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Anders D. Børglum

Aarhus University · DK
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Area of research
Genetics · Cognitive Neuroscience
Research interest
Research interests include Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, and Attention Deficit Hyperactivity Disorder.
h-index
102
citations
59,819
works
697
NIH funding
primary concept
Medicine
email

Recent publications

Mapping the genetic landscape across 14 psychiatric disorders
Nature 2025cited by 43position: middledoi
Associations between common genetic variants and income provide insights about the socio-economic health gradient
Nature Human Behaviour 2025cited by 24position: middledoi
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients
Biological Psychiatry Global Open Science 2025cited by 0position: middledoi
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
Nature Genetics 2024cited by 168position: middledoi
Systems biology dissection of PTSD and MDD across brain regions, cell types, and blood
Science 2024cited by 81position: middledoi
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease
Nature Cardiovascular Research 2024cited by 44position: middledoi
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
medRxiv 2024cited by 24position: middledoi
Neuropsychiatric polygenic scores are weak predictors of professional categories
Nature Human Behaviour 2024cited by 1position: middledoi
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Nature Genetics 2023cited by 731position: lastdoi
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature Medicine 2023cited by 296position: lastdoi
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Nature Medicine 2023cited by 173position: middledoi
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Nature Genetics 2023cited by 113position: middledoi
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores
Nature Communications 2023cited by 78position: middledoi
Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study
The Lancet Psychiatry 2023cited by 33position: middledoi
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder
Nature Genetics 2023cited by 25position: middledoi
Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Nature Genetics 2023cited by 14position: lastdoi
ENHANCING POLYGENIC PREDICTION WITH AN AGNOSTIC MULTI-PGS METHOD THAT LEVERAGES HUNDREDS OF POLYGENIC SCORES
European Neuropsychopharmacology 2023cited by 0position: middledoi
Rare coding variants in ten genes confer substantial risk for schizophrenia
Nature 2022cited by 863position: middledoi
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics 2022cited by 602position: middledoi
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis
Nature Genetics 2022cited by 317position: middledoi
Genetic correlates of phenotypic heterogeneity in autism
Nature Genetics 2022cited by 144position: middledoi
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
Molecular Psychiatry 2022cited by 133position: middledoi
The female protective effect against autism spectrum disorder
Cell Genomics 2022cited by 108position: middledoi
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Nature Genetics 2022cited by 74position: lastdoi
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
medRxiv 2022cited by 63position: lastdoi
Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis
Molecular Psychiatry 2022cited by 62position: middledoi
Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB
Journal of Allergy and Clinical Immunology 2022cited by 29position: middledoi
Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities
medRxiv 2022cited by 12position: lastdoi
Genetic analyses identify widespread sex-differential participation bias
Nature Genetics 2021cited by 266position: middledoi
Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits
Biological Psychiatry 2021cited by 85position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Preben Bo Mortensen · Lundbeck Foundation23 papers (2013–2023)David M. Hougaard · Statens Serum Institut21 papers (2013–2023)Jakob Grove · Aarhus University17 papers (2013–2025)Ole Mors · Broad Institute17 papers (2013–2023)Merete Nordentoft · Nordisk Fond for Miljø og Udvikling16 papers (2013–2023)Esben Agerbo · Virginia Commonwealth University14 papers (2015–2023)Jonas Bybjerg‐Grauholm · Statens Serum Institut10 papers (2017–2022)Manuel Mattheisen · Dalhousie University10 papers (2013–2022)Mark J. Daly · University of Helsinki8 papers (2016–2022)Benjamin M. Neale · Broad Institute8 papers (2016–2023)Andrew J. Schork · University of Copenhagen8 papers (2019–2023)Carsten Bøcker Pedersen · Aarhus University7 papers (2013–2021)Panos Roussos · Institute of Genetics6 papers (2016–2025)Bjarni J. Vilhjálmsson · Broad Institute6 papers (2015–2023)Ditte Demontis · Broad Institute6 papers (2013–2024)Wesley K. Thompson · Translational Genomics Research Institute6 papers (2018–2023)Thomas D. Als · Aarhus University Hospital5 papers (2017–2024)Naomi R. Wray · University of Oulu5 papers (2015–2021)Andrés Ingason · Aarhus University5 papers (2021–2023)Marianne Giørtz Pedersen · Aarhus University5 papers (2017–2023)
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