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Lista de obras de Naomi R. Wray

"Arte et Labore"-A Blackburn Rovers fan's legacy in human complex trait genetics

scientific article published on 01 July 2019

10 Years of GWAS Discovery: Biology, Function, and Translation

artículo científico publicado en 2017

A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families

artículo científico publicado en 2011

A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

artículo científico publicado en 2016

A DNA methylation biomarker of alcohol consumption.

artículo científico publicado en 2016

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

artículo científico publicado en 2017

A better coefficient of determination for genetic profile analysis

artículo científico publicado en 2012

A comparative study of techniques for differential expression analysis on RNA-Seq data

artículo científico publicado en 2014

A comparison of some simple methods to identify geographical areas with excess incidence of a rare disease such as childhood leukaemia

artículo científico publicado en 1999

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A direct test of the diathesis-stress model for depression.

artículo científico publicado en 2017

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

article

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.

artículo científico publicado en 2013

A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality

artículo científico publicado en 2010

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

artículo científico publicado en 2019

A genome-wide association study of sleep habits and insomnia

artículo científico publicado en 2013

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.

artículo científico publicado en 2012

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases

artículo científico publicado en 2016

A parsimonious model for mass-univariate vertex-wise analysis

artículo científico publicado en 2021

A recessive genetic model and runs of homozygosity in major depressive disorder

artículo científico publicado en 2014

A resource-efficient tool for mixed model association analysis of large-scale data

A resource-efficient tool for mixed model association analysis of large-scale data

scientific article published on 25 November 2019

A unified framework for association and prediction from vertex-wise grey-matter structure

scientific article published on 20 July 2020

A versatile gene-based test for genome-wide association studies

artículo científico publicado en 2010

A whole genome association study of neuroticism using DNA pooling

artículo científico publicado en 2007

ALS in Danish Registries: Heritability and links to psychiatric and cardiovascular disorders

scientific article published on 20 February 2020

ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

artículo científico publicado en 2013

Accounting for Mutation Effects in the Additive Genetic Variance-Covariance Matrix and Its Inverse

Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels

Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures

artículo científico publicado en 2009

Across-cohort QC analyses of GWAS summary statistics from complex traits

artículo científico publicado en 2016

Across-cohort QC analyses of genome-wide association study summary statistics from complex traits

article published in 2015

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

artículo científico publicado en 2013

Age at first birth in women is genetically associated with increased risk of schizophrenia

artículo científico publicado en 2018

Aggregation of childhood leukemia in geographic areas of Greece

artículo científico publicado en 1997

Allele frequencies and the r2 measure of linkage disequilibrium: impact on design and interpretation of association studies

artículo científico publicado en 2005

Analysis of DNA methylation associates the cystine-glutamate antiporter SLC7A11 with risk of Parkinson's disease

artículo científico publicado en 2020

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.

artículo científico publicado en 2018

Anxiety and comorbid measures associated with PLXNA2.

artículo científico publicado en 2007

Applying polygenic risk scores to postpartum depression

artículo científico publicado en 2014

Are surgical trials with negative results being interpreted correctly?

artículo científico publicado en 2012

Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

artículo científico publicado en 2013

Association analysis of the chromosome 4p-located G protein-coupled receptor 78 (GPR78) gene in bipolar affective disorder and schizophrenia

artículo científico publicado en 2006

Association analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophrenia

article

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

artículo científico publicado en 2010

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

artículo científico publicado en 2005

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

artículo científico publicado en 2017

Association of Mental Disorder in Childhood and Adolescence With Subsequent Educational Achievement

artículo científico publicado en 2020

Association of OPRD1 polymorphisms with heroin dependence in a large case-control series

artículo científico publicado en 2012

Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study

artículo científico publicado en 2019

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression

artículo científico publicado en 2008

Association study of candidate variants of COMT with neuroticism, anxiety and depression

artículo científico publicado en 2008

Assortative Mating in Autism Spectrum Disorder: Toward an Evidence Base From DNA Data, but Not There Yet

artículo científico publicado en 2019

Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits

artículo científico publicado en 2013

Asymptotic rates of response from index selection

article

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

scientific article published on 07 August 2018

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

scientific article published on 09 October 2020

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico publicado en 2022

Author Correction: Misestimation of heritability and prediction accuracy of male-pattern baldness

scientific article published in Nature Communications

Author reply to A commentary on Pitfalls of predicting complex traits from SNPs

artículo científico publicado en 2013

Bayesian reassessment of the epigenetic architecture of complex traits

artículo científico publicado en 2020

Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals

artículo científico publicado en 2020

Brain age predicts mortality.

