Demontis, D., Walters, G. B., Athanasiadis, G., Walters, R., Therrien, K.
, Nielsen, T. T., Farajzadeh, L., Voloudakis, G., Bendl, J., Zeng, B., Zhang, W.
, Grove, J., Als, T. D., Duan, J., Satterstrom, F. K., Bybjerg-Grauholm, J., Bækved-Hansen, M., Gudmundsson, O. O., Magnusson, S. H. ... ADHD Working Group of the Psychiatric Genomics Consortium (2023).
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
Nature Genetics,
55(2), 198-208.
https://doi.org/10.1038/s41588-022-01285-8
Del-Favero, J., Gestel, S. V.
, Børglum, A., Muir, W.
, Ewald, H., Mors, O., Ivezic, S., Oruc, L., Adolfsson, R., Blackwood, D., Kruse, T., Mendlewicz, J., Schalling, M. & Van Broeckhoven, C. (2002).
European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
European Journal of Human Genetics,
10(4), 276-80.
https://doi.org/10.1038/sj.ejhg.5200803
Deleuran, T.
, Olsen, I. M., Hansen, M. M.
, Zacharov, T. F., Børglum, A., Als, T. D. & Mors, O. (2008).
A significant association study of bipolar affective disorder on chrosome 12q24. Abstract from World Congress on Psychiatric Genetics XV, New York, United States.
Debost, J.-C., Petersen, L., Grove, J., Khashan, A.
, Henriksen, T., Mors, O., Hollegaard, M., Hougaard, D.
, Nyegaard, M., Børglum, A. & Mortensen, P. B. (2015).
Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia.
Psychoneuroendocrinology,
60, 18-27.
https://doi.org/10.1016/j.psyneuen.2015.05.013
Debost, J.-C., Debost, M.
, Grove, J., Mors, O., Hougaard, D. M.
, Børglum, A. D., Mortensen, P. B. & Petersen, L. (2017).
COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity.
Acta Psychiatrica Scandinavica,
136(1), 85-95.
https://doi.org/10.1111/acps.12761
Debost, J.-C. P. G., Thorsteinsson, E., Trabjerg, B., Benros, M. E.
, Albiñana, C., Vilhjalmsson, B. J., Børglum, A., Mors, O., Werge, T.
, Mortensen, P. B., Agerbo, E. & Petersen, L. (2022).
Genetic and psychosocial influence on the association between early childhood infections and later psychiatric disorders.
Acta Psychiatrica Scandinavica,
146(5), 406-419.
https://doi.org/10.1111/acps.13491
Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hämäläinen, E., Kajantie, E., Laivuori, H., Villa, P. M., Reynolds, R. M., Nystad, W., Håberg, S. E., London, S. J., O'Donnell, K. J., Garg, E., Meaney, M. J., Entringer, S., Wadhwa, P. D., Buss, C. ... Binder, E. B. (2019).
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns.
Nature Communications,
10, Article 2548.
https://doi.org/10.1038/s41467-019-10461-0
Corydon, T. J., Haagerup, A., Jensen, T. G., Binderup, H. G., Petersen, M. S.
, Kaltoft, K., Vestbo, J., Kruse, T. A.
& Børglum, A. (2007).
A functional CD86 polymorphism associated with asthma and related allergic disorders.
J Med. Genet,
8(44), 509-15.
Christensen, U., Haagerup, A., Binderup, H., Vestbo, J., Kruse, T.
& Børglum, A. D. (2006).
Family based association analysis of the IL2 and IL15 genes in allergic disorders.
Eur J Hum Genet,
14, 227-235.
Christensen, U., Møller-Larsen, S., Nyegaard, M., Haagerup, A., Hedemand, A., Brasch-Andersen, C., Kruse, T.
, Corydon, T. J., Deleuran, M. & Børglum, A. (2009).
Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21.
Human Genetics,
126(4), 549-557.
Christensen, J. H., Elfving, B., Müller, H. K., Fryland, T., Nyegaard, M., Corydon, T. J., Nielsen, A. L., Mors, O., Wegener, G. & Børglum, A. (2012).
The schizophrenia and bipolar disorder associated Brd1 gene is regulated upon chronic restraint stress.
European Neuropsychopharmacology,
22(9), 651-656.
Christensen, K. J.
, Dreier, J. W., Skotte, L., Feenstra, B.
, Grove, J., Børglum, A., Mitrovic, M., Cotsapas, C.
& Christensen, J. (2021).
Birth characteristics and risk of febrile seizures.
Acta Neurologica Scandinavica,
144(1), 51-57.
https://doi.org/10.1111/ane.13420
Christensen, K. J.
