Grotzinger, A. D., Mallard, T. T., Akingbuwa, W. A., Ip, H. F., Adams, M. J., Lewis, C. M., McIntosh, A. M.
, Grove, J., Dalsgaard, S., Lesch, K. P., Strom, N.
, Meier, S. M., Mattheisen, M., Børglum, A. D., Mors, O., Breen, G., iPSYCH, Tourette Syndrome and Obsessive Compulsive Disorder Working Group of the Psychiatric Genetics Consortium, Bipolar Disorder Working Group of the Psychiatric Genetics Consortium ... Nivard, M. G. (2022).
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis.
Nature Genetics,
54(5), 548-559.
https://doi.org/10.1038/s41588-022-01057-4
Gregersen, N., Buttenschøn, H. N., Nygaard, M.
, Kristensen, A. S., Woldbye, D., Joensen, S., Kruse, T. A.
, Børglum, A., Mors, O., Dahl, H. & Hedemand, A. (2009).
A PH sensitive sodium channel is a potential candidate gene for panic disorder. Poster session presented at World Congress of Psychiatric Genetics: Surfing the Wave of Discovery, San Diego, United States.
Gregersen, N., Børglum, A., Mors, O., Dahl, HA., Wang, AG., Nyegaard, M., Kruse, TA. & Als, TD. (2009).
A genome-wide association search for panic disorder susceptibility genes in the isolated population of Faroe Islands. Poster session presented at A genome-wide association search for panic disorder susceptibility genes in the isolated population of Faroe Islands.
Gregersen, N., Buttenschøn, H. N., Atli Dahl, H.
, Foldager, L., Kristensen, A. S., Woldby, D., Koefoed, P., Wang, AG., Joensen, S., Kruse, TA.
, Børglum, A. & Mors, O. (2010).
Markers on chromosome 19p13 associated with panic disorder.
XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., 288-289.
Gregersen, N., Buttenschøn, H. N., Dahl, H. A.
, Foldager, L., Als, T. D., Wang, A., Joensen, S.
, Kristensen, A. S., Woldbye, D., Koefoed, P., Kruse, T. A.
, Børglum, A. & Mors, O. (2010).
Association mellem markører på kromosom 19p13 og panikangst. Poster session presented at Psykiatriens 5. Forskningsdag, Risskov, Denmark.
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.
Gregersen, 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.
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., 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.
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.
Gregersen, N. O., Buttenschøn, H. N., Hedemand, A., Dahl, H. A.
, Kristensen, A. S., Clementsen, B.
, Woldbye, D. P. D., Koefoed, P., Erhardt, A., Kruse, T. A., Wang, A. G.
, Børglum, A. D. & Mors, O. (2014).
Are TMEM genes potential candidate genes for panic disorder? Psychiatric Genetics,
24(1), 37-41.
https://doi.org/10.1097/YPG.0000000000000022
Gregersen, N., Lescai, F., Liang, J., Li, Q.
, Als, T. D., Buttenschøn, H. N., Hedemand, A., Biskopstø, M., Wang, J., Wang, A.
, Børglum, A., Mors, O. & Demontis, D. (2016).
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
171(8), 1013-1022.
https://doi.org/10.1002/ajmg.b.32464
Gasse, C., Wimberley, T., Wang, Y.
, Mors, O., Børglum, A., Als, T. D., Werge, T., Nordentoft, M., Hougaard, D. M.
& Horsdal, H. T. (2019).
Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophrenia.
Schizophrenia Research,
212, 79-85.
https://doi.org/10.1016/j.schres.2019.08.008
Gasse, C., Thirstrup, J. P., Østergaard, S. D.
, Als, T. D., Köhler-Forsberg, O., Nordentoft, M.
, Mors, O. & Børglum, A. (2020).
GWAS of antidepressant treatment non-response in depression.. Poster session presented at ICPE All Access.
Gasse, C., Thirstrup, J. P., Als, T. D., Köhler-Forsberg, O., Nordentoft, M.
