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The Capital Region of Denmark - a part of Copenhagen University Hospital

Marie Bækvad-Hansen

(Former)

  1. 2020
  2. E-pub ahead of print

    Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years

    Skov, M., Baekvad-Hansen, M., Hougaard, D. M., Skogstrand, K., Lund, A. M., Pressler, T., Olesen, H. V. & Duno, M., 2020, In : Pediatric Pulmonology.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 2019
  4. E-pub ahead of print

    Genetic liability to ADHD and substance use disorders in individuals with ADHD

    Wimberley, T., Agerbo, E., Horsdal, H. T., Ottosen, C., Brikell, I., Als, T. D., Demontis, D., Børglum, A. D., Nordentoft, M., Mors, O., Werge, T., Hougaard, D., Bybjerg-Grauholm, J., Hansen, M. B., Mortensen, P. B., Thapar, A., Riglin, L., Langley, K. & Dalsgaard, S., 5 Dec 2019, In : Addiction (Abingdon, England).

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

    iPSYCH-Broad Consortium, Dec 2019, In : Nature Neuroscience. 22, 12, p. 1961-1965 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

    Nievergelt, C. M., Maihofer, A. X., Klengel, T., Atkinson, E. G., Chen, C-Y., Choi, K. W., Coleman, J. R. I., Dalvie, S., Duncan, L. E., Gelernter, J., Levey, D. F., Logue, M. W., Polimanti, R., Provost, A. C., Ratanatharathorn, A., Stein, M. B., Torres, K., Aiello, A. E., Almli, L. M., Amstadter, A. B., Andersen, S. B., Andreassen, O. A., Arbisi, P. A., Ashley-Koch, A. E., Austin, S. B., Avdibegovic, E., Babić, D., Bækvad-Hansen, M., Baker, D. G., Beckham, J. C., Bierut, L. J., Bisson, J. I., Boks, M. P., Bolger, E. A., Børglum, A. D., Bradley, B., Brashear, M., Breen, G., Bryant, R. A., Bustamante, A. C., Bybjerg-Grauholm, J., Calabrese, J. R., Caldas-de-Almeida, J. M., Dale, A. M., Daly, M. J., Daskalakis, N. P., Deckert, J., Delahanty, D. L., Dennis, M. F., Disner, S. G., Domschke, K., Dzubur-Kulenovic, A., Erbes, C. R., Evans, A., Farrer, L. A., Feeny, N. C., Flory, J. D., Forbes, D., Franz, C. E., Galea, S., Garrett, M. E., Gelaye, B., Geuze, E., Gillespie, C., Uka, A. G., Gordon, S. D., Guffanti, G., Hammamieh, R., Harnal, S., Hauser, M. A., Heath, A. C., Hemmings, S. M. J., Hougaard, D. M., Jakovljevic, M., Jett, M., Johnson, E. O., Jones, I., Jovanovic, T., Qin, X-J., Junglen, A. G., Karstoft, K-I., Kaufman, M. L., Kessler, R. C., Khan, A., Kimbrel, N. A., King, A. P., Koen, N., Kranzler, H. R., Kremen, W. S., Lawford, B. R., Lebois, L. A. M., Lewis, C. E., Linnstaedt, S. D., Lori, A., Lugonja, B., Luykx, J. J., Lyons, M. J., Maples-Keller, J., Marmar, C., Martin, A. R., Martin, N. G., Maurer, D., Mavissakalian, M. R., McFarlane, A., McGlinchey, R. E., McLaughlin, K. A., McLean, S. A., McLeay, S., Mehta, D., Milberg, W. P., Miller, M. W., Morey, R. A., Morris, C. P., Mors, O., Mortensen, P. B., Neale, B. M., Nelson, E. C., Nordentoft, M., Norman, S. B., O'Donnell, M., Orcutt, H. K., Panizzon, M. S., Peters, E. S., Peterson, A. L., Peverill, M., Pietrzak, R. H., Polusny, M. A., Rice, J. P., Ripke, S., Risbrough, V. B., Roberts, A. L., Rothbaum, A. O., Rothbaum, B. O., Roy-Byrne, P., Ruggiero, K., Rung, A., Rutten, B. P. F., Saccone, N. L., Sanchez, S. E., Schijven, D., Seedat, S., Seligowski, A. V., Seng, J. S., Sheerin, C. M., Silove, D., Smith, A. K., Smoller, J. W., Sponheim, S. R., Stein, D. J., Stevens, J. S., Sumner, J. A., Teicher, M. H., Thompson, W. K., Trapido, E., Uddin, M., Ursano, R. J., van den Heuvel, L. L., Van Hooff, M., Vermetten, E., Vinkers, C. H., Voisey, J., Wang, Y., Wang, Z., Werge, T., Williams, M. A., Williamson, D. E., Winternitz, S., Wolf, C., Wolf, E. J., Wolff, J. D., Yehuda, R., Young, R. M., Young, K. A., Zhao, H., Zoellner, L. A., Liberzon, I., Ressler, K. J., Haas, M. & Koenen, K. C., 8 Oct 2019, In : Nature Communications. 10, 1, p. 4558

