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., 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.
Horjales, E., Demontis, D., Lund, E. K.
, Vase, L., Finnerup, N. B., Børglum, A. D., Jensen, T. S. & Svensson, P. (2013).
Emotional modulation of muscle pain is associated with polymorphisms in the serotonin transporter gene.
Pain,
154(8), 1469-1476.
https://doi.org/10.1016/j.pain.2013.05.011
Børglum, A., Mors, O., Nyegaard, M., Christensen, J. H., Qvist, P., Rajkumar, A. P. & Wegener, G. (2013).
Heterozygous mouse with an inactivated brd1 allele and uses in psychiatry. (Patent No.
PCT/EP2013/069524).
https://patents.google.com/patent/WO2014044777A1/it
Grove, J., Foldager, L., Demontis, D., Hollegaard, M. V.
, Pedersen, C. B., Yolken, R. H., Hougaard, D. M.
, Mors, O., Mortensen, P. B., The Psychiatric Genomics Consortium – Schizophrenia
& Børglum, A. (2013).
Interaction between polygenic scores for schizophrenia and infection by herpes simples virus 1 and 2. Poster session presented at XXIst World Congress of Psychiatric Genetics, Boston, United States.
Horjales, E., Demontis, D., Lund, E. K.
, Finnerup, N. B., Børglum, A. D., Jensen, T. S., Svensson, P. & Vase, L. (2013).
Polymorphism in Serotonin Receptor 3B Is Associated with Pain Catastrophizing.
PLoS One,
8(11), Article e78889.
https://doi.org/10.1371/journal.pone.0078889
Harsløf, T., Frost, M., Nielsen, T. L.
, Husted, L. B., Nyegaard, M., Brixen, K.
, Børglum, A. D., Mosekilde, L., Andersen, M.
, Rejnmark, L. & Langdahl, B. L. (2013).
Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians.
Calcified Tissue International,
92(5), 467-76.
https://doi.org/10.1007/s00223-013-9702-1
Kruse, L. V., Nyegaard, M., Christensen, U., Møller-Larsen, S., Haagerup, A., Deleuran, M., Hansen, L. G., Venø, S. K., Goossens, D., Del-Favero, J.
& Børglum, A. D. (2012).
A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families.
European Journal of Human Genetics,
20(9), 965-72.
https://doi.org/10.1038/ejhg.2012.46
Gregersen, N., Dahl, H. A.
, Buttenschøn, H. N., Nyegaard, M., Hedemand, A., Als, T. D., Wang, A. G., Joensen, S., Woldbye, D. P., Koefoed, P.
, Kristensen, A. S., Kruse, T. A.
, Børglum, A. D. & Mors, O. (2012).
A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.
European Journal of Human Genetics,
20(1), 84-90.
https://doi.org/10.1038/ejhg.2011.148
Gregersen, N., Buttenschøn, H. N., Hedemand, A., Dahl, H. A.
, Kristensen, A. S., Joensen, S., Woldbye, D. P. D., Kofoed, P., Erhardt, A., Kruse, T. A., Wang, A. G.
, Børglum, A. & Mors, O. (2012).
Are TMEM genes potential candidate genes for panic disorder?. Poster session presented at XX World Congress of Psychiatric Genetics, Hamburg, Germany.
Rietschel, M., Mattheisen, M., Degenhardt, F., Kahn, R. S., Linszen, D. H., Os, J. V., Wiersma, D., Bruggeman, R., Cahn, W., de Haan, L., Krabbendam, L., Myin-Germeys, I., Mühleisen, T. W., Kirsch, P., Esslinger, C., Herms, S.
, Demontis, D., Steffens, M., Strohmaier, J. ... Cichon, S. (2012).
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.
Molecular Psychiatry,
17(9), 906–917.
https://doi.org/10.1038/mp.2011.80Elfving, B., Buttenschøn, H. N., Foldager, L., Poulsen, P. H. P., Andersen, J. H.
, Grynderup, M. B., Hansen, A. M.
, Kolstad, H. A., Kaerlev, L., Mikkelsen, S., Thomsen, J. F.
, Børglum, A. D., Wegener, G. & Mors, O. (2012).
Depression, the Val66Met polymorphism, age, and gender influence the serum BDNF level.
Journal of Psychiatric Research,
46(9), 1118-1125.
https://doi.org/10.1016/j.jpsychires.2012.05.003
Petersen, M., Andersen, J., Jimenez-Solem, E., Broedbaek, K.
, Afzal, S., Nyegaard, M., Børglum, A. D., Stender, S., Torp-Pedersen, C. T., Køber, L. V. & Poulsen, H. (2012).