, Mors, O. & Børglum, A. (2020).
GWAS of antidepressant treatment non-response in depression.
Pharmacoepidemiology and Drug Safety,
29(S3), Article 4653.
https://doi.org/10.1002/pds.5114
Gaspar, H. A., Gerring, Z., Hübel, C., Middeldorp, C. M., Derks, E. M., Breen, G. & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2019).
Using genetic drug-target networks to develop new drug hypotheses for major depressive disorder.
Translational Psychiatry,
9(1), Article 117.
https://doi.org/10.1038/s41398-019-0451-4
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
Fryland, T., Christensen, J. H., Pallesen, J., Mattheisen, M., Palmfeldt, J., Bak, M.
, Grove, J., Demontis, D., Blechingberg, J., Ooi, H. S., Nyegaard, M., Hauberg, M. E., Tommerup, N.
, Gregersen, N., Mors, O., Corydon, T. J., Nielsen, A. L. & Børglum, A. D. (2016).
Identification of the BRD1 interaction network and its impact on mental disorder risk.
Genome Medicine,
8(1), 53.
https://doi.org/10.1186/s13073-016-0308-x
Foss-Skiftesvik, J., Hagen, C. M., Mathiasen, R., Adamsen, D., Bækvad-Hansen, M.
, Børglum, A. D., Nordentoft, M., Werge, T., Christiansen, M., Schmiegelow, K.
, Juhler, M., Mortensen, P. B., Hougaard, D. M. & Bybjerg-Grauholm, J. (2021).
Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.
Child's Nervous System,
37(3), 819–830.
https://doi.org/10.1007/s00381-020-04946-3
Forstner, A. J., Awasthi, S., Wolf, C., Maron, E., Erhardt, A., Czamara, D., Eriksson, E., Lavebratt, C., Allgulander, C., Friedrich, N., Becker, J., Hecker, J., Rambau, S., Conrad, R., Geiser, F., McMahon, F. J., Moebus, S., Hess, T., Buerfent, B. C. ... Schumacher, J. (2021).
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.
Molecular Psychiatry,
26(8), 4179-4190.
https://doi.org/10.1038/s41380-019-0590-2
Foldager, L., Pedersen, C. B., Nyegaard, M., Zacharov, T. F., Nordentoft, M., Werge, T., Hougaard, DM., Sørensen, K. M.
, Mortensen, P. B., Mors, O. & Børglum, A. (2010).
Conditional logic regression: identifying SNP interactions from individually time-matched case-control data.
XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., 202-203.
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. (2010).
Conditional Logic Regression: identifying SNP Interactions from Individually time-matched Case-Control Data. Poster session presented at Psykiatriens 5. Forskningsdag, Risskov, 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 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.
Eyles, D. W., Trzaskowski, M., Vinkhuyzen, A. A. E.
, Mattheisen, M., Meier, S., Gooch, H., Anggono, V., Cui, X., Tan, M. C., Burne, T. H. J., Jang, S. E., Kvaskoff, D., Hougaard, D. M., Nørgaard-Pedersen, B., Cohen, A.
, Agerbo, E., Pedersen, C. B., Børglum, A. D., Mors, O. ... McGrath, J. J. (2018).
The association between neonatal vitamin D status and risk of schizophrenia.
Scientific Reports,
8(1), Article 17692.
https://doi.org/10.1038/s41598-018-35418-z
Esteller-Cucala, P., Maceda, I.
, Børglum, A. D., Demontis, D., Faraone, S. V., Cormand, B. & Lao, O. (2020).
Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples.
Scientific Reports,
10, Article 8622.
https://doi.org/10.1038/s41598-020-65322-4
Ernst, M., Rogers, S., Lausten-Thomsen, U., Bjorkbom, A., Laursen, S. S., Courraud, J.
, Borglum, A., Nordentoft, M., Werge, T.
, Mortensen, P. B., Hougaard, D. M. & Cohen, A. S. (2021).
