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Lista de obras de Anders D. Børglum

30. COMT Val158Met and MTHFR C677T Moderate Risk of Schizophrenia in Response to Childhood Trauma.

artículo científico publicado en 2017

A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring.

artículo científico publicado en 2010

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

artículo científico publicado en 2017

A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment

scientific journal article

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

A functional CD86 polymorphism associated with asthma and related allergic disorders.

artículo científico publicado en 2007

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

article

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 linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba

artículo científico publicado en 2006

A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families.

artículo científico publicado en 2012

A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.

artículo científico publicado en 2011

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

artículo científico publicado en 2020

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

scientific article published on 11 November 2019

A major role for common genetic variation in anxiety disorders

artículo científico publicado en 2019

A polygenic resilience score moderates the genetic risk for schizophrenia

artículo científico publicado en 2019

A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism

artículo científico publicado en 2009

ASD and ADHD have a similar burden of rare protein-truncating variants

Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells

artículo científico publicado en 2015

Adolescent residential mobility, genetic liability and risk of schizophrenia, bipolar disorder and major depression

artículo científico publicado en 2020

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

artículo científico publicado en 2016

An EcoRI polymorphism for the PLAUR gene ⬇️

artículo científico publicado el 11 de diciembre de 1991

An association study between the norepinephrine transporter gene and depression.

artículo científico publicado en 2013

An association study of suicide and candidate genes in the serotonergic system.

artículo científico publicado en 2013

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

artículo científico publicado en 2014

Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants.

artículo científico publicado en 2016

Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review

artículo científico publicado en 2016

Are TMEM genes potential candidate genes for panic disorder?

artículo científico publicado en 2014

Aromatic l-amino acid decarboxylase expression profiling and isoform detection in the developing porcine brain.

artículo científico publicado en 2009

Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2 ⬇️

artículo científico publicado el 1 de marzo de 1992

Association analyses suggestGPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia

article

Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders

article

Association between Mental Disorders and Subsequent Medical Conditions

artículo científico publicado en 2020

Association between genes on chromosome 19p13.2 and panic disorder.

artículo científico publicado en 2016

Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia

scientific article published on 01 November 2019

Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

artículo científico publicado en 2011

Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population.

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 of beta-adrenergic receptor polymorphisms and mortality in carvedilol-treated chronic heart-failure patients

artículo científico publicado en 2011

Association of the polygenic risk score for schizophrenia with mortality and suicidal behavior - A Danish population-based study.

artículo científico publicado en 2016

Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality

scientific article published on 04 January 2019

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

artículo científico publicado en 2019

Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins

scientific article published on 04 November 2016

Brain proteome changes in female Brd1 mice unmask dendritic spine pathology and show enrichment for schizophrenia risk

scientific article published on 24 December 2018

Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1 mice

artículo científico publicado en 2018

CACNA1C hypermethylation is associated with bipolar disorder.

artículo científico publicado en 2016

COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity.

artículo científico publicado en 2017

Changes in cognitive functions and cerebral grey matter and their associations with inflammatory markers, endocrine markers, and APOE genotypes in testicular cancer patients undergoing treatment.

artículo científico publicado en 2016

Common risk variants identified in autism spectrum disorder

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

artículo científico publicado en 2018

Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons

scientific article published on 04 November 2020

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Complex spatio-temporal distribution and genogeographic affinity of mitochondrial DNA haplogroups in 24,216 Danes

Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes

scientific article published in PLoS ONE

Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder

artículo científico publicado en 2020

Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes.

artículo científico publicado en 2016

Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers

artículo científico publicado en 2014

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

artículo científico publicado en 2017

Depression and BMI influences the serum vascular endothelial growth factor level

artículo científico publicado en 2014

Depression, the Val66Met polymorphism, age, and gender influence the serum BDNF level.

artículo científico publicado en 2012

Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls

scientific article published on 08 May 2018

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

artículo científico publicado en 2018

Dual association of a TRKA polymorphism with schizophrenia.

