List of works - Marie Bækvad-Hansen

A major role for common genetic variation in anxiety disorders

scientific article published on 20 November 2019

A polygenic resilience score moderates the genetic risk for schizophrenia

scientific article published on 06 September 2019

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

An epigenetic clock for gestational age at birth based on blood methylation data

scientific article

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

scientific article published on 25 November 2019

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

Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA

scientific article published on 02 November 2019

Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

scientific article published on 29 August 2017

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

scientific article published on 26 November 2018

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

scientific article published on 28 March 2018

Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality

scientific article

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

scientific article

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

scientific article published on 11 July 2015

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

scientific article published on 05 December 2019

Genetic liability to major depression and risk of childhood asthma

scientific article published on 28 July 2020

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

article

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

scientific article published on 26 April 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

scientific article published on 23 November 2020

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

scientific article

Genome-wide association study implicates CHRNA2 in cannabis use disorder

scientific article published on 17 June 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

scientific article published in June 2021

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals

scientific article

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

scientific article

Identification of common genetic risk variants for autism spectrum disorder

scientific article published on 25 February 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

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

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

scientific article published on 02 October 2020

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

RNA sequencing of archived neonatal dried blood spots

scientific article published on 24 December 2016

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

scientific article published on 07 October 2019

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

scientific article published in PLoS ONE

Surfactant protein B polymorphisms, pulmonary function and COPD in 10,231 individuals

scientific article published on 06 August 2010

The Duffy-null genotype and risk of infection

scientific article published on 22 September 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.

scientific article

List of works by Marie Bækvad-Hansen

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

An epigenetic clock for gestational age at birth based on blood methylation data

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

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

Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA

Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

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

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

Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality

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 liability to ADHD and substance use disorders in individuals with ADHD

Genetic liability to major depression and risk of childhood asthma

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

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals

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

Identification of common genetic risk variants for autism spectrum disorder

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

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

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

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

RNA sequencing of archived neonatal dried blood spots

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

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

Surfactant protein B polymorphisms, pulmonary function and COPD in 10,231 individuals

The Duffy-null genotype and risk of infection

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