Gestational age-dependent development of the neonatal metabolome.
Pediatric Research,
89(6), 1396-1404.
https://doi.org/10.1038/s41390-020-01149-z
Erlangsen, A., Appadurai, V., Wang, Y., Turecki, G.
, Mors, O., Werge, T.
, Mortensen, P. B., Starnawska, A., Børglum, A. D., Schork, A., Nudel, R., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hougaard, D. M.
, Thompson, W. K., Nordentoft, M.
& Agerbo, E. (2020).
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Molecular Psychiatry,
25, 2410-2421.
https://doi.org/10.1038/s41380-018-0218-y
Engemann, K., Pedersen, C. B., Agerbo, E., Arge, L., Børglum, A. D., Erikstrup, C., Hertel, O., Hougaard, D. M.
, McGrath, J. J., Mors, O., Mortensen, P. B., Nordentoft, M.
, Sabel, C. E., Sigsgaard, T., Tsirogiannis, C., Vilhjálmsson, B. J., Werge, T.
, Svenning, J.-C. & Horsdal, H. T. (2020).
Association Between Childhood Green Space, Genetic Liability, and the Incidence of Schizophrenia.
Schizophrenia Bulletin,
46(6), 1629-1637.
https://doi.org/10.1093/schbul/sbaa058
Eliasen, A. U., Pedersen, C. E. T., Rasmussen, M. A., Wang, N., Soverini, M., Fritz, A., Stokholm, J., Chawes, B. L., Morin, A., Bork-Jensen, J., Grarup, N., Pedersen, O., Hansen, T., Linneberg, A.
, Mortensen, P. B., Hougaard, D. M., Bybjerg-Grauholm, J., Bækvad-Hansen, M.
, Mors, O. ... Bønnelykke, K. (2022).
Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB.
Journal of Allergy and Clinical Immunology,
150(3), 622-630.
https://doi.org/10.1016/j.jaci.2022.03.019
Elfving, 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
Elfving, B., Buttenschøn, H. N., Foldager, L., Poulsen, P. H. P.
, Grynderup, M. B., Hansen, A. M.
, Kolstad, H. A., Kaerlev, L., Mikkelsen, S.
, Børglum, A. D., Wegener, G. & Mors, O. (2014).
Depression and BMI influences the serum vascular endothelial growth factor level.
International Journal of Neuropsychopharmacology,
17(9), 1409-1417.
https://doi.org/10.1017/S1461145714000273
Ejerskov, C., Krogh, K., Børglum, A., Østergaard, J. R. & Haagerup, A. (2018).
NF1 and the gastrointestinal canal: A high prevalence of gastrointestinal symptoms correlated to constipation.. Poster session presented at 18th European Neurofibromatosis Meeting, Paris, France.
Ejerskov, C., Gaustadnes, M., Østergaard, J. R., Krogh, K., Thorsen, K.
, Børglum, A. & Haagerup, A. (2020).
Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum. Abstract from 20th European NF Meeting, Rotterdam, Netherlands.
Ejerskov, C., Gaustadnes, M., Østergaard, J. R., Krogh, K., Thorsen, K., Børglum, A. & Haagerup, A. (2020).
Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum. Poster session presented at 20th European NF Meeting, Rotterdam, Netherlands.
Ejerskov, C., Gaustadnes, M., Ostergaard, J. R., Krogh, K., Thorsen, K., Borglum, A. D. & Haagerup, A. (2021).
Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum.
Scientific Reports,
11, Article 9179.
https://doi.org/10.1038/s41598-021-87686-x
Eising, E., Mirza-Schreiber, N., de Zeeuw, E. L., Wang, C. A., Truong, D. T., Allegrini, A. G., Shapland, C. Y., Zhu, G., Wigg, K. G., Gerritse, M. L., Molz, B., Alagoz, G., Gialluisi, A., Abbondanza, F., Rimfeld, K., van Donkelaar, M., Liao, Z., Jansen, P. R., Andlauer, T. F. M. ... Fisher, S. E. (2022).