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders

    Skogstrand, K., Hagen, C. M., Borbye-Lorenzen, N., Christiansen, M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Werge, T., Børglum, A., Mors, O., Nordentoft, M., Mortensen, P. B. & Hougaard, D. M., 7 Oct 2019, In : Translational psychiatry. 9, 1, p. 252

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. E-pub ahead of print

    A polygenic resilience score moderates the genetic risk for schizophrenia

    Schizophrenia Working Group of the Psychiatric Genomics Consortium, 6 Sep 2019, In : Molecular Psychiatry.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Genome-wide association study implicates CHRNA2 in cannabis use disorder

    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., Agerbo, E., Hougaard, D. M., Werge, T., Mors, O., Mortensen, P. B., Nordentoft, M., Daly, M. J., Stefansson, H., Stefansson, K., Nyegaard, M. & Børglum, A. D., Jul 2019, In : Nature Neuroscience. 22, 7, p. 1066-1074 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    GERAD1 Consortium:, Jul 2019, In : Nature Genetics. 51, 7, p. 1193

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations

    Wang, Y., Karstoft, K-I., Nievergelt, C. M., Maihofer, A. X., Stein, M. B., Ursano, R. J., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hougaard, D. M., Andreassen, O. A., Werge, T., Thompson, W. K. & Andersen, S. B., 1 Jun 2019, In : Journal of Affective Disorders. 252, p. 350-357 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Genome-wide association study identifies 30 loci associated with bipolar disorder

    eQTLGen Consortium, May 2019, In : Nature Genetics. 51, 5, p. 793-803 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

    iPSYCH-Broad ASD Group, 15 Apr 2019, In : Royal Society of London. Philosophical Transactions B. Biological Sciences. 374, 1770, p. 20180120

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Jan 2019, In : Nature Genetics. 51, 1, p. 63-75 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

    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., Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Adams, M. J., Agerbo, E., Air, T. M., Andlauer, T. F. M., Bacanu, S. A., Bækvad-Hansen, M., Beekman, A. T. F., Bigdeli, T. B., Binder, E. B., Blackwood, D. H. R., Bryois, J., Buttenschøn, H. N., Bybjerg-Grauholm, J., Cai, N., Castelao, E., Christensen, J. H., Clarke, T. K., Coleman, J. R. I., Colodro-Conde, L., Couvy-Duchesne, B., Craddock, N., Crawford, G. E., Davies, G., Deary, I. J., Degenhardt, F., Derks, E. M., Direk, N., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Hansen, T. F., Krogh, J., Thompson, W., Weinsheimer, S. M., Nordentoft, M., Werge, T. & 23andMe Research Team, 2019, In : Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 4, 1, p. 91-100

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. 2018
  17. Published

    Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes

    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., 13 Dec 2018, In : PLoS One. 13, 12, p. e0208829

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

    Hagen, C. M., Gonçalves, V. F., Hedley, P. L., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hansen, C. S., Kanters, J. K., Nielsen, J., Mors, O., Demur, A. B., Als, T. D., Nordentoft, M., Børglum, A., Mortensen, P. B., Kennedy, J., Werge, T. M., Hougaard, D. M. & Christiansen, M., 10 Dec 2018, In : PLoS One. 13, 12, p. e0208828

