Børglum, A. D., Flint, T., Tommerup, N., Fleckner, J.
, Justesen, J. & Kruse, T. A. (1996).
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32.
Cytogenetic and Genome Research,
73(1-2), 99-103.
Børglum, A. D., Demontis, D., Grove, J., Pallesen, J., Hollegaard, M. V.
, Pedersen, C. B., Hedemand, A., Mattheisen, M., Uitterlinden, A.
, Nyegaard, M., Orntoft, T., Wiuf, C., Didriksen, M., Nordentoft, M., Nöthen, M. M., Rietschel, M., Ophoff, R. A., Cichon, S., Yolken, R. H. ... GROUP Investigators (2014).
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.
Molecular Psychiatry,
Mar;19(3), 325-33.
https://doi.org/10.1038/mp.2013.2
Borbye-Lorenzen, N.
, Zhu, Z., Agerbo, E., Albiñana, C., Benros, M. E., Bian, B.
, Børglum, A. D., Bulik, C. M.
, Debost, J.-C. P. G., Grove, J., Hougaard, D. M., McRae, A. F.
, Mors, O., Mortensen, P. B., Musliner, K. L., Nordentoft, M.
, Petersen, L. V., Privé, F., Sidorenko, J.
... McGrath, J. J. (2023).
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders.
Cell Genomics,
3(12), 100457. Article 100457.
https://doi.org/10.1016/j.xgen.2023.100457
Bolund, L., Brunak, S., Brünner, N.
, Børglum, A., Pedersen, O. B., Danielsen, I., Flindt, E. N., Hansen, T., Jespersen, J., Kristiansen, K., Olesen, P., Sørensen, T.
& Ørntoft, T. F. (2015).
Paradigmeskifte i dansk sundhedsvidenskab: Nye muligheder i diagnostik og behandling.
Videnskab.dk.
Bolund, A. C. S., Starnawska, A., Miller, M. R.
, Schlünssen, V., Backer, V.
, Børglum, A. D., Christensen, K., Tan, Q.
, Christiansen, L. & Sigsgaard, T. (2017).
Lung function discordance in monozygotic twins and associated differences in blood DNA methylation.
Clinical Epigenetics (Print),
9(1), 132. Article 132.
https://doi.org/10.1186/s13148-017-0427-2
Blokland, G. A. M.
, Grove, J., Chen, C. Y., Cotsapas, C., Tobet, S., Handa, R., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Sex Differences Cross-Disorder Analysis Group of the Psychiatric Genomics Consortium & iPSYCH (2022).
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biological Psychiatry,
91(1), 102-117.
https://doi.org/10.1016/j.biopsych.2021.02.972
Blechingberg, J., Holm, I. E.
, Johansen, M. G., Børglum, A. & Nielsen, A. L. (2010).
Aromatic l-amino acid decarboxylase expression profiling and isoform detection in the developing porcine brain.
Brain Research,
1308, 1-13.
https://doi.org/10.1016/j.brainres.2009.10.051
Björkman, A.
, Qvist, P., Du, L., Bartish, M., Zaravinos, A., Georgiou, K.
, Børglum, A., Gatti, R. A., Törngren, T. & Pan-Hammerström, Q. (2015).
Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells.
Proceedings of the National Academy of Sciences,
112(7), 2157-2162.
https://doi.org/10.1073/pnas.1418947112
Bjarkam, C., Corydon, T., Olsen, I., Pallesen, J., Nyegaard, M., Fryland, T., Mors, O. & Børglum, A. (2009).
Further immunohistochemical characterization of BRD1 a new susceptibility gene for schizophrenia and bipolar affective disorder.
Brain Structure and Function (Print Edition),
214(1), 37-47.
https://doi.org/10.1007/s00429-009-0219-3
Besenbacher, S., Liu, S., Izarzugaza, J. M. G.
, Grove, J., Belling, K., Bork-Jensen, J., Huang, S.
, Als, T. D., Li, S., Yadav, R., Rubio-García, A.
, Lescai, F., Demontis, D., Rao, J., Ye, W.
, Mailund, T., Møllegaard Friborg, R., Pedersen, C. N. S., Xu, R. ... Rasmussen, S. (2015).
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios.
Nature Communications,
6, Article 5969.
https://doi.org/10.1038/ncomms6969
Bentzon, D. N., Nyegaard, M., Børglum, A., Ørntoft, T. F., Borre, M. & Dalsgaard Sørensen, K. (2012).
Replication of Prostate Cancer Risk Variants in a Danish Case-Control Association Study.
