Lista de obras -

A Comprehensive Analysis of Nuclear-Encoded Mitochondrial Genes in Schizophrenia

artículo científico publicado en 2018

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

artículo científico publicado en 2017

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 association study on medulloblastoma

artículo científico publicado en 2020

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

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

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

artículo científico

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

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

artículo científico publicado en 2019

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

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

DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study

artículo científico

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

Distinct DNA methylation patterns in cirrhotic liver and hepatocellular carcinoma

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

artículo científico publicado en 2018

Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021

Exploring Cuba's population structure and demographic history using genome-wide data

artículo científico publicado en 2018

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

artículo científico publicado en 2020

Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank

artículo científico

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 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 predisposition to hypertension is associated with preeclampsia in European and Central Asian women

scientific article published on 25 November 2020

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

artículo científico

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

artículo científico publicado en 2018

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 of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

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 dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

artículo científico publicado en 2016

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

scientific article published on 08 October 2019

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

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

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

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

article

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

artículo científico publicado en 2021

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

artículo científico publicado en 2020

Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations

artículo científico publicado en 2019

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

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

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

RNA sequencing of archived neonatal dried blood spots

artículo científico publicado en 2016

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

artículo científico publicado en 2019

Response to "Newborn dried blood spot samples in Denmark: the hidden figures of secondary use and research participation"

scientific article published on 28 June 2019

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

artículo científico publicado en 2011

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

The Duffy-null genotype and risk of infection

artículo científico publicado en 2020

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

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

artículo científico publicado en 2017

Lista de obras de

A Comprehensive Analysis of Nuclear-Encoded Mitochondrial Genes in Schizophrenia

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

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

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

A genome-wide association study on medulloblastoma

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

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

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

A major role for common genetic variation in anxiety disorders

A polygenic resilience score moderates the genetic risk for schizophrenia

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

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

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

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

Common risk variants identified in autism spectrum disorder

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

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

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

DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study

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

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

Distinct DNA methylation patterns in cirrhotic liver and hepatocellular carcinoma

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

Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021

Exploring Cuba's population structure and demographic history using genome-wide data

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

Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank

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

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

Genetic liability to major depression and risk of childhood asthma

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

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

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

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

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

Genome-wide association study implicates CHRNA2 in cannabis use disorder

Genome-wide association study implicatesCHRNA2in cannabis use disorder

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

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

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

Identification of common genetic risk variants for autism spectrum disorder

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

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

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

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

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

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

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

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

Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations

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

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

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

RNA sequencing of archived neonatal dried blood spots

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

Response to "Newborn dried blood spot samples in Denmark: the hidden figures of secondary use and research participation"

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

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

The Duffy-null genotype and risk of infection

The genetic architecture of sporadic and multiple consecutive miscarriage

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

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

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