, Dreier, J. W., Skotte, L., Feenstra, B.
, Grove, J., Børglum, A. D., Mitrovic, M., Cotsapas, C.
& Christensen, J. (2022).
Seasonal Variation and Risk of Febrile Seizures: A Danish Nationwide Cohort Study.
Neuroepidemiology,
56(2), 138-145.
https://doi.org/10.1159/000522065
Calle Sánchez, X., Helenius, D., Bybjerg-Grauholm, J.
, Pedersen, C., Hougaard, D. M.
, Børglum, A. D., Nordentoft, M.
, Mors, O., Mortensen, P. B., Geschwind, D. H., Montalbano, S., Raznahan, A., Thompson, W. K., Ingason, A. & Werge, T. (2022).
Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.
JAMA Psychiatry,
79(1), 59-69.
https://doi.org/10.1001/jamapsychiatry.2021.3392
Cabana-Domínguez, J., Llonga, N., Arribas, L., Alemany, S., Vilar-Ribó, L.
, Demontis, D., Fadeuilhe, C., Corrales, M., Richarte, V.
, Børglum, A. D., Ramos-Quiroga, J. A., Soler Artigas, M. & Ribasés, M. (2023).
Transcriptomic risk scores for attention deficit/hyperactivity disorder.
Molecular Psychiatry,
28(8), 3493-3502.
https://doi.org/10.1038/s41380-023-02200-1
Bybjerg-Grauholm, J., Hagen, C. M., Gonçalves, V. F., Bækvad-Hansen, M.
, Hansen, C. S., Hedley, P. L.
, Kanters, J. K., Nielsen, J., Theisen, M.
, Mors, O., Kennedy, J.
, Als, T. D., Demur, A. B., Nordentoft, M.
, Børglum, A., Mortensen, P. B., Werge, T. M., Hougaard, D. M.
& Christiansen, M. (2018).
Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes.
PLOS ONE,
13(12), Article e0208829.
https://doi.org/10.1371/journal.pone.0208829
Buttenschøn, H. N., Als, T. D., Daoud, A. E., Foldager, L., Wang, AG.
, Børglum, A., Kruse, TA., Lauritsen, MB.
& Mors, O. (2005).
The glutamate decarboxylase gene 1 as a potential candidate gene for autism.. Abstract from XIIIthWorld Congress on Psychiatric Genetics, The Westin Copley Place, Boston.
Buttenschøn, H. N., Lauritsen, M. B.
, Daoud, A. E., Hollegaard, M. V., Jørgensen, M.
, Tvedegaard, K. C., Hougaard, D. M.
, Børglum, A., Thorsen, P. & Mors, O. (2008).
A population based association study of GAD1 as a candidate gene for childhood autism. Poster session presented at The XV Wordl Congress of Psychiatric Genetics, New York, United States.
Buttenschøn, H. N., Lauritsen, M. B.
, Daoud, A. E., Hollegaard, M. V., Jørgensen, M.
, Tvedegaard, K. C., Hougaard, D. M.
, Børglum, A., Thorsen, P. & Mors, O. (2008).
A population based association study of GAD1 as a candidate gene for childhood autism. Poster session presented at Psykiatriens Forskningsdag, Risskov, Denmark.
Buttenschøn, H., Lauritsen, M.
, Daoud, A., Hollegaard, M., Jørgensen, M., Tvedegaard, K., Hougaard, D.
, Børglum, A., Thorsen, P. & Mors, O. (2009).
A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism.
Journal of Neural Transmission,
116(3), 381-388.
https://doi.org/10.1007/s00702-008-0142-4
Buttenschøn, H. N., Foldager, L., Zacharov, T. F., Olsen, I. M. L., Deleuran, T.
, Nyegaard, M., Hansen, M. M., Kallunki, P., Christensen, K. V., Blackwood, D. H., Muir, W. J., Straarup, S. E.
, Als, T. D., Nordentoft, M.
, Børglum, A. & Mors, O. (2010).
Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3.
Psychiatric Genetics,
20(3), 93-101.
https://doi.org/10.1097/YPG.0b013e32833a2066
Buttenschøn, H. N., Buch, H. N., Kristensen, A. S., Thomsen, JF., Mikkelsen, S., Bonde, JP., Kolsted, H., Kærlev, L., Kærgaard, A., Andersen, JH., Hansen, AM., Rugulies, R.
, Grynderup, M., Nygaard, KB., Boe, MH., Koefoed, P.
, Børglum, A., Erhardt, A., Woldby, D.
& Mors, O. (2010).
The norepinephrine transporter gene: a candidate gene for panic disorder.
XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., 292-293.
Buttenschøn, H. N., Buch, H. N., Kristensen, A. S., F. Thomsen, J., Mikkelsen, S., Bonde, J. P.
, Kolstad, H., Kærlev, L., Kærgaard, A., H. Andersen, J., Hansen, Å. M., Rugulies, R.
, Grynderup, M., B. Nygaard, K., B. Oddershede, M., Koefoed, P.
, Børglum, A., Erhardt, A., Woldbye, D.
& Mors, O. (2010).
Nordrenalin transportergenet er et kandidatgen for panikangst. Poster session presented at Psykiatriens 5. Forskningsdag, Risskov, Denmark.
Buttenschøn, H. N., Kristensen, A. S., Buch, H. N., Andersen, J. H., Bonde, J. P., Grynderup, M., Hansen, A. M., Kolstad, H., Kaergaard, A.
, Kaerlev, L., Mikkelsen, S., Thomsen, J. F.
, Koefoed, P., Erhardt, A.
, Woldbye, D. P. D., Børglum, A. D. & Mors, O. (2011).
The norepinephrine transporter gene is a candidate gene for panic disorder.
Journal of neural transmission (Vienna, Austria : 1996),
118(6), 969-976.
https://doi.org/10.1007/s00702-011-0624-7
Buttenschøn, H. N., Buch, H. N., Kristensen, A. S., Thomsen, J. F., Mikkelsen, S., Bonde, J. P.
, Kolstad, H., Kærlev, L., Kærgaard, A., Andersen, J., Hansen, A. M., Rugulies, R. E.
, Grynderup, M., Nygaard, K. B., Boe, M. H., Koefoed, P.
, Børglum, A., Erhardt, A., Woldbye, D.
& Mors, O. (2010).
The norepinephrine transporter gene: a candidate gene for panic disorder. Poster session presented at Dansk Psykiatrisk Selskabs Årsmøde 2011, Nyborg, Denmark.
Buttenschøn, H. N., Elfving, B., Foldager, L., Plougmann, P. H., Andersen, J. H., Bonde, J. P.
, Grynderup, M., Hansen, A. M.
, Kolstad, H., Kærgaard, A., Kærlev, L., Mikkelsen, S., Thomsen, J. F.
, Børglum, A., Wegener, G. & Mors, O. (2011).
Depression og Val66Met polymorfien påvirker serum BDNF niveauet. Poster session presented at Psykiatriens 6. Forskningsdag, Risskov, Denmark.
Buttenschøn, H. N., Flint, T. J.
, Foldager, L., Qin, P., Christoffersen, S., Hansen, N. F.
, Kristensen, I. B., Mortensen, P. B., Børglum, A. D. & Mors, O. (2013).
An association study of suicide and candidate genes in the serotonergic system.
Journal of Affective Disorders,
148(2-3), 291-8.
https://doi.org/10.1016/j.jad.2012.12.011
Buttenschøn, H. N., Jacobsen, I. S., Grynderup, M. B., Hansen, A. M.
, Kolstad, H. A., Kaerlev, L., Thomsen, J. F., Nordentoft, M., Silahtaroglu, A., Tommerup, N., Tümer, Z., Krogh, J.
, Børglum, A. D. & Mors, O. (2013).
An association study between the norepinephrine transporter gene and depression.
Psychiatric Genetics,
23(5), 217-221.
https://doi.org/10.1097/YPG.0000000000000003
Buttenschøn, H. N., Elfving, B., Foldager, L., Plougmann, P. H., Andersen, J. H.
, Grynderup, M. B., Kærgaard, A., Hansen, Å. M.
, Kolstad, H. A., Kærlev, L., Bonde, J. P., Mikkelsen, S., Thomsen, J. F.
, Børglum, A., Wegener, G. & Mors, O. (2013).
Depression and BMI influences the serum vascular endothelial growth factor level. Poster session presented at XXIst World Congress of Psychiatric Genetics, Boston, United States.
Buttenschøn, H. N., Demontis, D., Ollendorff, M. K., Elfving, B., Jensen, S. M., Gustafsen, C., Kærlev, L.
, Petersen, C. M., Børglum, A., Mors, O. & Pedersen, S. G. (2015).
Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF.
Translational Psychiatry,
5(e677).
https://doi.org/10.1038/tp.2015.167
Bulik-Sullivan, B. K., Loh, P.-R., Finucane, H. K., Ripke, S.
, Yang, J., Patterson, N., Daly, M. J., Price, A. L., Neale, B. M. & Schizophrenia Working Group of the Psychiatric Genomics Consortium (Anders Børglum and Ole Mors, members of -) (2015).