Open Journal of Urology,
2(2), 45-54.
https://doi.org/10.4236/oju.2012.22009
Benros, M. E.
, Trabjerg, B. B., Meier, S., Mattheisen, M., Mortensen, P. B., Mors, O., Børglum, A. D., Hougaard, D. M., Nørgaard-Pedersen, B., Nordentoft, M.
& Agerbo, E. (2016).
Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia.
Biological Psychiatry,
80(8), 609–616.
https://doi.org/10.1016/j.biopsych.2016.04.008
Bauer, A. E.
, Liu, X., Byrne, E. M., Sullivan, P. F., Wray, N. R.
, Agerbo, E., Nyegaard, M., Grove, J., Musliner, K. L., Ingstrup, K. G., Johannsen, B. M. W., Mægbæk, M. L., Wang, Y., Nordentoft, M.
, Mors, O., Børglum, A. D., Werge, T., Hougaard, D. M.
, Mortensen, P. B. ... Meltzer-Brody, S. (2019).
Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders.
Translational Psychiatry,
9(1), 288. Article 288.
https://doi.org/10.1038/s41398-019-0629-9
Barbu, M. C., Zeng, Y., Shen, X., Cox, S. R., Clarke, T.-K., Gibson, J., Adams, M. J., Johnstone, M., Haley, C. S., Lawrie, S. M., Deary, I. J., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, McIntosh, A. M. & Whalley, H. C. (2019).
Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank.
Biological psychiatry. Cognitive neuroscience and neuroimaging,
4(1), 91-100.
https://doi.org/10.1016/j.bpsc.2018.07.006
Bang Madsen, K., Liu, X., Albiñana, C., Jóhann Vilhjálmsson, B., Agerbo, E., Mortensen, P. B., Hougaard, D. M., Nordentoft, M., Werge, T.
, Mors, O., Børglum, A. D. & Munk-Olsen, T. (2023).
Genetic liability to posttraumatic stress disorder and its association with postpartum depression.
Psychological Medicine,
53(11), 5052-5059.
https://doi.org/10.1017/S0033291722002045
Bak, S. T., Staunstrup, N. H., Starnawska, A., Daugaard, T. F., Nyegaard, M., Nyengaard, J. R., Børglum, A., Mors, O., Dorph-Petersen, K.-A. & Nielsen, A. L. (2015).
Evaluating the Usability of Long-Term Stored Human Brain Bank Tissue for the Analysis of Epigenetic Markers. Poster session presented at Psykiatriens 10. forskningsdag, Risskov, Denmark.
Bak, S. T., Staunstrup, N. H., Starnawska, A., Daugaard, T. F., Nyengaard, J. R., Nyegaard, M., Børglum, A., Mors, O., Dorph-Petersen, K.-A. & Nielsen, A. L. (2018).
Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples.
Molecular Neurobiology,
55(1), 668-681.
https://doi.org/10.1007/s12035-016-0345-x
Backlund, L., Rosvall, L.
, Mors, O., Kockum, I., Traskman-Bendz, L., Frisén, L.
, Børglum, A., Mortensen, P., Isacsson, G., Agren, H., Schalling, M. & Osby, U. (2005).
Association between g72 haplotypes and bipolar disorder in a nordic sample. Abstract from Association between g72 haplotypes and bipolar disorder in a nordic sample.
Appadurai, V., Bybjerg-Grauholm, J., Krebs, M. D., Rosengren, A., Buil, A., Ingason, A.
, Mors, O., Børglum, A. D., Hougaard, D. M., Nordentoft, M.
, Mortensen, P. B., Delaneau, O., Werge, T. & Schork, A. J. (2023).
Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks.
Communications Biology,
6(1), Article 101.
https://doi.org/10.1038/s42003-023-04477-y
Andlauer, T. F. M., Guzman-Parra, J., Streit, F., Strohmaier, J., González, M. J., Gil Flores, S., Cabaleiro Fabeiro, F. J., Del Río Noriega, F., Perez, F. P., Haro González, J., Orozco Diaz, G., de Diego-Otero, Y., Moreno-Küstner, B., Auburger, G., Degenhardt, F., Heilmann-Heimbach, S., Herms, S., Hoffmann, P., Frank, J. ... Bipolar Disorder Working Group of the Psychiatric Genomics Consortium (2021).
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
Molecular Psychiatry,
26(4), 1286-1298.
https://doi.org/10.1038/s41380-019-0558-2
Andersen, P. S., Havndrup, O., Bundgaard, H., Moolman-Smook, J. C., Larsen, L. A.
