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Analysis of Shared Heritability in Common Disorders of the Brain
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Increased Prevalence of Diverse N -Methyl-D-Aspartate Glutamate Receptor Antibodies in Patients With an Initial Diagnosis of Schizophrenia
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Tourette's Syndrome and Migraine
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Migraine and Psychopathology
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Limitations of Diagnostic Criteria and Assessment Instruments for Mental Disorders
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The Structure of Genetic and Environmental Risk Factors for Common Psychiatric and Substance Use Disorders in Men and Women
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Personality and Major Depression
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Linguistic Ability in Early Life and Cognitive Function and Alzheimer's Disease in Late Life
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Depression and Risk of Stroke Morbidity and Mortality
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Linguistic ability in early life and cognitive function and Alzheimer's disease in late life. Findings from the Nun Study
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Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder
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Disorders and borders: Psychiatric genetics and nosology
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Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
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Long‐term outcome in anorexia nervosa in the community
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Adult attention deficit hyperactivity disorder is associated with migraine headaches
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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage
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Migraine Headache and Ischemic Stroke Risk: An Updated Meta-analysis
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Validity of the Executive Function Theory of Attention-Deficit/Hyperactivity Disorder: A Meta-Analytic Review
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Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?
inferredcites →https://doi.org/10.1016/j.jalz.2014.05.1757openalex-snapshot
Convergent genetic and expression data implicate immunity in Alzheimer's disease
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Comorbidity was associated with neurologic and psychiatric diseases: A general practice-based controlled study
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Epidemiology and comorbidity of headache
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Neuroinflammation in Parkinson's disease: a target for neuroprotection?
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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies
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Neuroinflammation in Alzheimer's disease
inferredcites →https://doi.org/10.1038/ejhg.2011.257openalex-snapshot
Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes
inferredcites →https://doi.org/10.1038/mp.2009.55openalex-snapshot
The heritability of general cognitive ability increases linearly from childhood to young adulthood
inferredcites →https://doi.org/10.1038/mp.2010.128openalex-snapshot
Meta-analysis of genome-wide association studies for personality
inferredcites →https://doi.org/10.1038/mp.2013.127openalex-snapshot
Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
inferredcites →https://doi.org/10.1038/mp.2013.16openalex-snapshot
Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system
inferredcites →https://doi.org/10.1038/mp.2015.197openalex-snapshot
Meta-analysis of genome-wide association studies of anxiety disorders
inferredcites →https://doi.org/10.1038/mp.2016.49openalex-snapshot
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci
inferredcites →https://doi.org/10.1038/nature08185openalex-snapshot
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
inferredcites →https://doi.org/10.1038/nature09534openalex-snapshot
A map of human genome variation from population-scale sequencing
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Genetic contributions to stability and change in intelligence from childhood to old age
inferredcites →https://doi.org/10.1038/nature11582openalex-snapshot
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot
Biological insights from 108 schizophrenia-associated genetic loci
inferredcites →https://doi.org/10.1038/nature14132openalex-snapshot
New genetic loci link adipose and insulin biology to body fat distribution
inferredcites →https://doi.org/10.1038/nature17671openalex-snapshot
Genome-wide association study identifies 74 loci associated with educational attainment
inferredcites →https://doi.org/10.1038/ncomms4339openalex-snapshot
Genome-wide association study reveals two new risk loci for bipolar disorder
inferredcites →https://doi.org/10.1038/ng.2238openalex-snapshot
Common variants at 12q15 and 12q24 are associated with infant head circumference
inferredcites →https://doi.org/10.1038/ng.2676openalex-snapshot
Genome-wide meta-analysis identifies new susceptibility loci for migraine