artículo científico publicado en 2017

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.

artículo científico publicado en 2015

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

COPD education and cognitive behavioral therapy group treatment for clinically significant symptoms of depression and anxiety in COPD patients: a randomized controlled trial

artículo científico publicado en 2007

Calculation of prediction error variances using sparse matrix methods

artículo científico publicado en 1994

Cardiovascular disease, psychiatric diagnosis and sex-differences in the multi-step hypothesis of ALS

artículo científico publicado en 2020

Causal associations between risk factors and common diseases inferred from GWAS summary data

artículo científico publicado en 2018

Causal associations between risk factors and common diseases inferred from GWAS summary data

Choosing the best tools for comparative analyses of texts

article

Cohort Profile Update: The Mater-University of Queensland Study of Pregnancy (MUSP).

artículo científico publicado en 2014

Cohort profile: the Australian genetics of depression study

artículo científico publicado en 2020

Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model

article

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion.

artículo científico publicado en 2012

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

artículo científico publicado en 2009

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

artículo científico publicado en 2018

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

article

Comorbid chronic pain and depression: Shared risk factors and differential antidepressant effectiveness

artículo científico publicado en 2020

Comparing apples and oranges: equating the power of case-control and quantitative trait association studies

artículo científico publicado en 2010

Comparison of Genotypic and Phenotypic Correlations: Cheverud's Conjecture in Humans.

artículo científico publicado en 2018

Complex Trait Prediction from Genome Data: Contrasting EBV in Livestock to PRS in Humans: Genomic Prediction

article

Concepts and Misconceptions about the Polygenic Additive Model Applied to Disease

artículo científico publicado en 2015

Concepts, estimation and interpretation of SNP-based heritability

artículo científico

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

artículo científico publicado en 2020

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

artículo científico publicado en 2015

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Conventional multipoint nonparametric linkage analysis is not necessarily inherently biased

artículo científico publicado en 2004

Correction to: Lifetime stress accelerates epigenetic aging in an urban, African American cohort: relevance of glucocorticoid signaling.

artículo científico publicado en 2018

Correction: GWAS on family history of Alzheimer's disease.

artículo científico publicado en 2019

Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

artículo científico publicado en 2020

Correction: Novel Genetic Analysis for Case-Control Genome-Wide Association Studies: Quantification of Power and Genomic Prediction Accuracy

artículo científico publicado en 2013

Corrigendum to: Sporadic cases are the norm for complex disease.

artículo científico publicado en 2010

Could Polygenic Risk Scores Be Useful in Psychiatry?: A Review

artículo científico publicado en 2020

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

artículo científico publicado en 2017

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies

article published in 2018

DNA methylation-based measures of biological age: meta-analysis predicting time to death

artículo científico publicado en 2016

DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

artículo científico publicado en 2014

Detection and quantification of inbreeding depression for complex traits from SNP data

artículo científico publicado en 2017

Discovery and implications of polygenicity of common diseases

artículo científico

Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease

artículo científico publicado en 2016

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

artículo científico publicado en 2022

Dissection of genetic variation and evidence for pleiotropy in male pattern baldness

artículo científico publicado en 2018

Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample

artículo científico publicado en 2010

Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

artículo científico publicado en 2017

EMX1 regulates NRP1-mediated wiring of the mouse anterior cingulate cortex.

artículo científico publicado en 2015

Embracing polygenicity: a review of methods and tools for psychiatric genetics research.

artículo científico

Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

article by Patrick F. Sullivan et al published 1 August 2006 in CrossRef Listing of Deleted DOIs

Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

article by Patrick F. Sullivan et al published August 2006 in Twin Research and Human Genetics

Epigenetic Signatures of Cigarette Smoking

artículo científico publicado en 2016

Epigenetic prediction of complex traits and death

article by Daniel L McCartney et al published 27 September 2018 in Genome Biology

