selected publications
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academic article
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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder.
Biological Psychiatry.
83.
2018
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.
Molecular Psychiatry.
23.
2018
Analysis of shared heritability in common disorders of the brain.
Science.
360.
2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Nature Genetics.
50.
2018
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium.
Biological Psychiatry.
84.
2018
Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
Genome Medicine.
10.
2018
Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.
Translational Psychiatry.
8.
2018
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Nature Genetics.
50.
2018
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.
Cell.
173.
2018
The anorexia nervosa genetics initiative (ANGI): Overview and methods.
Contemporary Clinical Trials.
74.
2018
The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.
Molecular Psychiatry.
23.
2018
The importance of data structure in statistical analysis of dendritic spine morphology.
Journal of Neuroscience Methods.
296.
2018
Assembly and analysis of 100 full MHC haplotypes from the Danish population.
Genome Research.
27.
2017
COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity.
Acta Psychiatrica Scandinavica.
136.
2017
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.
Biological Psychiatry.
81.
2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Nature Genetics.
49.
2017
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference.
Nature.
548.
2017
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.
Translational Psychiatry.
7.
2017
Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants.
JAMA Psychiatry.
73.
2016
CACNA1C hypermethylation is associated with bipolar disorder.
Translational Psychiatry.
6.
2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Nature Genetics.
48.
2016
High loading of polygenic risk in cases with chronic schizophrenia.
Molecular Psychiatry.
21.
2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.
PLoS ONE.
11.
2016
Identification of the BRD1 interaction network and its impact on mental disorder risk.
Genome Medicine.
8.
2016
LandScape: a simple method to aggregate p-values and other stochastic variables without a priori grouping.
Statistical Applications in Genetics and Molecular Biology.
15.
2016
Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.
European Neuropsychopharmacology.
26.
2016
Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder.
Bipolar Disorders.
17.
2015
Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia.
Psychoneuroendocrinology.
60.
2015
Low to Moderate Average Alcohol Consumption and Binge Drinking in Early Pregnancy: Effects on Choice Reaction Time and Information Processing Time in Five-Year-Old Children.
PLoS ONE.
10.
2015
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
American Journal of Human Genetics.
97.
2015
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios.
Nature Communications.
6.
2015
GWAS, Cytomegalovirus Infection, and Schizophrenia.
Current Behavioral Neuroscience Reports.
1.
2014
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.
Molecular Psychiatry.
19.
2014
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases.
American Journal of Human Genetics.
95.
2014
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dataset
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Supplementary Tables 1-8 from Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight.
the-royal-society.
2019
Supplementary Tables 1-8 from Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight.
the-royal-society.
2019
Additional file 3: of Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
springer-nature.
2018
Additional file 4: of Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
springer-nature.
2018
Additional file 12: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 14: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 16: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 9: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.
public-library-of-science.
2016
Associations between average maternal alcohol intake in pregnancy and choice reaction time (CRT) on the Sternberg task 1..
public-library-of-science.
2015
Associations between average maternal alcohol intake in pregnancy and slope 1 on the Sternberg task 2..
public-library-of-science.
2015
Maternal and child characteristics of participants and non-participants..
public-library-of-science.
2015
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hide from search
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Table S1 - Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk.
public-library-of-science.
2013
Amniotic fluid inflammatory cytokines: Potential markers of immunologic dysfunction in autism spectrum disorders.
The World Journal of Biological Psychiatry.
2013
Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
Molecular Genetics and Metabolism.
2013
Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk.
PLoS ONE.
2013
Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study.
BMC Medicine.
2013
Neonatal chemokine levels and risk of autism spectrum disorders: Findings from a Danish historic birth cohort follow-up study.
Cytokine.
2013
Neonatal levels of neurotrophic factors and risk of autism spectrum disorders.
Acta Psychiatrica Scandinavica.
2013
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preprint
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Common risk variants identified in autism spectrum disorder.
bioRxiv.
2017
Discovery of the first genome-wide significant risk loci for ADHD.
bioRxiv.
2017
Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
bioRxiv.
2017
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder.
bioRxiv.
2017
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder.
bioRxiv.
2017
Genome-wide association study implicates CHRNA2 in cannabis use disorder.
bioRxiv.
2017
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes.
bioRxiv.
2017
Social and non-social autism symptom and trait domains are genetically dissociable.
bioRxiv.
2017
The Anorexia Nervosa Genetics Initiative: Overview and Methods.
bioRxiv.
2017
The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders.
bioRxiv.
2017
Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape.
bioRxiv.
2016
Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.
bioRxiv.
2016
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
bioRxiv.
2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
bioRxiv.
2015