artículo científico publicado en 2011

EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions

artículo científico publicado en 2015

Effect of specific ADRB1/ADRB2/AGT genotype combinations on the association between survival and carvedilol treatment in chronic heart failure: a substudy of the ECHOS trial

artículo científico publicado en 2012

Electroconvulsive seizures regulates the Brd1 gene in the frontal cortex and hippocampus of the adult rat

scientific journal article

Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

artículo científico publicado en 2018

Endogenous and Antipsychotic-Related Risks for Diabetes Mellitus in Young People With Schizophrenia: A Danish Population-Based Cohort Study.

artículo científico publicado en 2017

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins.

artículo científico publicado en 2017

Epigenome-wide association study of depression symptomatology in elderly monozygotic twins

scientific article published on 02 September 2019

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder

artículo científico publicado en 2002

Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples.

artículo científico

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

artículo científico publicado en 2015

Exploring Genetic Variation That Influences Brain Methylation In Attention-Deficit/Hyperactivity Disorder

Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder

scientific article published on 03 October 2019

FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses

artículo científico publicado en 2020

Family based association analysis of the IL2 and IL15 genes in allergic disorders

article

Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp.

artículo científico publicado en 2004

Further immunohistochemical characterization of BRD1 a new susceptibility gene for schizophrenia and bipolar affective disorder.

artículo científico publicado en 2009

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

artículo científico publicado en 2019

GWAS, cytomegalovirus infection, and schizophrenia.

artículo científico publicado en 2014

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

article

Genetic Markers of ADHD-Related Variations in Intracranial Volume

artículo científico publicado en 2019

Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study

scientific article published on 22 May 2019

Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study

artículo científico publicado en 2020

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

scientific article published on 17 September 2018

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

scientific article published on 18 October 2018

Genetic liability to ADHD and substance use disorders in individuals with ADHD

artículo científico publicado en 2019

Genetic liability to major depression and risk of childhood asthma

artículo científico publicado en 2020

Genetic predictors of educational attainment and intelligence test performance predict voter turnout

scientific article published on 09 November 2020

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

scientific article published on 11 November 2019

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

article

Genome wide assessment of mRNA in astrocyte protrusions by direct RNA sequencing reveals mRNA localization for the intermediate filament protein nestin.

artículo científico publicado en 2013

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 DNA methylation profiling with MeDIP-seq using archived dried blood spots

artículo científico publicado en 2016

Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.

artículo científico publicado en 2018

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

artículo científico publicado en 2018

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

artículo científico publicado en 2013

Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci

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 implicates CHRNA2 in cannabis use disorder

artículo científico publicado en 2019

Genome-wide association study implicatesCHRNA2in cannabis use disorder

Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

artículo científico publicado en 2022

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 of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

artículo científico publicado en 2020

Genome-wide scans using archived neonatal dried blood spot samples.

artículo científico publicado en 2009

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

artículo científico publicado en 2003

Gestational age-dependent development of the neonatal metabolome

scientific article published on 17 September 2020

Hypomethylation of FAM63B in bipolar disorder patients.

artículo científico publicado en 2016

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Identification of the BRD1 interaction network and its impact on mental disorder risk

scientific journal article

Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders

artículo científico publicado en 2019

Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF.

artículo científico publicado en 2015

Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia

artículo científico publicado en 2016

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

artículo científico publicado en 2014

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019

Investigating causality between liability to ADHD and substance use, and liability to substance use and ADHD risk, using Mendelian randomization

scientific article published on 16 November 2019

Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia

artículo científico publicado en 2015

Investigating the association between body fat and depression via Mendelian randomization

artículo científico publicado en 2019

Investigating the causal relationship between neuroticism and depression via Mendelian randomization

artículo científico publicado en 2019

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

artículo científico publicado en 2014

Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

article published in 2018

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

artículo científico publicado en 2020

Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21

artículo científico publicado en 2009

Lung function discordance in monozygotic twins and associated differences in blood DNA methylation

artículo científico publicado en 2017

Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective

scientific article published in 2022

Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes

artículo científico publicado en 2011

Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia

artículo científico publicado en 2017

Mitochondrial DNA SNPs associated with Schizophrenia exhibit Highly Variable Inter-allelic Haplogroup Affiliation and Nuclear Genogeographic Affinity: Bi-Genomic Linkage Disequilibrium raises Major Concerns for Link to Disease