inferredcites →https://doi.org/10.1038/ng.2711openalex-snapshot
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
inferredcites →https://doi.org/10.1038/ng.2802openalex-snapshot
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
inferredcites →https://doi.org/10.1038/ng.3043openalex-snapshot
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
inferredcites →https://doi.org/10.1038/ng.3097openalex-snapshot
Defining the role of common variation in the genomic and biological architecture of adult human height
inferredcites →https://doi.org/10.1038/ng.3154openalex-snapshot
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
inferredcites →https://doi.org/10.1038/ng.3211openalex-snapshot
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3285openalex-snapshot
Meta-analysis of the heritability of human traits based on fifty years of twin studies
inferredcites →https://doi.org/10.1038/ng.3404openalex-snapshot
Partitioning heritability by functional annotation using genome-wide association summary statistics
inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot
An atlas of genetic correlations across human diseases and traits
inferredcites →https://doi.org/10.1038/ng.3552openalex-snapshot
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
inferredcites →https://doi.org/10.1038/ng.571openalex-snapshot
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
inferredcites →https://doi.org/10.1038/ng.784openalex-snapshot
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
inferredcites →https://doi.org/10.1038/ng1017-1558copenalex-snapshot
Erratum: Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
inferredcites →https://doi.org/10.1038/nrg3461openalex-snapshot
Pleiotropy in complex traits: challenges and strategies
inferredcites →https://doi.org/10.1038/tp.2015.96openalex-snapshot
Heritability estimates of the Big Five personality traits based on common genetic variants
inferredcites →https://doi.org/10.1056/nejmra052130openalex-snapshot
Multiple Sclerosis — The Plaque and Its Pathogenesis
inferredcites →https://doi.org/10.1073/pnas.1404623111openalex-snapshot
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
inferredcites →https://doi.org/10.1093/brain/awp262openalex-snapshot
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
inferredcites →https://doi.org/10.1093/hmg/dds491openalex-snapshot
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis
inferredcites →https://doi.org/10.1093/hmg/ddt030openalex-snapshot
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
inferredcites →https://doi.org/10.1093/schbul/sbn135openalex-snapshot
Psychiatric Comorbidities and Schizophrenia
inferredcites →https://doi.org/10.1111/j.1468-2982.2007.01460.xopenalex-snapshot
A review of the genetic relation between migraine and epilepsy.
inferredcites →https://doi.org/10.1111/j.1526-4610.2006.00469.xopenalex-snapshot
The Prevalence and Impact of Migraine Headache in Bipolar Disorder: Results From the Canadian Community Health Survey
inferredcites →https://doi.org/10.1126/science.1235488openalex-snapshot
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment
inferredcites →https://doi.org/10.1136/bmj.318.7196.1460openalex-snapshot
Evidence based cardiology: Psychosocial factors in the aetiology and prognosis of coronary heart disease: systematic review of prospective cohort studies
inferredcites →https://doi.org/10.1136/pgmj.2004.022012openalex-snapshot
Neurological channelopathies
inferredcites →https://doi.org/10.1161/01.cir.0000161822.83163.b6openalex-snapshot
Prospective Study of Body Mass Index and Risk of Stroke in Apparently Healthy Women
inferredcites →https://doi.org/10.1176/appi.ajp.157.5.708openalex-snapshot
Mental and Behavioral Disturbances in Dementia: Findings From the Cache County Study on Memory in Aging
inferredcites →https://doi.org/10.1176/appi.ajp.159.5.695openalex-snapshot
The Integration of Neurology, Psychiatry, and Neuroscience in the 21st Century
inferredcites →https://doi.org/10.1176/appi.ajp.160.1.4openalex-snapshot
Distinguishing Between the Validity and Utility of Psychiatric Diagnoses
inferredcites →https://doi.org/10.1176/appi.ajp.2007.07010045openalex-snapshot
The Relationship Between Depressive Personality Disorder and Major Depressive Disorder: A Population-Based Twin Study
inferredcites →https://doi.org/10.1176/appi.ajp.2015.15020266openalex-snapshot
Association Between ADHD and Obesity: A Systematic Review and Meta-Analysis
inferredcites →https://doi.org/10.1176/appi.ajp.2017.16121402openalex-snapshot
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
inferredcites →https://doi.org/10.1186/s13229-017-0137-9openalex-snapshot
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
inferredcites →https://doi.org/10.1212/01.wnl.0000058907.41080.54openalex-snapshot
Comorbidity of migraine and depression
inferredcites →https://doi.org/10.1212/wnl.64.10_suppl_2.s9openalex-snapshot
Migraine as an inflammatory disorder
inferredcites →https://doi.org/10.1375/twin.13.6.550openalex-snapshot
Externalizing Behaviors and Cigarette Smoking as Predictors for Use of Illicit Drugs: A Longitudinal Study Among Finnish Adolescent Twins
inferredcites →https://doi.org/10.1542/peds.2015-4654openalex-snapshot
Childhood Epilepsy, Febrile Seizures, and Subsequent Risk of ADHD
inferredcites →https://doi.org/10.4065/78.3.273openalex-snapshot
Discrepant Results Regarding Long-term Survival of Patients With Anorexia Nervosa?