Effect of specific ADRB1/ADRB2/AGT genotype combinations on the association between survival and carvedilol treatment in chronic heart failure: a substudy of the ECHOS trial.
Pharmacogenetics and Genomics,
22(10), 709-715.
https://doi.org/10.1097/FPC.0b013e3283540286
Fryland, T., Elfving, B., Christensen, J. H., Mors, O., Wegener, G. & Børglum, A. (2012).
Electroconvulsive Seizures Regulates the Brd1 Gene in the Frontal Cortex and Hippocampus of the Adult Rat.
Neuroscience Letters,
516(1), 110-113.
https://doi.org/10.1016/j.neulet.2012.03.069
Gregersen, N., Buttenschøn, H. N., Hedemand, A., Kristensen, A. S., Joensen, S.
, Woldbye, D. P. D., Koefoed, P., Erhardt , A., Dahl, HA., Wang, A. G.
, Børglum, A. & Mors, O. (2012).
Er TMEM-gener kandidatgener for panikangst?. Poster session presented at Psykiatriens 7. Forskningsdag, Risskov, Denmark.
Saetre, P.
, Grove, J., Børglum, A., Mors, O., Werge, T. M., Andreassen, O. A., Vares, M., Agartz, I., Terenius, L. & Jönsson, E. G. (2012).
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
159B(8).
Nyegaard, M., Overgaard, M. T., Søndergaard, M., Vranas, M., Behr, E. R., Hildebrandt, L., Lund, J., Hedley, P. L., Camm, A. J., Wettrell, G., Fosdal, I., Christiansen, M.
& Børglum, A. D. (2012).
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
American Journal of Human Genetics,
91(4), 703-12.
https://doi.org/10.1016/j.ajhg.2012.08.015
Nyegaard, M., Demontis, D., Thestrup, B. B., Hedemand, A., Sørensen, K. M., Hansen, T., Werge, T., Hougaard, D. M., Yolken, R. H.
, Mortensen, P. B., Mors, O. & Børglum, A. D. (2012).
No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia.
Psychiatric Genetics,
22(3), 146-8.
https://doi.org/10.1097/YPG.0b013e328353953c
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
Vassos, E., Steinberg, S., Cichon, S., Breen, G., Sigurdsson, E., Andreassen, O. A., Djurovic, S., Morken, G., Grigoroiu-Serbanescu, M., Diaconu, C. C., Czerski, P. M., Hauser, J., Babadjanova, G., Abramova, L. I., Mühleisen, T. W., Nöthen, M. M., Rietschel, M., McGuffin, P., Clair, D. S. ... GROUP Consortium (2012).
Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder.
Biological Psychiatry,
72(8), 645-650.
https://doi.org/10.1016/j.biopsych.2012.02.040Pedersen, C. B., Demontis, D., Pedersen, M. S., Agerbo, E., Mortensen, P. B., Børglum, A., Hougaard, D. M., Hollegaard, M. V.
, Mors, O. & Cantor-Graae, E. (2012).
Risk of schizophrenia in relation to parental origin and genome-wide divergence.
Psychological Medicine,
42(7), 1515-1521.
https://doi.org/10.1017/S0033291711002376
Pedersen, M. S., Benros, M. E.
, Agerbo, E., Børglum, A. D. & Mortensen, P. B. (2012).
Schizophrenia in patients with atopic disorders with particular emphasis on asthma: A Danish population-based study.
Schizophrenia Research,
138(1), 58-62.
https://doi.org/10.1016/j.schres.2012.02.019
Demontis, D., Nyegaard, M., Christensen, J. H., Severinsen, J., Hedemand, A., Hansen, T., Werge, T.
, Mors, O. & Børglum, A. D. (2012).
The gene encoding the melanin-concentrating hormone receptor 1 is associated with schizophrenia in a Danish case-control sample.
Psychiatric Genetics,
22(2), 62-9.
https://doi.org/10.1097/YPG.0b013e32834dc424
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.
Petersen, M., Andersen, J. T., Hjelvang, B. R., Broedbaek, K., Afzal, S.
, Nyegaard, M., Børglum, A. D., Stender, S., Køber, L. V., Torp-Pedersen, C. T. & Poulsen, H. E. (2011).
Association of beta-adrenergic receptor polymorphisms and mortality in carvedilol-treated chronic heart-failure patients.
British Journal of Clinical Pharmacology,
71(4), 556-565.
https://doi.org/10.1111/j.1365-2125.2010.03868.xDemontis, D., Nyegaard, M., Buttenschøn, H. N., Hedemand, A., Pedersen, C. B., Grove, J., Flint, T. J., Nordentoft, M., Werge, T., Hougaard, D. M., Sørensen, K. M., Yolken, R. H.