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Proceedings of the National Academy of Sciences,
119(35), Article e2202764119.
https://doi.org/10.1073/pnas.2202764119
Eickhardt, E. A., Als, T. D., Mattheisen, M., Hauberg, M. E., Grove, J., Børglum, A. & Lescai, F. (2015).
Genome-Wide Landscape of Genetic Variation with a Functional Impact on Predicted Binding Activity of Transcription Factor Binding Sites. Poster session presented at ESHG 2015, Glasgow, United Kingdom.
Donskov, J. G., Starnawska, A., Pallesen, J., Grove, J., Børglum, A. & Qvist, P. (2021).
Large-scale genomic data-mining implicates dysregulated nuclear receptor-mediated signaling in mental illness.
Journal of Translational Genetics and Genomics,
5(2), 136-162.
https://doi.org/10.20517/jtgg.2021.12
Direk, N., Williams, S., Smith, J. A., Ripke, S., Air, T., Amare, A. T., Amin, N., Baune, B. T., Bennett, D. A., Blackwood, D. H. R., Boomsma, D., Breen, G.
, Buttenschøn, H. N., Byrne, E. M., Børglum, A. D., Castelao, E., Cichon, S., Clarke, T.-K., Cornelis, M. C. ... Sullivan, P. F. (2017).
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.
Biological Psychiatry,
82(5), 322-329.
https://doi.org/10.1016/j.biopsych.2016.11.013
Demontis, 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
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
Demontis, D., Lescai, F., Børglum, A., Glerup, S., Østergaard, S. D., Mors, O., Li, Q., Liang, J., Jiang, H., Li, Y., Wang, J., Lesch, K.-P., Reif, A., Buitelaar, J. K. & Franke, B. (2016).
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder.
Journal of the American Academy of Child and Adolescent Psychiatry,
55(6), 521-3.
https://doi.org/10.1016/j.jaac.2016.03.009
Demontis, D., Walters, R. K., Martin, J.
, Mattheisen, M., Als, T. D., Agerbo, E., Baldursson, G., Belliveau, R., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Cerrato, F., Chambert, K., Churchhouse, C., Dumont, A., Eriksson, N., Gandal, M., Goldstein, J. I., Grasby, K. L.
, Grove, J. ... Børglum, A. D. (2019).
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Nature Genetics,
51(1), 63–75.
https://doi.org/10.1038/s41588-018-0269-7
Demontis, D., Rajagopal, V. M., Thorgeirsson, T. E.
, Als, T. D., Grove, J., Leppälä, K., Gudbjartsson, D. F.
, Pallesen, J., Hjorthøj, C., Reginsson, G. W., Tyrfingsson, T., Runarsdottir, V.
, Qvist, P., Christensen, J. H., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Huckins, L. M., Stahl, E. A.
, Timmermann, A. ... Børglum, A. D. (2019).
Genome-wide association study implicates CHRNA2 in cannabis use disorder.
Nature Neuroscience,
22, 1066-1074.
https://doi.org/10.1038/s41593-019-0416-1
Demontis, D., Walters, R. K.
, Rajagopal, V. M., Waldman, I. D.
, Grove, J., Als, T. D., Dalsgaard, S., Ribasas, M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Werge, T., Nordentoft, M.
, Mors, O., Mortensen, P. B., ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Cormand, B., Hougaard, D. M., Neale, B. M., Franke, B.
... Børglum, A. D. (2021).
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
Nature Communications,
12(1), Article 576.
https://doi.org/10.1038/s41467-020-20443-2
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., Werge, T., Nordentoft, M.
, Mors, O., Mortensen, P. B., ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Cormand, B., Hougaard, D. M., Neale, B. M., Franke, B.
... Børglum, A. D. (2021).
Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature communications (2021) 12 1 (576)).
Nature Communications,
12, Article 1166.
https://doi.org/10.1038/s41467-021-21566-w