inferredcites →https://doi.org/10.4065/78.3.278openalex-snapshot
Long-term Survival of Patients With Anorexia Nervosa: A Population-Based Study in Rochester, Minn
inferredcites →https://doi.org/10.4088/jcp.08m04807openalex-snapshot
Bipolar Disorder, Schizoaffective Disorder, and Schizophrenia Overlap
inferredcites →https://doi.org/10.4088/jcp.v64n0111openalex-snapshot
Screening for Bipolar Disorder in the Community
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Association Between Population Density and Genetic Risk for Schizophrenia
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Improving Genetic Association Analysis through Integration of Functional Annotations of the Human Genome
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Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population
inferred← citeshttps://doi.org/10.1002/ajmg.b.32652openalex-snapshot
Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data
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Early childhood adversities and risk of eating disorders in women: A Danish register‐based cohort study
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Quantitative mapping of genetic similarity in human heritable diseases by shared mutations
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Schizophrenia and the neurodevelopmental continuum:evidence from genomics
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Genetic Studies of Tic Disorders and Tourette Syndrome
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Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers
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Schizotypy and smooth pursuit eye movements as potential endophenotypes of obsessive-compulsive disorder
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Overweight in family members of probands with ADHD
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Co-occurrence Patterns and Transitions in Adolescents’ Depressive Symptoms and Problematic Smartphone Use: The Roles of Social Support and Self-control
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Polygene Varianten und Epigenetik bei Adipositas
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The Genetics of Gilles de la Tourette Syndrome: a Common Aetiological Basis with Comorbid Disorders?
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Restricted and Repetitive Behaviors in Autism Spectrum Disorder: a Review of Associated Features and Presentation Across Clinical Populations
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Genetics of obsessive-compulsive disorder and Tourette disorder
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Future directions in risk research
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Genetics of Eating and Weight Disorders
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A Powerful Approach to Estimating Annotation-Stratified Genetic Covariance via GWAS Summary Statistics
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Estimating SNP-Based Heritability and Genetic Correlation in Case-Control Studies Directly and with Summary Statistics
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Kynurenine pathway abnormalities are state-specific but not diagnosis-specific in schizophrenia and bipolar disorder
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Familial Liability to Epilepsy and Attention-Deficit/Hyperactivity Disorder: A Nationwide Cohort Study
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Association of Polygenic Risk for Attention-Deficit/Hyperactivity Disorder With Co-occurring Traits and Disorders
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Manifesto for a European research network into Problematic Usage of the Internet
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Autism Spectrum Symptoms in a Tourette’s Disorder Sample
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Association Between Childhood to Adolescent Attention Deficit/Hyperactivity Disorder Symptom Trajectories and Late Adolescent Disordered Eating
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The role of genetic variation of human metabolism for BMI, mental traits and mental disorders
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Exploring the genetic overlap between psychiatric illness and epilepsy: A review
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Schizophrenia risk alleles and neurodevelopmental outcomes in childhood: a population-based cohort study
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Gene–environment interplay in depressive symptoms: moderation by age, sex, and physical illness
inferred← citeshttps://doi.org/10.1017/s0033291717003440openalex-snapshot
Assessing the evidence for shared genetic risks across psychiatric disorders and traits
inferred← citeshttps://doi.org/10.1017/s0033291721000982openalex-snapshot
Insights into attention-deficit/hyperactivity disorder from recent genetic studies
inferred← citeshttps://doi.org/10.1017/s0033291721001744openalex-snapshot
Genetics of obsessive-compulsive disorder
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Efficacy of a transdiagnostic, prevention-focused program for at-risk young adults: a waitlist-controlled trial
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Classification of common human diseases derived from shared genetic and environmental determinants
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The implications of the shared genetics of psychiatric disorders
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Psychiatric genetics and the structure of psychopathology
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The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology
inferred← citeshttps://doi.org/10.1038/s41380-018-0115-4openalex-snapshot
Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder
inferred← citeshttps://doi.org/10.1038/s41398-017-0046-xopenalex-snapshot