, Mors, O., Børglum, A. D. & Mortensen, P. B. (2011).
Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
156(8), 913-922.
https://doi.org/10.1002/ajmg.b.31234
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.
Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T.
, Børglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietiläinen, O. P. H.
, Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N. ... Irish Schizophrenia Genomics Consortium (2011).
Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia.
Human Molecular Genetics,
20(20), 4076-81.
https://doi.org/10.1093/hmg/ddr325Foldager, L., Pedersen, C. B., Nyegaard, M., Zacharov, T. F., Nordentoft, M., Werge, T., M. Hougaard, D., M. Sørensen, K.
, Mortensen, P. B., Mors, O. & Børglum, A. (2011).
Conditional Logic Regression: identifying SNP Interactions from Individually time-matched Case-Control Data. Poster session presented at PhD Day 2011, Aarhus University, Faculty of Health Sciences, Aarhus, Denmark.
Foldager, L., Pedersen, C. B., Nyegaard, M., Zacharov, T. F., Nordentoft, M., Werge, T., M. Hougaard, D., M. Sørensen, K.
, Mortensen, P. B., Mors, O. & Børglum, A. (2011).
Conditional Logic Regression: identifying SNP Interactions from Individually time-matched Case-Control Data. Poster session presented at Dansk Psykiatrisk Selskabs Årsmøde 2011, Nyborg, Denmark.
Qvist, P., Huertas, P., Jimeno, S.
, Nyegaard, M., Hassan, M. J., Jackson, S. P.
& Børglum, A. (2011).
CtIP Mutations Cause Seckel and Jawad Syndromes.
PLoS Genetics,
7(10), e1002310.
https://doi.org/10.1371/journal.pgen.1002310
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.
Van Schijndel, J. E., Van Zweeden, M., Van Loo, K. M. J., Djurovic, S., Andreassen, O. A., Werge, T.
, Nyegaard, M., Sørensen, K. M., Nordentoft, M.
, Mortensen, P. B., Mors, O., Børglum, A. D., Del-Favero, J., Norrback, K.-F., Adolfsson, R., Hert, M. D., Claes, S., Cichon, S., Rietschel, M. ... Pedersen, J. T. (2011).
Dual association of a TRKA polymorphism with schizophrenia.
Psychiatric Genetics,
21(3), 125-131.
https://doi.org/10.1097/YPG.0b013e3283437194Gregersen, N., Buttenschøn, H. N., Nyegaard, M., Dahl, H. A.
, Hedemand, A., Kristensen, A. S., Woldbye, D., Wang, A. G., Joensen, S., Kruse, T.
, Børglum, A. & Mors, O. (2011).
Er en PH sensitiv natriumkanal medvirkende til panikangst?. Poster session presented at Dansk Psykiatrisk Selskabs Årsmøde 2011, Nyborg, Denmark.
Steinberg, S.
, Mors, O., Børglum, A. D., Gustafsson, O., Werge, T.
, Mortensen, P. B., Andreassen, O. A., Sigurdsson, E.
, Thorgeirsson, T. E., Böttcher, Y., Olason, P., Ophoff, R. A., Cichon, S., Gudjonsdottir, I. H., Pietiläinen, O. P. H.
, Nyegaard, M., Tuulio-Henriksson, A., Ingason, A.
, Hansen, T. ... Genetic Risk and Outcome in Psychosis (2011).
Expanding the range of ZNF804A variants conferring risk of psychosis.
Molecular Psychiatry,
16(1), 59-66.
https://doi.org/10.1038/mp.2009.149Ripke, S., Sanders, A. R., Kendler, K. S., Levinson, D. F., Sklar, P., Holmans, P. A., Lin, D.-Y., Duan, J., Ophoff, R. A., Andreassen, O. A., Scolnick, E., Cichon, S., St Clair, D., Corvin, A., Gurling, H., Werge, T., Rujescu, D., Blackwood, D. H. R., Pato, C. N. ... The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (2011).
Genome-wide association study identifies five new schizophrenia loci.
Nature Genetics,
43(10), 969-976.
https://doi.org/10.1038/ng.940Grove, J., Demontis, D., Hollegaard, M. V., Pedersen, C. B., Ørntoft, T. F., Yolken, R., Didriksen, M., Hougaard, D.
, Wiuf, C. H., Mors, O., Mortensen, P. B. & Børglum, A. (2011).
Genome-Wide Significant Interaction by Cytomegalovirus with Respect to Risk of Schizophrenia. Poster session presented at XIX World Congress on Psychiatric Genetics, Washington DC, United States.
Haubek, D., Gjørup, H., Jensen, L. G., Juncker, I., Nyegaard, M., Børglum, A., Poulsen, S. & Hertz, J. M. (2011).