Epigenetic prediction of complex traits and death

Erratum: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

article

Erratum: Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion

scholarly article published in Translational Psychiatry

Erratum: Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

article

Erratum: Meta-analysis of genome-wide association studies of anxiety disorders

article

Estimating Effects and Making Predictions from Genome-Wide Marker Data

article

Estimating Missing Heritability for Disease from Genome-wide Association Studies ⬇️

artículo científico publicado el 3 de marzo de 2011

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.

artículo científico publicado en 2012

Estimation and partition of heritability in human populations using whole-genome analysis methods.

artículo científico publicado en 2013

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

artículo científico publicado en 2014

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

artículo científico publicado en 2012

Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

artículo científico publicado en 2018

Estimation of SNP heritability from dense genotype data

artículo científico publicado en 2013

Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals

artículo científico publicado en 2020

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

artículo científico publicado en 2012

Evaluating the Impact of Nonrandom Mating: Psychiatric Outcomes Among the Offspring of Pairs Diagnosed With Schizophrenia and Bipolar Disorder

artículo científico publicado en 2019

Evidence for the involvement of the RSG2 gene in risk for anxiety and related phenotypes in an elderly population not selected for this trait

article

Evidence of CNIH3 involvement in opioid dependence.

artículo científico publicado en 2015

Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium

artículo científico publicado en 2019

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

artículo científico publicado en 2011

Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait

scientific article published on 30 April 2019

Explaining additional genetic variation in complex traits

artículo científico publicado en 2014

Exploring Boundaries for the Genetic Consequences of Assortative Mating for Psychiatric Traits

artículo científico publicado en 2016

Expression of eEF1A2 is associated with clear cell histology in ovarian carcinomas: overexpression of the gene is not dependent on modifications at the EEF1A2 locus.

artículo científico publicado en 2007

Extreme inbreeding in a European ancestry sample from the contemporary UK population

artículo científico publicado en 2019

Familiality of Psychiatric Disorders and Risk of Postpartum Psychiatric Episodes: A Population-Based Cohort Study

From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer

scientific article published on 30 September 2020

Future Directions in Genetics of Psychiatric Disorders

article

GCTA-GREML accounts for linkage disequilibrium when estimating genetic variance from genome-wide SNPs

artículo científico publicado en 2016

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

artículo científico publicado en 2018

GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression

artículo científico publicado en 2021

GWAS on family history of Alzheimer's disease.

artículo científico publicado en 2018

Gene action, genetic variation, and GWAS: A user-friendly web tool

artículo científico publicado en 2021

Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations.

artículo científico publicado en 2017

Genetic analyses of medication-use and implications for precision medicine

Genetic and Phenotypic Stability of Measures of Neuroticism Over 22 Years

Genetic and environmental exposures constrain epigenetic drift over the human life course

artículo científico publicado en 2014

Genetic and environmental influences on the co-morbidity between depression, panic disorder, agoraphobia, and social phobia: a twin study

artículo científico publicado en 2009

Genetic association study of childhood aggression across raters, instruments, and age

artículo científico publicado en 2021

Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins.

artículo científico publicado en 2011

Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression

artículo científico publicado en 2020

Genetic control of temperament traits across species: association of autism spectrum disorder risk genes with cattle temperament

scientific article published on 26 August 2020

Genetic correlates of social stratification in Great Britain

artículo científico publicado en 2019

Genetic correlations of polygenic disease traits: from theory to practice

artículo científico publicado en 2019

Genetic differences between five European populations

artículo científico

Genetic effects influencing risk for major depressive disorder in China and Europe

artículo científico publicado en 2017

Genetic overlap between diagnostic subtypes of ischemic stroke

artículo científico publicado en 2015

Genetic predisposition to schizophrenia associated with increased use of cannabis

artículo científico publicado en 2014

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic risk profiles for depression and anxiety in adult and elderly cohorts

artículo científico publicado en 2010

Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders

scientific article published on 11 November 2019

Genetic signatures of high-altitude adaptation in Tibetans

artículo científico publicado en 2017

Genetic stratification of depression in UK Biobank

scientific article published on 24 May 2020

Genetic studies of major depressive disorder: why are there no genome-wide association study findings and what can we do about it?

