interaction in the Etiology of Adult Antisocial Behaviors  Journal Article
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia  Journal Article
• Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2  Journal Article
• Meta-analysis of genome-wide association studies of anxiety disorders  Journal Article
• Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)  Journal Article
• Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018)  Journal Article
• Multiple Distinct Risk Loci for Nicotine Dependence Identified by Dense Coverage of the Complete Family of Nicotinic Receptor Subunit (CHRN) Genes  Journal Article
• Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth  Journal Article
• Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism  Journal Article
• New Approaches to Identifying Rare Genetic Variants Associated with Nicotine Dependence  Journal Article
• New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.  Journal Article
• No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes  Journal Article
• No association between MspI allele of the ADRA2A polymorphism and ADHD: meta-analysis of family-based studies  Journal Article
• On the parsing of statistical information in family-based association testing  Journal Article
• On the replication of genetic associations:: Timing can be everything!  Journal Article
• Partitioning the Genomic Components of Behavioral Disinhibition and Substance Use (Disorder) Using Genomic Structural Equation Modeling  Journal Article
• Perceived peer delinquency and the genetic predisposition for substance dependence vulnerability  Journal Article
• Personality Dimensions as Common and Broadband-Specific Features for Internalizing and Externalizing Disorders  Journal Article
• Phenotypic and genetic factors in motives for smoking  Journal Article
• Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways  Journal Article
• Population stratification in the candidate gene study: Fatal threat or red herring?  Journal Article
• Post-GWAS analysis of six substance use traits improves the identification and functional interpretation of genetic risk loci  Journal Article
• Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge  Journal Article
• Psychiatric comorbidity in children and adolescents with reading disability  Journal Article
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways  Journal Article
• Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit hyperactivity disorder  Journal Article
• REDUCED Chrna7 EXPRESSION IN MICE IS ASSOCIATED WITH DECREASES IN HIPPOCAMPAL MARKERS OF INHIBITORY FUNCTION: IMPLICATIONS FOR NEUROPSYCHIATRIC DISEASES  Journal Article
• Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans  Journal Article
• Reading disability: Evidence for a genetic etiology  Journal Article
• Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk  Journal Article
• Research on environmental effects in genetic studies of aging - Comments  Journal Article
• Resolving the paradox of common, harmful, heritable mental disorders: Which evolutionary genetic models work best?  Journal Article
• Right ventricular function and failure - Report of a National Heart, lung, and Blood Institute working group on cellular and molecular mechanisms of right heart failure  Journal Article
• Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor  Journal Article
• SNPs in CHRNA6 and CHRNB3 are associated with alcohol consumption in a nationally representative sample  Journal Article
• Sensation Seeking, Peer Deviance, and Genetic Influences on Adolescent Delinquency: Evidence for Person-Environment Correlation and Interaction  Journal Article
• Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility  Journal Article
• Serotonin transporter gene, stress and raphe-raphe interactions: a molecular mechanism of depression  Journal Article
• Setting priorities for genomic research  Journal Article
• Sibling-based association analyses of the serotonin transporter polymorphism and internalizing behavior problems in children  Journal Article
• Simple Sequence Repeats in the National Longitudinal Study of Adolescent Health: An Ethnically Diverse Resource for Genetic Analysis of Health and Behavior  Journal Article
• Social disorder, APOE-E4 genotype, and change in cognitive function among older adults living in Chicago  Journal Article
• Stressful Life Events and Depression among Adolescent Twin Pairs  Journal Article
• Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function  Journal Article
• Sun exposure, vitamin D receptor polymorphisms FokI and BsmI and risk of multiple primary melanoma  Journal Article
• Susceptibility to Phytophthora ramorum in a key infectious host: landscape variation in host genotype, host phenotype, and environmental factors.  Journal Article
• Susceptibility to glaucoma: differential comparison of the astrocyte transcriptome from glaucomatous African American and Caucasian American donors  Journal Article
• Symptom-level modelling unravels the shared genetic architecture of anxiety and depression  Journal Article
• Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database  Journal Article
• Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database  Journal Article
• Telomere Replication Stress Induced by POT1 Inactivation Accelerates Tumorigenesis  Journal Article
• Test of alternative hypotheses explaining the comorbidity between attention-deficit/hyperactivity disorder and conduct disorder  Journal Article
• Testing for neuropsychological endophenotypes in siblings discordant for attention-deficit/hyperactivity disorder  Journal Article
• The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language  Journal Article
• The Association Between Toddlerhood Self-Control and Later Externalizing Problems  Journal Article
• The CHRNA5/A3/B4 Gene Cluster and Tobacco, Alcohol, Cannabis, Inhalants and Other Substance Use Initiation: Replication and New Findings Using Mixture Analyses  Journal Article
• The CHRNA5/A3/B4 gene cluster variability as an important determinant of early alcohol and tobacco initiation in young adults  Journal Article
• The MUC5B-associated variant rs35705950 resides within an enhancer subject to lineage- and disease-dependent epigenetic remodeling  Journal Article
• The National Longitudinal Study of Adolescent to Adult Health (Add Health) Sibling Pairs Genome-Wide Data  Journal Article
• The Speed of Progression to Tobacco and Alcohol Dependence: A Twin Study  Journal Article
• The dynamic epigenome and its implications for behavioral interventions: a role for epigenetics to inform disorder prevention and health promotion  Journal Article
• The functional serotonin 1a receptor promoter polymorphism, rs6295, is associated with psychiatric illness and differences in transcription  Journal Article
• The human protein kinase C gamma gene (PRKCG) as a susceptibility locus for behavioral disinhibition  Journal Article
• The importance of family-based sampling for biobanks  Journal Article
• The role of genetic and environmental influences on the association between childhood ADHD symptoms and BMI  Journal Article
• The shared genetic architecture of modifiable risk for Alzheimer's disease: a genomic structural equation modelling study  Journal Article
• Trans-ancestry meta-analysis of genome wide association studies of inhibitory control  Journal Article
• Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders  Journal Article
• Transcriptome-Wide Structural Equation Modeling of 13 Major Psychiatric Disorders for Cross-Disorder Risk and Drug Repurposing  Journal Article
• Transcriptome-wide association study and eQTL colocalization identify potentially causal genes responsible for human bone mineral density GWAS associations  Journal Article
• Twin studies to GWAS: there and back again  Journal Article
• Understanding comorbidity: A twin study of reading disability and attention-deficit/hyperactivity disorder  Journal Article
• Understanding the Complex Etiologies of Developmental Disorders: Behavioral and Molecular Genetic Approaches  Journal Article
• Varieties of developmental reading disorder: Genetic and environmental influences  Journal Article
• What can genes tell us about the relationship between education and health?  Journal Article

broader concept

• Genotype  PubMed MeSh Term