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a danish five-generation family with a novel FAM83H nonsense mutation.
International Journal of Paediatric Dentistry (Print),
21, 407-412.
https://doi.org/10.1111/j.1365-263X.2011.01142.x.
Gregersen, N., Buttenschøn, H. N., Dahl, HA.
, Foldager, L., Kristensen, A. S., Woldbye, D. P. D., Kofoed, P., Joensen, S., Kruse, T. A., Wang, A. G.
, Børglum, A. & Mors, O. (2011).
Markers on chromosome 19p13 are associated with panic disorder. Poster session presented at PhD Day 2011, Aarhus University, Faculty of Health Sciences, Aarhus, Denmark.
Mortensen, P. B., Pedersen, CB., Hougaard, DM., Norgaard-Petersen, B.
, Mors, O., Børglum, A. & Yolken, RH. (2011).
Maternal antibodies to cytomegalovirus and schizophrenia risk. Abstract from 13th International Congress on Schizophrenia Research (ICOSR), Colorado Springs, United States.
Pers, T. H., Hansen, N. T., Hansen, K. L., Koefoed, P., Dworzynski, P., Miller, M. L.
, Zacharov, T. F., Mellerup, E. T., Dam, H. F., Andreassen, O. A., Djurovic, S., Melle, I.
, Børglum, A. D., Werge, T., Purcell, S., Ferreira, M. A., Kouskoumvekaki, I., Workman, C., Hansen, T. ... Brunak, S. (2011).
Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes.
Genetic Epidemiology,
35(5), 318-32.
https://doi.org/10.1002/gepi.20580Mortensen, P. B., Pedersen, C. B., McGrath, J. J., Hougaard, D. M., Nørgaard-Petersen, B.
, Mors, O., Børglum, A. D. & Yolken, R. H. (2011).
Neonatal antibodies to infectious agents and risk of bipolar disorder: a population-based case-control study.
Bipolar Disorders,
13(7-8), 624-629.
https://doi.org/10.1111/j.1399-5618.2011.00962.x
Harsløf, T., Husted, L. B., Nyegaard, M., Carstens, M., Stenkjær, L., Brixen, K., Eiken, P., Jensen, J.-E. B.
, Børglum, A., Mosekilde, L., Rejnmark, L. & Langdahl, B. L. (2011).
Polymorphisms in the ALOX12 gene and osteoporosis.
Osteoporosis International,
22(8), 2249-59.
https://doi.org/10.1007/s00198-010-1472-2
Harsløf, T., Tofteng, C. L.
, Husted, L. B., Nyegaard, M., Børglum, A., Carstens, M., Stenkjær, L., Brixen, K., Eiken, P., Jensen, J.-E. B.
, Mosekilde, L., Rejnmark, L. & Langdahl, B. L. (2011).
Polymorphisms of the peroxisome proliferator-activated receptor γ (PPARγ) gene are associated with osteoporosis.
Osteoporosis International,
22(10), 2655-66.
https://doi.org/10.1007/s00198-010-1491-z
Hollegaard, M. V., Grove, J., Grauholm, J., Kreiner-Moller, E., Bonnelykke, K.
, Nørgaard, M., Benfield, T. L., Norgaard-Pedersen, B.
, Mortensen, P. B., Mors, O., Sørensen, H. T., Harboe, Z. B.
, Børglum, A., Demontis, D., Ørntoft, T. F., Bisgaard, H. & Hougaard, D. M. (2011).
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.
BMC Genetics,
12(1), 58.
https://doi.org/10.1186/1471-2156-12-58
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., Bonnesen, S., Hedemand, A., Wu, T.
, Wang, X., Zhang, X., Brudek, T., Maric, R., Søndergaard, H., Sellebjerg, F. T.
... Pedersen, F. S. (2011).
The Etiology of Multiple Sclerosis: Genetic Evidence for the Involvement of the Human Endogenous Retrovirus HERV-Fc1.
PLoS One,
6(2), e16652.
https://doi.org/10.1371/journal.pone.0016652
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
Mortensen, P. B., Pedersen, C. B., Hougaard, D. M., Nørgaard-Petersen, B.
, Mors, O., Børglum, A. & Yolken, R. H. (2010).
A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring.
Schizophrenia Research,
122(1-3), 257-263.
https://doi.org/10.1016/j.schres.2010.06.010
Zacharov, T. F., Qin, P., Buttenschøn, H. N., Kristensen, I. B., Friis Hansen, N., Christoffersen, S.
, Foldager, L., Mortensen, P. B., Børglum, A. & Mors, O. (2010).
An association study of suicide and candidate genes in the serotonergic system.
XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., 231-232.