artículo científico publicado en 2014

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

artículo científico publicado en 2015

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

artículo científico publicado en 2016

Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.

artículo científico publicado en 2003

Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936

scientific article published on 18 July 2019

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

artículo científico publicado en 2020

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder

artículo científico publicado en 2016

Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes

artículo científico publicado en 2021

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

artículo científico publicado en 2016

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

artículo científico publicado en 2011

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

artículo científico publicado en 2008

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

artículo científico publicado en 2020

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

artículo científico

Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits

artículo científico publicado en 2020

Genome-wide association study of gastrointestinal disorders reinforces the link between the digestive tract and the nervous system

artículo científico publicado en 2019

Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

artículo científico publicado en 2010

Genome-wide association study of medication-use and associated disease in the UK Biobank

artículo científico publicado en 2019

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

artículo científico publicado en 2015

Genome-wide gene expression changes in postpartum depression point towards an altered immune landscape

artículo científico publicado en 2021

Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

article

Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

scientific article published on 23 January 2020

Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD.

artículo científico publicado en 2017

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands

artículo científico publicado en 2008

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

artículo científico publicado en 2019

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.: Supplementary Information

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

Genotype effects contribute to variation in longitudinal methylome patterns in older people

artículo científico publicado en 2018

Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank

scientific article published on 14 August 2019

Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank: Supplementary

Genotype-covariate correlation and interaction disentangled by a whole-genome multivariate reaction norm model

artículo científico publicado en 2019

Glutamate cysteine ligase (GCL) and self reported depression: an association study from the HUNT.

artículo científico publicado en 2011

Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder

article

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

artículo científico publicado en 2009

Heritability in the genomics era — concepts and misconceptions

artículo científico publicado en 2008

Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

artículo científico publicado en 2014

High loading of polygenic risk in cases with chronic schizophrenia

artículo científico publicado en 2015

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

artículo científico publicado en 2014

Identification of 55,000 Replicated DNA Methylation QTL

artículo científico publicado en 2018

Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms.

artículo científico publicado en 2011

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood.

artículo científico publicado en 2018

Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes

artículo científico publicado en 2012

Imprint of Assortative Mating on the Human Genome

Imprint of assortative mating on the human genome

scientific article published on 26 November 2018

Improved polygenic prediction by Bayesian multiple regression on summary statistics

scientific article published on 08 November 2019

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

scientific article published on 23 August 2019

Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations

artículo científico publicado en 2015

Improving genetic prediction by leveraging genetic correlations among human diseases and traits.

artículo científico publicado en 2018

Increasing long-term response to selection.

artículo científico publicado en 1994

Inference in Psychiatry via 2-Sample Mendelian Randomization-From Association to Causal Pathway?

artículo científico publicado en 2017

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

artículo científico publicado en 2016

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

artículo científico publicado en 2018

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

artículo científico publicado en 2013

Investigating the potential effect of antihypertensive medication on psychiatric disorders: a mendelian randomisation study

artículo científico publicado en 2020

Investigating the relationship between iron and depression

artículo científico

Is Schizophrenia a Risk Factor for Breast Cancer?—Evidence From Genetic Data

artículo científico publicado en 2019

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder

artículo científico publicado en 2015

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

artículo científico publicado en 2017

Large-scale genomics unveils the genetic architecture of psychiatric disorders

artículo científico publicado en 2014

Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction

artículo científico publicado en 2020

Lifetime stress accelerates epigenetic aging in an urban, African American cohort: relevance of glucocorticoid signaling.

artículo científico publicado en 2015

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Maternal depression and family adversity: Linked pathways to offspring depression?

artículo científico publicado en 2017

Meta-Analysis of Genome-Wide Association Studies of Anxiety Disorders

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

artículo científico publicado en 2012

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

artículo científico publicado en 2021

Meta-analysis of genome-wide association studies of anxiety disorders.

artículo científico publicado en 2016

Methods for predicting rates of inbreeding in selected populations

artículo científico publicado en 1990

Methylome-wide association study of early life stressors and adult mental health

artículo científico publicado en 2022

Misestimation of heritability and prediction accuracy of male-pattern baldness.