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Nature Genetics,
47(3), 291–295.
https://doi.org/10.1038/ng.3211
Bukowski, L., Chernomorchenko, A. M. F., Starnawska, A., Mors, O., Staunstrup, N. H., Børglum, A. D. & Qvist, P. (2020).
Neuropsin in mental health.
Journal of Physiological Sciences,
70(1), Article 26.
https://doi.org/10.1186/s12576-020-00753-2
Brikell, I., Wimberley, T., Albiñana, C., Pedersen, E. M., Vilhjálmsson, B. J., Agerbo, E., Demontis, D., Børglum, A. D., Schork, A. J., LaBianca, S., Werge, T.
, Mors, O., Hougaard, D. M., Thapar, A.
, Mortensen, P. B. & Dalsgaard, S. (2021).
Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD.
American Journal of Psychiatry,
178(9), 854-864.
https://doi.org/10.1176/appi.ajp.2020.20121686
Brikell, I., Wimberley, T., Albiñana, C., Vilhjálmsson, B. J., Agerbo, E., Børglum, A. D., Demontis, D., Schork, A. J., LaBianca, S., Werge, T., Hougaard, D. M., Nordentoft, M.
, Mors, O., Mortensen, P. B., Petersen, L. V. & Dalsgaard, S. (2023).
Interplay of ADHD Polygenic Liability With Birth-Related, Somatic, and Psychosocial Factors in ADHD: A Nationwide Study.
The American Journal of Psychiatry (Spanish Edition),
180(1), 73-88.
https://doi.org/10.1176/appi.ajp.21111105
Brasch-Andersen, C.
, Haagerup, A., Børglum, A. D., Vestbo, J. & Kruse, T. (2006).
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases.
J Med. Genet,
43, e10.
Brasch-Andersen, C., Tan, Q.
, Børglum, A. D., Haagerup, A., Larsen, T. R., Vestbo, J. & Kruse, T. (2006).
Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene.
Thorax,
61, 874-79.
Børglum, A., Kirov, G., Craddock, N.
, Mors, O., Muir, W., Murray, V., McKee, I., Collier, D. A.
, Ewald, H., Owen, M. J., Blackwood, D. & Kruse, T. A. (2003).
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
117B(1), 18-22.
Børglum, A., Nyegaard, M., Kvistgaard, AB., Mullaart, E., Uitterlinden, AG., Vijg, J. & Kruse, T. A. (1997).
Mapping of 34 minisatellite loci resolved by two-dimensional DNA typing. Cytogenetic and Genome Research,
79(3-4), 248-56.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=9605866&query_hl=1&itool=pubmed_docsum
Børglum, A., Vernesi, C.
, Jensen, P. K. A., Madsen, B., Haagerup, A. & Barbujani, G. (2007).
No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy.
American Journal of Physical Anthropology,
132(2), 278-84.
https://doi.org/10.1002/ajpa.20509
Børglum, A. D., Balslev, T., Haagerup, A., Birkebaek, N., Binderup, H., Kruse, T. A.
& Hertz, J. M. (2001).
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
European Journal of Human Genetics,
9(10), 753-7.
https://doi.org/10.1038/sj.ejhg.5200701
Børglum, A. D., Hampson, M.
, Kjeldsen, T. E., Muir, W., Murray, V.
, Ewald, H., Mors, O., Blackwood, D. & Kruse, T. A. (2001).
Dopa decarboxylase genotypes may influence age at onset of schizophrenia.
Molecular Psychiatry,
6(6), 712-7.
https://doi.org/10.1038/sj.mp.4000902
Børglum, A. D., Bruun, T. G.
, Kjeldsen, T. E., Ewald, H., Mors, O., Kirov, G., Russ, C., Freeman, B., Collier, D. A. & Kruse, T. A. (1999).
Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder.
Molecular Psychiatry,
4(6), 545-51.
Børglum, A. D., Byskov, A., Ragno, P., Roldan, A. L., Tripputi, P., Cassani, G., Danø, K., Blasi, F.
, Bolund, L. & Kruse, T. A. (1992).
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2.
American Journal of Human Genetics,
50(3), 492-7.
Børglum, A. D., Mullaart, E., Kvistgaard, A. B., Uitterlinden, A. G., Vijg, J. & Kruse, T. A. (1995).
Two-dimensional DNA typing as a genetic marker system in humans.
Cytogenetic and Genome Research,
71(3), 260-5.
Børglum, A. D., Flint, T., Madsen, P. S., Celis, J. E. & Kruse, T. A. (1995).
Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21.
Human Genetics,
96(5), 592-6.