Modeling the cooperativity of schizophrenia risk genes

scientific article published on 01 October 2019

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

artículo científico publicado en 2012

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

artículo científico publicado en 2016

No association of polymorphisms in the serotonin transporter gene with thermal pain sensation in healthy individuals

artículo científico publicado en 2014

No evidence of associations between genetic liability for schizophrenia and development of cannabis use disorder

artículo científico publicado en 2019

No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy.

artículo científico publicado en 2007

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios ⬇️

artículo científico publicado en 2015

Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample

artículo científico publicado en 2021

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 Risk and Progression to Bipolar or Psychotic Disorders Among Individuals Diagnosed With Unipolar Depression in Early Life

artículo científico publicado en 2020

Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder

artículo científico publicado en 2020

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

artículo científico publicado en 2017

Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians.

artículo científico publicado en 2013

Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.

artículo científico publicado en 2003

Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

scientific article published on 07 June 2018

Psychiatric Genomics: An Update and an Agenda

artículo científico publicado en 2017

Psychiatric Genomics: An Update and an Agenda

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: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

scientific article published on 01 June 2019

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

artículo científico publicado en 2019

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

Quantitative assessment of methyl-esterification and other side reactions in a standard propionylation protocol for detection of histone modifications

artículo científico publicado en 2016

Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders

artículo científico publicado en 2019

Replication of Prostate Cancer Risk Variants in a Danish Case-Control Association Study

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Roadmap for a precision-medicine initiative in the Nordic region

artículo científico publicado en 2019

STRATEGIES FOR THE STUDY OF GENE-ENVIRONMENT INTERACTIONS IN SCHIZOPHRENIA

article

Saliva as a Blood Alternative for Genome-Wide DNA Methylation Profiling by Methylated DNA Immunoprecipitation (MeDIP) Sequencing

Schizophrenia in patients with atopic disorders with particular emphasis on asthma: a Danish population-based study

artículo científico publicado en 2012

Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophrenia

artículo científico publicado en 2019

Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.

artículo científico publicado en 2016

Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

artículo científico publicado en 2018

Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.

artículo científico publicado en 2004

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

artículo científico publicado en 2017

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

scientific article published on 12 April 2020

Shared polygenetic variation between ASD and ADHD exerts opposite association patterns with educational attainment

Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene.

artículo científico publicado en 2006

Social and non-social autism symptoms and trait domains are genetically dissociable

scientific article published on 03 September 2019

Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain

artículo científico publicado en 2020

Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3.

artículo científico publicado en 2010

Support of association between BRD1 and both schizophrenia and bipolar affective disorder.

artículo científico publicado en 2010

Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function

artículo científico publicado en 2015

The Schizophrenia and Bipolar Disorder associated BRD1 gene is regulated upon chronic restraint stress

scientific journal article

The association between neonatal vitamin D status and risk of schizophrenia

scientific article published in Scientific Reports

The effect of hypoxia on ZEB1 expression in a mimetic system of the blood-brain barrier

artículo científico publicado en 2018

The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

artículo científico publicado en 2017

The importance of data structure in statistical analysis of dendritic spine morphology.

artículo científico publicado en 2017

The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark.

artículo científico publicado en 2017

Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR)

artículo científico publicado el 1 de julio de 1992

Two-dimensional DNA typing as a genetic marker system in humans ⬇️

artículo científico publicado el 1 de enero de 1995

Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

artículo científico publicado en 2019

Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder

article

Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population.

artículo científico publicado en 2016

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

artículo científico publicado en 2017

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

artículo científico publicado en 2022

[Genomics of mental disorders] ⬇️

artículo científico publicado en 2014

[Status of and perspectives on psychiatric genomic medicine]

scientific article published on 01 May 2005

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