Anders D. Børglum

Inserm — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

104h-index66.9kcitations688works10.32yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genetic Associations and Epidemiology(202), Genetics and Neurodevelopmental Disorders(124), Autism Spectrum Disorder Research(100), Attention Deficit Hyperactivity Disorder(73), Epigenetics and DNA Methylation(59)

Publications612 total

BRD1 haploinsufficiency alters early neuronal programming and disrupts maturation in human induced glutamatergic neurons
2025Open Access
Mapping the genetic landscape across 14 psychiatric disorders
Nature·2025· 16 citedOpen Access
Rare genetic variants confer a high risk of ADHD and implicate neuronal biology
Nature·2025· 2 citedOpen Access
As rates of ASD and ADHD rise, genetic contributions fall: Evidence for widening diagnostic criteria
2025· 1 citedOpen Access
Shared Genetic Architecture Between Endometriosis and Psychiatric Conditions May Explain Comorbidity
2025· 1 citedOpen Access
Porcine model of <i>BRD1</i> haploinsufficiency reveals neurodevelopmental, behavioral, and molecular alterations relevant to psychiatric disorders
2025· 1 citedOpen Access
W59. INTEGRATING GENOMIC AND EVOLUTIONARY PERSPECTIVES ON AUTISM SPECTRUM DISORDER
European Neuropsychopharmacology·2025
79. DISSECTING THE CONTRIBUTION OF RARE CODING VARIANTS TO RISK OF AUTISM AND ADHD
European Neuropsychopharmacology·2025
INVESTIGATING CROSS DISORDER GENE-ENVIRONMENT INTERACTIONS IN AUTISM AND RELATED DISORDERS: THE ROLE OF DIFFERENT TYPES OF MATERNAL INFECTIONS AND FEVER DURING PREGNANCY
European Neuropsychopharmacology·2025
W21. SHARED GENETIC ARCHITECTURE OF EARLY-LIFE NEURODEVELOPMENTAL CONDITIONS AND LATE-LIFE NEURODEGENERATIVE DISEASES
European Neuropsychopharmacology·2025Open Access
AUTISM GENETICS: TRANSLATING ASSOCIATION TO BIOLOGICAL UNDERSTANDING
European Neuropsychopharmacology·2025
T11. UNRAVELING THE GENETIC OVERLAP BETWEEN SCHIZOPHRENIA AND AUTISM SPECTRUM DISORDER
European Neuropsychopharmacology·2025
M15. GWAS OF MACRO-SCALE RESTING STATE FUNCTIONAL BRAIN NETWORKS IDENTIFY SHARED BIOLOGY WITH BRAIN STRUCTURE AND AUTISM
European Neuropsychopharmacology·2025
Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group
Molecular Psychiatry·2025· 4 citedOpen Access
A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activity
Molecular Psychiatry·2025Open Access
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·2025Open Access
Genetic risk effects on psychiatric disorders act in sets
2025· 1 citedOpen Access
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
UNC Libraries·2025Open Access
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
Utrecht University Repository (Utrecht University)·2025Open Access
Functional consequences of genetic risk for neuropsychiatric conditions at chr22q
2025· 1 citedOpen Access
page 1 of 31Next →

Frequent Co-authors

Ole Mors(31), Preben Bo Mortensen(30), David M. Hougaard(28), Merete Nordentoft(24), Thomas Werge(23), Jonas Bybjerg‐Grauholm(21), Jakob Grove(19), Mark J. Daly(18), Ditte Demontis(17), Manuel Mattheisen(16), Esben Agerbo(16), Benjamin M. Neale(16), Stephan Ripke(14), Thomas D. Als(13), Marie Bækvad‐Hansen(13), Carsten Bøcker Pedersen(13), Ole A. Andreassen(12), Hreinn Stefánsson(11), Raymond K. Walters(10), Patrick F. Sullivan(10)