, Mogensen, J., Brink, P. A.
, Børglum, A. D., Corfield, V. A., Kjeldsen, K., Vuust, J. & Christiansen, M. (2001).
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
Journal of Medical Genetics,
38(12), E43.
Als, T. D., TH, J.
, Børglum, A., Petersen, PA.
, Mors, O. & Wang, AG. (2006).
Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands.
Eur J Hum Genet,
14, 497-504.
Als, T. D., Dahl, HA.
, Wikman, F., Zacharov, T. F., Wang, AG., Marcheco-Teruel, B.
, Ørntoft, T. F., Børglum, A., Vang, M., Kruse, TA.
& Mors, O. (2006).
Cryptic Relatedness among cases and controls in two isolated populations. In
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics (Vol. 141B, pp. 744-744)
Als, T. D., Lescai, F., Dahl, H. A.
, Grove, J., Demontis, D., Wang, A. G., Andorsdottir, G., Biskopstø, M., Johansen, O.
, Nyegaard, M., Bolund, L., Mors, O., Wang, J.
& Børglum, A. (2014).
Population Structure & Cryptic Relatedness of the isolated Population of the Faroe Islands. Poster session presented at XXII World Congress of Psychiatric Genetics, København, Denmark.
Als, T. D., Lescai, F., Dahl, H.
, Demontis, D., Wang, A., Andorsdottir, G., Biskopstø, M., Johansen, O.
, Grove, J., Nyegaard, M., Bolund, L., Mors, O., Jun, W.
& Børglum, A. (2015).
Identifying Rare Variation in Cases of Schizophrenia in the Isolated Population of the Faroe Islands using Whole-genome Sequencing. Poster session presented at XXIII World Congress of Psychiatric Genetics, Toronto, Canada.
Als, T. D., Kurki, M. I.
, Grove, J., Voloudakis, G., Therrien, K., Tasanko, E.
, Nielsen, T. T., Naamanka, J., Veerapen, K., Levey, D. F., Bendl, J., Bybjerg-Grauholm, J., Zeng, B.
, Demontis, D., Rosengren, A., Athanasiadis, G., Bækved-Hansen, M.
, Qvist, P., Bragi Walters, G.
... Børglum, A. D. (2023).
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Nature Medicine,
29(7), 1832-1844.
https://doi.org/10.1038/s41591-023-02352-1
Allesøe, R. L., Nudel, R., Thompson, W. K., Wang, Y., Nordentoft, M.
, Børglum, A. D., Hougaard, D. M., Werge, T., Rasmussen, S. & Benros, M. E. (2022).
Deep learning-based integration of genetics with registry data for stratification of schizophrenia and depression.
Science Advances,
8(26), eabi7293. Article eabi7293.
https://doi.org/10.1126/sciadv.abi7293
Alderton, G. K., Joenje, H., Varon, R.
, Børglum, A., Jeggo, P. A. & O'Driscoll, M. (2004).
Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.
Human Molecular Genetics,
13(24), 3127-38.
https://doi.org/10.1093/hmg/ddh335
Albiñana, C., Grove, J., McGrath, J. J., Agerbo, E., Wray, N. R., Bulik, C. M., Nordentoft, M., Hougaard, D. M., Werge, T.
, Børglum, A. D., Mortensen, P. B., Privé, F. & Vilhjálmsson, B. J. (2021).
Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction.
American Journal of Human Genetics,
108(6), 1001-1011.
https://doi.org/10.1016/j.ajhg.2021.04.014
Albiñana, C., Zhu, Z., Borbye-Lorenzen, N., Boelt, S. G., Cohen, A. S., Skogstrand, K., Wray, N. R., Revez, J. A.
, Privé, F., Petersen, L. V., Bulik, C. M.
, Plana-Ripoll, O., Musliner, K. L., Agerbo, E., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Werge, T.
, Mortensen, P. B. ... McGrath, J. J. (2023).
Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots.
Nature Communications,
14(1), Article 852.
https://doi.org/10.1038/s41467-023-36392-5
Albiñana, C., Zhu, Z., Schork, A. J., Ingason, A., Aschard, H.
, Brikell, I., Bulik, C. M.
, Petersen, L. V., Agerbo, E., Grove, J., Nordentoft, M., Hougaard, D. M., Werge, T.
, Børglum, A. D., Mortensen, P. B., McGrath, J. J., Neale, B. M.
, Privé, F. & Vilhjálmsson, B. J. (2023).
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores.