artículo científico publicado en 2018

Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

artículo científico publicado en 2013

Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder.

artículo científico publicado en 2012

Multi-locus models of genetic risk of disease

artículo científico publicado en 2010

Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults

artículo científico publicado en 2020

Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series

scientific article published on 27 March 2020

NFIB-mediated repression of the epigenetic factor Ezh2 regulates cortical development

artículo científico publicado en 2014

Narrowing the boundaries of the genetic architecture of schizophrenia.

artículo científico publicado en 2009

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

Nick Martin and the Genetics of Depression: Sample Size, Sample Size, Sample Size

artículo científico publicado en 2020

Novel directions for G × E analysis in psychiatry

artículo científico publicado en 2014

Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy

artículo científico publicado en 2013

OSCA: a tool for omic-data-based complex trait analysis

article by Futao Zhang et al published 28 May 2019 in Genome Biology

Overlap of expression quantitative trait loci (eQTL) in human brain and blood

artículo científico publicado en 2014

PPD ACT: an app-based genetic study of postpartum depression

artículo científico publicado en 2018

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

artículo científico publicado en 2014

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

artículo científico publicado en 2013

Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method

artículo científico

Phenotypic and discordant-monozygotic analyses of stress and perceived social support as antecedents to or sequelae of risk for depression

artículo científico publicado en 2009

Phenotypic and genetic factors associated with differential consent to record linkage for prescription history in the Australian Genetics of Depression Study

artículo científico publicado en 2021

Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals

artículo científico publicado en 2021

Pitfalls of predicting complex traits from SNPs

artículo científico publicado en 2013

Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.

artículo científico publicado en 2015

Polygenic burden could explain high rates of affective disorders in a community with restricted founder population

artículo científico publicado en 2021

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants ⬇️

artículo científico publicado en 2013

Population density and childhood leukaemia: results of the EUROCLUS study

artículo científico publicado en 1999

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

artículo científico publicado en 2016

Prediction of individual genetic risk of complex disease

artículo científico publicado en 2008

Prediction of individual genetic risk to disease from genome-wide association studies

artículo científico publicado en 2007

Prediction of rates of inbreeding in selected populations

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

artículo científico publicado en 2019

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

scientific article published on 28 April 2020

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

artículo científico publicado en 2019

Publisher Correction: Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes

artículo científico publicado en 2021

Purification of neural precursor cells reveals the presence of distinct, stimulus-specific subpopulations of quiescent precursors in the adult mouse hippocampus

artículo científico publicado en 2015

Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder

artículo científico publicado en 2019

Quantitative genetics of disease traits

artículo científico

RICOPILI: Rapid Imputation for COnsortias PIpeLIne

artículo científico publicado en 2020

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study.

artículo científico publicado en 2016

Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies

artículo científico publicado en 2020

Reply to Kardos et al.: Estimation of inbreeding depression from SNP data

article published in the Proceedings of the National Academy of Sciences of the United States of America

Reply: To PMID 23177270.

artículo científico publicado en 2013

Research review: Polygenic methods and their application to psychiatric traits

artículo científico publicado en 2014

Research review: the role of cytokines in depression in adolescents: a systematic review

artículo científico

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.

artículo científico publicado en 2013

Response to Amar J. Klar: The Chromosome 1;11 Translocation Provides the Best Evidence Supporting Genetic Etiology for Schizophrenia and Bipolar Affective Disorders

artículo científico

Response to Amar J. Klar: The chromosome 1;11 translocation provides the best evidence supporting genetic etiology for schizophrenia and bipolar affective disorders.

artículo científico publicado en 2003

Response to Browning and Browning

artículo científico publicado en 2011

Risk in Relatives, Heritability, SNP-Based Heritability, and Genetic Correlations in Psychiatric Disorders: A Review

scientific article published on 10 June 2020

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

artículo científico publicado en 2016

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture

scientific article published on 23 September 2020

Schizophrenia polygenic risk scores in youth mental health: preliminary associations with diagnosis, clinical stage and functioning

artículo científico publicado en 2021

Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder

artículo científico publicado en 2015

Sex differences in symptoms of depression in unrelated individuals and opposite-sex twin and sibling pairs

artículo científico publicado en 2006

Shared temperament risk factors for anorexia nervosa: a twin study

artículo científico publicado en 2007

Signatures of negative selection in the genetic architecture of human complex traits

artículo científico publicado en 2018

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

artículo científico publicado en 2020

Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model

artículo científico publicado en 2015

Sizing up whole-genome sequencing studies of common diseases

Sleep Disorders and Risk of Incident Depression: A Population Case-Control Study

artículo científico publicado en 2019

Sporadic cases are the norm for complex disease

artículo científico publicado en 2009

Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples.

