Børglum, Anders D.

Genome-wide scans using archived neonatal dried blood spot samples

Hollegaard, M. V., Grauholm, J., Børglum, A., Nyegaard, M., Nørgaard-Pedersen, B., Ørntoft, T., Mortensen, P. B., Wiuf, C., Mors, O., Didriksen, M., et al. (2009) · BMC Genomics

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 89

Common risk variants identified in autism spectrum disorder

Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory)

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 89

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

Hollegaard, M. V., Grove, J., Grauholm, J., Kreiner-Møller, E., Bønnelykke, K., Nørgaard, M., Benfield, T. L., Nørgaard-Pedersen, B., Mortensen, P. B., Mors, O., et al. (2011) · BMC Genetics

Genetic Associations and EpidemiologyGenetic diversity and population structure

Cited by 83

The Etiology of Multiple Sclerosis: Genetic Evidence for the Involvement of the Human Endogenous Retrovirus HERV-Fc1

Nexø, B. A., Christensen, T., Frederiksen, J., Møller-Larsen, A., Oturai, A. B., Villesen, P., Hansen, B., Nissen, K. K., Laska, M. J., Petersen, T. S., et al. (2011) · PLoS ONE

Multiple Sclerosis Research StudiesGenetic Associations and Epidemiology

Cited by 83

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

Martin, J., Khramtsova, E. A., Goleva, S. B., Blokland, G. A. M., Traglia, M., Walters, R. K., Hübel, C., Coleman, J. R. I., Breen, G., Børglum, A. D., et al. (2021) · Biological Psychiatry

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 79

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

Starnawska, A., Tan, Q., McGue, M., Mors, O., Børglum, A. D., Christensen, K., Nyegaard, M., & Christiansen, L. (2017) · Frontiers in Aging Neuroscience

Epigenetics and DNA MethylationDementia and Cognitive Impairment Research

Cited by 54

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Demontis, D., Walters, R. K., Rajagopal, V. M., Waldman, I. D., Grove, J., Als, T. D., Dalsgaard, S., Ribasés, M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., et al. (2021) · Nature Communications

Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology

Cited by 50

Investigating the causal relationship between neuroticism and depression via Mendelian randomization

Speed, D., Hemani, G., Speed, M. S., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Børglum, A. D., & Østergaard, S. D. (2019) · Acta Psychiatrica Scandinavica

Genetic Associations and EpidemiologyPersonality Traits and Psychology

Cited by 38

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

Moses, M., Tiego, J., Demontis, D., Bragi Walters, G., Stefansson, H., Stefansson, K., Børglum, A. D., Arnatkeviciute, A., & Bellgrove, M. A. (2022) · Molecular Psychiatry

Attention Deficit Hyperactivity DisorderCognitive Abilities and Testing

Cited by 31

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

Rajkumar, A. P., Christensen, J. H., Mattheisen, M., Jacobsen, I., Bache, I., Pallesen, J., Grove, J., Qvist, P., McQuillin, A., Gurling, H. M., et al. (2015) · Bipolar Disorders

Bipolar Disorder and TreatmentSchizophrenia research and treatment

Cited by 24

Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1+/− mice

Qvist, P., Eskildsen, S. F., Hansen, B., Baragji, M., Ringgaard, S., Roovers, J., Paternoster, V., Molgaard, S., Corydon, T. J., Stødkilde-Jørgensen, H., et al. (2018) · Scientific Reports

Schizophrenia research and treatmentNeurotransmitter Receptor Influence on Behavior

Cited by 23

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology

Demontis, D., Duan, J., Hsu, Y.-H. H., Pintacuda, G., Grove, J., Nielsen, T. T., Thirstrup, J., Martorana, M., Botts, T., Satterstrom, F. K., et al. (2026) · Nature

Attention Deficit Hyperactivity DisorderGenetics and Neurodevelopmental Disorders

Cited by 17