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

    Generation Scotland & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 1 Dec 2018, In : PLoS One. 13, 12, e0209160.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

    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., 16 Aug 2018, In : Molecular Psychiatry.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published

    Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

    Olsen, L., Sparsø, T., Weinsheimer, S. M., Dos Santos, M. B. Q., Mazin, W., Rosengren, A., Sanchez, X. C., Hoeffding, L. K., Schmock, H., Baekvad-Hansen, M., Bybjerg-Grauholm, J., Daly, M. J., Neale, B. M., Pedersen, M. G., Agerbo, E., Mors, O., Børglum, A., Nordentoft, M., Hougaard, D. M., Mortensen, P. B., Geschwind, D. H., Pedersen, C., Thompson, W. K. & Werge, T., Jul 2018, In : The Lancet. Psychiatry. 5, 7, p. 573-580 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Ruderfer, D. M., Ripke, S., McQuillin, A., Boocock, J., Stahl, E. A., Pavlides, J. M. W., Mullins, N., Charney, A. W., Ori, A. P. S., Loohuis, L. M. O., Domenici, E., Di Florio, A., Papiol, S., Kalman, J. L., Trubetskoy, V., Adolfsson, R., Agartz, I., Agerbo, E., Akil, H., Albani, D., Albus, M., Alda, M., Alexander, M., Alliey-Rodriguez, N., Als, T. D., Amin, F., Anjorin, A., Arranz, M. J., Awasthi, S., Bacanu, S. A., Badner, J. A., Baekvad-Hansen, M., Bakker, S., Band, G., Barchas, J. D., Barroso, I., Bass, N., Bauer, M., Baune, B. T., Begemann, M., Bellenguez, C., Belliveau, R. A., Hansen, M., Hansen, T., Meier, S., Nordentoft, M., Olsen, L., Pers, T. H., Rasmussen, H. B., Werge, T., Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium douglas.ruderfer@vanderbilt.edu, Psychosis Endophenotypes International Consortium & Wellcome Trust Case-Control Consortium, 14 Jun 2018, In : Cell. 173, 7, p. 1705-1715.e16

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Adams, M. J., Agerbo, E., Air, T. M., Andlauer, T. M. F., Bacanu, S-A., Bækvad-Hansen, M., Beekman, A. F. T., Bigdeli, T. B., Binder, E. B., Blackwood, D. R. H., Bryois, J., Buttenschøn, H. N., Bybjerg-Grauholm, J., Cai, N., Castelao, E., Christensen, J. H., Clarke, T-K., Coleman, J. I. R., Colodro-Conde, L., Couvy-Duchesne, B., Craddock, N., Crawford, G. E., Crowley, C. A., Dashti, H. S., Davies, G., Deary, I. J., Degenhardt, F., Derks, E. M., Direk, N., Dolan, C. V., Dunn, E. C., Eley, T. C., Eriksson, N., Escott-Price, V., Kiadeh, F. H. F., Finucane, H. K., Forstner, A. J., Frank, J., Hansen, T. F., Krogh, J., Thompson, W., Weinsheimer, S. M., Nordentoft, M., Werge, T. & eQTLGen, May 2018, In : Nature Genetics. 50, 5, p. 668-681 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Elevated polygenic burden for autism is associated with differential DNA methylation at birth

    Hannon, E., Schendel, D., Ladd-Acosta, C., Grove, J., Hansen, C. S., Andrews, S. V., Hougaard, D. M., Bresnahan, M., Mors, O., Hollegaard, M. V., Bækvad-Hansen, M., Hornig, M., Mortensen, P. B., Børglum, A. D., Werge, T., Pedersen, M. G., Nordentoft, M., Buxbaum, J., Daniele Fallin, M., Bybjerg-Grauholm, J., Reichenberg, A., Mill, J. & iPSYCH-Broad ASD Group, 28 Mar 2018, In : Genome Medicine. 10, 1, p. 19