Nature Communications,
14(1), Article 4702.
https://doi.org/10.1038/s41467-023-40330-w
Albiñana, C., Zhu, Z., Borbye-Lorenzen, N., Boelt, S. G., Cohen, A. S.
, Skogstrand, K., Wray, N. R., Revez, J. A.
, Privé, F., Petersen, L. V., Bulik, C. M.
, Plana-Ripoll, O., Musliner, K. L., Agerbo, E., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Werge, T.
, Mortensen, P. B. ... McGrath, J. J. (2024).
Publisher Correction: Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots (Nature Communications, (2023), 14, 1, (852), 10.1038/s41467-023-36392-5).
Nature Communications,
15(1), Article 1741.
https://doi.org/10.1038/s41467-024-46199-7
Akingbuwa, W. A., Hammerschlag, A. R., Jami, E. S., Allegrini, A. G., Karhunen, V., Sallis, H., Ask, H., Askeland, R. B., Baselmans, B., Diemer, E., Hagenbeek, F. A., Havdahl, A., Hottenga, J.-J., Mbarek, H., Rivadeneira, F., Tesli, M., van Beijsterveldt, C., Breen, G., Lewis, C. M. ... and the Bipolar Disorder and Major Depressive Disorder Working Groups of the Psychiatric Genomics Consortium (2020).
Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42 998 Individuals: A Meta-analysis.
JAMA Psychiatry,
77(7), 715-728.
https://doi.org/10.1001/jamapsychiatry.2020.0527
Ahluwalia, T. S., Eliasen, A. U., Sevelsted, A., Pedersen, C.-E. T., Stokholm, J., Chawes, B., Bork-Jensen, J., Grarup, N., Pedersen, O., Hansen, T., Linneberg, A., Sharma, A., Weiss, S. T., Evans, M. D., Jackson, D. J., Morin, A., Krogfelt, K. A., Schjørring, S.
, Mortensen, P. B. ... Bønnelykke, K. (2020).
FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses.
Nature Communications,
11(1), Article 6398.
https://doi.org/10.1038/s41467-020-19814-6
Agerbo, E., Mortensen, P. B., Wiuf, C. H., Pedersen, MS., Hollegaard, M., Demiontis, D.
, Børglum, A., Hougaard, D.
, Mors, O. & Pedersen, CB. (2011).
Can SNP-variation across the whole-genome and across candidate genes explain the excess schizophrenia risk in offspring of parents with a severe psychiatric disorder?. Abstract from 13th International Congress on Schizophrenia Research (ICOSR), Colorado Springs, United States.
Agerbo, E., Sullivan, P. F.
, Vilhjálmsson, B. J., Pedersen, C. B., Mors, O., Børglum, A. D., Hougaard, D. M.
, Hollegaard, M. V., Meier, S., Mattheisen, M., Ripke, S., Wray, N. R.
& Mortensen, P. B. (2015).
Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.
J A M A Psychiatry.
https://doi.org/10.1001/jamapsychiatry.2015.0346
Agerbo, E., Trabjerg, B. B., Schork, A. J.
, Vilhjálmsson, B. J., Albiñana Climent, C., Wray, N. R., Werge, T.
, Børglum, A., Mors, O., Nordentoft, M., Hougaard, D.
, Musliner, K., Mortensen, P. B. & McGrath, J. J. (2019).
Absolute risk of major depression associated with the polygenic risk score for depression, parental socio-economic status and history of mental disorders: A danish population-based study . S87-S88. Abstract from World Congress of Psychiatric Genetics , Anaheim , California, United States.
Agerbo, E., Trabjerg, B. B., Børglum, A. D., Schork, A. J.
, Vilhjálmsson, B. J., Pedersen, C. B., Hakulinen, C., Albiñana, C., Hougaard, D. M.
, Grove, J., McGrath, J. J., Bybjerg-Grauholm, J.
, Mors, O., Plana-Ripoll, O., Werge, T., Wray, N. R.
, Mortensen, P. B. & Musliner, K. L. (2021).
Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status.
JAMA Psychiatry,
78(4), 387-397.
https://doi.org/10.1001/jamapsychiatry.2020.4172
Aarøe, L., Appadurai, V., Hansen, K. M., Schork, A. J., Werge, T.
, Mors, O., Børglum, A. D., Hougaard, D. M., Nordentoft, M.
, Mortensen, P. B., Thompson, W. K., Buil, A.
, Agerbo, E. & Petersen, M. B. (2021).
Genetic predictors of educational attainment and intelligence test performance predict voter turnout.
Nature Human Behavior,
5(2), 281-291.
https://doi.org/10.1038/s41562-020-00952-2