Childhood behaviour problems show the greatest gap between DNA-based and twin heritability
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A polygenic p factor for major psychiatric disorders
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Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder
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Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories
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Genetics and educational attainment
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Shared vulnerability for connectome alterations across psychiatric and neurological brain disorders
inferred← citeshttps://doi.org/10.1038/s41586-018-0566-4openalex-snapshot
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
inferred← citeshttps://doi.org/10.1038/s41588-018-0081-4openalex-snapshot
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
inferred← citeshttps://doi.org/10.1038/s41598-017-12325-3openalex-snapshot
Drug enrichment and discovery from schizophrenia genome-wide association results: an analysis and visualisation approach
inferred← citeshttps://doi.org/10.1038/tp.2017.115openalex-snapshot
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia
inferred← citeshttps://doi.org/10.1038/tp.2017.212openalex-snapshot
Investigating the genetic underpinnings of early-life irritability
inferred← citeshttps://doi.org/10.1055/s-0038-1676674openalex-snapshot
Polygene Formen der Adipositas und Störungs-übergreifende Analysen
inferred← citeshttps://doi.org/10.1093/schbul/sbx031openalex-snapshot
Genetic Overlap Between Schizophrenia and Developmental Psychopathology: Longitudinal and Multivariate Polygenic Risk Prediction of Common Psychiatric Traits During Development
inferred← citeshttps://doi.org/10.1098/rsob.170125openalex-snapshot
Statistical methods to detect pleiotropy in human complex traits
inferred← citeshttps://doi.org/10.1101/059519openalex-snapshot
Genomics implicates adaptive and innate immunity in Alzheimer’s and Parkinson’s
inferred← citeshttps://doi.org/10.1101/070730openalex-snapshot
Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data
inferred← citeshttps://doi.org/10.1101/088815openalex-snapshot
Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations
inferred← citeshttps://doi.org/10.1101/091264openalex-snapshot
Pathways analyses of schizophrenia GWAS focusing on known and novel drug targets
inferred← citeshttps://doi.org/10.1101/2020.06.04.20121061openalex-snapshot
A genome-wide association study of total child psychiatric problems scores
inferred← citeshttps://doi.org/10.1101/445874openalex-snapshot
Comparative genetic architectures of schizophrenia in East Asian and European populations
inferred← citeshttps://doi.org/10.1101/498097openalex-snapshot
Structural neuroimaging signatures of anorexia nervosa features in a mixed sample enriched for disease vulnerability
inferred← citeshttps://doi.org/10.1101/cshperspect.a028951openalex-snapshot
Genetics of Multiple Sclerosis: An Overview and New Directions
inferred← citeshttps://doi.org/10.1111/ejn.16162openalex-snapshot
Assessing non‐right‐handedness and atypical cerebral lateralisation as predictors of paediatric mental health difficulties
inferred← citeshttps://doi.org/10.1146/annurev-clinpsy-050817-084847openalex-snapshot
Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences
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Polygenic Risk for Depression Increases Risk of Ischemic Stroke
inferred← citeshttps://doi.org/10.1177/1087054719879499openalex-snapshot
Does Co-Occurring Anxiety Modulate ADHD-Related Cognitive and Neurophysiological Impairments?
inferred← citeshttps://doi.org/10.1177/1087054720914386openalex-snapshot
Parental Prenatal Symptoms of Depression and Offspring Symptoms of ADHD: A Genetically Informed Intergenerational Study
inferred← citeshttps://doi.org/10.1186/s10194-018-0856-0openalex-snapshot
Polygenic risk score: use in migraine research
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006933openalex-snapshot
Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer’s disease
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008009openalex-snapshot
Reverse GWAS: Using genetics to identify and model phenotypic subtypes
inferred← citeshttps://doi.org/10.1371/journal.pone.0193256openalex-snapshot
Statistical power and utility of meta-analysis methods for cross-phenotype genome-wide association studies
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Polygenic Risk, Personality Dimensions, and Adolescent Alcohol Use Problems: A Longitudinal Study
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Social communication deficits and restricted repetitive behavior symptoms in Tourette syndrome
inferred← citeshttps://doi.org/10.3389/fnins.2016.00340openalex-snapshot
Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis
inferred← citeshttps://doi.org/10.3389/fnmol.2017.00083openalex-snapshot
Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD)
inferred← citeshttps://doi.org/10.3410/f.727880805.793537708openalex-snapshot
Faculty Opinions recommendation of Classification of common human diseases derived from shared genetic and environmental determinants.
inferred← citeshttps://doi.org/10.3410/f.732656134.793563017openalex-snapshot
Faculty Opinions recommendation of Polygenic risk for depression increases risk of ischemic stroke: from the stroke genetics network study.
inferred← citeshttps://doi.org/10.3410/f.733499086.793567847openalex-snapshot
Faculty Opinions recommendation of The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology.
inferred← citeshttps://doi.org/10.3410/f.733675894.793549439openalex-snapshot
Faculty Opinions recommendation of Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
inferred← citeshttps://doi.org/10.46278/j.ncacn.20220422openalex-snapshot
Lignes directrices pour l’examen diagnostique des troubles neurodéveloppementaux chez l'adulte en neuropsychologie
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