artículo científico publicado en 2014

Students', colleagues' and research partners' experience about work and accomplishments from collaborating with Robin Thompson

scientific article published on 01 July 2019

Study protocol for the Australian autism biobank: an international resource to advance autism discovery research

article

Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression

scientific article published on April 2009

Synthetic associations created by rare variants do not explain most GWAS results

artículo científico publicado en 2011

Testing the role of circadian genes in conferring risk for psychiatric disorders

artículo científico publicado en 2014

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

The association between family history of mental disorders and general cognitive ability.

artículo científico publicado en 2014

The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects

artículo científico publicado en 2015

The association between neonatal vitamin D status and risk of schizophrenia

scientific article published in Scientific Reports

The contribution of genetic variants to disease depends on the ruler

artículo científico publicado en 2014

The epigenetic clock and telomere length are independently associated with chronological age and mortality

artículo científico publicado en 2016

The epigenetic clock and telomere length are independently associated with chronological age and mortality

artículo científico publicado en 2017

The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936

artículo científico publicado en 2015

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

artículo científico publicado en 2011

The genetic interpretation of area under the ROC curve in genomic profiling

artículo científico publicado en 2010

The heritability of delusional-like experiences

artículo científico publicado en 2012

The neuroprogressive nature of major depressive disorder: pathways to disease evolution and resistance, and therapeutic implications

artículo científico publicado en 2012

The value of polygenic analyses in psychiatry

artículo científico publicado en 2018

Trajectories of inflammatory biomarkers over the eighth decade and their associations with immune cell counts and epigenetic ageing

scholarly article published 24 August 2018

Trajectories of inflammatory biomarkers over the eighth decade and their associations with immune cell profiles and epigenetic ageing

article by Anna J Stevenson et al published 20 December 2018 in Clinical epigenetics

Trajectories of maternal depression: a 27-year population-based prospective study

artículo científico publicado en 2016

Trans-eQTLs identified in whole blood have limited influence on complex disease biology

artículo científico publicado en 2018

Translation elongation factor eEF1A2 is a potential oncoprotein that is overexpressed in two-thirds of breast tumours

artículo científico publicado en 2005

Underestimated effect sizes in GWAS: fundamental limitations of single SNP analysis for dichotomous phenotypes

artículo científico publicado en 2011

Understanding genetic risk factors for common side effects of antidepressant medications

artículo científico publicado en 2021

Understanding genetic risk factors for common side effects of antidepressant medications

artículo científico

Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study

artículo científico publicado en 2012

Use of Monozygotic Twins to Investigate the Relationship between 5HTTLPR Genotype, Depression and Stressful Life Events: An Application of Item Response Theory

article

Use of monozygotic twins to investigate the relationship between 5HTTLPR genotype, depression and stressful life events: an application of Item Response Theory

artículo científico publicado en 2008

Using information of relatives in genomic prediction to apply effective stratified medicine.

artículo científico publicado en 2017

Using summary data from the Danish National Registers to estimate heritabilities for schizophrenia, bipolar disorder, and major depressive disorder ⬇️

artículo científico publicado el 2 de julio de 2012

What do we know about the variability in survival of patients with amyotrophic lateral sclerosis?

artículo científico publicado en 2020

Where GWAS and Epidemiology Meet: Opportunities for the Simultaneous Study of Genetic and Environmental Risk Factors in Schizophrenia ⬇️

artículo científico publicado el 1 de agosto de 2013

Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort

artículo científico publicado en 2017

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

artículo científico publicado en 2017

Widespread signatures of natural selection across human complex traits and functional genomic categories

artículo científico publicado en 2021

Widespread signatures of negative selection in the genetic architecture of human complex traits

scholarly article published 3 June 2017

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