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Pardiñas, A. F., Holmans, P., Pocklington, A. J., Escott-Price, V., Ripke, S., Carrera, N., Legge, S. E., Bishop, S., Cameron, D., Hamshere, M. L., Han, J., Hubbard, L., Lynham, A., Mantripragada, K., Rees, E., MacCabe, J. H., McCarroll, S. A., Baune, B. T., Breen, G., Byrne, E. M., Dannlowski, U., Eley, T. C., Hayward, C., Martin, N. G., McIntosh, A. M., Plomin, R., Porteous, D. J., Wray, N. R., Caballero, A., Geschwind, D. H., Huckins, L. M., Ruderfer, D. M., Santiago, E., Sklar, P., Stahl, E. A., Won, H., Agerbo, E., Als, T. D., Andreassen, O. A., Bækvad-Hansen, M., Mortensen, P. B., Pedersen, C. B., Børglum, A. D., Bybjerg-Grauholm, J., Djurovic, S., Durmishi, N., Pedersen, M. G., Golimbet, V., Nordentoft, M., Werge, T. & GERAD1 Consortium:, Mar 2018, In : Nature Genetics.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. 2017
  27. Published

    Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

    Starnawska, A., Hansen, C. S., Sparsø, T., Mazin, W., Olsen, L., Bertalan, M., Demur, A. A. B., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hougaard, D. M., Mortensen, P. B., Pedersen, C. B., Nyegaard, M., Werge, T. & Weinsheimer, S., 29 Aug 2017, In : Translational psychiatry. 7, 8, p. e1221

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. 2016
  29. Published

    An epigenetic clock for gestational age at birth based on blood methylation data

    Knight, A. K., Craig, J. M., Theda, C., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hansen, C. S., Hollegaard, M. V., Hougaard, D. M., Mortensen, P. B., Weinsheimer, S. M., Werge, T. M., Brennan, P. A., Cubells, J. F., Newport, D. J., Stowe, Z. N., Cheong, J. L. Y., Dalach, P., Doyle, L. W., Loke, Y. J., Baccarelli, A. A., Just, A. C., Wright, R. O., Téllez-Rojo, M. M., Svensson, K., Trevisi, L., Kennedy, E. M., Binder, E. B., Iurato, S., Czamara, D., Räikkönen, K., Lahti, J. M. T., Pesonen, A-K., Kajantie, E., Villa, P. M., Laivuori, H., Hämäläinen, E., Park, H. J., Bailey, L. B., Parets, S. E., Kilaru, V., Menon, R., Horvath, S., Bush, N. R., LeWinn, K. Z., Tylavsky, F. A., Conneely, K. N. & Smith, A. K., 7 Oct 2016, In : Genome Biology (Online Edition). 17, 1, p. 206

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. Published

    High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

    Poulsen, J. B., Lescai, F., Grove, J., Bækvad-Hansen, M., Christiansen, M., Hagen, C. M., Maller, J., Stevens, C., Li, S., Li, Q., Sun, J., Wang, J., Nordentoft, M., Werge, T. M., Mortensen, P. B., Børglum, A. D., Daly, M., Hougaard, D. M., Bybjerg-Grauholm, J. & Hollegaard, M. V., 2016, In : P L o S One. 11, 4, p. e0153253

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. 2012
  32. Published

    Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals

    Bækvad-Hansen, M., Nordestgaard, B. G. & Dahl, M., 2012, In : Respiratory Research. 13, p. 67

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. Published
  34. 2011
  35. Published

    Surfactant protein B polymorphisms, pulmonary function and COPD in 10,231 individuals

    Bækvad-Hansen, M., Nordestgaard, B. G. & Dahl, M., 2011, In : European Respiratory Journal. 37, 4, p. 791-9 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. 2010
  37. Published

    Two novel mutations in surfactant protein-C, lung function and obstructive lung disease

    Bækvad-Hansen, M., Nordestgaard, B. G., Tybjaerg-Hansen, A. & Dahl, M., 1 Mar 2010, In : Respiratory medicine. 104, 3, p. 418-25 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  38. Published

ID: 32195698